1-Triacontanol (BioDeep_00000017372)

Secondary id: BioDeep_00000000548, BioDeep_00000860134

human metabolite PANOMIX_OTCML-2023 Volatile Flavor Compounds

代谢物信息卡片

1-Triacontanol 100 microg/mL in Methyl-tert-butyl ether

化学式: C30H62O (438.48004019999996)
中文名称: 三十烷醇, 三十醇, 1-三十烷醇
谱图信息: 最多检出来源 Viridiplantae(plant) 1.09%

分子结构信息

SMILES: C(CCCCCCCCCCCCCO)CCCCCCCCCCCCCCCC
InChI: InChI=1S/C30H62O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31/h31H,2-30H2,1H3

描述信息

Triacontan-1-ol is an ultra-long-chain primary fatty alcohol that is triacontane in which one of the terminal methyl hydrogens is replaced by a hydroxy group. It is a fatty alcohol 30:0 and an ultra-long-chain primary fatty alcohol.
1-Triacontanol is a natural product found in Haplophyllum bucharicum, Euphorbia dracunculoides, and other organisms with data available.
See also: Saw Palmetto (part of); Iris versicolor root (part of).

同义名列表

29 个代谢物同义名

1-Triacontanol 100 microg/mL in Methyl-tert-butyl ether; TRICONTANOL (CONSTITUENT OF SAW PALMETTO) [DSC]; TRICONTANOL (CONSTITUENT OF SAW PALMETTO); 1-Triacontanol, >=98\\% (capillary GC); 1-triacontanol, aluminum salt; MYRICYL ALCOHOL [INCI]; Myricyl alcohol (VAN); 1-Hydroxytriacontane; triacontanyl alcohol; 1-Triacontanol, 96\\%; 1-TRIACONTANOL [MI]; 1-Triacontanol,(S); Triacontyl alcohol; Melissyl alcohol; Triacontan-1-ol; Myricyl alcohol; 1-Triacontanol; 1-?Triacontanol; 1-Triacontanol; n-Triacontanol; Triacontanol-1; triacontanol; tricontanol; Well-Bloom; AI3-20480; miraculan; FOH 30:0; ULTRIA; Triacontan-1-ol

数据库引用编号

19 个数据库交叉引用编号

ChEBI: CHEBI:28409
KEGG: C08392
PubChem: 68972
HMDB: HMDB0244015_nmr_one_3920
ChEMBL: CHEMBL1079147
Wikipedia: 1-Triacontanol
LipidMAPS: LMFA05000006
MeSH: 1-triacontanol
ChemIDplus: 0000593500
CAS: 28351-05-5
CAS: 593-50-0
medchemexpress: HY-N6933
MetaboLights: MTBLC28409
PubChem: 10588
KNApSAcK: C00001269
NIKKAJI: J6.767I
KNApSAcK: 28409
LOTUS: LTS0026833
wikidata: Q4860821

