BAY 1316957)

BAY 1316957) Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:BAY-1316957
CAS:1613264-40-6
Purity:98.00% Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Nantong HI-FUTURE Biology Co., Ltd.
Tel: +undefined18051384581
Email: sales@chemhifuture.com
Products Intro: Product Name:BAY 1316957)
CAS:1613264-40-6
Purity:98%+ HPLC Package:100MG,500MG,1G,5G,10G 50MG
Company Name: Aladdin Scientific
Tel: +1-833-552-7181
Email: sales@aladdinsci.com
Products Intro: Product Name:BAY-1316957
CAS:1613264-40-6
Purity:98% Package:$150.9/5mg;$250.9/10mg;$550.9/25mg;$950.9/50mg;$1550.9/100mg;Bulk package Remarks:98%
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Products Intro: Product Name:BAY 1316957
CAS:1613264-40-6
Purity:98% Package:5mg
Company Name: ShangHai Biochempartner Co.,Ltd  
Tel: 17754423994 17754423994
Email: 2853530910@QQ.com
Products Intro: Product Name:BAY 1316957
CAS:1613264-40-6
Purity:98% HPLC LCMS Package:100MG;1G
BAY 1316957) Basic information
Product Name:BAY 1316957)
Synonyms:BAY 1316957);BAY-1316957 (BAY1316957;1H-Benzimidazole-5-carboxylic acid, 2-(9-ethyl-6-methyl-9H-carbazol-3-yl)-1-(2-methoxyethyl)-4-methyl-
CAS:1613264-40-6
MF:C27H27N3O3
MW:441.52
EINECS:
Product Categories:
Mol File:1613264-40-6.mol
BAY 1316957) Structure
BAY 1316957) Chemical Properties
Boiling point 646.3±65.0 °C(Predicted)
density 1.26±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 100 mg/mL (226.49 mM; Need ultrasonic)
pka2.10±0.30(Predicted)
Safety Information
MSDS Information
BAY 1316957) Usage And Synthesis
Biological ActivityBAY-1316957 is a potent, selective and orally active prostaglandin E2 receptor subtype 4 (EP4-R) antagonist with an IC50 of 15.3 nM for human EP4-R. BAY-1316957 has excellent drug metabolism and pharmacokinetics properties, and can be used for endometriosis research[1]. BAY-1316957 (Compound 32) shows high solubility and permeability using the Caco-2 cellular assay[1]. BAY-1316957 (Compound 32; 0.2-5 mg/kg; oral administration; once) treatment significantly reduces mechanical allodynia in dmPGE2 pain model[1].The pharmacokinetic parameters of BAY-1316957 (Compound 32) shows a low clearance, long half-life, and high bioavailability (F%=90%) in Wistar rats. Investigation of the metabolic pathways of BAY-1316957 (Compound 32) in human, rat, mouse, dog, and monkey hepatocytes revealed that the formation of the acyl glucuronide was also the common and predominant route of biotransformation, mainly catalyzed by UGT1A1 and to a lesser extent by UGT1A3[1].
References[1]. B?urle S, et al. Identification of a Benzimidazolecarboxylic Acid Derivative (BAY 1316957) as a Potent and Selective Human Prostaglandin E2 Receptor Subtype 4 (hEP4-R) Antagonist for the Treatment of Endometriosis. J Med Chem. 2019 Mar 14;62(5):2541-2563.
BAY 1316957) Preparation Products And Raw materials
Tag:BAY 1316957)(1613264-40-6) Related Product Information
BAY1895344 2HCl BAY-2402234 BAY-1125976. BAY-885 BAY-985 BAY-1163877 BAY1895344 HCl BAY-1895344 Benzamide, N-[5-(3,5-dicyano-1,4-dihydro-1,2,6-trimethyl-4-pyridinyl)-6-fluoro-7-methyl-1H-indazol-3-yl]-2-ethyl- BAY 2666605 BAY 2416964