all-trans-4-Oxoretinoic acid (BioDeep_00001874726)
Main id: BioDeep_00000019605
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C20H26O3 (314.1881846)
中文名称: 4-氧代-维A酸
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1C(C)(C)C(/C=C/C(=C/C=C/C(=C/C(=O)O)/C)/C)=C(C)C(=O)C1
InChI: InChI=1S/C20H26O3/c1-14(7-6-8-15(2)13-19(22)23)9-10-17-16(3)18(21)11-12-20(17,4)5/h6-10,13H,11-12H2,1-5H3,(H,22,23)/b8-6+,10-9+,14-7+,15-13+
描述信息
A retinoid that consists of all-trans-retinoic acid bearing an oxo substituent at position 4 on the cyclohexenyl ring.
D020011 - Protective Agents > D000975 - Antioxidants > D002338 - Carotenoids
all-trans-4-Oxoretinoic acid, an active metabolite of vitamin A, induces gene transcription via binding to nuclear retinoic acid receptors (RARs).
同义名列表
数据库引用编号
11 个数据库交叉引用编号
- ChEBI: CHEBI:80656
- KEGG: C16678
- PubChem: 6437063
- ChEMBL: CHEMBL104049
- LipidMAPS: LMPR01090026
- CAS: 1346606-26-5
- CAS: 38030-57-8
- MetaboLights: MTBLC80656
- PubChem: 51091001
- NIKKAJI: J362.532J
- medchemexpress: HY-107494A
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)
0 个相关的物种来源信息
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
- Poonam Sonawane, Hwang Eui Cho, Ashujit Tagde, Dattesh Verlekar, Alice L Yu, C Patrick Reynolds, Min H Kang. Metabolic characteristics of 13-cis-retinoic acid (isotretinoin) and anti-tumour activity of the 13-cis-retinoic acid metabolite 4-oxo-13-cis-retinoic acid in neuroblastoma.
British journal of pharmacology.
2014 Dec; 171(23):5330-44. doi:
10.1111/bph.12846
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The British journal of dermatology.
2009 Sep; 161(3):664-70. doi:
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2006; 20(16):2497-504. doi:
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Journal of lipid research.
2002 Jul; 43(7):1133-42. doi:
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Journal of chromatography. B, Biomedical sciences and applications.
1997 Jun; 694(1):83-92. doi:
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Journal of chromatography. B, Biomedical sciences and applications.
1997 Mar; 691(1):43-58. doi:
10.1016/s0378-4347(96)00434-3
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British journal of cancer.
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Journal of nutritional science and vitaminology.
1995 Aug; 41(4):493-8. doi:
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Toxicology and applied pharmacology.
1994 Mar; 125(1):34-41. doi:
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Biochemical pharmacology.
1994 Feb; 47(4):737-41. doi:
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Archives of toxicology.
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The Journal of nutrition.
1991 Jul; 121(7):1016-25. doi:
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1991 Mar; 24(3):425-8. doi:
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. [PMID: 1829464] - C Eckhoff, H Nau. Identification and quantitation of all-trans- and 13-cis-retinoic acid and 13-cis-4-oxoretinoic acid in human plasma.
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. [PMID: 2275606] - W L Davis, L A Crawford, O J Cooper, G R Farmer, D Thomas, B L Freeman. Generation of radical oxygen species by neural crest cells treated in vitro with isotretinoin and 4-oxo-isotretinoin.
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. [PMID: 2749577] - W B Howard, C C Willhite, S T Omaye, R P Sharma. Comparative distribution, pharmacokinetics and placental permeabilities of all-trans-retinoic acid, 13-cis-retinoic acid, all-trans-4-oxo-retinoic acid, retinyl acetate and 9-cis-retinal in hamsters.
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. [PMID: 2730336] - R Wyss, F Bucheli. Quantitative analysis of retinoids in biological fluids by high-performance liquid chromatography using column switching. I. Determination of isotretinoin and tretinoin and their 4-oxo metabolites in plasma.
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