| Weight | 149.215 g/mol |
|---|---|
| Formula | C5H11NO2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
DL-Penicillamine (52-67-5, 52-66-4)
Score:
#628 in Biochemistry
,
#1799 in Biology
,
#2141 in Chemistry
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- Chemical mechanisms underlying the vasodilator and platelet anti-aggregating properties of S-nitroso-N-acetyl-DL-penicillamine and S-nitrosoglutathione (Bioorganic & Medicinal Chemistry, 1995)
- Controlled photoinitiated release of nitric oxide from polymer films containing S-nitroso-N-acetyl-DL-penicillamine derivatized fumed silica filler. (Journal of the American Chemical Society, 2004)
- N-ACETYL-DL-PENICILLAMINE, A NEW ORAL PROTECTIVE AGENT AGAINST THE LETHAL EFFECTSOF MERCURIC CHLORIDE (Journal of Pharmacology and Experimental Therapeutics, 1959)
- DL-penicillamine as a cause of optic axial neuritis. (JAMA, 1963)
- Enhanced release of nitric oxide causes increased cytotoxicity of S-nitroso-N-acetyl-dl-penicillamine and sodium nitroprusside under hypoxic conditions (Biochemical Journal, 1996)
- Organotin (IV) derivatives of L-cysteine and DL-penicillamine (Journal of Organometallic Chemistry, 1978)
-
Predict GHS Hazards for Any Chemical in silico.
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SMILESCC(C)(C(C(=O)O)N)S
-
InChIKeyVVNCNSJFMMFHPL-UHFFFAOYSA-N
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