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BAY 1316957)

CAS No.
1613264-40-6
Chemical 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-
CBNumber:
CB54844522
Molecular Formula:
C27H27N3O3
Molecular Weight:
441.52
MDL Number:
MFCD31813801
MOL File:
1613264-40-6.mol
Last updated:2024-07-02 08:55:11

BAY 1316957) 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)
form Solid
pka 2.10±0.30(Predicted)
color White to off-white

BAY 1316957) price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ChemScene CS-0087003 BAY-1316957 1613264-40-6 5mg $150 2021-12-16 Buy
ChemScene CS-0087003 BAY-1316957 1613264-40-6 10mg $250 2021-12-16 Buy
ChemScene CS-0087003 BAY-1316957 1613264-40-6 25mg $550 2021-12-16 Buy
ChemScene CS-0087003 BAY-1316957 1613264-40-6 50mg $950 2021-12-16 Buy
ChemScene CS-0087003 BAY-1316957 1613264-40-6 100mg $1550 2021-12-16 Buy
Product number Packaging Price Buy
CS-0087003 5mg $150 Buy
CS-0087003 10mg $250 Buy
CS-0087003 25mg $550 Buy
CS-0087003 50mg $950 Buy
CS-0087003 100mg $1550 Buy

BAY 1316957) Chemical Properties,Uses,Production

Biological Activity

BAY-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

Raw materials

Preparation Products

BAY 1316957) Suppliers

Global( 16)Suppliers
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TargetMol Chemicals Inc.
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Nantong HI-FUTURE Biology Co., Ltd.
+undefined18051384581 sales@chemhifuture.com China 3136 58
Aladdin Scientific
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Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9707 58
ShangHai Biochempartner Co.,Ltd 17754423994 17754423994 2853530910@QQ.com China 8014 62
Shanghai Rechem science Co., Ltd. 21-31433387 15618786686 sales@rechemscience.com China 2991 58
Beijing Solarbio Science & Tecnology Co., Ltd. 010-50973130 4009686088 3193328036@qq.com China 29786 68
Zhaoqing Wanwei New Material Technology Co., Ltd. 0755-1328880-4488 13068786899 13288804488@163.com China 625 58
Fan De(Beijing) Biotechnology Co., Ltd. 15911056312 liming@bio-fount.com China 9730 58
DC Chemicals 021-58447131 13564518121 sales@dcchemicals.com China 9412 58
BAY 1316957) BAY-1316957 (BAY1316957 1H-Benzimidazole-5-carboxylic acid, 2-(9-ethyl-6-methyl-9H-carbazol-3-yl)-1-(2-methoxyethyl)-4-methyl- 1613264-40-6