Glisoxepide (BioDeep_00000033315)
human metabolite blood metabolite
代谢物信息卡片
化学式: C20H27N5O5S (449.1732812000001)
中文名称: 格列派特
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC1=CC(=NO1)C(=O)NCCC1=CC=C(C=C1)S(=O)(=O)NC(=O)NN1CCCCCC1
InChI: InChI=1S/C20H27N5O5S/c1-15-14-18(23-30-15)19(26)21-11-10-16-6-8-17(9-7-16)31(28,29)24-20(27)22-25-12-4-2-3-5-13-25/h6-9,14H,2-5,10-13H2,1H3,(H,21,26)(H2,22,24,27)
描述信息
Glisoxepide is one of the sulphonamide-derived oral antidiabetic drugs. It inhibits the uptake of bile acids into isolated rat hepatocytes. However it inhibits taurocholate uptake only in the absence of sodium ions. Glisoxepide uptake could be further inhibited by blockers of the hepatocellular monocarboxylate transporter, by the loop diuretic bumetanide, by 4,4-diisothiocyano-2,2-stilbenedisulfonate (DIDS) and by sulphate. These results are consistent with the transport of glisoxepide via the transport system for the unconjugated bile acid cholate. (PMID:1618280, 9017793).
A - Alimentary tract and metabolism > A10 - Drugs used in diabetes > A10B - Blood glucose lowering drugs, excl. insulins > A10BB - Sulfonylureas
C78276 - Agent Affecting Digestive System or Metabolism > C29711 - Anti-diabetic Agent > C97936 - Sulfonylurea Antidiabetic Agent
同义名列表
数据库引用编号
9 个数据库交叉引用编号
- ChEBI: CHEBI:135731
- PubChem: 32778
- HMDB: HMDB0015406
- DrugBank: DB01289
- ChEMBL: CHEMBL2106618
- Wikipedia: Glisoxepide
- chemspider: 30380
- CAS: 25046-79-1
- RefMet: Glisoxepide
分类词条
相关代谢途径
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代谢反应
0 个相关的代谢反应过程信息。
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1 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。
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文献列表
- Tobie D Lee, Olivia W Lee, Kyle R Brimacombe, Lu Chen, Rajarshi Guha, Sabrina Lusvarghi, Bethilehem G Tebase, Carleen Klumpp-Thomas, Robert W Robey, Suresh V Ambudkar, Min Shen, Michael M Gottesman, Matthew D Hall. A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Molecular pharmacology.
2019 11; 96(5):629-640. doi:
10.1124/mol.119.115964
. [PMID: 31515284] - Cornelius Hess, Frank Musshoff, Burkhard Madea. Simultaneous identification and validated quantification of 11 oral hypoglycaemic drugs in plasma by electrospray ionisation liquid chromatography-mass spectrometry.
Analytical and bioanalytical chemistry.
2011 Apr; 400(1):33-41. doi:
10.1007/s00216-011-4698-8
. [PMID: 21327875] - Toshiaki Sato, Alexandre D T Costa, Tomoaki Saito, Takehiko Ogura, Hideyuki Ishida, Keith D Garlid, Haruaki Nakaya. Bepridil, an antiarrhythmic drug, opens mitochondrial KATP channels, blocks sarcolemmal KATP channels, and confers cardioprotection.
The Journal of pharmacology and experimental therapeutics.
2006 Jan; 316(1):182-8. doi:
10.1124/jpet.105.094029
. [PMID: 16174795] - Guillaume Hoizey, Denis Lamiable, Thierry Trenque, Arnaud Robinet, Laurent Binet, Matthieu L Kaltenbach, Sandrine Havet, Hervé Millart. Identification and quantification of 8 sulfonylureas with clinical toxicology interest by liquid chromatography-ion-trap tandem mass spectrometry and library searching.
Clinical chemistry.
2005 Sep; 51(9):1666-72. doi:
10.1373/clinchem.2005.050864
. [PMID: 16020498] - Hans H Maurer, Carsten Kratzsch, Thomas Kraemer, Frank T Peters, Armin A Weber. Screening, library-assisted identification and validated quantification of oral antidiabetics of the sulfonylurea-type in plasma by atmospheric pressure chemical ionization liquid chromatography-mass spectrometry.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
2002 Jun; 773(1):63-73. doi:
10.1016/s1570-0232(01)00618-3
. [PMID: 12015271]