SC-51322

SC-51322 Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: 3B Pharmachem (Wuhan) International Co.,Ltd.  
Tel: 18930552037
Email: 3bsc@sina.com
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Tel: 021-50135380
Email: shchemsky@sina.com
Company Name: Guangzhou Isun Pharmaceutical Co., Ltd  
Tel: 020-39119399 18927568969
Email: isunpharm@qq.com
Company Name: EMMX Biotechnology LLC  
Tel: 888-539-0666
Email: info@emmx.com

SC-51322 manufacturers

  • SC 51322
  • SC 51322 pictures
  • $69.00
  • 2026-05-11
  • CAS:146032-79-3
  • Purity:
  • Supply Ability: 10g
SC-51322 Basic information
Product Name:SC-51322
Synonyms:SC-51322;8-Chloro-2-[3-[(2-furanylmethyl)thio]-1-oxopropyl]-dibenz(Z)[b,f][1,4]oxazepine-10(11H)-carboxylicacidhydrazide;8-Chloro-dibenz[b,f][1,4]oxazepine-10(11H)-carboxylic Acid 2-[3-[(2-FuranylMethyl) thio]-1-oxopropyl]hydrazide;Dibenz[b,f][1,4]oxazepine-10(11H)-carboxylic acid, 8-chloro-, 2-[3-[(2-furanylmethyl)thio]-1-oxopropyl]hydrazide;SC-51322, EP1 receptor antagonist
CAS:146032-79-3
MF:C22H20ClN3O4S
MW:457.93
EINECS:
Product Categories:Amines;Heterocycles;Inhibitors;Intermediates & Fine Chemicals;Pfizer compounds;Pharmaceuticals;Sulfur & Selenium Compounds
Mol File:Mol File
SC-51322 Structure
SC-51322 Chemical Properties
Melting point 112-114°C
RTECS HQ4002000
storage temp. Store at +4°C
solubility DMSO: ≥10mg/mL
form powder
color white to off-white
InChI1S/C22H20ClN3O4S/c23-16-7-8-20-18(12-16)26(13-15-4-1-2-6-19(15)30-20)22(28)25-24-21(27)9-11-31-14-17-5-3-10-29-17/h1-8,10,12H,9,11,13-14H2,(H,24,27)(H,25,28)
InChIKeyCQBVTZDISUKDSX-UHFFFAOYSA-N
SMILESClc1ccc2Oc3ccccc3CN(C(=O)NNC(=O)CCSCc4ccco4)c2c1
Safety Information
Hazard Codes T
Risk Statements 25
Safety Statements 45
RIDADR UN 2811 6.1 / PGIII
WGK Germany 3
HazardClass 6.1
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
MSDS Information
SC-51322 Usage And Synthesis
DescriptionThe 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 PropertiesOff-White Solid
UsesA selective E-prostanoid receptor subtype 1 (EP1) receptor antagonist which shows antihypertensive effects.
IC 50EP2: 8.1 (pA2)
storageStore at -20°C
References[1] E. ANN HALLINAN. Aminoacetyl Moiety as a Potential Surrogate for Diacylhydrazine Group of SC-51089, a Potent PGE2 Antagonist, and Its Analogs[J]. Journal of Medicinal Chemistry, 1996, 39 2: 609-613. DOI: 10.1021/jm950454k
[2] N FOUDI. Vasorelaxation induced by prostaglandin E2 in human pulmonary vein: role of the EP4 receptor subtype[J]. British Journal of Pharmacology, 2009, 154 8: 1631-1639. DOI: 10.1038/bjp.2008.214
SC-51322 Preparation Products And Raw materials
Tag:SC-51322(146032-79-3) Related Product Information
PROSTAGLANDIN F1ALPHA Latanoprost Misoprostol Acid PROSTAGLANDIN D2 Sulprostone PROSTAGLANDIN B1 Fluprostenol Prostaglandin F2a PROSTAGLANDIN A1 13,14-Dihydro-prostaglandin E1 (PGE0) PROSTAGLANDIN B2 Leukotriene B4 dimethyl amide 6(R)-(4-Carboxyphenylthio)-5(S)-hydroxy-7(E),9(E),11(Z),14(Z)-eicosatetraenoic acid Leukotriene d4 SC-51089 U-75302 L-161,982 11BETA-PROSTAGL AND IN F2ALPHA