Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D0T7UP
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| Former ID |
DNC000060
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| Drug Name |
3-fluorovinylglycine
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| Synonyms |
Fluorovinylglycine; 3-Fluorovinylglycine; FVGly; ACMC-20melc; 3-Butenoic acid, 2-amino-3-fluoro-, (S)-; AC1MIW53; 2-amino-3-fluorobut-3-enoic acid; 2-Amino-3-fluoro-3-butenoic acid; 111687-18-4; AKOS006361808; 3-Butenoic acid, 2-amino-3-fluoro-, (+-)-
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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 |
C4H6FNO2
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| Canonical SMILES |
C=C(C(C(=O)O)N)F
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| InChI |
1S/C4H6FNO2/c1-2(5)3(6)4(7)8/h3H,1,6H2,(H,7,8)
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| InChIKey |
HMOXWHQSNHKKFM-UHFFFAOYSA-N
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| CAS Number |
CAS 111581-52-3
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| PubChem Compound ID | ||||
| PubChem Substance ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Mycobacterium Biosynthetic alanine racemase (MycB alr) | Target Info | Inhibitor | [1] |
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Mechanism-based inactivation of alanine racemase by 3-halovinylglycines. J Biol Chem. 1991 Nov 15;266(32):21657-65. | |||
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