Betulone (BioDeep_00000397294)
Chemicals and Drugs natural product
代谢物信息卡片
化学式: C30H48O2 (440.36541079999995)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C=C(C)[C@@H]1CC[C@]2(CO)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CCC(=O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12
InChI: InChI=1S/C30H48O2/c1-19(2)20-10-15-30(18-31)17-16-28(6)21(25(20)30)8-9-23-27(5)13-12-24(32)26(3,4)22(27)11-14-29(23,28)7/h20-23,25,31H,1,8-18H2,2-7H3/t20-,21+,22-,23+,25+,27-,28+,29+,30+/m0/s1
描述信息
Betulone is a triterpenoid. It has a role as a metabolite. It derives from a hydride of a lupane.
Betulone is a natural product found in Euonymus carnosus, Salacia chinensis, and other organisms with data available.
A natural product found in Cupania cinerea.
同义名列表
5 个代谢物同义名
(1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one; (1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-1-isopropenyl-5a,5b,8,8,11a-pentamethyl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one; 28-hydroxy-lup-20(29)-en-3-one; 3-Oxobetulin; Betulone
数据库引用编号
7 个数据库交叉引用编号
- ChEBI: CHEBI:67824
- PubChem: 10411004
- ChEMBL: CHEMBL469284
- CAS: 7020-34-0
- medchemexpress: HY-N9378
- MetaboLights: MTBLC67824
- LOTUS: LTS0222075
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)
42 个相关的物种来源信息
- 3808 - Acacia: LTS0222075
- 4294 - Aquifoliaceae: LTS0222075
- 3504 - Betula: LTS0222075
- 216994 - Betula lenta: 10.1515/HFSG.1991.45.4.265
- 216994 - Betula lenta: LTS0222075
- 3505 - Betula pendula: LTS0222075
- 1689654 - Betula pendula subsp. mandshurica: 10.1248/CPB.44.1033
- 1689654 - Betula pendula subsp. mandshurica: LTS0222075
- 78630 - Betula platyphylla: 10.1248/CPB.44.1033
- 78630 - Betula platyphylla: LTS0222075
- 216988 - Betula platyphylla var. japonica: 10.1248/CPB.44.1033
- 216988 - Betula platyphylla var. japonica: LTS0222075
- 216986 - Betula schmidtii: 10.1248/CPB.46.1051
- 216986 - Betula schmidtii: LTS0222075
- 3514 - Betulaceae: LTS0222075
- 4305 - Celastraceae: LTS0222075
- 61134 - Ceriops: LTS0222075
- 61143 - Ceriops tagal: 10.1080/10286020.2010.485566
- 61143 - Ceriops tagal: LTS0222075
- 3954 - Combretaceae: LTS0222075
- 2759 - Eukaryota: LTS0222075
- 3803 - Fabaceae: LTS0222075
- 4295 - Ilex: LTS0222075
- 58305 - Ilex macropoda: 10.1007/BF02976931
- 58305 - Ilex macropoda: LTS0222075
- 3398 - Magnoliopsida: LTS0222075
- 2364055 - Monteverdia: LTS0222075
- 115001 - Platypodium: LTS0222075
- 115002 - Platypodium elegans: 10.1016/S0367-326X(00)00279-3
- 115002 - Platypodium elegans: LTS0222075
- 40029 - Rhizophoraceae: LTS0222075
- 4319 - Salacia: LTS0222075
- 1009589 - Salacia chinensis: 10.1016/J.TET.2008.05.054
- 1009589 - Salacia chinensis: LTS0222075
- 670368 - Salacia cordata: 10.1021/NP50081A020
- 381101 - Senegalia mellifera: 10.1016/J.PHYTOCHEM.2004.03.002
- 35493 - Streptophyta: LTS0222075
- 39992 - Terminalia: LTS0222075
- 1924228 - Terminalia glabrescens: 10.1590/S0103-50532003000300021
- 1924228 - Terminalia glabrescens: LTS0222075
- 58023 - Tracheophyta: LTS0222075
- 33090 - Viridiplantae: LTS0222075
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
- Lía S Valencia-Chan, Isabel García-Cámara, Luis W Torres-Tapia, Rosa E Moo-Puc, Sergio R Peraza-Sánchez. Lupane-Type Triterpenes of Phoradendron vernicosum.
Journal of natural products.
2017 11; 80(11):3038-3042. doi:
10.1021/acs.jnatprod.7b00177
. [PMID: 29120172] - Oliver Callies, Luis M Bedoya, Manuela Beltrán, Alejandro Muñoz, Patricia Obregón Calderón, Alex A Osorio, Ignacio A Jiménez, José Alcamí, Isabel L Bazzocchi. Isolation, Structural Modification, and HIV Inhibition of Pentacyclic Lupane-Type Triterpenoids from Cassine xylocarpa and Maytenus cuzcoina.
Journal of natural products.
2015 May; 78(5):1045-55. doi:
10.1021/np501025r
. [PMID: 25927586] - Jian Zhou, Chuang-Jun Li, Jing-Zhi Yang, Jie Ma, Yan Li, Xiu-Qi Bao, Xiao-Guang Chen, Dan Zhang, Dong-Ming Zhang. Lupane triterpenoids from the stems of Euonymus carnosus.
Journal of natural products.
2014 Feb; 77(2):276-84. doi:
10.1021/np400851k
. [PMID: 24467317]