20410-95-1
20410-95-1 structure
- Name: 6-Alpha Naloxol
- Chemical Name: 6 α-naloxol
- CAS Number: 20410-95-1
- Molecular Formula: C19H23NO4
- Molecular Weight: 329.39000
- Catalog: Signaling Pathways GPCR/G Protein Opioid Receptor
- Create Date: 2017-11-30 20:53:55
- Modify Date: 2025-09-07 18:31:43
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6-Alpha Naloxol(Alpha-Naloxol) is an opioid antagonist closely related to naloxone; a human metabolite of naloxone.IC50 value:Target: opioid antagonistWhen responding over the entire 30 min operant session was examined, naloxone was only 5-fold more potent than 6-alpha-naloxol in suppressing operant responding under Morphine Na ve conditions, but this increased to a 65-fold potency difference after Single or Repeat Morphine pretreatment. Examination of the relative potency of these antagonists in the Early Phase of operant testing (5-15 min post-antagonist) revealed an even greater 100-fold potency difference between naloxone and 6-alpha-naloxol, but in the Late Phase of testing (25-35 min post-antagonist), this had declined to a 9-fold potency difference, comparable to the relative potency of naloxone to 6-alpha-naloxol under Morphine-Na ve conditions.
| Name | 6 α-naloxol |
|---|---|
| Synonyms |
6a-Naloxol
6-Alpha Naloxol |
| Description | 6-Alpha Naloxol(Alpha-Naloxol) is an opioid antagonist closely related to naloxone; a human metabolite of naloxone.IC50 value:Target: opioid antagonistWhen responding over the entire 30 min operant session was examined, naloxone was only 5-fold more potent than 6-alpha-naloxol in suppressing operant responding under Morphine Na ve conditions, but this increased to a 65-fold potency difference after Single or Repeat Morphine pretreatment. Examination of the relative potency of these antagonists in the Early Phase of operant testing (5-15 min post-antagonist) revealed an even greater 100-fold potency difference between naloxone and 6-alpha-naloxol, but in the Late Phase of testing (25-35 min post-antagonist), this had declined to a 9-fold potency difference, comparable to the relative potency of naloxone to 6-alpha-naloxol under Morphine-Na ve conditions. |
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| Related Catalog | |
| References |
[1]. Weinstein SH, et al. Metabolites of naloxone in human urine. J Pharm Sci. 1971 Oct;60(10):1567-8. |
| Density | 1.43g/cm3 |
|---|---|
| Boiling Point | 532.5ºC at 760mmHg |
| Molecular Formula | C19H23NO4 |
| Molecular Weight | 329.39000 |
| Flash Point | 275.8ºC |
| Exact Mass | 329.16300 |
| PSA | 73.16000 |
| LogP | 1.03110 |
| Vapour Pressure | 3.62E-12mmHg at 25°C |
| Index of Refraction | 1.701 |
|
~93%
20410-95-1 |
| Literature: MALLINCKRODT INC. Patent: WO2008/137672 A1, 2008 ; Location in patent: Page/Page column 25 ; |
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~%
20410-95-1 |
| Literature: Rezaie, Robert; Bailey, Timothy S. Patent: US2010/36128 A1, 2010 ; Location in patent: Page/Page column 7 ; |
|
~63%
20410-95-1 |
| Literature: Hosztafi, Sandor; Berenyi, Sandor; Toth, Geza; Makleit, Sandor Monatshefte fuer Chemie, 1992 , vol. 123, # 5 p. 435 - 442 |
|
~%
20410-95-1 |
| Literature: Hahn; Fishman Journal of Organic Chemistry, 1975 , vol. 40, # 1 p. 31 - 34 |
|
~%
20410-95-1 |
| Literature: Hosztafi, Sandor; Berenyi, Sandor; Toth, Geza; Makleit, Sandor Monatshefte fuer Chemie, 1992 , vol. 123, # 5 p. 435 - 442 |
|
~%
20410-95-1 |
| Literature: Hosztafi, Sandor; Berenyi, Sandor; Toth, Geza; Makleit, Sandor Monatshefte fuer Chemie, 1992 , vol. 123, # 5 p. 435 - 442 |
| Precursor 5 | |
|---|---|
| DownStream 0 | |