Identification | Back 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 Properties | Back 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 |
Hazard Information | Back 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. | [storage]
Store at -20°C |
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Company Name: |
BOC Sciences
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Tel: |
1-631-485-4226; 16314854226 |
Website: |
https://www.bocsci.com |
Company Name: |
Energy Chemical
|
Tel: |
021-58432009 400-005-6266 |
Website: |
http://www.energy-chemical.com |
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