Morphine-7,8-oxide

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==Description==
==Description==
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increased analgesic activity compared to parent; RN given refers to (5alpha,6alpha,7beta,8beta)-isomer; structure in first source
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Increased analgesic activity compared to parent; RN given refers to (5alpha,6alpha,7beta,8beta)-isomer; structure in first source.
 +
Morphine-7,8-oxide (morphine epoxide) is assumed to be a metabolite of morphine. Morphine epoxide in antinociceptive action was practically as potent as morphine. The development of tolerance in antinociceptive action was slower in the rats treated with morphine epoxide than in the rats with morphine. Furthermore, morphine epoxide was less potent than morphine in the inhibition of abstinence syndrome.
==General Properties==
==General Properties==

Revision as of 04:14, 5 May 2009

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Morphine-7,8-oxide
Systematic (IUPAC) name
N/A
Identifiers
CAS number  ?
ATC code  ?
PubChem 15977129
Chemical data
Formula C17H19NO4
Mol. mass 301.33706
SMILES eMolecules & PubChem
Pharmacokinetic data
Bioavailability  ?
Metabolism  ?
Half life  ?
Excretion  ?
Therapeutic considerations
Pregnancy cat.

?

Legal status
Routes  ?

Description

Increased analgesic activity compared to parent; RN given refers to (5alpha,6alpha,7beta,8beta)-isomer; structure in first source. Morphine-7,8-oxide (morphine epoxide) is assumed to be a metabolite of morphine. Morphine epoxide in antinociceptive action was practically as potent as morphine. The development of tolerance in antinociceptive action was slower in the rats treated with morphine epoxide than in the rats with morphine. Furthermore, morphine epoxide was less potent than morphine in the inhibition of abstinence syndrome.

General Properties

*Molecular Weight

301.33706

*Molecular Formula

C17H19NO4

*IUPAC NAME

N/A

*Canonical Smiles

CN1CCC23C4C1CC5=C2C(=C(C=C5)O)OC3C(C6C4O6)O

*Isomeric Smiles

CN1CC[C@]23[C@@H]4[C@@H]1CC5=C2C(=C(C=C5)O)O[C@H]3[C@H](C6C4O6)O

*XLogP

0

*Topological Polar Surface Area

65.5

External Links

Link to BIAdb Database