| Weight | 311.381 g/mol |
|---|---|
| Formula | C19H21NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
THEBAINE (115-37-7)
Score:
#2340 in Biochemistry
,
#4649 in Biology
,
#5897 in Chemistry
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- Novel analgesics and molecular rearrangements in the morphine-thebaine group. III. Alcohols of the 6,14-endo-ethenotetrahydrooripavine series and derived analogs of N-allylnormorphine and -norcodeine (Journal of the American Chemical Society, 1967)
- Novel analgesics and molecular rearrangements in the morphine-thebaine group. I.. Ketones derived from 6,14-endo-ethenotetrahydrothebaine (Journal of the American Chemical Society, 1967)
- Antagonism of the convulsant effects of heroin, d-propoxyphene, meperidine, normeperidine and thebaine by naloxone in mice. (Journal of Pharmacology and Experimental Therapeutics, 1975)
- Novel analgesics and molecular rearrangements in the morphine-thebaine group. II. Alcohols derived from 6,14-endo-etheno- and 6,14-endo-ethanotetrahydrothebaine (Journal of the American Chemical Society, 1967)
- Determination of thebaine in water samples, biological fluids, poppy capsule, and narcotic drugs, using electromembrane extraction followed by high-performance liquid chromatography analysis. (Analytica Chimica Acta, 2011)
- Transformation of thebaine to oripavine, codeine, and morphine by rat liver, kidney, and brain microsomes. (Proceedings of the National Academy of Sciences of the United States of America, 1988)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCN1CCC23C4C(=CC=C2C1CC5=C3C(=C(C=C5)OC)O4)OC
-
InChIKeyFQXXSQDCDRQNQE-UHFFFAOYSA-N
- Pubchem - THEBAINE
- Wikipedia - Thebaine
Thebaine (paramorphine), also known as codeine methyl enol ether, is an opiate alkaloid, its name coming from the Greek , Thbai (Thebes), an ancient city in Upper Egypt. A minor constituent of opium, thebaine is chemically similar to both morphine and codeine, but has stimulatory rather than depressant effects. At high doses, it causes convulsions similar to strychnine poisoning.
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