7-Ketocholesterol (BioDeep_00000018887)
Secondary id: BioDeep_00000405287
human metabolite PANOMIX_OTCML-2023 Endogenous blood metabolite natural product
代谢物信息卡片
化学式: C27H44O2 (400.3341124)
中文名称: 胆甾-3-羟基-5-烯-7-酮
谱图信息:
最多检出来源 Chinese Herbal Medicine(otcml) 0.57%
分子结构信息
SMILES: CC(C)CCCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C
InChI: InChI=1S/C27H44O2/c1-17(2)7-6-8-18(3)21-9-10-22-25-23(12-14-27(21,22)5)26(4)13-11-20(28)15-19(26)16-24(25)29/h16-18,20-23,25,28H,6-15H2,1-5H3/t18-,20?,21?,22+,23+,25+,26+,27-/m1/s1
描述信息
7-Ketocholesterol is a major oxidation product of cholesterol (oxysterol) found in human atherosclerotic plaque and is more atherogenic than cholesterol in some animal studies. Oxysterols (oxygenated forms of cholesterol) are present at low levels in the circulation and accumulate is plasma and tissues in some pathologies. In atherosclerotic lesions, 7-oxygenated oxysterols, predominantly 7-ketocholesterol, accumulate and have been implicated in the pathology of the disease. There is some in vivo and in vitro evidence that sterol 27-hydroxylase acts on 7-ketocholesterol to initiate its degradation to more polar, water-soluble products. Recent studies indicate an alternative mechanism, in which 7-ketocholesterol is reduced to 7 beta-hydroxycholesterol by 11 beta-hydroxysteroid dehydrogenase type 1. 7-Ketocholesterol can inhibit cholesterol 7 alpha-hydroxylase, the rate-limiting step in bile acid biosynthesis, as well as strongly inhibiting HMG-CoA reductase, the rate-limiting enzyme in cholesterol biosynthesis. It has even been suggested that 7-ketocholesterol is formed enzymically as an endogenous regulator of cholesterol biosynthesis. However, when tested as a pharmacological cholesterol-lowering agent, inhibition of HMG-CoA reductase was rapidly overcome and the 7-ketocholesterol metabolised. In vitro, 7-ketocholesterol has wide-ranging and potent effects, most of which have the potential to contribute to atherosclerosis. For example, 7-ketocholesterol can be cytotoxic and can induce apoptosis in vascular cells. These effects, either individually or more likely, in combination, all implicate 7-ketocholesterol in the initiation and development of atherosclerosis, but further work is needed to establish whether or not its role is a direct causal one. 7-Ketocholesterol is the second most abundant oxysterol found in human atherosclerotic plaque, after the enzymically formed 27-hydroxycholesterol (cholest-5-ene-3beta,27-diol). 7-Ketocholesterol differs from cholesterol by a ketone functional group present at the 7-position. It is produced from cholesterol via the epimeric cholesterol 7-hydroperoxides (cholest-5-ene-3beta-ol-7-hydroperoxide) which decompose to the epimeric 7-hydroxycholesterols (cholest-5-ene-3beta,7-diol) and 7-ketocholesterol. 7-Ketocholesterol is a major dietary oxysterol. It has also been widely suggested that 7-ketocholesterol present in atherosclerotic tissue may be derived from the diet. Certainly, 7-ketocholesterol is a major oxysterol found in cholesterol-rich processed foodstuffs. Dietary 7-ketocholesterol is rapidly metabolised by the liver to 7beta-hydroxycholesterol (cholest-5-ene-3beta,7beta-diol), unusual bile acids and perhaps even cholesterol itself. Its conversion to 7beta-hydroxycholesterol is well documented. (PMID: 15798369, 10224662).
7-Ketocholesterol is a major oxidation product of cholesterol (oxysterol) found in human atherosclerotic plaque and is more atherogenic than cholesterol in some animal studies. Oxysterols (oxygenated forms of cholesterol) are present at low levels in the circulation and accumulate is plasma and tissues in some pathologies. In atherosclerotic lesions, 7-oxygenated oxysterols, predominantly 7-ketocholesterol, accumulate and have been implicated in the pathology of the disease. There is some in vivo and in vitro evidence that sterol 27-hydroxylase acts on 7-ketocholesterol to initiate its degradation to more polar, water-soluble products. Recent studies indicate an alternative mechanism, in which 7-ketocholesterol is reduced to 7 beta-hydroxycholesterol by 11 beta-hydroxysteroid dehydrogenase type 1.
7-Ketocholesterol, toxic oxysterol, inhibits the rate-limiting step in bile acid biosynthesis cholesterol 7 alpha-hydroxylase, as well as strongly inhibiting HMG-CoA reductase (the rate-limiting enzyme in cholesterol biosynthesis). 7-Ketocholesterol induces cell apoptosis[1].