分类词条

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

87 个相关的物种来源信息

342581 - Abies spectabilis: 10.1002/JPS.2600551130
1217423 - Acacia suma: 10.4268/CJCMM20101114
300953 - Andrachne: 10.4268/CJCMM20150419
13339 - Apocynum cannabinum: 10.1007/S10600-011-9801-Z
377125 - Apocynum venetum: 10.1007/S10600-011-9801-Z
587400 - Ardisia humilis: 10.1021/NP040041Z
78371 - Arisaema triphyllum: 10.1139/CJR34-013
35708 - Arundo donax:
4442 - Camellia sinensis: 10.1002/JSFA.2740430305
542762 - Camellia sinensis var. sinensis: 10.1016/S0031-9422(00)91295-0
622458 - Capparis decidua:
1819373 - Capparis spinosa var. ovata: 10.1055/S-0028-1099537
1524680 - Chamaecrista kleinii: 10.1016/S0031-9422(01)00114-5
159034 - Clausena anisata: 10.1002/HLCA.200390259
1224754 - Clausena dunniana: 10.1002/HLCA.200390259
2807180 - Cnestis ferruginea: 10.1016/0378-8741(82)90058-7
1329283 - Convolvulus microphyllus: 10.1515/ZNB-1978-0231
267599 - Convolvulus prostratus: 10.1515/ZNB-1978-0231
60117 - Cornus capitata: 10.1021/NP50046A034
140997 - Crataegus monogyna: 10.1016/S0021-9673(96)01091-6
205937 - Crinum asiaticum: 10.1016/0031-9422(90)85365-M
323034 - Croton californicus: 10.1021/NP50003A016
2815093 - Croton tetradenius: 10.1002/HLCA.200900201
66014 - Cymbopogon citratus: 10.1055/S-0028-1097851
557061 - Delavaya toxocarpa: 10.4028/WWW.SCIENTIFIC.NET/AMR.554-556.1845
396369 - Elephantopus scaber: 10.1016/S0031-9422(00)85888-4
46385 - Eleutherococcus trifoliatus: 10.1016/S0031-9422(00)90113-4
1408201 - Eschenbachia blinii: 10.3987/COM-98-8408
627158 - Eucalyptus robusta: 10.1002/CJOC.19860040110
183855 - Eucalyptus tereticornis: 10.1016/0031-9422(93)85412-K
38845 - Euphorbia dendroides:
1008446 - Euphorbia dracunculoides: 10.4268/CJCMM20142015
318062 - Euphorbia hirta: 10.1246/BCSJ.39.2532
1333928 - Euphorbia micractina: 10.1021/NP900305J
1333944 - Euphorbia rothiana:
90528 - Fagonia cretica: 10.1111/J.2042-7158.1965.TB07741.X
1818589 - Fernandoa adenophylla: 10.1055/S-0028-1099423
1471565 - Gymnosporia montana: 10.1021/NP50017A026
256095 - Gymnosporia senegalensis: 10.1021/NP50017A026
1604314 - Gynura japonica: 10.1002/JCCS.200400211
1006069 - Haplophyllum bucharicum: 10.1007/BF02238348
49577 - Hellenia speciosa: 10.1016/S0031-9422(00)81170-X
229543 - Hibiscus cannabinus: 10.1002/1099-1565(200011/12)11:6<345::AID-PCA540>3.0.CO;2-T
