中草药  2017, Vol. 48 Issue (4): 808-842
0
  PDF    
2014年新天然活性化合物简介
侯文彬, 单淇, 江纪武, 郑礼胜, 廖茂梁, 华洁, 周福军, 王淼, 潘明佳, 陈常青     
天津药物研究院, 天津 300193
摘要: 化合物名称规范化非常重要,规范化的原则是科学性、系统性、单义性、开放性、回译性、词根对译、简单易记等。从11种国外期刊和4种国内期刊检索2014年发表的论文222篇,检索到新天然活性化合物592个。对于新化合物的命名,可能存在争议,592个新化合物的名称均按上述命名原则进行规范。
关键词: 新天然活性化合物     命名原则     单义性     开放性     回译性     词根对译    
Profile of new natural active compounds in 2014
HOU Wen-bin, SHAN Qi, JIANG Ji-wu, ZHENG Li-sheng, LIAO Mao-liang, HUA Jie, ZHOU Fu-jun, WANG Miao, PAN Ming-jia, CHEN Chang-qing     
Tianjin Institute of Pharmaceutical Research, Tianjin 300193, China
Abstract: The standardization of compound nomenclature is of vital importance. The principles of standardization include scientificity, systematization, monosemy, openness, and back-translatability. The standardized compound names should also be cross-translatable from roots of the words and easy to remember. The article indexed 592 new active natural compounds, referencing 222 papers from 11 leading foreign periodicals and four domestic journals. The names of new compounds in the paper may be controversial, but the nomenclature was complied with the above principles of standardization.
Key words: new natural active compounds     naming principles     monosemy     open     back translation     root of translation    

中药是中华民族的瑰宝,中药约86%是植物药,其次是动物药和矿物药。中药活性成分是新药研发的热门领域,获得诺贝尔奖的青蒿素就是其中的突出代表。在信息化的潮流中,新天然活性化合物就是瑰宝中的“钻石矿”,宜集中优势科技人员,在大数据和云计算等先进科技指引下,通过信息服务抢得先机,创新性地实现“人在干、数在转、云在算”大协作精神,促进新药研发的现代化。

本文从11种国外期刊和4种国内期刊检索2014年发表的论文222篇,检索到新天然活性化合物592个。化合物名称规范化非常重要,规范化的原则是科学性、系统性、单义性、开放性、回译性、词根对译、简单易记等,如词尾为“in”,译成素,按单义性原则,就不能译成苷(oside)等;如生物碱词尾应为“ine”。本文在此思想指导下,将2014年期刊中报道的新天然活性化合物进行简要介绍。

1 收录期刊简介

查阅11种国外期刊和4种中国大陆期刊,检索文献222篇,新天然活性化合物592个。各期刊的文献和化合物数量见表 1。查阅过的期刊尚有《中国药学杂志》《中国中药杂志》和《中国药物化学杂志》,但未见新活性化合物。

表 1 收录期刊简介 Table 1 Profiles of included journals

2 新天然化合物名称命名原则

化合物名称命名原则是科学性、系统性、单义性、开放性、回译性、翻得过来、译得过去、简单易记、名从主人等。每个国家都有权按其本国文字对其新发现的化合物命名一个得体的俗名(化学名不算俗名),以便记忆和信息交流。中国不应放弃对新化合物的命名权,增强话语权,不论在发表的中文和英文论文中,对发现的新化合物,按名从主人原则,命名一个中文俗名,然后按回译性原则翻译成英文俗名。如表 2中化合物491,在原文中只有很长的化学名,未命名中英文俗名,笔者代拟中英文俗名链霉氨酸(streptaminoic acid)。又如化合物452、453,在文章标题和摘要中为sinomacutine A、B,但在正文中为salisonine A、B,前后不一致,salisonine词义为何,如何译成中文,使读者困扰。是否可命名为青藤亭碱(sinomacutine)A、B。

表 2 2014年新发现的天然活性化合物 Table 2 New natural active compounds found in 2014

592个新天然活性化合物按英文名称字母顺序排列,列出中英文名称、类别、分子式、物理性质、生物来源、生物活性和参考文献,具体见表 2。其中,萜类199个,苷类113个,生物碱类77个,柠檬苦素类25个,根皮酚类25个,木脂素类24个,黄酮类19个,缩酚酸酮类18个,甾体类16个,苯丙素类10个,肽类10个,聚酮类8个,x±s酮类5个,其他类43个。每个化合物只属于一类(归属到一类),跨类者不重计,如黄酮苷、萜苷不计入黄酮和萜类。

3 结语

本文检索到的2014年新活性天然化合物592个,还有很多未被本文收录的新活性化合物,再加上未报道活性的新化合物就更多了。一年有这么多的新化合物被发现,可见从自然界寻找新活性化合物仍然是新药研究的热门领域。这么多的新化合物,极大多数只命名英文名,而没有中文名,如何将这些英文名翻译成规范的中文名,是本文的重要内容。中文名称规范化的原则是科学性、系统性、单义性、开放性、回译性等,并按形义兼顾、词根对译的方法,将500多个新化合物外文名翻译出比较合理的中文名称,这是一件既繁又难的工作,以期专家学者指正,以便逐步完善。

参考文献
[1] El-Desoky A H, Kato H, Eguchi K, et al. Acantholactam and pre-neo-kauluamine, manzamine-related alkaloids from the indonesian marine sponge Acanthostrongylophora ingens[J]. J Nat Prod, 2014, 77(6): 1536–1540. DOI:10.1021/np500290a
[2] Furusato A, Kato H, Nehira T, et al. Acanthomanzamines A-E with new manzamine frameworks from the marine sponge Acanthostrongylophora ingens[J]. Org Lett, 2014, 16(15): 3888–3891. DOI:10.1021/ol5015569
[3] Xu X, Bai H, Zhou L, et al. Three new cucurbitane triterpenoids from Hemsleya penxianensis and their cytotoxic activities[J]. Bioorg Med Chem Lett, 2014, 24(9): 2159–2162. DOI:10.1016/j.bmcl.2014.03.027
[4] Hwang B S, Kim H S, Yih W, et al. Acuminolide A: structure and bioactivity of a new polyether macrolide from dinoflagellate Dinophysis acuminata[J]. Org Lett, 2014, 16(20): 5362–5365. DOI:10.1021/ol502567g
[5] Kusama T, Tanaka N, Sakai K, et al. Agelamadins A and B, dimeric bromopyrrole alkaloids from a marine sponge Agelas sp[J]. Org Lett, 2014, 16(15): 3916–3918. DOI:10.1021/ol501664b
[6] Sun Y, Takada K, Nogi Y, et al. Lower homologues of ahpatinin, aspartic protease inhibitors, from a marine Streptomyces sp[J]. J Nat Prod, 2014, 77(7): 1749–1752. DOI:10.1021/np500337m
[7] 王乐飞, 赵军, 唐文照, 等. 臭椿根皮中1个新的达玛烷型三萜[J]. 中草药, 2014, 45(2):161–163.