同义名列表
9 个代谢物同义名
(1S,2R,10S,11S,15R)-5-hydroxy-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one; 3-hydroxy-10,13-dimethyl-17-(6-methylheptan-2-yl)-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one; 3beta-Hydroxy-5-cholestene-7-one; Delta5-Cholesten-3b-ol-7-one; 3b-Hydroxycholest-5-en-7-one; 5-Cholesten-3 beta-ol-7-one; Cholest-5-en-3b-ol-7-one; 7-KETOCHOLESTEROL; 7-Oxocholesterol
数据库引用编号
8 个数据库交叉引用编号
- PubChem: 53477696
- HMDB: HMDB0000501
- foodb: FDB022079
- chemspider: 59651438
- CAS: 566-28-9
- PMhub: MS000012080
- medchemexpress: HY-113342
- LOTUS: LTS0051197
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)
73 个相关的物种来源信息
- 3319 - Abies: LTS0051197
- 56046 - Abies pinsapo: LTS0051197
- 928731 - Abies pinsapo var. marocana: 10.1016/S0031-9422(00)94835-0
- 928731 - Abies pinsapo var. marocana: LTS0051197
- 186623 - Actinopteri: LTS0051197
- 7898 - Actinopterygii: LTS0051197
- 8292 - Amphibia: LTS0051197
- 77184 - Ancorinidae: LTS0051197
- 6656 - Arthropoda: LTS0051197
- 6525 - Biomphalaria: LTS0051197
- 112528 - Biomphalaria tenagophila: 10.1007/BF02534802
- 112528 - Biomphalaria tenagophila: LTS0051197
- 7089 - Bombycidae: LTS0051197
- 7090 - Bombyx: LTS0051197
- 7091 - Bombyx mori: 10.1248/CPB.32.3003
- 7091 - Bombyx mori: LTS0051197
- 10205 - Bryozoa: LTS0051197
- 3071 - Chlorella: LTS0051197
- 3077 - Chlorella vulgaris: 10.1248/BPB.19.573
- 3077 - Chlorella vulgaris: LTS0051197
- 35461 - Chlorellaceae: LTS0051197
- 3041 - Chlorophyta: LTS0051197
- 7711 - Chordata: LTS0051197
- 76785 - Cliona: LTS0051197
- 395614 - Cliona copiosa: 10.1021/NP50089A005
- 395614 - Cliona copiosa: LTS0051197
- 76786 - Cliona viridis: 10.1021/NP50089A005
- 76786 - Cliona viridis: LTS0051197
- 76784 - Clionaidae: LTS0051197
- 4630 - Costaceae: LTS0051197
- 4631 - Costus: LTS0051197
- 2172426 - Costus tonkinensis: 10.1016/S0031-9422(97)00101-5
- 2172426 - Costus tonkinensis: LTS0051197
- 558754 - Cryptosula: LTS0051197
- 558755 - Cryptosula pallasiana: 10.3390/MD9020162
- 558755 - Cryptosula pallasiana: LTS0051197
- 558762 - Cryptosulidae: LTS0051197
- 6042 - Demospongiae: LTS0051197
- 2759 - Eukaryota: LTS0051197
- 2806 - Florideophyceae: LTS0051197
- 6448 - Gastropoda: LTS0051197
- 10206 - Gymnolaemata: LTS0051197
- 9606 - Homo sapiens: -
- 50557 - Insecta: LTS0051197
- 4447 - Liliopsida: LTS0051197
- 3398 - Magnoliopsida: LTS0051197
- 1917068 - Melanothamnus: LTS0051197
- 1917069 - Melanothamnus somalensis: 10.1016/0031-9422(96)00027-1
- 1917069 - Melanothamnus somalensis: LTS0051197
- 33208 - Metazoa: LTS0051197
- 6447 - Mollusca: LTS0051197
- 118318 - Myxillidae: LTS0051197
- 3070 - Oocystaceae: LTS0051197
- 3318 - Pinaceae: LTS0051197
- 58019 - Pinopsida: LTS0051197
- 6524 - Planorbidae: LTS0051197
- 6040 - Porifera: LTS0051197
- 8399 - Rana: LTS0051197
- 8407 - Rana temporaria: 10.1080/14786419.2010.484391
- 8407 - Rana temporaria: LTS0051197
- 8397 - Ranidae: LTS0051197
- 2803 - Rhodomelaceae: LTS0051197
- 2763 - Rhodophyta: LTS0051197
- 253167 - Stelletta: LTS0051197
- 35493 - Streptophyta: LTS0051197
- 72045 - Syngnathidae: LTS0051197
- 32443 - Teleostei: LTS0051197
- 58023 - Tracheophyta: LTS0051197
- 161593 - Trachyrhamphus: LTS0051197
- 161594 - Trachyrhamphus serratus: 10.1007/S10600-011-9966-5
- 161594 - Trachyrhamphus serratus: LTS0051197
- 75966 - Trebouxiophyceae: LTS0051197
- 33090 - Viridiplantae: LTS0051197
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。