9606 - Homo sapiens: -
65561 - Hypericum perforatum: 10.1021/NP50030A025
1321360 - Hypericum wightianum: 10.1080/10286020310001595935
139741 - Ipomoea nervosa: 10.1016/S0031-9422(00)86474-2
217685 - Iresine diffusa: 10.1002/MRC.1550
2833435 - Jatropha mollissima: 10.1016/S0305-1978(03)00140-6
126435 - Lantana camara: 10.1055/S-0028-1099554
649173 - Lantana strigocamara: 10.1055/S-0028-1099554
300998 - Leptopus chinensis: 10.1007/S10600-005-0207-7
475890 - Lithodora fruticosa: 10.1021/NP50034A043
344083 - Litsea acutivena: 10.1002/JCCS.200700071
566153 - Lonicera quinquelocularis: 10.1016/S0031-9422(99)00426-4
389206 - Mandragora autumnalis: 10.1002/HLCA.19420250402
33117 - Mandragora officinarum: 10.1002/HLCA.19420250402
353996 - Mansoa alliacea: 10.1006/BIOO.1993.1007
155640 - Melia azedarach: 10.1055/S-0028-1097188
40337 - Mucuna pruriens var. utilis: 10.1016/0031-9422(96)86994-9
463667 - Nanodea muscosa: 10.1021/NP020513E
296034 - Phyllanthus niruri: 10.1016/0378-8741(85)90026-1
296035 - Phyllanthus urinaria: 10.1055/S-2006-958083
538264 - Piper eucalyptifolium: 10.1016/0031-9422(89)80275-4
2138340 - Piper schmidtii: 10.1021/NP50068A032
1548623 - Pluchea arguta: 10.1016/0031-9422(86)80034-6
102697 - Prosopis glandulosa: 10.1055/S-0028-1097595
32242 - Prunus laurocerasus: 10.1016/0031-9422(96)00241-5
106626 - Rhizophora apiculata: 10.1016/0031-9422(93)85036-Q
4202 - Sambucus nigra: 10.1055/S-0028-1097541
233893 - Scutellaria lateriflora: 10.1021/NP900068T
875646 - Senegalia polyacantha: 10.4268/CJCMM20101114
72401 - Senna didymobotrya: 10.1016/0031-9422(93)85192-T
992784 - Senna petersiana: 10.1016/S0367-326X(00)00155-6
185195 - Smallanthus maculatus: 10.1007/S10600-006-0193-4
119830 - Solanum torvum: 10.1016/S0031-9422(00)80080-1
199523 - Solidago sempervirens: 10.1016/0031-9422(83)85058-4
13274 - Stellaria media: 10.1016/0031-9422(94)00935-M
153544 - Styrax officinalis: 10.1055/S-0028-1099499
680229 - Tecomella undulata:
1292371 - Tephrosia strigosa: 10.1055/S-0028-1097619
161594 - Trachyrhamphus serratus: 10.1007/S10600-011-9966-5
1117634 - Vachellia jacquemontii: 10.1016/0040-4020(79)85042-5
138038 - Vachellia pennatula: 10.1007/S10600-005-0133-8
237943 - Viburnum jucundum: 10.1055/S-2001-17357
552636 - Xanthium strumarium var. canadense: 10.1016/S0031-9422(00)97296-0
241841 - Xylocarpus granatum: 10.1080/14786410902726183

