11b,17a,21-Trihydroxypreg-nenolone (BioDeep_00000896078)
Main id: BioDeep_00000637540
human metabolite Endogenous
代谢物信息卡片
化学式: C21H32O5 (364.2249622)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC12CC(O)C3C(CC=C4CC(O)CCC34C)C1CC[C@]2(O)C(=O)CO
InChI: InChI=1S/C21H32O5/c1-19-7-5-13(23)9-12(19)3-4-14-15-6-8-21(26,17(25)11-22)20(15,2)10-16(24)18(14)19/h3,13-16,18,22-24,26H,4-11H2,1-2H3/t13-,14-,15-,16-,18+,19-,20-,21-/m0/s1
描述信息
11beta,17alpha,21-Trihydroxypregnenolone is an intermediate in C21-Steroid hormone metabolism. 11beta,17alpha,21-Trihydroxypregnenolone is the 4th to last step in the synthesis of Cortol and is converted from 17alpha,21-Dihydroxypregnenolone via the enzyme cytochrome P450 (EC:1.14.15.4). It is then converted to Cortisol via the enzyme 3beta-hydroxy-delta5-steroid dehydrogenase (EC 1.1.1.145) and the enzyme steroid delta-isomerase (EC 5.3.3.1). [HMDB]
11beta,17alpha,21-Trihydroxypregnenolone is an intermediate in C21-Steroid hormone metabolism. 11beta,17alpha,21-Trihydroxypregnenolone is the 4th to last step in the synthesis of Cortol and is converted from 17alpha,21-Dihydroxypregnenolone via the enzyme cytochrome P450 (EC:1.14.15.4). It is then converted to Cortisol via the enzyme 3beta-hydroxy-delta5-steroid dehydrogenase (EC 1.1.1.145) and the enzyme steroid delta-isomerase (EC 5.3.3.1).
同义名列表
6 个代谢物同义名
2-hydroxy-1-[(17R)-3,11,17-trihydroxy-10,13-dimethyl-1,2,3,4,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl]ethanone; 2-hydroxy-1-[(14R)-5,14,17-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-14-yl]ethan-1-one; 2-hydroxy-1-[(14R)-5,14,17-trihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-14-yl]ethanone; 11beta,17alpha,21-Trihydroxypreg-nenolone; 11beta,17alpha,21-trihydroxypregnenolone; 11b,17a,21-Trihydroxypreg-nenolone
数据库引用编号
13 个数据库交叉引用编号
- ChEBI: CHEBI:171954
- ChEBI: CHEBI:27783
- KEGG: C05489
- PubChem: 11966170
- PubChem: 440708
- HMDB: HMDB0006760
- foodb: FDB024064
- chemspider: 389583
- CAS: 1050-84-6
- PubChem: 7848
- LipidMAPS: LMST02030166
- 3DMET: B05061
- NIKKAJI: J2.756.014H
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
34 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(34)
- Steroidogenesis:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Adrenal Hyperplasia Type 3 or Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia Due to 17 alpha-Hydroxylase Deficiency:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 17-alpha-Hydroxylase Deficiency (CYP17):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 11-beta-Hydroxylase Deficiency (CYP11B1):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 21-Hydroxylase Deficiency (CYP21):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Corticosterone Methyl Oxidase I Deficiency (CMO I):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Corticosterone Methyl Oxidase II Deficiency (CMO II):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Apparent Mineralocorticoid Excess Syndrome:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 3-beta-Hydroxysteroid Dehydrogenase Deficiency:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Steroidogenesis:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Adrenal Hyperplasia Type 3 or Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia Due to 17 alpha-Hydroxylase Deficiency:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 17-alpha-Hydroxylase Deficiency (CYP17):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 11-beta-Hydroxylase Deficiency (CYP11B1):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 21-Hydroxylase Deficiency (CYP21):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Corticosterone Methyl Oxidase I Deficiency (CMO I):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Corticosterone Methyl Oxidase II Deficiency (CMO II):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Apparent Mineralocorticoid Excess Syndrome:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 3-beta-Hydroxysteroid Dehydrogenase Deficiency:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Steroidogenesis:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Steroidogenesis:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Adrenal Hyperplasia Type 3 or Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Adrenal Hyperplasia Type 5 or Congenital Adrenal Hyperplasia Due to 17 alpha-Hydroxylase Deficiency:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Congenital Lipoid Adrenal Hyperplasia (CLAH) or Lipoid CAH:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 17-alpha-Hydroxylase Deficiency (CYP17):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 11-beta-Hydroxylase Deficiency (CYP11B1):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 21-Hydroxylase Deficiency (CYP21):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Corticosterone Methyl Oxidase I Deficiency (CMO I):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Corticosterone Methyl Oxidase II Deficiency (CMO II):
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- Apparent Mineralocorticoid Excess Syndrome:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
- 3-beta-Hydroxysteroid Dehydrogenase Deficiency:
Cortexolone + Oxygen + Reduced adrenal ferredoxin ⟶ Cortisol + Oxidized adrenal ferredoxin + Water
PharmGKB(0)
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- 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。
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