[8] Jin H G, Kim A R, Ko H J, et al. Three new lignan glycosides with IL-6 inhibitory activity from Akebia quinata[J]. Chem Pharm Bull, 2014, 62(3): 288–293. DOI:10.1248/cpb.c13-00668
[9] Ferreira E A, Reigada J B, Correia M V, et al. Antifungal and cytotoxic 2-acylcyclohexane-1, 3-diones from Peperomia alata and P. trineura[J]. J Nat Prod, 2014, 77(6): 1377–1382. DOI:10.1021/np500130x
[10] Barrosa K H, Pinto E G, Tempone A G, et al. Alchornedine, a new anti-trypanosomal guanidine alkaloid from Alchornea glandulosa[J]. Planta Med, 2014, 80(15): 1310–1314. DOI:10.1055/s-00000058
[11] Sun J, Zhang P, Wei Q, et al. Amarusine A, a new dioxaspiro [4. 4] nonane derivative with a butyrolactone ring from Pleioblastus amarus[J]. Tetrahedron Lett, 2014, 55(33): 4529–4531. DOI:10.1016/j.tetlet.2014.04.031
[12] Luo J G, Yin H, Fan B Y, et al. Labdane diterpenoids from the roots of Amomum maximum and their cytotoxic evaluation[J]. Helv Chim Acta, 2014, 97(8): 1140–1145. DOI:10.1002/hlca.v97.8
[13] Zhu G Y, Chen G, Liu L, et al. C-17 lactam-bearing limonoids from the twigs and leaves of Amoora tsangii[J]. J Nat Prod, 2014, 77(4): 983–989. DOI:10.1021/np401089h
[14] Nuzzo G, Cutignano A, Sardo A, et al. Antifungal amphidinol 18 and its 7-sulfate derivative from the marine dinoflagellate Amphidinium carterae[J]. J Nat Prod, 2014, 77(6): 1524–1527. DOI:10.1021/np500275x
[15] Ccana-Ccapatinta G V, Stolz E D, da Costa P F, et al. Acylphloroglucinol derivatives from Hypericum andinum: antidepressant-like activity of andinin A[J]. J Nat Prod, 2014, 77(10): 2321–2325. DOI:10.1021/np500426m
[16] Fu Y, Di Y, He H, et al. Angustifonines A and B, cytotoxic bisindole alkaloids from Bousigonia angustifolia[J]. J Nat Prod, 2014, 77(1): 57–62. DOI:10.1021/np4005823
[17] Zhang X, Tan Y, Li Y, et al. Aphanamixins A-F, acyclic diterpenoids from the stem bark of Aphanamixis polystachya[J]. Chem Pharm Bull, 2014, 62(5): 494–498. DOI:10.1248/cpb.c14-00056
[18] Cai J Y, Chen D Z, Luo S H, et al. Limonoids from Aphanamixis polystachya and their antifeedant activity[J]. J Nat Prod, 2014, 77(3): 472–482. DOI:10.1021/np400678h
[19] Fan B Y, Gu Y C, He Y, et al. Cytotoxic resin glycosides from Ipomoea aquatica and their effects on intracellular Ca2+ concentrations[J]. J Nat Prod, 2014, 77(10): 2264–2272. DOI:10.1021/np5005246
[20] 王宇, 李占林, 刘涛, 等. 海洋来源真菌Aspergillus aculeatus 中一个新的具有长交叉共轭系统的甾体[J]. 药学学报, 2014, 49(1):68–71.
[21] Zhou M, Miao M M, Du G, et al. Aspergillines A-E, highly oxygenated hexacyclic indole-tetrahydrofuran-tetramic acid derivatives from Aspergillus versicolor[J]. Org Lett, 2014, 16(19): 5016–5019. DOI:10.1021/ol502307u
[22] Miao F P, Liang X R, Liu X H, et al. Aspewentins A-C, norditerpenes from a cryptic pathway in an algicolous strain of Aspergillus wentii[J]. J Nat Prod, 2014, 77(2): 429–432. DOI:10.1021/np401047w
[23] Patiño C L P, Muniain C, Knott M E, et al. Bromopyrrole alkaloids isolated from the patagonian bryozoan Aspidostoma giganteum[J]. J Nat Prod, 2014, 77(5): 1170–1178. DOI:10.1021/np500012y
[24] 徐基伟, 车茜, 朱天骄, 等. 曲霉属真菌Aspergillussclerotiorum XJW-56中抗肿瘤活性次级代谢产物研究[J]. 中国海洋药物, 2014, 33(2):13–18.
[25] Xu J, Zhang Q, Wang M, et al. Bioactive clerodane diterpenoids from the twigs of Casearia balansae[J]. J Nat Prod, 2014, 77(10): 2182–2189. DOI:10.1021/np5003516
[26] Portmann C, Sieber S, Wirthensohn S, et al. Balgacyclamides, antiplasmodial heterocyclic peptides from Microcystis aeruguinosa EAWAG 251[J]. J Nat Prod, 2014, 77(3): 557–562. DOI:10.1021/np400814w
[27] Yang J H, Wang W G, Du X, et al. Heterodimeric ent-kauranoids from Isodon tenuifolius[J]. J Nat Prod, 2014, 77(11): 2444–2453. DOI:10.1021/np5005196
[28] Park J E, Woo K W, Sang U C, et al. Two new cytotoxic spirostane-steroidal saponins from the roots of Bletilla striata[J]. Helv Chim Acta, 2014, 45(18): 56–63.
[29] da Rocha C Q, Queiroz E F, Meira C S, et al. Dimeric flavonoids from Arrabidaea brachypoda and assessment of their anti-trypanosoma cruzi activity[J]. J Nat Prod, 2014, 77(6): 1345–1350. DOI:10.1021/np401060j
[30] Suzuki R, Irie R, Harntaweesup Y, et al. Brevisulcatic acids, marine ladder-frame polyethers from the red tide dinoflagellate Karenia brevisulcata in New Zealand[J]. Org Lett, 2014, 16(22): 5850–5853. DOI:10.1021/ol502700h
[31] Meng L H, Li X M, Lv C T, et al. Brocazines A-F, cytotoxic bisthiodiketopiperazine derivatives from Penicillium brocae MA-231, an endophytic fungus derived from the marine mangrove plant Avicennia marina[J]. J Nat Prod, 2014, 77(8): 1921–1927. DOI:10.1021/np500382k
[32] Ono M, Takigawa A, Kanemaru Y, et al. Calysolins V-IX, resin glycosides from Calystegia soldanella and their antiviral activity toward herpes[J]. Chem Pharm Bull, 2014, 62(1): 97–105. DOI:10.1248/cpb.c13-00610
[33] Ono M, Kawakami G, Takigawa A, et al. Calysolins X-XIII, resin glycosides from Calystegia soldanella, and their antiviral activity toward herpes simplex virus[J]. Chem Pharm Bull, 2014, 62(8): 839–844. DOI:10.1248/cpb.c14-00356
[34] Wang X B, Yang C S, Zhang C, et al. Ten new calyxins from Alpinia katsumadai: a systematically studies on the stereochemistry of calyxins[J]. Tetrahedron, 2014, 70(45): 8714–8722. DOI:10.1016/j.tet.2014.09.027
[35] Yu L, Trujillo M E, Miyanaga S, et al. Campechic acids A and B: anti-invasive polyether polyketides from a soil-derived Streptomyces[J]. J Nat Prod, 2014, 77(4): 976–982. DOI:10.1021/np401071x
[36] Matsumoto T, Nakamura S, Nakashima S, et al. Lignan dicarboxylates and terpenoids from the flower buds of Cananga odorata and their inhibitory effects on melanogenesis[J]. J Nat Prod, 2014, 77(4): 990–999. DOI:10.1021/np401091f
[37] 魏建国, 杨大松, 陈维云, 等. 粤蛇葡萄的化学成分及其抗血管生成活性研究[J]. 中草药, 2014, 45(7):900–905.
[38] Fu P, Johnson M, Chen H, et al. Carpatamides A-C, cytotoxic arylamine derivatives from a marine-derived Streptomyces sp[J]. J Nat Prod, 2014, 77(5): 1245–1248. DOI:10.1021/np500207p
[39] Yang Y X, Shan L, Liu Q X, et al. Carpedilactones A-D, four new isomeric sesquiterpene lactone dimers with potent cytotoxicity from Carpesium faberi[J]. Org Lett, 2014, 16(16): 4216–4219. DOI:10.1021/ol501923k
[40] Melek F R, Kassem I A A, Miyase T, et al. Caspicaosides E-K, triterpenoid saponins and cytotoxic acylated saponins from fruits of Gleditsia caspica Desf[J]. Phytochemistry, 2014, 100: 110–119. DOI:10.1016/j.phytochem.2014.01.019
[41] Feng Y, Ren F, Niu S, et al. Guanacastane diterpenoids from the plant endophytic fungus Cercospora sp[J]. J Nat Prod, 2014, 77(4): 873–881. DOI:10.1021/np4009688
[42] Li R J, Lin Z M, Kang Y Q, et al. Cembrane-type diterpenoids from the Chinese liverworts Chandonanthus hirtellus and C. birmensis[J]. J Nat Prod, 2014, 77(2): 339–345. DOI:10.1021/np400936t
[43] Yin J L, Fang X, Liu E D, et al. Phragmalin limonoids from the stem barks of Chukrasia tabularis var. velutina[J]. Planta Med, 2014, 80(15): 1304–1309. DOI:10.1055/s-00000058
[44] Cheng G G, Cai X H, Zhang B H, et al. Cinchona alkaloids from Cinchona succirubra and Cinchona ledgeriana[J]. Planta Med, 2014, 80(2/3): 223–230.
