N139
(−)-Normetazocine
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About This Item
Empirical Formula (Hill Notation):
C14H19NO
CAS Number:
Molecular Weight:
217.31
MDL number:
UNSPSC Code:
41116107
drug control
regulated under CDSA - not available from Sigma-Aldrich Canada
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
format
neat
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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M D Aceto et al.
Journal of pharmaceutical sciences, 73(12), 1864-1866 (1984-12-01)
alpha-(-)-, (+)-, and (+/-)-N-4-Methylpentyl-, (-)- and (+)-N-cis-3-chloroallyl-, and (-)- and (+)-N-propynyl-N-normetazocine (I, II, and III, respectively) have been prepared from alpha-(-)-, (+)-, and (+/-)-N-normetazocine (IV) and tested for antinociceptive activity in mice and in morphine-dependent rhesus monkeys. The results obtained
S W Mascarella et al.
Journal of medicinal chemistry, 38(3), 565-569 (1995-02-03)
sigma 1 receptor ligands have potential pharmacological significance as antipsychotic drugs, as tools in the study of drug-induced motor function disorders, and as radiopharmaceutical imaging agents for the noninvasive imaging of malignant tumors in human subjects. A series of substituted
J M Walker et al.
European journal of pharmacology, 231(1), 61-68 (1993-01-26)
Three novel benzomorphans, (+)-N-benzylnormetazocine, (-)-deoxy-N-benzylnormetazocine, and (-)-deoxypentazocine were tested for their ability to produce circling behavior in rats following intranigral microinjections. Dose studies revealed the following rank order of potency: (-)-deoxypentazocine > (-)-deoxy-N-benzylnormetazocine > (+)-N-benzylnormetazocine. This rank order approximates that
G Ronsisvalle et al.
Journal of medicinal chemistry, 36(13), 1860-1865 (1993-06-25)
A series of phenyl carboxyl esters 5a-d derived from N-(cyclopropylmethyl)normetazocine was synthesized and evaluated for its selectivity at mu, kappa, and delta opioid receptors. Compound 5a, although 43 times less potent than the reference compound U50488, was specific for kappa
B de Costa et al.
Journal of medicinal chemistry, 35(12), 2221-2230 (1992-06-12)
Unlabeled fluoro- and iodo-substituted ligands exhibiting very high affinity and selectivity for sigma receptors were synthesized based on three different structural classes of sigma receptor ligands. These compounds were evaluated for sigma receptor affinity and specificity in order to assess
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