| Weight | 321.804 g/mol |
|---|---|
| Formula | C17H20ClNO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
Hydromorphone HCL (71-68-1)
Hydromorphone · Dilaudid · Dihydromorphinone
Score:
#823 in Neuroscience
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#3621 in Biology
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#4547 in Chemistry
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- Opioids and the Management of Chronic Severe Pain in the Elderly: Consensus Statement of an International Expert Panel with Focus on the Six Clinically Most Often Used World Health Organization step III Opioids (Buprenorphine, Fentanyl, Hydromorphone, Methadone, Morphine, Oxycodone) (Pain Practice, 2008)
- Opioid rotation in patients with cancer pain: A retrospective comparison of dose ratios between methadone, hydromorphone, and morphine (Cancer, 1996)
- Neuroexcitatory effects of morphine and hydromorphone: Evidence implicating the 3-glucuronide metabolites (Clinical and Experimental Pharmacology and Physiology, 2000)
- Enadoline, a selective kappa opioid agonist: comparison with butorphanol and hydromorphone in humans (Psychopharmacology, 2001)
- Comparing the subjective, psychomotor, and physiological effects of intravenous hydromorphone and morphine in healthy volunteers (Psychopharmacology, 2000)
- CYP2D6 phenotype determines the metabolic conversion of hydrocodone to hydromorphone. (Clinical Pharmacology & Therapeutics, 1993)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Hydromorphone
- Dilaudid
- Dihydromorphinone
- Hydromorphone Hydrochloride
- Palladone
- Hydromorphon
- Laudacon
-
SMILES[H+].CN1CCC23C4C1CC5=C2C(=C(C=C5)O)OC3C(=O)CC4.[Cl-]
-
InChIKeyXHILEZUETWRSHC-UHFFFAOYSA-N
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