426 Results for "

CDK 2

" in MedChemExpress (MCE) Product Catalog:
Products (426)

426 Results for "CDK 2" in MCE Product Catalog:

Cat. No.: HY-P3730
CAS No.: 237392-84-6
Target:  

CDK

Research Areas:  

Cancer

Cdk2/Cyclin Inhibitory Peptide I (Tat-LFG), a CDK2 inhibitor, kills U2OS osteosarcoma cells in a dose-dependent manner .
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Cat. No.: HY-178007
CAS No.: 3099145-52-2
Target:  

CDK

Research Areas:  

Cancer

CDK2 degrader 8 is a selective cyclin-dependent kinase 2 (CDK2) degrader. CDK2 degrader 8 can be used in studies related to CDK2 degradation and HR + HER2 - breast cancer .
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Cat. No.: HY-151580S
CAS No.: 2498658-25-4
CDK2-IN-14-d3 is a potent and selective CDK2 inhibitor. CDK2-IN-14-d3 can be used in research of cancer .
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Cat. No.: HY-178756
Target:  

CDK

Research Areas:  

Cancer

CDK2-IN-48 (Compound 109) is a CDK2 inhibitor with IC50 values for CDK2 and CDK1 of respectively < 0.05 and > 1 μM. CDK2-IN-48 can be used for the study of CDK2-dependent cancers .
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Cat. No.: HY-151580
CAS No.: 2862836-22-2
Target:  

CDK

Research Areas:  

Cancer

CDK2-IN-14 (compound 4f) is a highly selective CDK2 inhibitor. CDK2-IN-14 can be used in research of cancer .
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Cat. No.: HY-178112
Target:  

CDK Apoptosis

Research Areas:  

Cancer

CDK2-IN-47 is a potent CDK2 inhibitor with an IC50 of 0.21 μM. CDK2-IN-47 exhibits outstanding anticancer activity against MCF-7, HCT-116, and MGC-803 cell lines. CDK2-IN-47 effectively induces G1 cell cycle arrest, retinoblastoma protein (Rb) dephosphorylation, and significant apoptosis. CDK2-IN-47 can be used for the studies of breast cancer, colorectal cancer and gastric cancer .
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Cat. No.: HY-169048
CAS No.: 3034898-59-1
Target:  

CDK

Research Areas:  

Cancer

CDK2/4-IN-2 (compound 56) is a CDK2 and CDK4 dual inhibitor with IC50s less than 100 nM. CDK2/4-IN-2 can be used in the study of cancer .
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Cat. No.: HY-E70672
Target:  

CDK

Research Areas:  

Cancer

CDK2 is a cyclin-dependent kinase involved in the control of the cell cycle. CDK2/CycE1 Recombinant Human Active Protein Kinase is an ortholog of CDK2 .
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Cat. No.: HY-173124
Target:  

CDK VEGFR PDGFR Apoptosis

Research Areas:  

Cancer

CDK2/FLT4/PDGFRA-IN-1 (Compound 4a) is a potent inhibitor of CDK2/cyclin A, FLT4 (VEGFR3) and PDGFRA, with IC50s of 1.672, 0.554, and 0.629 μM, respectively. CDK2/FLT4/PDGFRA-IN-1 exhibits potent antiproliferative effects against cancer cells (lung EBC-1, pancreatic ductal adenocarcinoma AsPC-1, colorectal HT-29 cells). CDK2/FLT4/PDGFRA-IN-1 can also induce apoptosis in cancer cells .
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Cat. No.: HY-176124
CAS No.: 3030281-30-9
Research Areas:  

Cancer

CDK2 ligand-2 is a PROTAC target protein ligand (Ligands for Target Protein for PROTAC). CDK2 ligand-2 combined with E3 Ligase Ligand-linker Conjugate 184 (HY-176125) can be used to synthesize PROTAC degrader (CDK2 degrader 2 (HY-163815)) .
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Cat. No.: HY-RS02374
Research Areas:  

Others

CDK2 Human Pre-designed siRNA Set A contains three designed siRNAs for CDK2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS02375
Research Areas:  

Others

Cdk2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Cdk2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS02376
Research Areas:  

Others

Cdk2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Cdk2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-144810
CAS No.: 2919216-36-5
Target:  

CDK

Research Areas:  

Cancer

CDK2-IN-8 is a potent CDK2 inhibitor with an IC50 of 1.74 µM. CDK2-IN-8 shows antiproliferative activity. CDK2-IN-8 has the potential for the research of melanoma .
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Cat. No.: HY-160643
CAS No.: 2927473-94-5
Target:  

CDK

Research Areas:  

Cancer

CDK2-IN-27 (compound 1) is a potent CDK2 inhibitor with IC50 values of <10, >10-20 nM for CDK2/cyclin E1, CDK2/cyclin B1, respectively .
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Cat. No.: HY-144811
CAS No.: 2919216-33-2
Target:  

CDK Apoptosis

Research Areas:  

Cancer

CDK2-IN-9 is a potent CDK2 inhibitor with an IC50 of 0.63 µM. CDK2-IN-9 shows antiproliferative activity. CDK2-IN-9 induces apoptosis and cell cycle arrest at S and G2/M phase. CDK2-IN-9 has the potential for the research of melanoma .
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Cat. No.: HY-179161
Research Areas:  

Cancer

CDK2-IN-49 (Compound 5j) is a CDK2 inhibitor with an IC50 of 0.25 μM. CDK2-IN-49 shows potent activity against CDK7 with an IC50 of 0.14 μM. CDK2-IN-49 induces Apoptosis by raising the levels of p53 and Bax protein expression while reducing the amount of Bcl-2. CDK2-IN-49 inhibits cell division. CDK2-IN-49 can be used in the research of cancer .
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Cat. No.: HY-176174S
CAS No.: 2498658-21-0
CDK2-IN-46 (compound 5g) is a selective CDK2 inhibitor with an IC50 of 0.3 nM. CDK2-IN-46 has a selectivity of >200-fold for CDK1, CDK7, CDK9, CDK4, and CDK6. CDK2-IN-46 shows improves rat and cyno pharmacokinetic profiles .
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Cat. No.: HY-148651
CAS No.: 1219915-83-9
Target:  

CDK

Research Areas:  

Cardiovascular Disease Cancer

CDK2-IN-15 (Compound 19) is an inhibitor of CDK2 with an IC50 of 2.9 μM. CDK2-IN-15 can be used for cancer research .
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Cat. No.: HY-173203
Target:  

CDK

Research Areas:  

Cancer

CDK2-IN-43 (Compound 3a) is a CDK2-cyclin E2 inhibitor with an IC50 value of 6.0 nM. CDK2-IN-43 can be used in the research of the anti-cancer field .
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