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Country: China (Mainland)
Business Type:Trading Company
Tel: +86-371- 86259723
Tel: 17734809689
Tel: 17734809689
Tel: 86-371-86259723
Tel: 17734809689
Tel: 17734809689
Mobile: 17734809689
Tel: +86-371- 86259723
Fax: +86-371- 86259723
Province/state: HENAN
City: ZHENGZHOU
Street: Mingmen International Center, NO.222 Dongming Road,Zhengzhou,Henan,China
MaxCard:
CAS NO.127191-97-3
1.Certificate Of Analysis (COA)
2.Material Safety Data Sheet (MSDS)
3.Route of synthesis (ROS)
4.Method of Aanlysis(MOA)
5.Nuclear Magnetic Resonance(NMR)
About Service
1. Quality control, before shipment, free sample for test.
2. Prompt shipment with professional documents
3. Packing as your request, with photo before shipment
4. Mixed containers with different mixed items in one container
About Company
Product Name: | KN-62 |
Synonyms: | KN-62;4-[(2S)-2-[(5-ISOQUINOLINYLSULFONYL)METHYLAMINO]-3-OXO-3-(4-PHENYL-1-PIPERAZINYL)PROPYL] PHENYL ISOQUINOLINESULFONIC ACID ESTER;1-[N,O-BIS-(5-ISOQUINOLINESULFONYL)-N-METHYL-L-TYROSYL]-4-PHENYLPIPERAZINE;(S)-5-ISOQUINOLINESULFONIC ACID 4-(2-[(5-ISOQUINOLINYLSULFONYL)METHYLAMINO]- 3-OXO-3-[4-PHENYL-1-PIPERAZINYL]PROPYL)PHENYL ESTER;1-(N,O-BIS-(5-ISOQUINOLINESULFONYL)-*N-M ETHYL-L-TYR;KN-62 97%;KN-62, 99+%;4-((2S)-2-((5-isoquinolinylsulfonyl)methylamino)-3-oxo-3-(4-phenyl-1-piperazinyl)propyl)phenylisoquinolinesulfonicacid |
CAS: | 127191-97-3 |
MF: | C38H35N5O6S2 |
MW: | 721.84 |
EINECS: | |
Product Categories: | Protein Kinase Inhibitors and Activators;Protein Kinase;Inhibitor |
Mol File: | 127191-97-3.mol |
KN-62 Chemical Properties |
mp | 92-94°C |
density | 1.388 |
storage temp. | −20°C |
solubility | 45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: 0.93 mg/mL |
form | solid |
color | white |
CAS DataBase Reference | 127191-97-3(CAS DataBase Reference) |
Safety Information |
Safety Statements | 24/25 |
WGK Germany | 3 |
MSDS Information |
Provider | Language |
---|---|
ACROS | English |
SigmaAldrich | English |
KN-62 Usage And Synthesis |
Chemical Properties | Yellow Solid |
Usage | A specific inhibitor of Ca2+/Calmodulin-dependent protein kinase II |
Usage | selectively inhibits rat brain Ca2+/cadmodulin-dependent protein kinase II, |
Biological Activity | Selective, cell-permeable inhibitor of CaM kinase II (IC 50 = 0.9 μ M). Binds directly to the calmodulin binding site of the enzyme. Potent non-competitive antagonist at the P2X 7 receptor (IC 50 = 15 nM). Also available as part of the Mixed Kinase Inhibitor Tocriset™ . |
KN-62 Preparation Products And Raw materials |