BAY-876

BAY-876 Structure
CAS No.
1799753-84-6
Chemical Name:
BAY-876
Synonyms
BAY-876;CS-2442;BAY876;BAY 876;BAY-876 >=98% (HPLC);N4-(1-(4-cyanobenzyl)-5-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl)-7-fluoroquinoline-2,4-dicarboxamide;N4-[1-[(4-cyanophenyl)methyl]-5-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]-7-fluoro-2,4-Quinolinedicarboxamide;2,4-Quinolinedicarboxamide, N4-[1-[(4-cyanophenyl)methyl]-5-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]-7-fluoro-;Inhibitor,metabolism,transporter,ovarian,BAY876,BAY 876,glycolytic,cancer,Glucose transporter,glucose,inhibit,BAY-876,orally,GLUT
CBNumber:
CB73133472
Molecular Formula:
C24H16F4N6O2
Molecular Weight:
496.42
MOL File:
1799753-84-6.mol
MSDS File:
SDS
Modify Date:
2023/6/30 15:45:59

BAY-876 Properties

Melting point >250oC (dec.)
Boiling point 632.3±55.0 °C(Predicted)
Density 1.48±0.1 g/cm3(Predicted)
storage temp. 2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
form powder
pka 10.33±0.70(Predicted)
color white to beige

BAY-876 price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) SML1774 BAY-876 ≥98% (HPLC) 1799753-84-6 5MG ₹19452.53 2022-06-14 Buy
Sigma-Aldrich(India) SML1774 BAY-876 ≥98% (HPLC) 1799753-84-6 25MG ₹78134.85 2022-06-14 Buy
Product number Packaging Price Buy
SML1774 5MG ₹19452.53 Buy
SML1774 25MG ₹78134.85 Buy

BAY-876 Chemical Properties,Uses,Production

Description

BAY-876 is a potent, highly selective, cell-permeable inhibitor of glucose transporter GLUT1. It had an IC50 value of 2 nM in vitro and inhibited glucose uptake by Hela-MaTu cells with an IC50 value of 3.2 nM. BAY-876 was at least 130-fold selective for GLUT1 relative to GLUT2, GLUT3, GLUT4 and a panel of 18 kinases and 68 proteins.BAY-588 is used as a negative control and is available from Sigma.

Uses

BAY-876 is a potent and selective inhibitor of glucose transporter 1 (Glut1) with IC50 values of 2, 10,800, 1,670, and 290 nM for Glut1, Glut2, Glut3, and Glut4, respectively, in CHO cells expressing human recombinant receptors.1 It shows low metabolic clearance and has high permeability in vitro. In vivo, BAY-876 displays low plasma clearance and high oral bioavailability in rats and dogs.

Biological Activity

Potent and selective GLUT1 inhibitor (IC50 = 2 nM). Displays selectivity for GLUT1 over GLUT2/3/4 (IC50 values are 10.8, 1.67 and 0.29 μM, respectively). Induces cell death in hypoxic conditions in vitro. Inhibits glucose uptake by Hela-MaTu cells. Cell permeable and orally bioavailable.

BAY-876 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 78)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
ATK CHEMICAL COMPANY LIMITED +undefined-21-51877795 China 32836 60 Inquiry
BOC Sciences +1-631-485-4226 United States 19553 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29824 58 Inquiry
Zhejiang J&C Biological Technology Co.,Limited +1-2135480471 +1-2135480471 China 10522 58 Inquiry
Labnetwork lnc. +86-27-50766799 +8618062016861 China 19994 58 Inquiry
InvivoChem +1-708-310-1919 +1-13798911105 United States 6393 58 Inquiry
LEAP CHEM CO., LTD. +86-852-30606658 China 24738 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 United States 19973 58 Inquiry
ShenZhen Trendseen Biological Technology Co.,Ltd. 13417589054 China 11681 58 Inquiry
Wuhan Topule Biopharmaceutical Co., Ltd +8618327326525 China 8474 58 Inquiry

1799753-84-6(BAY-876)Related Search:

N4-[1-[(4-cyanophenyl)methyl]-5-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]-7-fluoro-2,4-Quinolinedicarboxamide BAY-876 N4-(1-(4-cyanobenzyl)-5-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl)-7-fluoroquinoline-2,4-dicarboxamide CS-2442 BAY876;BAY 876 BAY-876 >=98% (HPLC) 2,4-Quinolinedicarboxamide, N4-[1-[(4-cyanophenyl)methyl]-5-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]-7-fluoro- Inhibitor,metabolism,transporter,ovarian,BAY876,BAY 876,glycolytic,cancer,Glucose transporter,glucose,inhibit,BAY-876,orally,GLUT 1799753-84-6