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Biochemical Reagents
Agonist Inhibitors
GSK J2
GSK J2
Product Name
GSK J2
CAS
1394854-52-4
MF
C22H23N5O2
MW
389.45
EINECS
MOL File
1394854-52-4.mol
Chemical Properties
Boiling point
609.9±55.0 °C(Predicted)
Density
1.292±0.06 g/cm3(Predicted)
storage temp.
Desiccate at RT
solubility
DMSO:40.47(Max Conc. mg/mL);103.91(Max Conc. mM)
form
Powder
pka
4.22±0.10(Predicted)
color
White to off-white
Usage And Synthesis
Uses
GSK J2 is the inactive isomer of GSK J1(G797553), which is a selective and potent inhibitor of JMJDE and UTX demethylases.
Definition
ChEBI: 3-[[2-(3-pyridinyl)-6-(1,2,4,5-tetrahydro-3-benzazepin-3-yl)-4-pyrimidinyl]amino]propanoic acid is an organonitrogen heterocyclic compound.
storage
Desiccate at RT
GSK J2 Supplier
BOC Sciences
Tel
1-631-485-4226; 16314854226
Email
info@bocsci.com
RuiErKang Pharmaceuticals, Inc.
Tel
2921645477
Email
2921645477@qq.com
Haoyuan Chemexpress Co., Ltd.
Tel
021-58950125
Email
info@chemexpress.com
LETOPHARM LIMITED
Tel
+86-21-5821 5861
Email
sales@letopharm.com
SPIRO PHARMA
Tel
Email
eric_feng1954@126.com
GSK J2 manufacturers
GSK-J2
Purity: 98.13%
$65.00
Inquiry
GSK-J2
Purity: 98.13%
$65.00
Inquiry
Related Product Information
GSK J1
GSK J4 HCl
GSK J5
Di-2-pyridyl ketone
5-Carboxy-8-hydroxyquinoline
Deferiprone
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