bauerenol (BioDeep_00000308892)

代谢物信息卡片

bauerenol

化学式: C30H50O (426.386145)
中文名称: 降香萜烯醇
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1CCC2(C)CCC3(C)C4=CCC5C(C)(C)C(O)CCC5(C)C4CCC3(C)C2C1C
InChI: InChI=1S/C30H50O/c1-19-11-14-27(5)17-18-29(7)22-9-10-23-26(3,4)24(31)13-15-28(23,6)21(22)12-16-30(29,8)25(27)20(19)2/h9,19-21,23-25,31H,10-18H2,1-8H3/t19-,20+,21+,23+,24+,25-,27-,28-,29-,30+/m1/s1

描述信息

同义名列表

1 个代谢物同义名

bauerenol

数据库引用编号

4 个数据库交叉引用编号

PubChem: 111220
KNApSAcK: C00035252
CAS: 6466-94-0
PMhub: MS000078333

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)

26 个相关的物种来源信息

3702 - Arabidopsis thaliana: 10.1016/S0040-4039(00)01347-2
693367 - Ardisia elliptica: 10.1055/S-0028-1097577
276775 - Ardisia japonica:
1073919 - Ardisia solanacea: 10.1055/S-0028-1097577
35608 - Artemisia annua: 10.1016/0031-9422(94)85021-6
482930 - Bosistoa brassii: 10.1021/NP50091A007
354489 - Bosistoa medicinalis: 10.1021/NP50091A007
114282 - Cichorium spinosum: 10.1021/JF025848G
570484 - Diospyros ebenum:
570488 - Diospyros kirkii: 10.1016/S0031-9422(97)01020-0
1948899 - Diospyros melanoxylon: 10.1016/S0305-1978(98)00061-1
413760 - Diospyros mespiliformis: 10.1016/S0031-9422(97)01020-0
1333925 - Euphorbia macroclada: 10.4268/CJCMM20142015
3494 - Ficus carica:
4298 - Ilex aquifolium: 10.1055/S-0028-1097405
318058 - Ixeris chinensis: 10.1248/CPB.44.509
189245 - Jacobaea arnautorum: 10.1135/CCCC19820664
453901 - Kopsia arborea: 10.1248/CPB.7.129
278673 - Petasites hybridus: 10.1135/CCCC19621393
212690 - Picris hieracioides: 10.1248/CPB.43.1634
1331808 - Raulinoa echinata: 10.1078/0944-7113-00016
189242 - Senecio nemorensis: 10.1135/CCCC19811048
2707859 - Solidago chilensis: 10.1016/0031-9422(92)80433-F
3979 - Suregada multiflora: 10.1016/0031-9422(89)80205-5
13702 - Symphoricarpos albus: 10.1016/S0031-9422(00)80074-6
118778 - Tussilago farfara: 10.1016/J.BSE.2007.07.003

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

Jung Yeon Han, Hye-Jeong Jo, Eun Kyung Kwon, Yong Eui Choi. Cloning and Characterization of Oxidosqualene Cyclases Involved in Taraxasterol, Taraxerol and Bauerenol Triterpene Biosynthesis in Taraxacum coreanum. Plant & cell physiology. 2019 Jul; 60(7):1595-1603. doi: 10.1093/pcp/pcz062. [PMID: 31020326]
Perumal Sathish Kumar, Madepalli Byrappa Gowdu Viswanathan, Muthappan Venkatesan, Kedike Balakrishna. Bauerenol, a triterpenoid from Indian Suregada angustifolia: Induces reactive oxygen species-mediated P38MAPK activation and apoptosis in human hepatocellular carcinoma (HepG2) cells. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine. 2017 Apr; 39(4):1010428317698387. doi: 10.1177/1010428317698387. [PMID: 28443465]
Cristina Setim Freitas, Cristiane Hatsuko Baggio, Ana Cristina Dos Santos, Bárbara Mayer, André Twardowschy, Ana Paula Luiz, Rodrigo Marcon, Cristian Soldi, Moacir G Pizzolatti, Elide Pereira Dos Santos, Maria Consuelo Andrade Marques, Adair R S Santos. Antinociceptive properties of the hydroalcoholic extract, fractions and compounds obtained from the aerial parts of Baccharis illinita DC in mice. Basic & clinical pharmacology & toxicology. 2009 Apr; 104(4):285-92. doi: 10.1111/j.1742-7843.2008.00367.x. [PMID: 19281601]
Irene M Villaseñor, Arlyn P Canlas, Karen M Faustino, Katherine G Plana. Evaluation of the bioactivity of triterpene mixture isolated from Carmona retusa (Vahl.) Masam leaves. Journal of ethnopharmacology. 2004 May; 92(1):53-6. doi: 10.1016/j.jep.2004.01.017. [PMID: 15099847]