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ChemicalBook--->CAS DataBase List--->2099681-31-7

2099681-31-7

2099681-31-7 Structure

2099681-31-7 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]-
[CAS]

2099681-31-7
[Synonyms]

AT 121,AT121
Sulfamide, N-[2-[1,2-dihydro-1'-[cis-4-(1-methylethyl)cyclohexyl]-3-oxospiro[isoquinoline-4(3H),4'-piperidin]-2-yl]ethyl]-
[Molecular Formula]

C24 H38 N4 O3 S
[MDL Number]

MFCD34469231
[MOL File]

2099681-31-7.mol
[Molecular Weight]

462.65
Chemical PropertiesBack Directory
[Boiling point ]

650.6±65.0 °C(Predicted)
[density ]

1.25±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Chloroform: 10 mg/ml; DMF: miscible; DMSO: miscible; Ethanol: miscible; Ethanol:PBS (pH 7.2) (1:20): 50μg/ml
[form ]

Liquid
[pka]

10.81±0.60(Predicted)
[color ]

Colorless to light yellow
Safety DataBack Directory
[Symbol(GHS) ]


GHS06,GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H302-H310-H331-H315-H319-H351-H361-H372
[Precautionary statements ]

P201-P202-P260-P262-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P310-P308+P313-P321-P314-P330-P361+P364-P332+P313-P337+P313-P403+P233-P405-P501
Hazard InformationBack Directory
[Description]

AT-121 is a dual μ-opioid and nociceptin receptor partial agonist (Kis = 16.49 and 3.67 nM, respectively).1 It stimulates [35S]GTPγS binding to cell membranes expressing μ-opioid or nociceptin receptors (EC50s = 19.6 and 34.7 nM, respectively). AT-121 (0.003-0.03 mg/kg) decreases capsaicin-induced thermal allodynia without increasing scratching activity in rhesus monkeys in a dose-dependent manner. It lacks reinforcing effects, a marker of abuse potential, and reduces oxycodone, but not food pellet, reinforcement in a drug self-administration assay in rhesus monkeys when administered at doses ranging from 0.3 to 10 μg/kg per injection. AT-121 (0.01 or 0.03 mg/kg) does not induce hyperalgesia, a marker of tolerance development, in rhesus monkeys.
[References]

1. Ding, H., Kiguchi, N., Yasuda, D., et al. A bifunctional nociceptin and mu opioid receptor agonist is analgesic without opioid side effects in nonhuman primates Sci. Transl. Med. 10(456),eaar3483(2018).
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