8 Results for "

pyrazolopyrimidine

" in MedChemExpress (MCE) Product Catalog:
Products (8)

8 Results for "pyrazolopyrimidine" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-10520
CAS No.: 522629-08-9
Purity:  98.71%
Target:  

MNK Apoptosis

Research Areas:  

Cancer

CGP 57380 is a cell-permeable pyrazolo-pyrimidine compound that acts as a selective inhibitor of Mnk1 with IC50 of 2.2 μM, but has no inhibitory activity against p38, JNK1, ERK1/2, PKC, or Src-like kinases.
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Cat. No.: HY-117882
CAS No.: 147676-50-4
Synonyms: Piperidino-acetildenafil
Target:  

Drug Intermediate

Research Areas:  

Others

Piperiacetildenafil (compound 3) is an intermediate for the preparation of pyrazolopyrimidines .
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Cat. No.: HY-157487
Target:  

Drug Derivative

Research Areas:  

Cancer

Anticancer agent 185 (compound 9d) is a glycohybrid derivative of pyrazolopyrimidine [1,5-a]. Anticancer agent 185 has good anti-breast cancer activity. Anticancer agent 185 shows good cytotoxic activity against MCF-7 cells with IC50 value of 15.3 μM .
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Cat. No.: HY-153246
CAS No.: 2414149-20-3
Research Areas:  

Cancer

ALK2-IN-5, pyrazolopyrimidine compound, is an ALK2 inhibitor. ALK2-IN-5 can inhibit ALK2 activity and FGFR activity. ALK2-IN-5 can be used for the research of disorders associated with ALK2 activity and/or FGFR activity, such as cancer .
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Cat. No.: HY-164413
CAS No.: 1312024-59-1
Target:  

VEGFR EGFR RET Apoptosis

Research Areas:  

Cancer

CLM3, a pyrazolopyrimidine derivative, is a multiple tyrosine kinase inhibitor. CLM3 shows antiproliferative and proapoptotic activity on endothelial and cancer cells, synergistically enhanced by SN38 (HY-13704). These effects are mainly due to its inhibition of phosphorylation of VEGFR-2, EGFR and RET tyrosine kinases and their related signaling pathways .
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Cat. No.: HY-163267
Target:  

Fluorescent Dye

Research Areas:  

Others

ZNL0325 is a covalent probe based on pyrazolopyrimidine. ZNL0325 features an acrylamide side chain at the C3 position, which is capable of forming covalent bonds with multiple kinases that possess a cysteine at the αD-1 position, including BTK, EGFR, BLK, and JAK3. ZNL0325 can be used in the research of creating structurally distinct covalent kinase inhibitors .
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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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Cat. No.: HY-10520R
CAS No.: 522629-08-9
Research Areas:  

Cancer

CGP 57380 (Standard) is the analytical standard of CGP 57380 (HY-10520). This product is intended for research and analytical applications. CGP 57380 is a cell-permeable pyrazolo-pyrimidine compound that acts as a selective inhibitor of Mnk1 with IC50 of 2.2 μM, but has no inhibitory activity against p38, JNK1, ERK1/2, PKC, or Src-like kinases.
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