[45] Zeng J, Xue Y, Shu P, et al. Diterpenoids with immunosuppressive activities from Cinnamomum cassia[J]. J Nat Prod, 2014, 77(8): 1948–1954. DOI:10.1021/np500465g
[46] Wu G G, Sun X H, Yu G H, et al. Cladosins A-E, hybrid polyketides from a deep-sea-derived fungus, Cladosporium sphaerospermum[J]. J Nat Prod, 2014, 77(2): 270–275. DOI:10.1021/np400833x
[47] Gu H S, Ma S G, Li Y H, et al. Claoxylones A-I, prenylbisabolane diterpenoids with anti-coxsackie B virus activity from the branches and leaves of Claoxylon polot[J]. Tetrahedron, 2014, 70(41): 7476–7483. DOI:10.1016/j.tet.2014.08.021
[48] Xia H M, Li C J, Yang J Z, et al. A, D-seco-limonoids from the stems of Clausena emarginata[J]. J Nat Prod, 2014, 77(4): 784–791. DOI:10.1021/np400797s
[49] Deng H D, Mei W L, Guo Z K, et al. Monoterpenoid coumarins from the peels of Clausena lansium[J]. Planta Med, 2014, 80(11): 955–958. DOI:10.1055/s-00000058
[50] Pham V C, Mai H D T, Litaudon M, et al. Cytotoxic aryltetralin lignans from fruits of Cleistanthus indochinensis[J]. Planta Med, 2014, 80(8/9): 695–702.
[51] Guan S C, Fan G Y. Diterpenoids from aerial parts of Clerodendranthus spicatus and their cytotoxic activity[J]. Helv Chim Acta, 2014, 97(12): 1708–1713. DOI:10.1002/hlca.201400106
[52] Cui B S, Qiao Y Q, Yuan Y, et al. Hepatoprotective saikosaponin homologs from Comastoma pedunculatum[J]. Planta Med, 2014, 80(17): 1647–1656. DOI:10.1055/s-00000058
[53] Kim C K, Song I H, Park H Y, et al. Suvanine sesterterpenes and deacyl irciniasulfonic acids from a tropical Coscinoderma sp. sponge[J]. J Nat Prod, 2014, 77(6): 1396–1403. DOI:10.1021/np500156n
[54] Miron-Lopez G, Bazzocchi I L, Jimenez-Diaz I A, et al. Cytotoxic diterpenes from roots of Crossopetalum gaumeri, a Celastraceae species from Yucatan peninsula[J]. Bioorg Med Chem Lett, 2014, 24(9): 2105–2109. DOI:10.1016/j.bmcl.2014.03.051
[55] Liu C P, Xu J B, Zhao J X, et al. Diterpenoids from Croton laui and their cytotoxic and antimicrobial activities[J]. J Nat Prod, 2014, 77(4): 1013–1020. DOI:10.1021/np500042c
[56] Han W B, Lu Y H, Zhang A H, et al. Curvulamine, a new antibacterial alkaloid incorporating two undescribed units from a Curvularia species[J]. Org Lett, 2014, 16(20): 5366–5369. DOI:10.1021/ol502572g
[57] Peng F, Fandong K, Xia L, et al. Cyanogramide with a new spiro [indolinone-pyrroloimidazole] skeleton from Actinoalloteichus cyanogriseus[J]. Org Lett, 2014, 16(14): 3708–3711. DOI:10.1021/ol501523d
[58] Fu P, Kong F, Li X, et al. Cyanogramide with a new npiro [indolinone-pyrroloimidazole] skeleton from Actinoalloteichus cyanogriseus[J]. Org Lett, 2014, 16(14): 3708–3711. DOI:10.1021/ol501523d
[59] Jelassi A, Zardi-Bergaoui A, Nejma A B, et al. Two new unusual monoterpene acid glycosides from Acacia cyclops with potential cytotoxic activity[J]. Bioorg Med Chem Lett, 2014, 24(16): 3777–3781. DOI:10.1016/j.bmcl.2014.06.075
[60] Xiao-Peng W, Xiao-Po Z, Guo-Xu M, et al. A new ursane-type triterpene, cymosic acid from Rosa cymosa[J]. J Asian Nat Prod Res, 2014, 16(4): 422–425. DOI:10.1080/10286020.2014.885507
[61] Piao X L, Xing S F, Lou C X, et al. Novel dammarane saponins from Gynostemma pentaphyllum and their cytotoxic activities against HepG2 cells[J]. Bioorg Med Chem Lett, 2014, 24(20): 4831–4833. DOI:10.1016/j.bmcl.2014.08.059
[62] Luo J G, Wang X B, Xu Y M, et al. Delitschiapyrone A, a pyrone-naphthalenone adduct bearing a new pentacyclic ring system from the leaf-associated fungus Delitschia sp. FL1581[J]. Org Lett, 2014, 16(22): 5944–5947. DOI:10.1021/ol502973c
[63] Li Y, Wang C L, Zhao H J, et al. Eight new bibenzyl derivatives from Dendrobium candidum[J]. J Asian Nat Prod Res, 2014, 16(11): 1035–1043. DOI:10.1080/10286020.2014.967230
[64] Song Y, Li Q, Liu X, et al. Cyclic hexapeptides from the deep south china sea-derived Streptomyces scopuliridis SCSIO ZJ46 active against pathogenic gram-positive bacteria[J]. J Nat Prod, 2014, 77(8): 1937–1941. DOI:10.1021/np500399v
[65] Jing S X, Luo S H, Li C H, et al. Biologically active dichapetalins from Dichapetalum gelonioides[J]. J Nat Prod, 2014, 77(4): 882–893. DOI:10.1021/np400971r
[66] Thorroad S, Worawittayanont P, Khunnawutmanotham N, et al. Three new lycopodium alkaloids from Huperzia carinata and Huperzia squarrosa[J]. Tetrahedron, 2014, 70(43): 8017–8022. DOI:10.1016/j.tet.2014.08.042
[67] Tang Y, Xue Y, Zhou L, et al. New norclerodane diterpenoids from the tubers of Dioscorea bulbifera[J]. Chem Pharm Bull, 2014, 62(7): 719–724. DOI:10.1248/cpb.c14-00057
[68] Zheng K Y, Zhang Z X, Zhou W, et al. New phenanthrene glycosides from Dioscorea opposita[J]. J Asian Nat Prod Res, 2014, 16(2): 148–152. DOI:10.1080/10286020.2013.837459
[69] Tian W J, Qiu Y Q, Yao X J, et al. Dioxasampsones A and B, two polycyclic polyprenylated acylphloroglucinols with unusual epoxy-ring-fused skeleton from Hypericum sampsonii[J]. Org Lett, 2014, 16(24): 6346–6349. DOI:10.1021/ol503122m
[70] Chen C J, Jiang R, Wang G, et al. Oligostilbenoids with acetylcholinesterase inhibitory activity from Dipterocarpus alatus[J]. Planta Med, 2014, 80(17): 1641–1646. DOI:10.1055/s-00000058
[71] Jia S H, Lv F, Dai R J, et al. C-21 steroidal glycosides from Dregea sinensis[J]. J Asian Nat Prod Res, 2014, 16(8): 836–840. DOI:10.1080/10286020.2014.921910
[72] Ge Y Z, Zhang H, Liu H C, et al. Cytotoxic dinorditerpenoids from Drypetes perreticulata[J]. Phytochemistry, 2014, 100: 120–125. DOI:10.1016/j.phytochem.2014.01.013
[73] Yin T P, Cai L, He J M, et al. Three new diterpenoid alkaloids from the roots of Aconitum duclouxii[J]. J Asian Nat Prod Res, 2014, 16(4): 345–350. DOI:10.1080/10286020.2014.881802
[74] Jiao W H, Xu T T, Yu H B, et al. Dysideanones A-C, unusual sesquiterpene quinones from the South China Sea sponge Dysidea avara[J]. J Nat Prod, 2014, 77(2): 346–350. DOI:10.1021/np4009392
