10 Results for "

Pyrrolopyrimidine

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "Pyrrolopyrimidine" in MCE Product Catalog:

12
12 Cited Publications
Cat. No.: HY-15764
CAS No.: 364042-47-7
Purity:  99.75%
Synonyms: RK-20449
Target:  

Src Apoptosis

Research Areas:  

Cancer

A 419259 is a broad-spectrum pyrrolo-pyrimidine inhibitor, has high selectivity towards the Src family. A 419259 shows inhibitory effect for Src, Lck and Lyn with IC50 of 9 nM, <3 nM and <3 nM, respectively .
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Cat. No.: HY-69047
CAS No.: 84955-31-7
Target:  

IKK

Research Areas:  

Others

6-Chloro-7-deazaguanine is an inactive molecule of IKK (lacking the critical 5-cyano group). IKKβ and IKKα are core molecules in the canonical NF-κB pathway and non-canonical NF-κB pathway, respectively .
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Cat. No.: HY-149530
CAS No.: 3055550-22-3
Purity:  99.92%
Target:  

EGFR Apoptosis

Research Areas:  

Cancer

EGFR-IN-86 (compound 4i) is an EGFR inhibitor (IC50: 1.5 nM) with high activity against glioblastoma. EGFR-IN-86 induces apoptosis and arrests the U87 cell cycle in the G2/M phase .
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Cat. No.: HY-175428
CAS No.: 518063-75-7
Target:  

Antifolate

Research Areas:  

Cancer

Antifolate agent 1 is a 6-substituted pyrrolopyrimidine antifolate with a 1-carbon bridge. Antifolate agent 1 shows no activity against cells expressing FRα and FRβ, and has no GARFTase inhibitory activity. Antifolate agent 1 can be used as a negative control in the development of folate receptor-targeted antifolates .
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Cat. No.: HY-W059210
CAS No.: 952518-97-7
Research Areas:  

Others

Ruxolitinib impurity-1 is a pyrrolopyrimidine derivative and also an impurity of Ruxolitinib (HY-50856). Ruxolitinib serves as a synthetic intermediate for TDM-180967, a dual JAK1/Tyk2 inhibitor, and can also be used as an impurity reference standard for drug quality control .
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Cat. No.: HY-150021
CAS No.: 2410793-22-3
Research Areas:  

Others

GRK5-IN-3 is a covalent inhibitor of GRK5 (G Protein-Coupled Receptor Kinase 5). GRK5-IN-3 shows potent inhibitory effect to GRK5 and GRK6 with IC50s of 0.22 μM and 0.41 μM, respectively .
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Cat. No.: HY-150022
CAS No.: 2410794-89-5
Synonyms: CCG-265328
GRK5-IN-4 (Compound 16d, CCG-265328) is a potent and and selective covalent GRK5 (G protein-coupled receptor kinase 5) inhibitor, with an IC50 of 1.1 μM. GRK5-IN-4 shows 90-fold selectivity over GRK2. GRK5-IN-4 can be used for heart failure research . GRK5-IN-4 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Cat. No.: HY-150752
CAS No.: 2820426-92-2
Target:  

Btk Pyroptosis

Research Areas:  

Cancer

BTK-IN-15 (compound 42) is a potent Bruton's tyrosine kinase (BTK) inhibitor with high oral absorption. BTK-IN-15 inhibits BTK with an IC50 value of 0.7 nM. BTK-IN-15 displays excellent kinase selectivity, antitumor activity, and induces apoptosis .
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Cat. No.: HY-111147
CAS No.: 914496-19-8
Target:  

HIV

Research Areas:  

Infection

RDEA-427 is a pyrrolopyrimidine derivative and also a HIV-1 non-nucleoside reverse transcriptase inhibitor (NNRTI). RDEA-427 acts on wild-type and NNRTI-resistant mutant HIV-1. RDEA-427 can be used in research related to HIV infection .
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Cat. No.: HY-P11927
Target:  

GSK-3

Research Areas:  

Cancer

BiS3 is a selective hyperbivalent macrocyclic peptide GSK3β inhibitor, with a Kd of 0.28 nM and an IC50 of 4.8 nM against GSK3β. BiS3 is applicable to studies related to GSK3β signaling and colorectal cancer .
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