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ChemicalBook--->CAS DataBase List--->146032-79-3

146032-79-3

146032-79-3 Structure

146032-79-3 Structure
IdentificationBack Directory
[Name]

SC-51322
[CAS]

146032-79-3
[Synonyms]

SC-51322
8-Chloro-dibenz[b,f][1,4]oxazepine-10(11H)-carboxylic Acid 2-[3-[(2-FuranylMethyl) thio]-1-oxopropyl]hydrazide
8-Chloro-2-[3-[(2-furanylmethyl)thio]-1-oxopropyl]-dibenz(Z)[b,f][1,4]oxazepine-10(11H)-carboxylicacidhydrazide
Dibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 8-chloro-, 2-[3-[(2-furanylmethyl)thio]-1-oxopropyl]hydrazide
[Molecular Formula]

C22H20ClN3O4S
[MDL Number]

MFCD00916246
[MOL File]

146032-79-3.mol
[Molecular Weight]

457.93
Chemical PropertiesBack Directory
[Melting point ]

112-114°C
[RTECS ]

HQ4002000
[storage temp. ]

Store at +4°C
[solubility ]

DMSO: ≥10mg/mL
[form ]

powder
[color ]

white to off-white
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

25
[Safety Statements ]

45
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
[HazardClass ]

6.1
Hazard InformationBack Directory
[Description]

The prostaglandin E2 (PGE2) receptor (EP1) is involved in triggering PGE2-mediated pain as well as neuronal survival and growth. SC-51322 is a selective EP1 antagonist that inhibits PGE2 signaling in a guinea pig ileum muscle strip assay with a pA2 value of 8.1 and demonstrates analgesic activity in a mouse writhing assay with an ED50 value of 0.9 mg/kg. It is pharmacologically similar to SC-51089, but does not release hydrazine, a known carcinogen to rats, as does SC-51089. SC-51322 potentiates the vasorelaxation of human pulmonary vein induced by PGE2 with an EC50 value of 7.75 μM.
[Chemical Properties]

Off-White Solid
[Uses]

A selective E-prostanoid receptor subtype 1 (EP1) receptor antagonist which shows antihypertensive effects.
[IC 50]

EP2: 8.1 (pA2)
[storage]

Store at -20°C
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