[75] Nugroho A E, Momota T, Sugiura R, et al. Dysotriflorins A-M, triterpenoids from Dysoxylum densiflorum[J]. Tetrahedron, 2014, 70(51): 9661–9667. DOI:10.1016/j.tet.2014.10.070
[76] Gu J, Cheng G G, Qian S Y, et al. Dysoxydensins A-G, seven new clerodane diterpenoids from Dysoxylum densiflorum[J]. Planta Med, 2014, 80(12): 1017–1022. DOI:10.1055/s-00000058
[77] Liu Z G, Li Z L, Bai J, et al. Anti-inflammatory diterpenoids from the roots of Euphorbia ebracteolata[J]. J Nat Prod, 2014, 77(4): 792–799. DOI:10.1021/np400873v
[78] Mitsui T, Ishihara R, Hayashi K, et al. New cassane-type diterpenoids of Caesalpinia echinata (Leguminosae) exhibiting NF-κB inhibitory activities[J]. Chem Pharm Bull, 2014, 62(3): 267–273. DOI:10.1248/cpb.c13-00812
[79] Cao F, Shao C L, Chen M, et al. Antiviral C-25 epimers of 26-acetoxy steroids from the South China Sea gorgonian Echinogorgia rebekka[J]. J Nat Prod, 2014, 77(6): 1488–1493. DOI:10.1021/np500252q
[80] Heine D, Martin K, Hertweck C. Genomics-guided discovery of endophenazines from Kitasatospora sp. HKI 714[J]. J Nat Prod, 2014, 77(4): 1083–1087. DOI:10.1021/np400915p
[81] Jin Q, Lee C, Lee J W, et al. 2-Phenoxychromones and prenylflavonoids from Epimedium koreanum and their inhibitory effects on LPS-induced nitric oxide and interleukin-1β production[J]. J Nat Prod, 2014, 77(7): 1724–1728. DOI:10.1021/np400831p
[82] Li W, Zhou W, Song S B, et al. Sterol fatty acid esters from the mushroom Hericium erinaceum and their PPAR transactivational effects[J]. J Nat Prod, 2014, 77(12): 2611–2618. DOI:10.1021/np500234f
[83] Qi W Y, Zhang W Y, Shen Y, et al. Ingol-type diterpenes from Euphorbia antiquorum with mouse 11β-hydroxysteroid dehydrogenase type 1 inhibition activity[J]. J Nat Prod, 2014, 77(6): 1452–1458. DOI:10.1021/np5002237
[84] Rawal M K, Shokoohinia Y, Chianese G, et al. Jatrophanes from euphorbia squamosa as potent inhibitors of candida albicans multidrug transporters[J]. J Nat Prod, 2014, 77(12): 2700–2706. DOI:10.1021/np500756z
[85] Zhao J X, Liu C P, Qi W Y, et al. Eurifoloids A-R, structurally diverse diterpenoids from Euphorbia neriifolia[J]. J Nat Prod, 2014, 77(10): 2224–2233. DOI:10.1021/np5004752
[86] Yu S, Ye X, Xin W, et al. Fatsioside A, a rare baccharane-type glycoside inhibiting the growth of glioma cells from the fruits of Fatsia japonica[J]. Planta Med, 2014, 80(4): 315–320. DOI:10.1055/s-00000058
[87] Shao T M, Zheng C J, Han C R, et al. Lactones from Ficus auriculata and their effects on the proliferation function of primary mouse osteoblasts in vitro[J]. Bioorg Med Chem Lett, 2014, 24(16): 3952–3955. DOI:10.1016/j.bmcl.2014.06.035
[88] Xu F Q, Xu F C, Hou B, et al. Cytotoxic bibenzyl dimers from the stems of Dendrobium fimbriatum Hook[J]. Bioorg Med Chem Lett, 2014, 24(22): 5268–5273. DOI:10.1016/j.bmcl.2014.09.052
[89] Huang X J, Tang J Q, Li M M, et al. riterpenoid saponins from the rhizomes of Anemone flaccida and their inhibitory activities on LPS-induced NO production in macrophage RAW264. 7 cells[J]. J Asian Nat Prod Res, 2014, 16(9): 910–921. DOI:10.1080/10286020.2014.954554
[90] Chao C H, Cheng J C, Hwang T L, et al. Trinorditerpenes from the roots of Flueggea virosa[J]. Bioorg Med Chem Lett, 2014, 24(2): 447–449. DOI:10.1016/j.bmcl.2013.12.051
[91] Peng X R, Liu J Q, Wang C F, et al. Hepatoprotective effects of triterpenoids from Ganoderma cochlear[J]. J Nat Prod, 2014, 77(4): 737–743. DOI:10.1021/np400323u
[92] Xu J, Song Y C, Guo Y, et al. Fumigaclavines D-H, New ergot alkaloids from endophytic Aspergillus fumigatus[J]. Planta Med, 2014, 80(13): 1131–1137. DOI:10.1055/s-00000058
[93] Ma K, Ren J, Han J, et al. Ganoboninketals A-C, antiplasmodial 3,4-seco-27-norlanostane triterpenes from Ganoderma boninense Pat[J]. J Nat Prod, 2014, 77(8): 1847–1852. DOI:10.1021/np5002863
[94] Zhang H, Zhang D D, Lao Y Z, et al. Cytotoxic and anti-inflammatory prenylated benzoylphloroglucinols and xanthones from the twigs of Garcinia esculenta[J]. J Nat Prod, 2014, 77(7): 1700–1707. DOI:10.1021/np5003498
[95] Yamashita-Higuchi Y, Sugimoto S, Matsunami K, et al. Grevillosides J-Q, Arbutin derivatives from the leaves of Grevillea robusta and their melanogenesis inhibitory activity[J]. Chem Pharm Bull, 2014, 62(4): 364–372. DOI:10.1248/cpb.c13-00962
[96] Xiao S J, Lei X X, Xia B, et al. Two novel polycyclic spiro lignans from Gymnotheca involucrata[J]. Tetrahedron Lett, 2014, 55(43): 5949–5951. DOI:10.1016/j.tetlet.2014.09.044
[97] Li W, Zhou W, Lee D S, et al. Hericirine, a novel anti-inflammatory alkaloid from Hericium erinaceum[J]. Tetrahedron Lett, 2014, 55(30): 4086–4090. DOI:10.1016/j.tetlet.2014.05.117
[98] Lin Z M, Guo Y X, Wang S Q I, et al. Diterpenoids from the chinese Liverwort heteroscyphus tener and their antiproliferative effects[J]. J Nat Prod, 2014, 77(6): 1336–1344. DOI:10.1021/np5000507
[99] Umeyama A, Ohta C, Shino Y, et al. Three lanostane triterpenoids with antitrypanosomal activity from the fruiting body of Hexagonia tenuis[J]. Tetrahedron, 2014, 70(44): 8312–8315. DOI:10.1016/j.tet.2014.09.013
[100] Qi Q Y, Bao L, Ren J W, et al. Sterhirsutins A and B, two new heterodimeric sesquiterpenes with a new skeleton from the culture of Stereum hirsutum collected in tibet plateau[J]. Org Lett, 2014, 16(19): 5092–5095. DOI:10.1021/ol502441n
[101] Huang B, Xiao C J, Huang Z Y, et al. Hispidanins A-D: four new asymmetric dimeric diterpenoids from the rhizomes of Isodon hispida[J]. Org Lett, 2014, 16(13): 3552–3555. DOI:10.1021/ol501417k
[102] Kim C S, Shin B, Kwon O W, et al. Holophyllin A, a rearranged abietane-type diterpenoid from the trunk of Abies holophylla[J]. Tetrahedron Lett, 2014, 55(47): 6504–6507. DOI:10.1016/j.tetlet.2014.10.030
[103] Ma Q, Min K, Li H L, et al. Horsfiequinones A-F, dimeric diarylpropanoids from Horsfieldia tetratepala[J]. Planta Med, 2014, 80(8/9): 688–694.
