7 Results for "

2-aminopyrimidine compound

" in MedChemExpress (MCE) Product Catalog:
Products (7)

7 Results for "2-aminopyrimidine compound" in MCE Product Catalog:

Cat. No.: HY-41340
CAS No.: 109-12-6
2-Aminopyrimidine is an important heterocyclic intermediate. 2-Aminopyrimidine can undergo various reactions such as alkylation and acylation, and can be used for the synthesis of other active compounds .
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Cat. No.: HY-41340R
CAS No.: 109-12-6
2-Aminopyrimidine (Standard) is the analytical standard of 2-Aminopyrimidine (HY-41340). This product is intended for research and analytical applications. 2-Aminopyrimidine is an important heterocyclic intermediate. 2-Aminopyrimidine can undergo various reactions such as alkylation and acylation, and can be used for the synthesis of other active compounds.
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Cat. No.: HY-W720946
CAS No.: 2733146-01-3
2-Aminopyrimidine-d2 is the deuterium labeled 2-Aminopyrimidine (HY-41340). 2-Aminopyrimidine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-162530
CAS No.: 3033950-84-1
Target:  

CDK

Research Areas:  

Cancer

CDK4/6-IN-20 (Compound II-5) is a CDK4/CDK6 inhibitor with IC50 values ​​of 1.9, 14.2 nM, respectively. CDK4/6-IN-20 also inhibits cell proliferation and can be used in cancer research .
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Cat. No.: HY-149889
CAS No.: 3042104-73-1
Purity:  99.57%
Target:  

Apoptosis EGFR

Research Areas:  

Cancer

EGFR-IN-78 (compound A5),a 2-aminopyrimidine derivative,is a reversible inhibitor of EGFR C797S-TK,and also an inducer of apoptosis. EGFR-IN-78 shows anti-proliferative activity,inhibits EGFR phosphorylation and arrests cell cycle at G2/M phase .
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Cat. No.: HY-162529
CAS No.: 3033950-86-3
Target:  

CDK

Research Areas:  

Cancer

CDK4/6-IN-19 (Compound II-7) is a CDK4/CDK6 inhibitor with IC50 values ​​of 0.2, 5.0 nM, respectively. CDK4/6-IN-19 also inhibits cell proliferation and can be used in cancer research .
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Cat. No.: HY-123599
CAS No.: 1884209-98-6
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

IACS-4619 (compound 4) is a highly selective 2-aminopyrimidine-based MTH1 (MutT homolog 1) inhibitor (IC50=0.2 nM). IACS-4619 inhibits MTH1 by blocking its hydrolysis of oxidized purine nucleotides such as 8-oxo-dGTP, thereby preventing MTH1 from inhibiting the incorporation of oxidized nucleotides into DNA. IACS-4619 significantly inhibits endogenous MTH1 activity in MTH1-overexpressing U2OS cells, but without antiproliferative or cytotoxic effects on various human cancer and normal cell lines. IACS-4619 can be used in oncology research related to the MTH1 target .
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