| Weight | 116.164 g/mol |
|---|---|
| Formula | C5H12N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Valinamide (4540-60-7, 20108-78-5)
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- Peptide models. 3. Conformational potential energy hypersurface of formyl-L-valinamide (Journal of the American Chemical Society, 1993)
- Synthesis and biological activity of analogues of the antimicrotubule agent N, , -trimethyl-L-phenylalanyl-N1-[(1S, 2E)-3-carboxy-1-isopropylbut-2-enyl]-N1, 3 -dimethyl-L-valinamide (HTI-286) (Journal of Medicinal Chemistry, 2004)
- CONCURRENT INDUCTION AND MECHANISM-BASED INACTIVATION OF CYP3A4 BY AN L-VALINAMIDE DERIVATIVE (Drug Metabolism and Disposition, 2003)
- Optimized preparation of deca(L-Alanyl)-L-valinamide by 9-fluorenylmethyloxycarbonyl (fmoc) solid-phase synthesis on polyethylene glycol-polystyrene (PEG-PS) graft supports, with 1,8-diazobicyclo[5.4.0]-undec-7-ene (DBU) deprotection (Peptide research, 1996)
- Effect of the Bulky Side Chain on the Backbone Structure of the Amino Acid Derivative Valinamide (Journal of Physical Chemistry A, 2002)
- Peptide Models XXXI. Conformational Properties of Hydrophobic Residues Shaping the Core of Proteins. An Ab Initio Study of N-Formyl-L-Valinamide and N-Formyl-L-Phenylalaninamide (Journal of Computational Chemistry, 2001)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H317: May cause an allergic skin reaction
Warning Sensitization, Skin - Category 1 -
SMILESCC(C)C(C(=O)N)N
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InChIKeyXDEHMKQLKPZERH-UHFFFAOYSA-N
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