[104] Zhu H, Chen C, Yang J, et al. Bioactive acylphloroglucinols with adamantyl skeleton from Hypericum sampsonii[J]. Org Lett, 2014, 16(24): 6322–6325. DOI:10.1021/ol5030579
[105] Tian W J, Qiu Y Q, Jin X J, et al. Novel polycyclic polyprenylated acylphloroglucinols from Hypericum sampsonii[J]. Tetrahedron, 2014, 70(43): 7912–7916. DOI:10.1016/j.tet.2014.08.062
[106] Zhang J J, Yang J, Liao Y, et al. Hyperuralones A and B, new acylphloroglucinol derivatives with intricately caged cores from Hypericum uralum[J]. Org Lett, 2014, 16(18): 4912–4915. DOI:10.1021/ol502425f
[107] Yang X W, Ding Y, Zhang J J, et al. New acylphloroglucinol derivatives with diverse architectures from Hypericum henryi[J]. Org Lett, 2014, 16(9): 2434–2437. DOI:10.1021/ol500808p
[108] Li L, Feng L S, He Y X. Cytotoxic triterpenesaponins from Ilex pubescens[J]. J Asian Nat Prod Res, 2014, 16(8): 830–835. DOI:10.1080/10286020.2014.920012
[109] Liu C, Zhao C, Pan H H, et al. Chemical constituents from Inonotus obliquus and their biological activities[J]. J Nat Prod, 2014, 77(1): 35–41. DOI:10.1021/np400552w
[110] Zhang G J, Li Y H, Jiang J D, et al. Diterpenes and sesquiterpenes with anti-Coxsackie virus B3 activity from the stems of Illicium jiadifengpi[J]. Tetrahedron, 2014, 70(30): 4494–4499. DOI:10.1016/j.tet.2014.05.006
[111] Han L, Gao C, Jiang Y, et al. Jiangrines A-F and jiangolide from an actinobacterium, Jiangella gansuensis[J]. J Nat Prod, 2014, 77(12): 2605–2610. DOI:10.1021/np500402a
[112] Yu Z, Wang X S, Hu Z H. Dammarane-type saponins from Ziziphus jujube[J]. J Asian Nat Prod Res, 2014, 16(2): 200–205. DOI:10.1080/10286020.2013.866098
[113] Takemoto K, Kamisuki S, Chia P T, et al. Bioactive dihydronaphthoquinone derivatives from Fusarium solani[J]. J Nat Prod, 2014, 77(9): 1992–1996. DOI:10.1021/np500175j
[114] Shimada M, Ozawa M, Iwamoto K, et al. A lanostane triterpenoid and three cholestane sterols from Tilia kiusiana[J]. Chem Pharm Bull, 2014, 62(9): 937–941. DOI:10.1248/cpb.c14-00200
[115] Li H, Li M M, Su X Q, et al. Anti-inflammatory labdane diterpenoids from Lagopsis supina[J]. J Nat Prod, 2014, 77(4): 1047–1053. DOI:10.1021/np5001329
[116] Shi Y M, Yang J, Xu L, et al. Structural characterization and antioxidative activity of Lancifonins: unique nortriterpenoids from Schisandra lancifolia[J]. Org Lett, 2014, 16(5): 1370–1373. DOI:10.1021/ol5001186
[117] Wang W G, Yan B C, Li X N, et al. -Seco-ent-kaurane-type diterpenoids from Isodon eriocalyx var. laxiflora[J]. Tetrahedron, 2014, 70(41): 7445–7453. DOI:10.1016/j.tet.2014.08.018
[118] Ye M, Xiong J, Zhu J J, et al. Leonurusoleanolides E-J, minor spirocyclic triterpenoids from Leonurus japonicus fruits[J]. J Nat Prod, 2014, 77(1): 178–182. DOI:10.1021/np400838a
[119] Razafimahefa S, Mutulis F, Mutule I, et al. Libiguins A and B: novel phragmalin limonoids isolated from Neobeguea mahafalensis causing profound enhancement of sexual activity[J]. Planta Med, 2014, 80(4): 306–314. DOI:10.1055/s-00000058
[120] Kim K H, Moon E, Ha S K, et al. Bioactive lignan constituents from the twigs of Lindera glauca[J]. Chem Pharm Bull, 2014, 62(11): 1136–1140. DOI:10.1248/cpb.c14-00381
[121] Wang H, Ning R, Yu S, et al. Lithocarpic acids A-N, 3, 4-seco-cycloartane derivatives from the cupules of Lithocarpus polystachyus[J]. J Nat Prod, 2014, 77(8): 1910–1920. DOI:10.1021/np500379f
[122] Wu W M, Zhu Y Y, Li H R, et al. Two new alkaloids from the bulbs of Lycoris sprengeri[J]. J Asian Nat Prod Res, 2014, 16(2): 192–199. DOI:10.1080/10286020.2013.864639
[123] Lee C L, Hwang T L, Yang J C, et al. Anti-Inflammatory spirostanol and furostanol saponins from Solanum macaonense[J]. J Nat Prod, 2014, 77(8): 1770–1783. DOI:10.1021/np500057b
[124] Choi J H, Suzuki T, Kawaguchi T, et al. Makomotines A to D from Makomotake, Zizania latifolia infected with Ustilago esculenta[J]. Tetrahedron Lett, 2014, 55(26): 3596–3599. DOI:10.1016/j.tetlet.2014.04.125
[125] Belofsky G, Aronica M, Foss E, et al. Antimicrobial and antiinsectan phenolic metabolites of Dalea searlsiae[J]. J Nat Prod, 2014, 77(5): 1140–1149. DOI:10.1021/np401083g
[126] Campana P R V, Coleman C M, Teixeira M M, et al. TNF-α inhibition elicited by mansoins A and B, heterotrimeric flavonoids isolated from Mansoa hirsuta[J]. J Nat Prod, 2014, 77(4): 824–830. DOI:10.1021/np400929g
[127] Zhang J, Fan P, Zhu R, et al. Marsupellins A-F, ent-longipinane-type sesquiterpenoids from the Chinese liverwort Marsupella alpine with acetylcholinesterase inhibitory activity[J]. J Nat Prod, 2014, 77(4): 1031–1036. DOI:10.1021/np4009255
[128] Assis P A D, Theodoro P N E T, Paula J E D, et al. Antifungal ether diglycosides from Matayba guianensis Aublet[J]. Bioorg Med Chem Lett, 2014, 24(5): 1414–1416. DOI:10.1016/j.bmcl.2014.01.022
[129] Wang W, Song W, Lan X, et al. Merremins A-G, Resin glycosides from Merremia hederacea with multidrug resistance reversal activity[J]. J Nat Prod, 2014, 77(10): 2234–2240. DOI:10.1021/np500483d
[130] Li Y, Liu Y B, Liu Y L, et al. Mollanol A, a diterpenoid with a new C-nor-D-homograyanane skeleton from the fruits of Rhododendron molle[J]. Org Lett, 2014, 16(8): 4320–4323.
[131] Dendup T, Prachyawarakorn V, Pansanit A, et al. α-Glucosidase inhibitory activities of isoflavanones, isoflavones, and pterocarpans from Mucuna pruriens[J]. Planta Med, 2014, 80(7): 604–608. DOI:10.1055/s-00000058
[132] Shi S, Liu J, Kadouh H, et al. Three new anti-proliferative annonaceous acetogenins with mono-tetrahydrofuran ring from graviola fruit (Annona muricata)[J]. Bioorg Med Chem Lett, 2014, 24(42): 2773–2776.
