CAS 16808-86-9
:6,14-Etenomorfinano-7-metanolo, 17-(ciclopropilmetil)-4,5-epossi-18,19-diidro-3-idrossi-6-metossi-α,α-dimetil-, cloridrato (1:1), (5α,7α)-
Descrizione:
6,14-Etenomorfinano-7-metanolo, 17-(ciclopropilmetil)-4,5-epossi-18,19-diidro-3-idrossi-6-metossi-α,α-dimetil-, cloridrato (1:1), (5α,7α)-, identificato dal numero CAS 16808-86-9, è un composto sintetico appartenente alla classe degli alcaloidi morfinani. Questa sostanza presenta una struttura molecolare complessa caratterizzata da più gruppi funzionali, inclusi gruppi metanolo, epossido e idrossile, che contribuiscono alle sue proprietà farmacologiche. Si incontra tipicamente nel contesto di ricerche relative agli analgesici e potenziali agenti terapeutici a causa della sua interazione con i recettori oppioidi. La presenza del gruppo ciclopropilmetile può influenzare la sua affinità di legame e selettività, impattando la sua efficacia e profilo di sicurezza. Come sale cloridrato, è probabile che sia più solubile in acqua, facilitando il suo utilizzo in varie formulazioni. Le precauzioni di sicurezza e gestione sono essenziali, così come per molti composti di questa classe, a causa dei potenziali effetti psicoattivi e delle considerazioni normative.
Formula:C26H35NO4·ClH
InChI:InChI=1S/C26H35NO4.ClH/c1-23(2,29)18-13-24-8-9-26(18,30-3)22-25(24)10-11-27(14-15-4-5-15)19(24)12-16-6-7-17(28)21(31-22)20(16)25;/h6-7,15,18-19,22,28-29H,4-5,8-14H2,1-3H3;1H/t18-,19-,22-,24-,25+,26-;/m1./s1
InChI key:InChIKey=UNPUINKKJUSSDZ-UVGWPQHUSA-N
SMILES:O(C)[C@@]12[C@]3([C@]45[C@@]([C@](N(CC6CC6)CC4)(CC7=C5C(O3)=C(O)C=C7)[H])(C[C@@H]1[C@@](C)(C)O)CC2)[H].Cl
Sinonimi:- (5alpha,7alpha)-17-(Cyclopropylmethyl)-4,5-epoxy-18,19-dihydro-3-hydroxy-6-methoxy-alpha,alpha-dimethyl-6,14-ethenomorphinan-7-methanol hydrochloride
- 6,14-Ethenomorphinan-7-methanol, 17-(cyclopropylmethyl)-4,5-epoxy-18,19-dihydro-3-hydroxy-6-methoxy-α,α-dimethyl-, hydrochloride (1:1), (5α,7α)-
- 6,14-Ethenomorphinan-7-methanol, 17-(cyclopropylmethyl)-4,5-epoxy-18,19-dihydro-3-hydroxy-6-methoxy-α,α-dimethyl-, hydrochloride, (5α,7α)-
- 6,14-Ethenomorphinan-7-methanol, 18,19-dihydro-17-(cyclopropylmethyl)-alpha,alpha-dimethyl-4,5-epoxy-3-hydroxy-6-methoxy-, hydrochloride, (5-alpha,7-alpha)-
- 6,14-endo-Ethanetetrahydrooripavine, 21-cyclopropyl-7-alpha-(1-hydroxy-1-methylethyl)-, HCl
- 6,14-endo-Ethanotetrahydrooripavine, 21-cyclopropyl-7α-(1-hydroxy-1-methylethyl)-, hydrochloride
- Diprenorphine hydrochloride
- Revivon
Ordinare per
Purezza (%)
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100
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50
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90
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95
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100
4 prodotti.
Diprenorphine Hydrochloride (1 mg/ml in Methanol)
CAS:Prodotto controllatoFormula:C26H35NO4·ClHColore e forma:Single SolutionPeso molecolare:462.02Diprenorphine-d3 Hydrochloride
CAS:Prodotto controllato<p>Applications Labelled Diprenorphine (D492100). Diprenorphine is a narcotic antagonist. Diprenorphine is closely related to Cyprenorphine.<br>References Blane, G.F., et al.: J. Pharm. Pharmacol., 19, 367 (1967), Grange, M., et al.: Rev. Med. Vet., 124, 899 (1973), Pert, C.B., et al.: Life Sci., 16, 1849 (1975), Duggett, N.S., et al.: Toxicol. Appl. Pharmacol., 31, 141 (1977),<br></p>Formula:C26H33D3ClNO4Colore e forma:NeatPeso molecolare:465.04Diprenorphine Hydrochloride
CAS:Prodotto controllato<p>Applications Diprenorphine is a narcotic antagonist. Diprenorphine is closely related to Cyprenorphine.<br>References Blane, G.F., et al.: J. Pharm. Pharmacol., 19, 367 (1967), Grange, M., et al.: Rev. Med. Vet., 124, 899 (1973), Pert, C.B., et al.: Life Sci., 16, 1849 (1975), Duggett, N.S., et al.: Toxicol. Appl. Pharmacol., 31, 141 (1977),<br></p>Formula:C26H35NO4·ClHColore e forma:NeatPeso molecolare:462.02Diprenorphine hydrochloride
CAS:Prodotto controllato<p>Diprenorphine hydrochloride is a drug that belongs to the class of opioids. It is used as an antidote for opioid overdose and has been shown to be effective in reducing the severity of withdrawal symptoms. Diprenorphine hydrochloride has been shown to inhibit P-glycoprotein (P-gp), which is a membrane protein that transports certain substances from the brain back into the blood. This inhibition leads to increased concentrations of dopamine in the brain, which may contribute to its clinical relevance as an anti-psychotic agent. Diprenorphine hydrochloride also has binding affinity for μ-, κ-, δ-, and ν-opioid receptors, which can lead to decreased locomotor activity, antinociceptive effects, and sedation.</p>Formula:C26H36ClNO4Purezza:Min. 95%Colore e forma:PowderPeso molecolare:462.02 g/mol