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

文献列表

Tunisha Verma, Savita Bhardwaj, Ali Raza, Ivica Djalovic, Pv Vara Prasad, Dhriti Kapoor. Mitigation of salt stress in Indian mustard (Brassica juncea L.) by the application of triacontanol and hydrogen sulfide. Plant signaling & behavior. 2023 12; 18(1):2189371. doi: 10.1080/15592324.2023.2189371. [PMID: 36934336]
Adam Yasgar, Danielle Bougie, Richard T Eastman, Ruili Huang, Misha Itkin, Jennifer Kouznetsova, Caitlin Lynch, Crystal McKnight, Mitch Miller, Deborah K Ngan, Tyler Peryea, Pranav Shah, Paul Shinn, Menghang Xia, Xin Xu, Alexey V Zakharov, Anton Simeonov. Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products. ACS pharmacology & translational science. 2023 May; 6(5):683-701. doi: 10.1021/acsptsci.2c00194. [PMID: 37200814]
Izabela Weremczuk-Jeżyna, Katarzyna Hnatuszko-Konka, Liwia Lebelt, Dorota G Piotrowska, Izabela Grzegorczyk-Karolak. The Effect of the Stress-Signalling Mediator Triacontanol on Biochemical and Physiological Modifications in Dracocephalum forrestii Culture. International journal of molecular sciences. 2022 Dec; 23(23):. doi: 10.3390/ijms232315147. [PMID: 36499476]
Shakil Ahmed, Maria Ahmad, Rehana Sardar, Muhammad Amir Ismail. Triacontanol priming as a smart strategy to attenuate lead toxicity in Brassica oleracea L. International journal of phytoremediation. 2022 Nov; ?(?):1-16. doi: 10.1080/15226514.2022.2143478. [PMID: 36384370]
Giovanni Mian, Nicola Belfiore, Rita Musetti, Diego Tomasi, Pierpaolo Cantone, Lorenzo Lovat, Stefania Lupinelli, Lucilla Iacumin, Emilio Celotti, Fabrizio Golinelli. Effect of a triacontanol-rich biostimulant on the ripening dynamic and wine must technological parameters in Vitis vinifera cv. 'Ribolla Gialla'. Plant physiology and biochemistry : PPB. 2022 Oct; 188(?):60-69. doi: 10.1016/j.plaphy.2022.07.032. [PMID: 35987022]
Rehana Sardar, Shakil Ahmed, Muhammad Akbar, Nasim Ahmad Yasin, Guihua Li. Alleviation of cadmium phytotoxicity in triacontanol treated Coriandrum sativum L. by modulation of physiochemical attributes, oxidative stress biomarkers and antioxidative system. Chemosphere. 2022 May; 295(?):133924. doi: 10.1016/j.chemosphere.2022.133924. [PMID: 35149022]
Mubeen Sarwar, Sumreen Anjum, Muhammad Waqar Alam, Qurban Ali, C M Ayyub, Muhammad Saleem Haider, M Irfan Ashraf, Wajid Mahboob. Triacontanol regulates morphological traits and enzymatic activities of salinity affected hot pepper plants. Scientific reports. 2022 03; 12(1):3736. doi: 10.1038/s41598-022-06516-w. [PMID: 35260596]
Aarifa Nabi, Tariq Aftab, M Masroor, A Khan, M Naeem. Exogenous triacontanol provides tolerance against arsenic-induced toxicity by scavenging ROS and improving morphology and physiological activities of Mentha arvensis L. Environmental pollution (Barking, Essex : 1987). 2022 Feb; 295(?):118609. doi: 10.1016/j.envpol.2021.118609. [PMID: 34896400]
H Faiz, O Khan, I Ali, T Hussain, S T Haider, T Siddique, M Liaquat, A Noor, R W Khan, S Ashraf, S Rashid, A Noreen, S Asghar, Q S Anjum. Foliar application of triacontanol ameliorates heat stress through regulation of the antioxidant defense system and improves yield of eggplant. Brazilian journal of biology = Revista brasleira de biologia. 2022; 84(?):e253696. doi: 10.1590/1519-6984.253696. [PMID: 35043836]
Mubeen Sarwar, Sumreen Anjum, Qurban Ali, Muhammad Waqar Alam, Muhammad Saleem Haider, Wajid Mehboob. Triacontanol modulates salt stress tolerance in cucumber by altering the physiological and biochemical status of plant cells. Scientific reports. 2021 12; 11(1):24504. doi: 10.1038/s41598-021-04174-y. [PMID: 34969963]
Javed Ahmad, Arlene A Ali, Asma A Al-Huqail, M Irfan Qureshi. Triacontanol attenuates drought-induced oxidative stress in Brassica juncea L. by regulating lignification genes, calcium metabolism and the antioxidant system. Plant physiology and biochemistry : PPB. 2021 Sep; 166(?):985-998. doi: 10.1016/j.plaphy.2021.07.009. [PMID: 34265697]
