Weight | 425.569 g/mol |
---|---|
Formula | C26H35NO4 |
Hydrogen Acceptors | 5 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 4 |
Diprenorphine (14357-78-9)
Revivon · Diprenorphine Hydrochloride
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#731 in Neuroscience
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#3217 in Biology
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#4025 in Chemistry
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- Central poststroke pain and reduced opioid receptor binding within pain processing circuitries: a [11C]diprenorphine PET study. (Pain, 2004)
- An autoradiographic map of (3H)diprenorphine binding in rat brain: effects of social interaction (Brain Research Bulletin, 1981)
- Cerebral decreases in opioid receptor binding in patients with central neuropathic pain measured by [11C]diprenorphine binding and PET (European Journal of Pain, 2004)
- The role of opioids in restless legs syndrome: an [11C]diprenorphine PET study (Brain, 2005)
- Compartmental Analysis of Diprenorphine Binding to Opiate Receptors in the Rat in vivo and its Comparison with Equilibrium Data in vitro (Journal of Cerebral Blood Flow and Metabolism, 1991)
- Quantification of Human Opiate Receptor Concentration and Affinity Using High and Low Specific Activity [11C]Diprenorphine and Positron Emission Tomography (Journal of Cerebral Blood Flow and Metabolism, 1991)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Revivon
- Diprenorphine Hydrochloride
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SMILESCC(C)(C1CC23CCC1(C4C25CCN(C3CC6=C5C(=C(C=C6)O)O4)CC7CC7)OC)O
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InChIKeyOIJXLIIMXHRJJH-UHFFFAOYSA-N
- Pubchem - Diprenorphine
- Wikipedia - diprenorphine
Diprenorphine (brand name Revivon; former developmental code name M5050), also known as diprenorfin, is a non-selective, high-affinity, weak partial agonist of the - (MOR), - (KOR), and -opioid receptor (DOR) (with equal affinity) that is employed in veterinary medicine as an opioid antagonist. It is used to reverse the effects of super-potent opioid analgesics such as etorphine and carfentanil that are used for tranquilizing large animals. The drug is not approved for use in humans.
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