lanostane (BioDeep_00000636736)
代谢物信息卡片
化学式: C30H54 (414.4225)
中文名称: 羊毛甾烷
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1CCC(C)(C)[C@]2([H])CC[C@]3([H])[C@@]([H])([C@]21C)CC[C@]1(C)[C@@]([H])([C@H](C)CCCC(C)C)CC[C@]13C
InChI: InChI=1S/C30H54/c1-21(2)11-9-12-22(3)23-15-19-30(8)25-13-14-26-27(4,5)17-10-18-28(26,6)24(25)16-20-29(23,30)7/h21-26H,9-20H2,1-8H3/t22-,23-,24+,25-,26+,28-,29-,30+/m1/s1
数据库引用编号
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
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)
0 个相关的物种来源信息
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。
| 亚细胞结构定位 | 关联基因列表 |
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文献列表
- Naïm Stiti, Marie-Andrée Hartmann. Nonsterol Triterpenoids as Major Constituents of Olea europaea.
Journal of lipids.
2012; 2012(?):476595. doi:
10.1155/2012/476595. [PMID: 22523691] - Ulrike Grienke, Judit Mihály-Bison, Daniela Schuster, Taras Afonyushkin, Markus Binder, Shu-hong Guan, Chun-ru Cheng, Gerhard Wolber, Hermann Stuppner, De-an Guo, Valery N Bochkov, Judith M Rollinger. Pharmacophore-based discovery of FXR-agonists. Part II: identification of bioactive triterpenes from Ganoderma lucidum.
Bioorganic & medicinal chemistry.
2011 Nov; 19(22):6779-91. doi:
10.1016/j.bmc.2011.09.039. [PMID: 22014750] - Bingji Ma, Wei Ren, Yan Zhou, Jinchuan Ma, Yuan Ruan, Chun-Nan Wen. Triterpenoids from the spores of Ganoderma lucidum.
North American journal of medical sciences.
2011 Nov; 3(11):495-8. doi:
10.4297/najms.2011.3495. [PMID: 22361494] - Biswanath Dinda, Sudhan Debnath, Bikas Chandra Mohanta, Yoshihiro Harigaya. Naturally occurring triterpenoid saponins.
Chemistry & biodiversity.
2010 Oct; 7(10):2327-580. doi:
10.1002/cbdv.200800070. [PMID: 20963775] - Xian-Wen Yang, Su-Mei Li, Liang Wu, Yong-Li Li, Lin Feng, Yun-Heng Shen, Jun-Mian Tian, Jian Tang, Ning Wang, Yonghong Liu, Wei-Dong Zhang. Abiesatrines A-J: anti-inflammatory and antitumor triterpenoids from Abies georgei Orr.
Organic & biomolecular chemistry.
2010 Jun; 8(11):2609-16. doi:
10.1039/c001885f. [PMID: 20372737] - Lu Lu, Jian-Chao Chen, He-Jiao Song, Yan Li, Yin Nian, Ming-Hua Qiu. Five new triterpene bisglycosides with acyclic side chains from the rhizomes of Cimicifuga foetida L.
Chemical & pharmaceutical bulletin.
2010 May; 58(5):729-33. doi:
10.1248/cpb.58.729. [PMID: 20460805] - Ninh Khac Ban, Bui Van Thanh, Phan Van Kiem, Chau Van Minh, Nguyen Xuan Cuong, Nguyen Xuan Nhiem, Hoang Thanh Huong, Ha Tuan Anh, Eun-Jeon Park, Dong Hwan Sohn, Young Ho Kim. Dibenzocyclooctadiene lignans and lanostane derivatives from the roots of Kadsura coccinea and their protective effects on primary rat hepatocyte injury induced by t-butyl hydroperoxide.
Planta medica.
2009 Sep; 75(11):1253-7. doi:
10.1055/s-0029-1185537. [PMID: 19350485] - Carla C Mendes, Luciana Q Sandes, Frederico G Cruz, Nídia F Roque. New (9betaH)-lanostanes and lanostanes from Mikania aff. jeffreyi (Asteraceae).
Chemistry & biodiversity.
2009 Sep; 6(9):1463-70. doi:
10.1002/cbdv.200800269. [PMID: 19774608] - Dang Ngoc Quang, Toshihiro Hashimoto, Masami Tanaka, Yoshinori Asakawa. Tyromycic acids F and G: two new triterpenoids from the mushroom Tyromyces fissilis.
Chemical & pharmaceutical bulletin.
2003 Dec; 51(12):1441-3. doi:
10.1248/cpb.51.1441. [PMID: 14646328] - Hong-Jie Zhang, Ghee Teng Tan, Vu Dinh Hoang, Nguyen Van Hung, Nguyen Manh Cuong, D Doel Soejarto, John M Pezzuto, Harry H S Fong. Natural anti-HIV agents. Part IV. Anti-HIV constituents from Vatica cinerea.
Journal of natural products.
2003 Feb; 66(2):263-8. doi:
10.1021/np020379y. [PMID: 12608862] - S I Wada, A Iida, R Tanaka. Triterpene constituents from the stem bark of Pinus luchuensis and their DNA topoisomerase II inhibitory effect.
Planta medica.
2001 Oct; 67(7):659-64. doi:
10.1055/s-2001-17360. [PMID: 11582546]
