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NU6102

CAS No.
444722-95-6
Chemical Name:
NU6102
Synonyms
NU6102;CDK1/2 INHIBITOR II;O6-CYCLOHEXYLMETHYL-2-(4-SULFAMOYLANILINO)PURINE;6-CYCLOHEXYLMETHOXY-2-(4'-SULFAMOYLANILINO)PURINE;4-[[6-(Cyclohexylmethoxy)-1H-purin-2-yl]amino]benzenesulfonamide;Benzenesulfonamide, 4-[[6-(cyclohexylmethoxy)-9H-purin-2-yl]amino]-
CBNumber:
CB0811835
Molecular Formula:
C18H22N6O3S
Molecular Weight:
402.47
MDL Number:
MFCD08702693
MOL File:
Mol file
Last updated:2023-06-30 15:45:59

NU6102 Properties

Melting point 152-154℃ (water )
storage temp. Store at -20°C
solubility DMSO:1.0(Max Conc. mg/mL);2.5(Max Conc. mM)
form White to off-white solid.
color White to off-white
FDA UNII X5J53DR704

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS08
Signal word  Warning
Hazard statements  H341
Precautionary statements  P201-P202-P280-P308+P313-P405-P501

NU6102 price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 217713 Cdk1/2 Inhibitor II, NU6102 - CAS 444722-95-6 - Calbiochem 444722-95-6 1mg $172 2024-03-01 Buy
Sigma-Aldrich 217713 Cdk1/2 Inhibitor II, NU6102 - CAS 444722-95-6 - Calbiochem 444722-95-6 5mg $322 2023-01-07 Buy
Cayman Chemical 13317 NU 6102 ≥95% 444722-95-6 1mg $54 2024-03-01 Buy
Cayman Chemical 13317 NU 6102 ≥95% 444722-95-6 5mg $168 2024-03-01 Buy
TRC N925290 NU6102 444722-95-6 50mg $835 2021-12-16 Buy
Product number Packaging Price Buy
217713 1mg $172 Buy
217713 5mg $322 Buy
13317 1mg $54 Buy
13317 5mg $168 Buy
N925290 50mg $835 Buy

NU6102 Chemical Properties,Uses,Production

Uses

Cyclin-dependent kinases (CDKs) play a key role in regulating cell division by phosphorylating distinct substrates in different phases of the cell cycle. Cell cycle deregulation in many cancers often results from altered CDK activity. Thus, CDKs are potential pharmacological targets for anticancer agents. NU 6102 is a potent inhibitor of Cdk1 and Cdk2 with Ki values of 9 and 6 nM and IC50 values of 9.5 and 5.4 nM, respectively. NU 6102 inhibits Cdk4 activity with an IC50 value of 1.6 μM, suggesting it is most selective for Cdk2. Time-lapse videomicroscopy reveals that 20 μM NU 6102 delays cell entry into mitosis where most cells appear to eventually complete mitotic division but cannot correctly undergo cytokinesis, and hence become binucleated with an abnormal number of centrosomes. In SKUT-1B cancer cells a 24 h exposure to NU 6102 induced G2 arrest, inhibition of target protein phosphorylation, and cytotoxicity with an LC50 value of 2.6 μM.

Uses

NU6102 is a known potent inhibitor of CDK1, CDK2 and CDK7. Cyclin-dependent kinases play a key role in the regulation of cell division which is controlled by the phosphorylation of distinct substrates in different phases of the cell cycle. In any circumstance where the cell cycle is deregulated, cyclin-dependent kinases activities are altered. Since NU6102 is known to exert inhibitory activities against CDKs, it has potential to act as a control in the cell cycle, especially in various cancers. NU6102 is known to be an anticancer agent use to repress the expression of breast cancer cells.

storage

+4°C

NU6102 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 45)Suppliers
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TargetMol Chemicals Inc.
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Aladdin Scientific
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J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
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AdooQ BioScience, LLC +1 (866) 930-6790 info@adooq.com United States 2784 58
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Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9709 58
Shanghai Changyan Chem & Tech Co., Ltd. 021-021-20242659 18930833303 order@changyanchem.com China 5008 55
Shenzhen Polymeri Biochemical Technology Co., Ltd. +86-400-002-6226 13028896684 sales@rrkchem.com China 55827 58
6-CYCLOHEXYLMETHOXY-2-(4'-SULFAMOYLANILINO)PURINE CDK1/2 INHIBITOR II NU6102 O6-CYCLOHEXYLMETHYL-2-(4-SULFAMOYLANILINO)PURINE 4-[[6-(Cyclohexylmethoxy)-1H-purin-2-yl]amino]benzenesulfonamide Benzenesulfonamide, 4-[[6-(cyclohexylmethoxy)-9H-purin-2-yl]amino]- 444722-95-6