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AZD 5438

CAS No.
602306-29-6
Chemical Name:
AZD 5438
Synonyms
AZD;CS-1903;AZD 5438;AZD5438, >=98%;AZD 5438; AZD5438;AZD 5438 USP/EP/BP;AZD5438 >=97% (HPLC);4-[2-Methyl-1-(1-Methylethyl)-1H-iMidazol-5-yl]-N-[4-(Methylsulfonyl)phenyl]-;4-[2-Methyl-1-isopropyl-1H-imidazol-5-yl]-N-[4-(methylsulfonyl)phenyl]-2-pyrimidinamine;4-[2-Methyl-1-(1-methylethyl)-1H-imidazol-5-yl]-N-[4-(methylsulfonyl)phenyl]-2-pyrimidinamine
CBNumber:
CB61512498
Molecular Formula:
C18H21N5O2S
Molecular Weight:
371.46
MDL Number:
MFCD11112135
MOL File:
602306-29-6.mol
Last updated:2023-06-30 15:45:59

AZD 5438 Properties

Boiling point 655.2±65.0 °C(Predicted)
Density 1.31
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility insoluble in H2O; ≥18.55 mg/mL in DMSO; ≥42.1 mg/mL in EtOH
form solid
pka 4.08±0.50(Predicted)
FDA UNII 276Z913G29

SAFETY

Risk and Safety Statements

Hazard statements  H401
Precautionary statements  P273-P501

AZD 5438 price More Price(33)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML1855 AZD5438 ≥97% (HPLC) 602306-29-6 5MG $105 2024-03-01 Buy
Sigma-Aldrich SML1855 AZD5438 ≥97% (HPLC) 602306-29-6 25MG $424 2024-03-01 Buy
Cayman Chemical 21598 AZD 5438 ≥98% 602306-29-6 5mg $89 2024-03-01 Buy
Cayman Chemical 21598 AZD 5438 ≥98% 602306-29-6 10mg $168 2024-03-01 Buy
Cayman Chemical 21598 AZD 5438 ≥98% 602306-29-6 25mg $374 2024-03-01 Buy
Product number Packaging Price Buy
SML1855 5MG $105 Buy
SML1855 25MG $424 Buy
21598 5mg $89 Buy
21598 10mg $168 Buy
21598 25mg $374 Buy

AZD 5438 Chemical Properties,Uses,Production

Uses

AZD 5438 is a potent oral inhibitor of cyclin-dependent kinases 1, 2, and 9, which leads to leads to pharmacodynamic changes and potent antitumor effects in human tumor xenografts.

Definition

ChEBI: 4-(2-methyl-3-propan-2-yl-4-imidazolyl)-N-(4-methylsulfonylphenyl)-2-pyrimidinamine is a sulfonamide.

Biological Activity

azd5438 is a potent small molecule inhibitor of cyclin-dependent kinase (cdk) 1, 2 and 9 with half maximal inhibitory concentration ic50 of 16 nmol/l, 6 nmol/l and 20 nmol/l respectively. azd5438 has also been found to potently inhibit the human cyclin e/cdk2 complex, the cyclin b1/cdk1 complex and the cyclin a/cdk2 complex with ic50 of 0.006 μm, 0.016 μm and 0.045 μm respectively. in previous studies, azd5438 has exhibited significant anti-proliferative activity in a few human tumor cell lines with ic50 ranging from 0.2 μmol/l to 1.7 μmol/l, in which the phosphorylation of a few proteins, including cdk substrates prb, nucleolin, protein phosphatase 1a and rna polymerase ii cooh-terminal domain, and cell cycling at g2-m, s and g1 phases were inhibited.

storage

Desiccate at RT

References

[1]camidge dr1, smethurst d, growcott j, barrass nc, foster jr, febbraro s, swaisland h, hughes a. a first-in-man phase i tolerability and pharmacokinetic study of the cyclin-dependent kinase-inhibitor azd5438 in healthy male volunteers. cancer chemother pharmacol. 2007 aug;60(3):391-8. epub 2006 nov 18.
[2]byth kf, thomas a, hughes g, forder c, mcgregor a, geh c, oakes s, green c, walker m, newcombe n, green s, growcott j, barker a, wilkinson rw. azd5438, a potent oral inhibitor of cyclin-dependent kinases 1, 2, and 9, leads to pharmacodynamic changes and potent antitumor effects in human tumor xenografts. mol cancer ther. 2009 jul;8(7):1856-66. doi: 10.1158/1535-7163.mct-08-0836. epub 2009 jun 9.

AZD 5438 Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 137)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Biochempartner
0086-13720134139 candy@biochempartner.com CHINA 967 58
Hubei xin bonus chemical co. LTD
86-13657291602 linda@hubeijusheng.com CHINA 22968 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63711 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
career henan chemical co
+86-0371-86658258 15093356674; factory@coreychem.com China 29826 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
ANHUI WITOP BIOTECH CO., LTD
+8615255079626 eric@witopchemical.com China 23556 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29271 58

View Lastest Price from AZD 5438 manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
AZD 5438 pictures 2019-12-26 AZD 5438
602306-29-6
US $9.80 / KG 1g ≥99% 100kg Career Henan Chemical Co
  • AZD 5438 pictures
  • AZD 5438
    602306-29-6
  • US $9.80 / KG
  • ≥99%
  • Career Henan Chemical Co

AZD 5438 Spectrum

2-Pyrimidinamine,4-[2-methyl-1-(1-methylethyl)-1H-imidazol-5-yl]-N-[4-(methylsulfonyl)phenyl]- AZD 5438 4-[2-Methyl-1-(1-methylethyl)-1H-imidazol-5-yl]-N-[4-(methylsulfonyl)phenyl]-2-pyrimidinamine 4-[2-Methyl-1-(1-Methylethyl)-1H-iMidazol-5-yl]-N-[4-(Methylsulfonyl)phenyl]- 2-Pyrimidinamine,4-[2-methyl-1-(1-methylethyl)-1H-imidazol-5-yl]-N-[4-(methylsulfonyl)phenyl]-(AZD 5438) 4-[2-Methyl-1-isopropyl-1H-imidazol-5-yl]-N-[4-(methylsulfonyl)phenyl]-2-pyrimidinamine 4-[2-Methyl-1-isopropyl-1H-imidazol-5-yl]-N-[4-(methylsulfonyl)phenyl]-2-pyrimidinamine AZD 5438 AZD 5438 4-[2-Methyl-1-isopropyl-1H-imidazol-5-yl]-N-[4-(methylsulfonyl)phenyl]-2-pyrimidinamine AZD5438, >=98% AZD 5438 USP/EP/BP AZD5438 >=97% (HPLC) AZD 5438; AZD5438 CS-1903 AZD 602306-29-6 C18H21N5O2S Inhibitors API intermediates Potent inhibitor of cyclin-dependent kinase (cdk) 1, 2 and 9.