[133] Cao M M, Huang S D, Di Y T, et al. Myrifabine, the first dimeric myrioneuron alkaloid from Myrioneuron faberi[J]. Org Lett, 2014, 16(2): 528–531. DOI:10.1021/ol403408m
[134] Fu Y, Wu P, Xue J, et al. Cytotoxic and antibacterial quinone sesquiterpenes from a Myrothecium fungus[J]. J Nat Prod, 2014, 77(8): 1791–1799. DOI:10.1021/np500142g
[135] Ma G X, Wu H F, Yuan J Q, et al. Further diterpenes from the seeds of Caesalpinia minax Hance[J]. Helv Chim Acta, 2014, 97(4): 581–586. DOI:10.1002/hlca.v97.4
[136] Lajter I, Vasas A, Beéni Z, et al. Sesquiterpenes from Neurolaena lobata and their antiproliferative and anti-inflammatory activities[J]. J Nat Prod, 2014, 77(3): 576–582. DOI:10.1021/np400834c
[137] Chen Q B, Xin X L, Yang Y, et al. Highly conjugated norditerpenoid and pyrroloquinoline alkaloids with potent PTP1B inhibitory activity from Nigella glandulifera[J]. J Nat Prod, 2014, 77(4): 807–812. DOI:10.1021/np4009078
[138] Liu X, Kunert O, Blunder M, et al. Polyyne Hybrid compounds from Notopterygium incisum with peroxisome proliferator-activated receptor gamma agonistic effects[J]. J Nat Prod, 2014, 77(11): 2513–2521. DOI:10.1021/np500605v
[139] Wang S, Li R J, Zhu R X, et al. Notolutesins A-J, dolabrane-type diterpenoids from the Chinese liverwort Notoscyphus lutescens[J]. J Nat Prod, 2014, 77(9): 2081–2087. DOI:10.1021/np5004559
[140] Zhang H, Tao L, Fu W W, et al. Prenylated benzoylphloroglucinols and xanthones from the leaves of Garcinia oblongifolia with antienteroviral activity[J]. J Nat Prod, 2014, 77(4): 1037–1046. DOI:10.1021/np500124e
[141] Wang K B, Di Y T, Bao Y, et al. Peganumine A, a β-carboline dimer with a new octacyclic scaffold from Peganum harmala[J]. Org Lett, 2014, 16(15): 4028–4031. DOI:10.1021/ol501856v
[142] Li X, Zhao J, Peng C, et al. Cytotoxic triterpenoid glycosides from the roots of Camellia oleifera[J]. Planta Med, 2014, 80(7): 590–598. DOI:10.1055/s-00000058
[143] Hu X L, Bian X Q, Wu X, et al. Penioxalamine A, a novel prenylated spiro-oxindole alkaloid from Penicillium oxalicum TW01-1[J]. Tetrahedron Lett, 2014, 55(29): 3864–3867. DOI:10.1016/j.tetlet.2014.05.104
[144] Li C S, Li X M, An C Y, et al. Prenylated indole alkaloid derivatives from marine sediment-derived fungus Penicillium paneum SD-44[J]. Helv Chim Acta, 2014, 97(10): 1440–1444. DOI:10.1002/hlca.v97.10
[145] Kubo M, Liu Y, Ishida M, et al. A new spiroindene pigment from the medicinal fungus Phellinus ribis[J]. Chem Pharm Bull, 2014, 62(1): 122–124. DOI:10.1248/cpb.c13-00722
[146] Ren Y, Lantvit D D, Deng Y, et al. Potent cytotoxic arylnaphthalene lignan lactones from Phyllanthus poilanei[J]. J Nat Prod, 2014, 77(6): 1494–1504. DOI:10.1021/np5002785
[147] Huang X X, Liu Q B, Wu J, et al. Antioxidant and tyrosinase inhibitory effects of neolignan glycosides from Crataegus pinnatifida seeds[J]. Planta Med, 2014, 80(18): 1732–1738. DOI:10.1055/s-00000058
[148] Zhang Z M, Wang C H, Zeng X J, et al. Sesquiterpenoids and lignans from the roots of Syringa pinnatifolia[J]. Chem Pharm Bull, 2014, 62(10): 1009–1012. DOI:10.1248/cpb.c14-00320
[149] Luyen B T T, Tai B H, Thao N P, et al. A new phenylpropanoid and an alkylglycoside from Piper retrofractum leaves with their antioxidant and α-glucosidase inhibitory activity[J]. Bioorg Med Chem Lett, 2014, 24(17): 4120–4124. DOI:10.1016/j.bmcl.2014.07.057
[150] Reis M A, Paterna A, Mónico A, et al. Diterpenes from euphorbia piscatoria: synergistic interaction of lathyranes with doxorubicin on resistant cancer cells[J]. Planta Med, 2014, 80(18): 1739–1745. DOI:10.1055/s-00000058
[151] Qiao Y, Sun W W, Wang J F, et al. Flavonoids from Podocarpus macrophyllus and their cardioprotective activities[J]. J Asian Nat Prod Res, 2014, 16(2): 222–229. DOI:10.1080/10286020.2013.861821
[152] Han Y, Di X, Li H, et al. Podoimbricatin A, a cytotoxic diterpenoid with an unprecedented 6/6/5/6-fused tetracyclic ring system from the twigs and leaves of Podocarpus imbricatus[J]. Bioorg Med Chem Lett, 2014, 24(6): 3326–3328.
[153] Rajachan O, Kanokmedhakul S, Kanokmedhakul K, et al. Bioactive depsidones from the fungus Pilobolus heterosporus[J]. Planta Med, 2014, 80(17): 1635–1640. DOI:10.1055/s-00000058
[154] Yan S L, Su Y F, Chen L, et al. Polygonumosides A-D, stilbene derivatives from processed roots of Polygonum multiflorum[J]. J Nat Prod, 2014, 77(2): 397–401. DOI:10.1021/np400720y
[155] Du L, Robles A J, King J B, et al. Cytotoxic dimeric epipolythiodiketopiperazines from the ascomycetous fungus Preussia typharum[J]. J Nat Prod, 2014, 77(6): 1459–1466. DOI:10.1021/np5002253
[156] Liu C C, Lei C, Zhong Y, et al. Novel grayanane diterpenoids from Rhododendron principis[J]. Tetrahedron, 2014, 70(29): 4317–4322. DOI:10.1016/j.tet.2014.05.019
[157] Boonnak N, Chantrapromma S, Fun H K, et al. Three types of cytotoxic natural caged-scaffolds: pure enantiomers or partial racemates[J]. J Nat Prod, 2014, 77(7): 1562–1571. DOI:10.1021/np400996k
[158] Liu Y, Wang J S, Wang X B, et al. Absolute configuration study of a new dimeric indole alkaloid from the leaves and twigs of Psychotria henryi[J]. J Asian Nat Prod Res, 2014, 16(1): 29–33. DOI:10.1080/10286020.2013.870996
[159] Suthiwong J, Pitchuanchom S, Wattanawongdon W, et al. Terpenoids from the root bark of Pterolobium macropterum[J]. J Nat Prod, 2014, 77(11): 2432–2437. DOI:10.1021/np500476h
[160] Tadesse M, Svenson J, Sepčić K, et al. Isolation and synthesis of pulmonarins A and B, acetylcholinesterase inhibitors from the colonial ascidian Synoicum pulmonaria[J]. J Nat Prod, 2014, 77(2): 364–369. DOI:10.1021/np401002s
[161] Yang H, Liu D Q, Liang T J, et al. Racemosin C, a novel minor bisindole alkaloid with protein tyrosine phosphatase-1B inhibitory activity from the green alga Caulerpa racemosa[J]. J Asian Nat Prod Res, 2014, 16(12): 1158–1165. DOI:10.1080/10286020.2014.965162
[162] Zhan K X, Jiao W H, Yang F, et al. Reniochalistatins A-E, cyclic peptides from the marine sponge Reniochalina stalagmitis[J]. J Nat Prod, 2014, 77(12): 2678–2684. DOI:10.1021/np5006778
[163] 杨宁线, 梁光义, 曹佩雪. 石岩枫中两个新的木脂素类化合物[J]. 天然产物研究与开发, 2014, 26(7):983–986.
