Camelliol C (BioDeep_00000013090)

human metabolite Endogenous natural product

代谢物信息卡片

4,6,6-trimethyl-5-[(3Z,7E,11Z)-3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraen-1-yl]cyclohex-3-en-1-ol

化学式: C30H50O (426.386145)
中文名称:
谱图信息: 最多检出来源 Bos taurus(blood) 38.46%

分子结构信息

SMILES: CC(C)=CCC/C(C)=C/CC/C(C)=C/CC/C=C(\C)CC[C@@H]1C(C)=CC[C@H](O)C1(C)C
InChI: InChI=1S/C30H50O/c1-23(2)13-11-16-25(4)18-12-17-24(3)14-9-10-15-26(5)19-21-28-27(6)20-22-29(31)30(28,7)8/h13-15,18,20,28-29,31H,9-12,16-17,19,21-22H2,1-8H3/b24-14+,25-18-,26-15-

描述信息

Camelliol C is found in fats and oils. Camelliol C is a constituent of sasanqua oil (Camellia sasanqua).
Constituent of sasanqua oil (Camellia sasanqua). Camelliol C is found in tea and fats and oils.

同义名列表

3 个代谢物同义名

4,6,6-trimethyl-5-[(3Z,7E,11Z)-3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraen-1-yl]cyclohex-3-en-1-ol; 4,6,6-trimethyl-5-[(3Z,7E,11Z)-3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraenyl]cyclohex-3-en-1-ol; Camelliol C

数据库引用编号

15 个数据库交叉引用编号

ChEBI: CHEBI:62452
KEGG: C19835
PubChem: 131751388
PubChem: 78412146
PubChem: 6476390
HMDB: HMDB0033195
Metlin: METLIN73388
ChEMBL: CHEMBL463552
KNApSAcK: C00045251
foodb: FDB011207
chemspider: 35013558
CAS: 220359-76-2
PMhub: MS000027476
PubChem: 135626302
LOTUS: LTS0089201

分类词条

代谢反应

1 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(1)

Triterpenoid Biosynthesis: Hydrogen Ion + NADPH + Presqualene diphosphate ⟶ NADP + Pyrophosphate + Squalene

PharmGKB(0)

22 个相关的物种来源信息

4441 - Camellia: LTS0089201
4443 - Camellia japonica: 10.1007/S11745-999-0466-5
4443 - Camellia japonica: LTS0089201
385388 - Camellia oleifera:
385388 - Camellia oleifera: 10.1007/S11745-999-0466-5
385388 - Camellia oleifera: 10.1021/NP980336A
385388 - Camellia oleifera: LTS0089201
182300 - Camellia sasanqua:
182300 - Camellia sasanqua: 10.1007/S11745-999-0466-5
182300 - Camellia sasanqua: 10.1021/NP980336A
182300 - Camellia sasanqua: LTS0089201
2759 - Eukaryota: LTS0089201
3990 - Euphorbia: LTS0089201
334664 - Euphorbia antiquorum: 10.1021/NP010377Y
334664 - Euphorbia antiquorum: LTS0089201
3977 - Euphorbiaceae: LTS0089201
9606 - Homo sapiens: -
3398 - Magnoliopsida: LTS0089201
35493 - Streptophyta: LTS0089201
27065 - Theaceae: LTS0089201
58023 - Tracheophyta: LTS0089201
33090 - Viridiplantae: LTS0089201

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

Ruoshi Huang, Duan Wu, Zhongju Ji, Baolian Fan, Yaru She, Xiande Zhang, Lixin Duan, Qi Shen. Characterization of a Group of 2,3-Oxidosqualene Cyclase Genes Involved in the Biosynthesis of Diverse Triterpenoids of Perilla frutescens. Journal of agricultural and food chemistry. 2023 Feb; 71(5):2523-2531. doi: 10.1021/acs.jafc.2c07716. [PMID: 36705014]
Guo-Yan Mo, Fang Huang, Yin Fang, Lin-Tao Han, Kayla K Pennerman, Li-Jing Bu, Xiao-Wei DU, Joan W Bennett, Guo-Hua Yin. Transcriptomic analysis in Anemone flaccida rhizomes reveals ancillary pathway for triterpene saponins biosynthesis and differential responsiveness to phytohormones. Chinese journal of natural medicines. 2019 Feb; 17(2):131-144. doi: 10.1016/s1875-5364(19)30015-9. [PMID: 30797419]
T Akihisa, J Ogihara, J Kato, K Yasukawa, M Ukiya, S Yamanouchi, K Oishi. Inhibitory effects of triterpenoids and sterols on human immunodeficiency virus-1 reverse transcriptase. Lipids. 2001 May; 36(5):507-12. doi: 10.1007/s11745-001-0750-4. [PMID: 11432464]