| Weight | 357.45 g/mol |
|---|---|
| Formula | C21H27NO4 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
nalbuphine (20594-83-6)
Nubain · Nalbuphine Hydrochloride · EN-2234A
Score:
#536 in Neuroscience
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#2448 in Biology
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#3049 in Chemistry
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- A new reagent for the selective, high-yield N-dealkylation of tertiary amines: improved syntheses of naltrexone and nalbuphine (Journal of Organic Chemistry, 1984)
- The kappa opioid nalbuphine produces gender- and dose-dependent analgesia and antianalgesia in patients with postoperative pain (Pain, 1999)
- Ceiling effect for respiratory depression by nalbuphine (Clinical Pharmacology & Therapeutics, 1980)
- Analgesic and respiratory depressant activity of nalbuphine: a comparison with morphine. (Anesthesiology, 1982)
- The enflurane sparing effect of morphine, butorphanol, and nalbuphine. (Anesthesiology, 1982)
- Evaluation of nalbuphine for abuse potential. (Clinical Pharmacology & Therapeutics, 1972)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Nubain
- Nalbuphine Hydrochloride
- EN-2234A
- EN 2234A
- EN2234A
- SERB brand of nalbuphine
- Nalbuphine Serb
- nalbuphine SERB brand
-
SMILESC1CC(C1)CN2CCC34C5C(CCC3(C2CC6=C4C(=C(C=C6)O)O5)O)O
-
InChIKeyNETZHAKZCGBWSS-UHFFFAOYSA-N
- Pubchem - nalbuphine
- Wikipedia - nalbuphine
Nalbuphine is a semi-synthetic opioid agonist-antagonist used commercially as an analgesic under a variety of trade names, including Nubain and Manfine.
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