| Weight | 168.583 g/mol |
|---|---|
| Formula | C7H5ClN2O |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
Zoxazolamine (61-80-3)
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- Sigma-Aldrich - Zoxazolamine29.20 - 254.00 USD
- Fisher Scientific - Search for Zoxazolamine
- TCI - Search for Zoxazolamine
- The effect of dibenzoxanthenes on the paralyzing action of zoxazolamine (Naturwissenschaften, 1975)
- Genetic Expression of Aryl Hydrocarbon Hydroxylase Induction: Presence or Absence of Association with Zoxazolamine, Diphenylhydantoin, and Hexobarbital Metabolism (Molecular Pharmacology, 1974)
- Zoxazolamine: physiological disposition, uricosuric properties. (The American Journal of Medicine, 1958)
- Contrasting effects of thyroxin on zoxazolamine and hexobarbital metabolism. (Biochemical Pharmacology, 1961)
- THE METABOLIC FATE OF ZOXAZOLAMINE (FLEXIN) IN MAN (Journal of Pharmacology and Experimental Therapeutics, 1960)
- In vivo activation of zoxazolamine metabolism by flavone (Science, 1982)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C(C=C1Cl)N=C(O2)N
-
InChIKeyYGCODSQDUUUKIV-UHFFFAOYSA-N
- Pubchem - Zoxazolamine
- Wikipedia - zoxazolamine
Zoxazolamine (INN, USAN, BAN) (brand name Contrazole, Deflexol, Flexin, Miazol, Uri-Boi, Zoxamine, Zoxine) is a muscle relaxant that is no longer marketed. It was synthesized in 1953 and introduced clinically in 1955 but was withdrawn due to hepatotoxicity. One of its active metabolites, chlorzoxazone, was found to show less toxicity, and was subsequently marketed in place of zoxazolamine.
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benzo[d]oxazol-6-amine
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[(5-chloro-6-methyl-1,3-benzoxazol-2-yl)methyl]amine hydrochloride
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benzo[d]oxazol-4-amine
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benzooxazol-4-ol
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potassium 1,3-benzoxazole-2-carboxylate
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Zoxazolamine
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