[164] Thao N P, Luyen B T T, Tai B H, et al. Rat intestinal sucrase inhibition of constituents from the roots of Rosa rugosa Thunb[J]. Bioorg Med Chem Lett, 2014, 24(4): 1192–1196. DOI:10.1016/j.bmcl.2013.12.098
[165] Zhao S M, Wang Z, Zeng G Z, et al. New cytotoxic naphthohydroquinone dimers from Rubia alata[J]. Org Lett, 2014, 16(21): 5576–5579. DOI:10.1021/ol502603f
[166] Huang M B, Zhao S M, Zeng G Z, et al. Rubischumanins A-C, new cytotoxic cyclopeptides from Rubia schumanniana[J]. Tetrahedron, 2014, 70(42): 7627–7631. DOI:10.1016/j.tet.2014.07.105
[167] Zhang C, Shu W, Zeng K W, et al. Rupestonic acids B-G, NO inhibitory sesquiterpenoids from Artemisia rupestris[J]. Bioorg Med Chem Lett, 2014, 24(17): 4318–4322. DOI:10.1016/j.bmcl.2014.07.008
[168] He J, Yang Y N, Jiang J, et al. Saffloflavonesides A and B, two rearranged derivatives of flavonoid C-glycosides with a furan-tetrahydrofuran ring from Carthamus tinctorius[J]. Org Lett, 2014, 16(21): 5714–5717. DOI:10.1021/ol502789x
[169] Chen J J, Chen C J, Yao X J, et al. Eremophilane-type sesquiterpenoids with diverse skeletons from Ligularia sagitta[J]. J Nat Prod, 2014, 77(6): 1329–1335. DOI:10.1021/np5003302
[170] Jiang Z Y, Li W J, Jiao L X, et al. New clerodane diterpenes from Tinospora sagittata var. yunnanensis[J]. Planta Med, 2014, 80(5): 419–425. DOI:10.1055/s-00000058
[171] Nguyen M T T, Nguyen N T, Nguyen K D H, et al. Geranyl dihydrochalcones from Artocarpus altilis and their antiausteric activity[J]. Planta Med, 2014, 80(2/3): 193–200.
[172] Li Y H, Li H M, Li Y, et al. New alkaloids sinomacutines A-E, and cephalonine-2-O-β-d-glucopyranoside from rhizomes of Sinomenium acutum[J]. Tetrahedron, 2014, 70(46): 8893–8899. DOI:10.1016/j.tet.2014.09.088
[173] Wang Y, Zhang C L, Liu Y F, et al. Hepatoprotective triterpenoids and saponins of Schefflera kwangsiensis[J]. Planta Med, 2014, 80(2/3): 215–222.
[174] Long Z, Zhang Y, Guo Z, et al. Amide alkaloids from Scopolia tangutica[J]. Planta Med, 2014, 80(13): 1124–1130. DOI:10.1055/s-00000058
[175] Do Thi T, Do Thi P, Hanh T T H, et al. Two new neoclerodane diterpenoids from Scutellaria barbata D. Don growing in Vietnam[J]. J Asian Nat Prod Res, 2014, 16(4): 364–369. DOI:10.1080/10286020.2014.882912
[176] Liu X, Luo H B, Huang Y Y, et al. Selaginpulvilins A-D, new phosphodiesterase-4 inhibitors with an unprecedented skeleton from Selaginella pulvinata[J]. Org Lett, 2014, 16(1): 282–285. DOI:10.1021/ol403282f
[177] Williams R B, Du L, Norman V L, et al. Diterpenes from the endangered goldenrod Solidago shortii[J]. J Nat Prod, 2014, 77(6): 1438–1444. DOI:10.1021/np500178s
[178] Cheng S Y, Shih N L, Chuang C T, et al. Sinugyrosanolide A, an unprecedented C-4 norcembranoid, from the Formosan soft coral Sinularia gyrosa[J]. Bioorg Med Chem Lett, 2014, 24(6): 1562–1564. DOI:10.1016/j.bmcl.2014.01.073
[179] Li G S, Yao F, Zhang L, et al. New sesquiterpenoid derivatives from Solanum lyratum and their cytotoxicities[J]. J Asian Nat Prod Res, 2014, 16(2): 129–134. DOI:10.1080/10286020.2013.839664
[180] Zhang C L, Wang Y, Liu Y F, et al. Iridal-type triterpenoids with neuroprotective activities from Iris tectorum[J]. J Nat Prod, 2014, 77(2): 411–415. DOI:10.1021/np400937f
[181] Niu S, Liu D, Hu X, et al. Spiromastixones A-O, antibacterial chlorodepsidones from a deep-sea-derived Spiromastix sp. fungus[J]. J Nat Prod, 2014, 77(4): 1021–1030. DOI:10.1021/np5000457
[182] Kamauchi H, Kon T, Kinoshita K, et al. Three new terpenoids, sterebins O, P1, and P2, isolated from Stevia rebaudiana fermented by Saccharomyces cerevisiae[J]. Tetrahedron Lett, 2014, 55(52): 7203–7205. DOI:10.1016/j.tetlet.2014.11.012
[183] 蒋秋龙, 杨志钧, 饶敏, 等. 一株链霉菌产生的抗肿瘤活性产物[J]. 天然产物研究与开发, 2014, 26(1):1–5.
[184] Tchinda A T, Jansen O, Nyemb J N, et al. Strychnobaillonine, an unsymmetrical bisindole alkaloid with an unprecedented skeleton from Strychnos icaja roots[J]. J Nat Prod, 2014, 77(4): 1078–1082. DOI:10.1021/np400908u
[185] Song W H, Cheng Z H, Chen D F. Anticomplement monoterpenoid glucosides from the root bark of Paeonia suffruticosa[J]. J Nat Prod, 2014, 77(1): 42–48. DOI:10.1021/np400571x
[186] Geng C A, Chen X L, Zhou N J, et al. LC-MS guided isolation of (±)-sweriledugenin A, a pair of enantiomeric lactones, from Swertia leducii[J]. Org Lett, 2014, 16(2): 370–373. DOI:10.1021/ol403198d
[187] Cheng Y B, Chien Y T, Lee J C, et al. Limonoids from the seeds of Swietenia macrophylla with inhibitory activity against dengue virus 2[J]. J Nat Prod, 2014, 77(11): 2367–2374. DOI:10.1021/np5002829
[188] Gong J, Sun P, Jiang N, et al. New steroids with a rearranged skeleton as (h) P300 inhibitors from the sponge Theonella swinhoei[J]. Org Lett, 2014, 16(8): 2224–2227. DOI:10.1021/ol5007345
[189] Ma K, Wang J S, Luo J, et al. Tabercarpamines A-J, Apoptosis-inducing indole alkaloids from the leaves of Tabernaemontana corymbosa[J]. J Nat Prod, 2014, 77(5): 1156–1163. DOI:10.1021/np401098y
[190] Sim D S Y, Chong K W, Nge C E, et al. Cytotoxic vobasine, tacaman, and corynanthe-tryptamine bisindole alkaloids from Tabernaemontana and structure revision of tronoharine[J]. J Nat Prod, 2014, 77(11): 2504–2512. DOI:10.1021/np500589u
[191] He J W, Mu Z Q, Gao H, et al. New polyesters from Talaromyces flavus[J]. Tetrahedron, 2014, 70(29): 4425–4430. DOI:10.1016/j.tet.2014.02.060
[192] Zhao C, Gan C C, Jin M N, et al. Antitumor metastasis pregnane alkaloids from Pachysandra terminalis[J]. J Asian Nat Prod Res, 2014, 16(5): 440–446. DOI:10.1080/10286020.2014.893511
[193] Lv H W, Zhu M D, Luo J G, et al. Antihyperglycemic glucosylated coumaroyltyramine derivatives from Teucrium viscidum[J]. J Nat Prod, 2014, 77(2): 200–205. DOI:10.1021/np400487a