Basmah M Alharbi, Awatif Mahfouz Abdulmajeed, Heba Hassan. Biochemical and Molecular Effects Induced by Triacontanol in Acquired Tolerance of Rice to Drought Stress. Genes. 2021 07; 12(8):. doi: 10.3390/genes12081119. [PMID: 34440293]
Mirka Macel, Isabella G S Visschers, Janny L Peters, Nicole M van Dam, Rob M de Graaf. High Concentrations of Very Long Chain Leaf Wax Alkanes of Thrips Susceptible Pepper Accessions (Capsicum spp). Journal of chemical ecology. 2020 Dec; 46(11-12):1082-1089. doi: 10.1007/s10886-020-01226-x. [PMID: 33089351]
S A Shoba, I V Gorepekin, G N Fedotov, T A Gracheva. Plant Growth Hormones Increase the Stimulation Efficiency of Seedlings Development for Spring Wheat Seeds upon Pre-sowing Treatment. Doklady biological sciences : proceedings of the Academy of Sciences of the USSR, Biological sciences sections. 2020 Jul; 493(1):128-131. doi: 10.1134/s0012496620040080. [PMID: 32894427]
Yimeng Zhou, Ning Li, Zhixia Qiu, Xiaoyu Lu, Min Fang, Xijing Chen, Lili Ren, Guangji Wang, Pingkai Ouyang. Superior anti-neoplastic activities of triacontanol-PEG conjugate: synthesis, characterization and biological evaluations. Drug delivery. 2018 Nov; 25(1):1546-1559. doi: 10.1080/10717544.2018.1477864. [PMID: 30022695]
Stefania Sut, Clizia Franceschi, Gregorio Peron, Gabriele Poloniato, Stefano Dall'Acqua. Development and Validation of an HPLC-ELSD Method for the Quantification of 1-Triacontanol in Solid and Liquid Samples. Molecules (Basel, Switzerland). 2018 Oct; 23(11):. doi: 10.3390/molecules23112775. [PMID: 30373135]
Xiaoyu Lu, Min Fang, Yu Dai, Yue Yang, Ali Fan, Jiaqiu Xu, Zhiying Qin, Yang Lu, Di Zhao, Xijing Chen, Ning Li. Quantification of triacontanol and its PEGylated prodrug in rat plasma by GC-MS/MS: Application to a pre-clinical pharmacokinetic study. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2018 Jul; 1089(?):8-15. doi: 10.1016/j.jchromb.2018.04.037. [PMID: 29738967]
Elham Asadi Karam, Viviana Maresca, Sergio Sorbo, Batool Keramat, Adriana Basile. Effects of triacontanol on ascorbate-glutathione cycle in Brassica napus L. exposed to cadmium-induced oxidative stress. Ecotoxicology and environmental safety. 2017 Oct; 144(?):268-274. doi: 10.1016/j.ecoenv.2017.06.035. [PMID: 28633105]
Kan Chen, Chang-Qian Wang, Yu-Qi Fan, Zhi-Hua Han, Yue Wang, Lin Gao, Hua-Su Zeng. [Lipid-lowering effect of seven traditional Chinese medicine monomers in zebrafish system]. Sheng li xue bao : [Acta physiologica Sinica]. 2017 Feb; 69(1):55-60. doi: . [PMID: 28217808]
Muhammad Waqas, Raheem Shahzad, Abdul Latif Khan, Sajjad Asaf, Yoon-Ha Kim, Sang-Mo Kang, Saqib Bilal, Muhammad Hamayun, In-Jung Lee. Salvaging effect of triacontanol on plant growth, thermotolerance, macro-nutrient content, amino acid concentration and modulation of defense hormonal levels under heat stress. Plant physiology and biochemistry : PPB. 2016 Feb; 99(?):118-25. doi: 10.1016/j.plaphy.2015.12.012. [PMID: 26744997]
Divya Pulivarthi, Kelly Marie Steinberg, Lianet Monzote, Abel Piñón, William N Setzer. Antileishmanial Activity of Compounds Isolated from Sassafras albidum. Natural product communications. 2015 Jul; 10(7):1229-30. doi: . [PMID: 26411017]
Chunfeng Wang, Ali Fan, Xiaojie Zhu, Yang Lu, Shuhua Deng, Wenchao Gao, Wei Zhang, Qi Liu, Xijing Chen. Trace quantification of 1-triacontanol in beagle plasma by GC-MS/MS and its application to a pharmacokinetic study. Biomedical chromatography : BMC. 2015 May; 29(5):749-55. doi: 10.1002/bmc.3351. [PMID: 25331188]
Chunfeng Wang, Ali Fan, Shuhua Deng, Wenchao Gao, Wei Zhang, Wei Yang, Xiaojie Zhu, Yang Lu, Xijing Chen. Investigation on pharmacokinetics, tissue distribution and excretion of 1-triacontanol in rats by gas chromatography-tandem mass spectrometry (GC-MS/MS). Xenobiotica; the fate of foreign compounds in biological systems. 2015 Jan; 45(1):71-8. doi: 10.3109/00498254.2014.943334. [PMID: 25080280]
