GSK180

GSK180 Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: CAS:1799725-26-0
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:GSK180
CAS:1799725-26-0
Purity:98.00% Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: InvivoChem
Tel: +1-708-310-1919 +1-13798911105
Email: sales@invivochem.cn
Products Intro: Product Name:GSK180
CAS:1799725-26-0
Purity:98% Package:10mg Remarks:V32226
Company Name: Suzhou ARTK Medchem Co., Ltd.
Tel: +86-512-68323967 +86-18015559028
Email: sales1@artkmedchem.com
Products Intro: Product Name:GSK-180
CAS:1799725-26-0
Purity:0.98 Package:100KG;25KG;10KG;1KG
Company Name: Shanghai Chaolan Chemical Technology Center  
Tel: QQ:65489617 15618227136
Email: info@SuperLan-chem.com
Products Intro: Product Name:GSK180
CAS:1799725-26-0
Purity:98% HPLC Package:5MG;10MG;50MG;100MG,1G,5G,500G
GSK180 Basic information
Product Name:GSK180
Synonyms:GSK180 (GSK 180;3(2H)-Benzoxazolepropanoic acid, 5,6-dichloro-2-oxo-;GSK180
CAS:1799725-26-0
MF:C10H7Cl2NO4
MW:276.07
EINECS:
Product Categories:
Mol File:1799725-26-0.mol
GSK180 Structure
GSK180 Chemical Properties
Boiling point 483.8±55.0 °C(Predicted)
density 1.626±0.06 g/cm3(Predicted)
solubility ≥27.6 mg/mL in DMSO; insoluble in H2O; ≥14.04 mg/mL in EtOH with ultrasonic
form solid
pka4.34±0.10(Predicted)
Safety Information
MSDS Information
GSK180 Usage And Synthesis
Biological Activitygsk180 is a potent, selective and competitive inhibitor of kynurenine-3-monooxygenase (kmo) with an ic50 of ~6 nm. [1]gsk180 inhibited endogenous kmo action in primary human hepatocytes with similar potency (ic50 = 2.6 μm). gsk180 is proper for i.v. administration. gsk180 inhibited rat kmo mildly less potently than it did the human enzyme with an ic50 of 7 μm. gsk180 exhibited a concentration-dependent displacement of tryptophan from plasma proteins. [1]gsk180 was dosed to kmowt and kmonull mice as a bolus injection at 30 mg/kg, which delivered plasma levels 1 h after dosage of 263 ± 98 μm and 351 ± 87 μm, respectively. gsk180 resulted in a promotion in kynurenine in kmowt mice, but no change was detected in the kmonull mice, which confirms that this increase results from the inhibition of kmo. gsk180 caused an evident reduction in circulating tryptophan levels in both kmowt and kmonull mice, suggesting that the chemical had an additional effect unrelated to kmo inhibition. gsk180 is excepted from rat erythrocytes (blood:plasma ratio of 0.46), and it is modestly bound to rat plasma proteins (free fraction 7.7% at 1 mm, n = 2), meaning that the top free drug levels in plasma (92 μm) are >12-fold above the ic50 in cells. treatment with gsk180 resulted in a rapid promotion in the circulating levels of both kynurenine and kynurenic acid, which restablished to baseline as the drug levels dropped. the fierce inflammatory cell infiltrate in ap consisted of mpo-positive neutrophils and monocytes positive for the ed1 antigen, the rat ortholog of cd68, which were present to the same extent in the pancreas tissue of rats with induced ap and rats with induced ap treated with gsk180. [1][1]. kynurenine-3-monooxygenase inhibition prevents multiple organ failure in rodent models of acute pancreatitis.nat med. 2016 feb;22(2):202-9.
GSK180 Preparation Products And Raw materials
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