ChemicalBook--->CAS DataBase List--->603151-83-3

603151-83-3

603151-83-3 Structure

603151-83-3 Structure
IdentificationBack Directory
[Name]

NBI 35965 hydrochloride
[CAS]

603151-83-3
[Synonyms]

NBI-35965 Mesylate
NBI 35965 hydrochloride
[Molecular Formula]

C22H26Cl2N4O3S
[MOL File]

603151-83-3.mol
[Molecular Weight]

497.438
Chemical PropertiesBack Directory
[Melting point ]

167 °C
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO > 10 mM
[form ]

Powder
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P321-P362+P364-P332+P313-P337+P313-P403+P233-P405-P501
Hazard InformationBack Directory
[Uses]

Corticotropin-releasing hormone, also known as corticotropin-releasing factor (CRF) or corticoliberin, is a peptide hormone and neurotransmitter involved in the stress response. It is secreted from the hypothalamus and is the major regulator of pituitary corticotropin-release and consequent glucocorticoid secretion. NBI 35965 is a selective CRF receptor 1 (CRF1) antagonist with a Ki value of 4 nM. It does not inhibit CRF2 (Ki = >10,000 nM). NBI 35965 inhibits cAMP accumulation and adrenocorticotropic hormone (ACTH) production in vitro (pIC50s = 7.1 and 6.9, respectively) and reduces CRF- and stress-induced ACTH production in vivo. In animal models of stress, NBI 35965 administration produces anxiolytic effects.[Cayman Chemical]
[Uses]

NBI 35965 Hydrochloride is a potent and selective corticotropin-releasing factor 1 (CRF1) antagonist.
[Uses]

NBI 35965 Mesylate is a selective corticotropin-releasing factor (CRF1) receptor antagonist involved in stress response.
[in vivo]

NBI 35965 methanesulfonate (20 mg/kg; oral gavage; once) reduces stress induced ACTH production in mice[1].
In rats, NBI 35965 methanesulfonate (Compound 12a; 10 mg/kg) has a volume of distribution 17.8 L/kg, a plasma clearance of 17 mL/min/kg, and a half-life of 12 h. The estimated oral bioavailability is 34% with a mean maximal plasma concentration at 1 h of 560 ng/mL. NBI 35965 methanesulfonate also penetrated the blood-brain barrier, resulting in a mean maximal brain concentration of 700 ng/g[1].

Animal Model:Male CD-1 mice (24-26 g) bearing restraint stress[1]
Dosage:20 mg/kg (10 mL/kg 5% mannitol-d (w/v) in water)
Administration:Oral gavage; 60 min prior to the initiation of the stressor
Result:Reduced stress induced ACTH production in vivo.
[IC 50]

CRFR1: 4 nM (Ki); CRFR1: 8.5 (pKi)
[storage]

Store at -20°C
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