Weight | 202.637 g/mol |
---|---|
Formula | C9H11ClO3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 4 |
chlorphenesin (104-29-0)
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LabBot
- Optimization of chlorphenesin emulgel formulation (Aaps Journal, 2004)
- Chlorphenesin: A New Inhibitor of IgE-Mediated Histamine Release (Journal of Immunology, 1969)
- THE METABOLISM OF CHLORPHENESIN CARBAMATE (Journal of Pharmacology and Experimental Therapeutics, 1964)
- Comparative Pharmacokinetics of Chlorphenesin Carbamate and Methocarbamol in Man (Journal of Pharmaceutical Sciences, 1971)
- Evaluation of sustained-release granules of chlorphenesin carbamate in dogs and humans (International Journal of Pharmaceutics, 1993)
- The absorption, excretion, and metabolism of chlorphenesin carbamate in the dog (Biochemical Pharmacology, 1966)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC=C1OCC(CO)O)Cl
-
InChIKeyMXOAEAUPQDYUQM-UHFFFAOYSA-N
- Pubchem - chlorphenesin
- Wikipedia - chlorphenesin
Chlorphenesin carbamate (Maolate, Musil) is a centrally acting muscle relaxant used to treat muscle pain and spasms. Chlorphenesin is no longer used for this purpose in most developed nations due to the availability of much safer spasmolytics such as benzodiazepines. It is a naturally occurring compound found in Bull Semen.
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