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2099681-71-5

2099681-71-5 Structure

2099681-71-5 Structure
IdentificationBack Directory
[Name]

Sulfamide, N-[2-[1,2-dihydro-1'-[cis-4-(1-methylethyl)cyclohexyl]-3-oxospiro[isoquinoline-4(3H),4'-piperidin]-2-yl]ethyl]-, hydrochloride (1:1)
[CAS]

2099681-71-5
[Synonyms]

AT-121 hydrochloride
Sulfamide, N-[2-[1,2-dihydro-1'-[cis-4-(1-methylethyl)cyclohexyl]-3-oxospiro[isoquinoline-4(3H),4'-piperidin]-2-yl]ethyl]-, hydrochloride (1:1)
[Molecular Formula]

C24H39ClN4O3S
[MOL File]

2099681-71-5.mol
[Molecular Weight]

499.11
Hazard InformationBack Directory
[Description]

AT-121 hydrochloride is a bifunctional nociception and mu opioid receptor agonist. It is a safe, non-addictive analgesic, and shows antinociceptive and antiallodynic effects.
[Uses]

AT-121 hydrochloride is a bifunctional nociception and mu opioid receptor agonist, with Kis of 3.67 and 16.49 nM, respectively. AT-121 hydrochloride is a safe, non-addictive analgesic, and shows antinociceptive and antiallodynic effects[1].
[in vivo]

AT-121 hydrochloride (0.003-0.03 mg/kg; s.c.) produces potent antinociceptive effect[1].

Animal Model:Adult male and female rhesus monkeys[1]
Dosage:0.003-0.03 mg/kg
Administration:Subcutaneous
Result:Produced antinociceptive effects against an acute noxious stimulus, 50 °C water, in a dose-dependent.
[IC 50]

μ Opioid Receptor/MOR
[References]

[1] Ding H, et al. A bifunctional nociceptin and mu opioid receptor agonist is analgesic without opioid side effects in nonhuman primates. Sci Transl Med. 2018;10(456):eaar3483. DOI:10.1126/scitranslmed.aar3483
Spectrum DetailBack Directory
[Spectrum Detail]

Sulfamide, N-[2-[1,2-dihydro-1'-[cis-4-(1-methylethyl)cyclohexyl]-3-oxospiro[isoquinoline-4(3H),4'-piperidin]-2-yl]ethyl]-, hydrochloride (1:1)(2099681-71-5)1HNMR
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