Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0L0ZP
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| Former ID |
DNC006469
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| Drug Name |
3-methoxy-4-(oxazol-5-yl)aniline
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| Synonyms |
3-methoxy-4-(oxazol-5-yl)aniline; 198821-79-3; 3-METHOXY-4-(1,3-OXAZOL-5-YL)ANILINE; Benzenamine, 3-methoxy-4-(5-oxazolyl)-; 3-methoxy-4-(5-oxazolyl)aniline; CHEMBL45870; 5-(4-amino-2-methoxyphenyl)oxazole; AK116113; A1-00139; SCHEMBL1353846; CTK4E2632; KS-00000NNJ; DTXSID80572997; MolPort-006-666-066; KYCMMXMEXWSPCV-UHFFFAOYSA-N; ZINC2518269; FCH848314; 3-methoxy-4-(oxazol-5-yl) aniline; BDBM50127715; 3-Methoxy-4-oxazol-5-yl-phenylamine; AKOS006278384; CS-W005501; MP-1879; DS-2798; 3-methoxy-4-(oxazol-5-yl)benzenamine; AJ-37081
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C10H10N2O2
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| Canonical SMILES |
COC1=C(C=CC(=C1)N)C2=CN=CO2
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| InChI |
1S/C10H10N2O2/c1-13-9-4-7(11)2-3-8(9)10-5-12-6-14-10/h2-6H,11H2,1H3
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| InChIKey |
KYCMMXMEXWSPCV-UHFFFAOYSA-N
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| CAS Number |
CAS 198821-79-3
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Inosine-5'-monophosphate dehydrogenase 2 (IMPDH2) | Target Info | Inhibitor | [1] |
| BioCyc | Purine nucleotides degradation | |||
| Urate biosynthesis/inosine 5'-phosphate degradation | ||||
| Guanosine nucleotides de novo biosynthesis | ||||
| Superpathway of purine nucleotide salvage | ||||
| Purine nucleotides de novo biosynthesis | ||||
| Guanosine ribonucleotides de novo biosynthesis | ||||
| KEGG Pathway | Purine metabolism | |||
| Drug metabolism - other enzymes | ||||
| Metabolic pathways | ||||
| Panther Pathway | De novo purine biosynthesis | |||
| Reactome | Purine ribonucleoside monophosphate biosynthesis | |||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Low molecular weight indole fragments as IMPDH inhibitors. Bioorg Med Chem Lett. 2006 May 1;16(9):2535-8. | |||
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