Sugey López-Martínez, Gabriel Navarrete-Vázquez, Samuel Estrada-Soto, Ismael León-Rivera, María Yolanda Rios. Chemical constituents of the hemiparasitic plant Phoradendron brachystachyum DC Nutt (Viscaceae). Natural product research. 2013; 27(2):130-6. doi: 10.1080/14786419.2012.662646. [PMID: 22360797]
M K Akitha Devi, G Sakthivelu, P Giridhar, G A Ravishankar. Protocol for augmented shoot organogenesis in selected variety of soybean [Glycine max L. (Merr.)]. Indian journal of experimental biology. 2012 Oct; 50(10):729-34. doi: . [PMID: 23214267]
Veeramuthu Duraipandiyan, Naif Abdullah Al-Harbi, Savarimuthu Ignacimuthu, Chinnasamy Muthukumar. Antimicrobial activity of sesquiterpene lactones isolated from traditional medicinal plant, Costus speciosus (Koen ex.Retz.) Sm. BMC complementary and alternative medicine. 2012 Mar; 12(?):13. doi: 10.1186/1472-6882-12-13. [PMID: 22397713]
Vijaya Ravinayagam, Ravindran Jaganathan, Sachdanandam Panchanadham, Shanthi Palanivelu. Potential Antioxidant Role of Tridham in Managing Oxidative Stress against Aflatoxin-B(1)-Induced Experimental Hepatocellular Carcinoma. International journal of hepatology. 2012; 2012(?):428373. doi: 10.1155/2012/428373. [PMID: 22518320]
Niranjan Das, Basudev Achari, Yoshihiro Harigaya, Biswanath Dinda. A new flavonol glucoside from the aerial parts of Sida glutinosa. Journal of Asian natural products research. 2011 Oct; 13(10):965-71. doi: 10.1080/10286020.2011.602343. [PMID: 21972814]
Sumayya Saied, Shazia Shah, Zulfiqar Ali, Ajmal Khan, Bishnu P Marasini, Muhammad Iqbal Choudhary. Chemical constituents of Cichorium intybus and their inhibitory effects against urease and alpha-chymotrypsin enzymes. Natural product communications. 2011 Aug; 6(8):1117-20. doi: . [PMID: 21922913]
Dong Min Jung, Mi Jin Lee, Suk Hoo Yoon, Mun Yhung Jung. A gas chromatography-tandem quadrupole mass spectrometric analysis of policosanols in commercial vegetable oils. Journal of food science. 2011 Aug; 76(6):C891-9. doi: 10.1111/j.1750-3841.2011.02232.x. [PMID: 22417487]
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Berit Ebert, Daniela Zöller, Alexander Erban, Ines Fehrle, Jürgen Hartmann, Annette Niehl, Joachim Kopka, Joachim Fisahn. Metabolic profiling of Arabidopsis thaliana epidermal cells. Journal of experimental botany. 2010 Mar; 61(5):1321-35. doi: 10.1093/jxb/erq002. [PMID: 20150518]
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Pinar Karacakaya, Nur Koçberber Kiliç, Ergin Duygu, Gönül Dönmez. Stimulation of reactive dye removal by cyanobacteria in media containing triacontanol hormone. Journal of hazardous materials. 2009 Dec; 172(2-3):1635-9. doi: 10.1016/j.jhazmat.2009.08.037. [PMID: 19740608]
Daniela Haim, Miriam Berríos, Alfonso Valenzuela, Luis A Videla. Trace quantification of 1-octacosanol and 1-triacontanol and their main metabolites in plasma by liquid-liquid extraction coupled with gas chromatography-mass spectrometry. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2009 Dec; 877(32):4154-8. doi: 10.1016/j.jchromb.2009.10.034. [PMID: 19931494]
Neena Srivastava, Sayadda Khatoon, A K S Rawat, Vartika Rai, Shanta Mehrotra. Chromatographic estimation of p-coumaric acid and triacontanol in an Ayurvedic root drug patala (Stereospermum suaveolens Roxb.). Journal of chromatographic science. 2009 Nov; 47(10):936-9. doi: 10.1093/chromsci/47.10.936. [PMID: 19930809]
Wendong Xu, Chenggen Zhu, Wei Cheng, Xiaona Fan, Xiaoguang Chen, Sen Yang, Ying Guo, Fei Ye, Jiangong Shi. Chemical Constituents of the Roots of Euphorbia micractina. Journal of natural products. 2009 Sep; 72(9):1620-6. doi: 10.1021/np900305j. [PMID: 19702283]
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