Drug Information
Drug General Information | Top | |||
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Drug ID |
D0R7BT
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Former ID |
DNC003138
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Drug Name |
1-(2,2'-bithiophen-5-yl)methanamine
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Synonyms |
4380-96-5; [2,2'-Bithiophen]-5-ylmethanamine; 2,2'-bithiophene-5-methylamine; 2,2'-bithiophen-5-ylmethanamine; [2,2'-Bithiophene]-5-methanamine; 1-(2,2'-bithiophen-5-yl)methanamine; 2,2-Bithiophene-5-methylamine; CHEMBL538940; (5-(2-thienyl)-2-thienyl)methylamine; [5-(Thiophen-2-Yl)Thiophen-2-Yl]Methanamine; SDCCGMLS-0065983.P001; AC1MCQYM; SCHEMBL2690127; CTK1D7717; DTXSID50380066; MolPort-000-142-515; FHYTVXBZSXZMGD-UHFFFAOYSA-N; ZINC158800; 2,2''-bithiophen-5-ylmethanamine; AC1Q5409; QC-966; SBB091920; BDBM50294164
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C9H9NS2
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Canonical SMILES |
C1=CSC(=C1)C2=CC=C(S2)CN
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InChI |
1S/C9H9NS2/c10-6-7-3-4-9(12-7)8-2-1-5-11-8/h1-5H,6,10H2
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InChIKey |
FHYTVXBZSXZMGD-UHFFFAOYSA-N
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CAS Number |
CAS 4380-96-5
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Leukotriene A-4 hydrolase (LTA4H) | Target Info | Inhibitor | [1] |
BioCyc | Leukotriene biosynthesis | |||
KEGG Pathway | Arachidonic acid metabolism | |||
Metabolic pathways | ||||
Pathwhiz Pathway | Arachidonic Acid Metabolism | |||
WikiPathways | Arachidonic acid metabolism | |||
Eicosanoid Synthesis |
References | Top | |||
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REF 1 | The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42. |
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