[194] Joshi K R, Devkota H P, Watanabe T, et al. Thotneosides A, B and C: potent antioxidants from Nepalese crude drug, leaves of Aconogonon molle[J]. Chem Pharm Bull, 2014, 62(2): 191–195. DOI:10.1248/cpb.c13-00748
[195] Lin T T, Huang Y Y, Tang G H, et al. Prenylated coumarins: natural phosphodiesterase-4 inhibitors from Toddalia asiatica[J]. J Nat Prod, 2014, 77(4): 955–962. DOI:10.1021/np401040d
[196] Zhao W, Huang X X, Yu L H, et al. Tomensides A-D, new antiproliferative phenylpropanoid sucrose esters from Prunus tomentosa leaves[J]. Bioorg Med Chem Lett, 2014, 24(11): 2459–2462. DOI:10.1016/j.bmcl.2014.04.018
[197] Cheng Z B, Lu X, Bao J M, et al. (±)-Torreyunlignans A-D, rare 8-9′ linked neolignan enantiomers as phosphodiesterase-9A inhibitors from Torreya yunnanensis[J]. J Nat Prod, 2014, 77(12): 2651–2657. DOI:10.1021/np500528u
[198] Lin K H, Tseng Y J, Chen B W, et al. Tortuosenes A and B, new diterpenoid metabolites from the Formosan soft coral Sarcophyton tortuosum[J]. Org Lett, 2014, 16(5): 1314–1317. DOI:10.1021/ol403723b
[199] Liu C P, Xu J B, Han Y S, et al. Trichiconins A-C, limonoids with new carbon skeletons from Trichilia connaroides[J]. Org Lett, 2014, 16(20): 5478–5481. DOI:10.1021/ol5027552
[200] Chen J J, Wang S W, Hsiao H Y, et al. Aliphatic phenolic ethers from Trichobotrys effusa[J]. J Nat Prod, 2014, 77(5): 1097–1101. DOI:10.1021/np400776y
[201] Waterman C, Calcul L, Mutka T, et al. A potent antimalarial trichothecene from hyphomycete species[J]. Tetrahedron Lett, 2014, 55(29): 3989–3991. DOI:10.1016/j.tetlet.2014.05.056
[202] Ferreira E A, Reigada J B, Correia M V, et al. Antifungal and cytotoxic 2-acylcyclohexane-1,3-diones from Peperomia alata and P. trineura[J]. J Nat Prod, 2014, 77(6): 1377–1382. DOI:10.1021/np500130x
[203] Li D Y, Wei J X, Hua H M, et al. Antimicrobial constituents from the flowers of Trollius chinensis[J]. J Asian Nat Prod Res, 2014, 16(10): 1018–1023. DOI:10.1080/10286020.2014.927868
[204] Qin Z B, Zhang J, Wu X D, et al. Sesquiterpenoids from Tussilago farfara and their inhibitory effects on nitric oxide production[J]. Planta Med, 2014, 80(8/9): 703–709.
[205] Song W, Si L, Ji S, et al. Uralsaponins M-Y, antiviral triterpenoid saponins from the roots of Glycyrrhiza uralensis[J]. J Nat Prod, 2014, 77(7): 1632–1643. DOI:10.1021/np500253m
[206] Wei P Y, Li L, Yang C G, et al. A novel oxybis cresol verticilatin with highly varying degrees of biological activities from the insect pathogenic fungus Paecilomyces verticillatus[J]. J Asian Nat Prod Res, 2014, 16(12): 1153–1157. DOI:10.1080/10286020.2014.959438
[207] Cao F, Shao C L, Wang Y, et al. Polyhydroxylated sterols from the South China Sea gorgonian Verrucella umbraculum[J]. Helv Chim Acta, 2014, 97(6): 900–908. DOI:10.1002/hlca.v97.6
[208] Gao X, Shao L D, Dong L B, et al. Vibsatins A and B, two new tetranorvibsane-type diterpenoids from Viburnum tinus cv. variegatus[J]. Org Lett, 2014, 16(3): 980–983. DOI:10.1021/ol403707a
[209] Cheng G G, Zhao Y L, Zhang Y, et al. Indole alkaloids from cultivated Vinca major[J]. Tetrahedron, 2014, 70(45): 8723–8729. DOI:10.1016/j.tet.2014.09.026
[210] Myobatake Y, Takemoto K, Kamisuki S, et al. Cytotoxic alkylated hydroquinone, phenol, and cyclohexenone derivatives from Aspergillus violaceofuscus Gasperini[J]. J Nat Prod, 2014, 77(5): 1236–1240. DOI:10.1021/np401017g
[211] Lou Z H, Li H M, Gao L H, et al. Antioxidant lignans from the seeds of Vitex negundo var. cannabifolia[J]. J Asian Nat Prod Res, 2014, 16(9): 963–969. DOI:10.1080/10286020.2014.929574
[212] Lou H, Zheng S, Li T, et al. Vulgarisin A, a new diterpenoid with a rare 5/6/4/5 ring skeleton from the Chinese medicinal plant Prunella vulgaris[J]. Org Lett, 2014, 16(10): 2696–2699. DOI:10.1021/ol5009763
[213] Cretton S, Breant L, Pourrez L, et al. Antitrypanosomal quinoline alkaloids from the roots of Waltheria indica[J]. J Nat Prod, 2014, 77(10): 2304–2311. DOI:10.1021/np5006554
[214] Yin G P, Li L C, Zhang Q Z, et al. INOS inhibitory activity of sesquiterpenoids and a monoterpenoid from the rhizomes of Curcuma wenyujin[J]. J Nat Prod, 2014, 77(10): 2161–2169. DOI:10.1021/np400984c
[215] Wu H Y, Zhan R, Wang W G, et al. Cytotoxic ent-kaurane diterpenoids from Isodon wikstroemioides[J]. J Nat Prod, 2014, 77(4): 931–941. DOI:10.1021/np4010135
[216] Trisuwan K, Boonyaketgoson S, Rukachaisirikul V, et al. Oxygenated xanthones and biflavanoids from the twigs of Garcinia xanthochymus[J]. Tetrahedron Lett, 2014, 55(26): 3600–3602. DOI:10.1016/j.tetlet.2014.04.105
[217] Zhou Z F, Liu H L, Zhang W, et al. Bioactive rearranged limonoids from the Chinese mangrove Xylocarpus granatum Koenig[J]. Tetrahedron, 2014, 70(37): 6444–6449. DOI:10.1016/j.tet.2014.07.027
[218] Wu Y B, Xia Q, Huo C H, et al. Xylomexicanins E-H, new limonoids from Xylocarpus granatum[J]. Tetrahedron, 2014, 70(30): 4557–4562. DOI:10.1016/j.tet.2014.04.062
[219] Kang J, Cui X Q, Wang H Q, et al. Two new diels-alder-type adducts from the stem barks of Morus yunanensis[J]. J Asian Nat Prod Res, 2014, 16(6): 617–622. DOI:10.1080/10286020.2014.923407
[220] Ji K L, Zhang P, Hu H B, et al. Limonoids from the leaves and twigs of Walsura yunnanensis[J]. J Nat Prod, 2014, 77(8): 1764–1769. DOI:10.1021/np400976p
[221] Li W, Yang S Y, Yan X T, et al. NF-κB inhibitory activities of glycosides and alkaloids from Zanthoxylum schinifolium stems[J]. Chem Pharm Bull, 2014, 62(2): 196–202. DOI:10.1248/cpb.c13-00759
[222] Wang J F, Deng Y H, Yang S H, et al. Characterization and biological evaluation of six new dimeric lignans with an unusual α, β-unsaturated ketone motif from Zanthoxylum simulans[J]. Bioorg Med Chem Lett, 2014, 24(19): 4667–4671. DOI:10.1016/j.bmcl.2014.08.042