| Weight | 110.116 g/mol |
|---|---|
| Formula | C5H6N2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
1H-Pyrrole-2-carboxamide (4551-72-8)
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- Kinesin spindle protein (KSP) inhibitors. 9. Discovery of (2S)-4-(2,5-difluorophenyl)-n-[(3R,4S)-3-fluoro-1-methylpiperidin-4-yl]-2-(hydroxymethyl)-N-methyl-2-phenyl-2,5-dihydro-1H-pyrrole-1-carboxamide (MK-0731) for the treatment of taxane-refractory cancer. (Journal of Medicinal Chemistry, 2008)
- Synthesis and D2-like binding affinity of new derivatives of N-(1-ethyl-2-pyrrolidinylmethyl)-4,5-dihydro-1H-benzo[g]indole-3-carboxamide and related 4H-[1]benzothiopyrano[4,3-b]pyrrole and 5,6-dihydro-4H-benzo[6,7]cyclohepta[b]pyrrole-3-carboxamide analogues (Bioorganic & Medicinal Chemistry, 2002)
- A Catalyst System, Copper/N-Methoxy-1H-pyrrole-2-carboxamide, for the Synthesis of Phenothiazines in Poly(ethylene glycol) (Synthesis, 2014)
- 1,4-Phenylene-bis-(3,4-dichloro-5-phenylcarbamoyl-1H-pyrrole-2- carboxamide) bis(tetrabutylammonium chloride) acetonitrile disolvate (Acta Crystallographica Section E-structure Reports Online, 2005)
- Design, synthesis and biological evaluation of 4,5-dibromo-N-(thiazol-2-yl)-1H-pyrrole-2-carboxamide derivatives as novel DNA gyrase inhibitors (Bioorganic & Medicinal Chemistry, 2017)
- 1-Benzyl-N-methyl-1H-pyrrole-2-carboxamide. (Acta Crystallographica Section E-structure Reports Online, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CNC(=C1)C(=O)N
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InChIKeyRLOQBKJCOAXOLR-UHFFFAOYSA-N
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1H-Pyrrole-2-carboxamide
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