WH-4-023

WH-4-023 Basic information
Product Name:WH-4-023
Synonyms:WH-4-023;2,6-DIMETHYLPHENYL 2,4-DIMETHOXYPHENYL(2-(4-(4-METHYLPIPERAZIN-1-YL)PHENYLAMINO)PYRIMIDIN-4-YL)CARBAMATE;Carbamic acid, N-(2,4-dimethoxyphenyl)-N-[2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-4-pyrimidinyl]-, 2,6-dimethylphenyl ester;KIN001-112;KIN112;2,6-dimethylphenyl (2,4-dimethoxyphenyl)(2-((4-(4-methylpiperazin-1-yl)phenyl)amino)pyrimidin-4-yl)carbamate WH-4-023;WH-4-023 2,6-DIMETHYLPHENYL 2,4-DIMETHOXYPHENYL(2-(4-(4-METHYLPIPERAZIN-1-YL)PHENYLAMINO)PYRIMIDIN-4-YL)CARBAMATE;WH-4-023, >=98%
CAS:837422-57-8
MF:C32H36N6O4
MW:568.67
EINECS:
Product Categories:Inhibitors;API
Mol File:837422-57-8.mol
WH-4-023 Structure
WH-4-023 Chemical Properties
Boiling point 743.2±70.0 °C(Predicted)
density 1.247±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility Soluble in DMSO (60 mg/ml)
form powder
pka7.89±0.42(Predicted)
color white to beige
Stability:Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 2 month.
Safety Information
RIDADR UN 2811 6.1 / PGIII
MSDS Information
WH-4-023 Usage And Synthesis
DescriptionWH-4-23 (837422-57-8) is a potent and selective inhibitor of Src family kinases Lck and Src, IC50=2 and 6 nM respectively.1,2 Also inhibits SIK, IC50=10, 22 and 60 nM for SIK 1, 2 and 3 respectively.3 May be used along with PD-325901 and CHIR-99021 to support self-renewal of na?ve human embryonic stem cells.4
UsesWH-4-023 is a potent and selective dual lymphocyte-specific kinase (Lck) inhibitor.
DefinitionChEBI: N-(2,4-dimethoxyphenyl)-N-[2-[4-(4-methyl-1-piperazinyl)anilino]-4-pyrimidinyl]carbamic acid (2,6-dimethylphenyl) ester is a member of piperazines.
Biochem/physiol ActionsWH-4-023 (KIN112) is a potent and selective inihbitor of the tyrosine kinases Lck and Src with IC50 values of 2 nM for Lck and 6 nM for Src. WH-4-023 is a somewhat less potent inhibitor of salt-inducible kinases (SIKs) with IC50 values of 10, 22 and 60 nM for SIK 1, 2 and 3 respectively. WH-4-023 was found to support self-renewal of naive human embryonic stem cells, in particular in combination with PD 0325901 (PZ0162), CHIR99021 (SML1046), and SB-590885 (SML0501).
storageStore at -20°C
ReferencesMartin et al. (2006), Novel 2-aminopyrimidine carbamates as potent and orally active inhibitors of Lck: synthesis, SAR, and in vivo anti-inflammatory activity; J. Med. Chem., 49 4981 Moroco et al. (2015), A discovery Strategy for Selective Inhibitors of c-Src in Complex with the Focal Adhesion Kinase SH3/SH2-binding Region; Chem. Biol. Drug. Des., 86 144 Clark et al. (2012), Phosphorylation of CRTC3 by the salt-inducible kinases controls the interconversion of classically activated and regulatory macrophages; Proc. Natl. Acad. Sci. USA, 109 16986 Theunissen et al. (2014), Systemic identification of culture conditions for introduction and maintenance of na?ve human pluripotency; Cell Stem Cell, 15 471
WH-4-023 Preparation Products And Raw materials
JX401 Olaparib Phenol, 3-[(6,7-diMethoxy-4-quinazolinyl)aMino]- JAK3 INHIBITOR II 2,4-Thiazolidinedione,5-(1,3-benzodioxol-5-ylmethylene)- ZM 306416 hydrochloride 7-BROMO-1,2,3,4-TETRAHYDRO-QUINOLINE HYDROCHLORIDE GW441756 IM-12 4-AMINO-3-CYANO-1,2,5,6-TETRAHYDROPYRIDINE 4-PHENYLAMINO-6,7-DIMETHOXYQUINAZOLINE PD 0325901 SB590885 Saracatinib JAK3 INHIBITOR I Y27632 (hydrochloride)

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