11 Results for "

CDK9-IN-2

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "CDK9-IN-2" in MCE Product Catalog:

7
7 Cited Publications
Cat. No.: HY-16462
CAS No.: 1263369-28-3
Target:  

CDK

Research Areas:  

Cancer

CDK9-IN-2 is a special cyclin-dependent kinase 9 (CDK9) inhibitor, extracted from patent WO/2012131594A1, compound CDKI(8), has an IC50 of 5 nM and 7 nM in H929 multiple myeloma(MM) cell line (72 hours) and A2058 skin cell line (72 hours), respectively.
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Cat. No.: HY-112811
CAS No.: 2435721-30-3
Target:  

PROTACs CDK

Research Areas:  

Cancer

PROTAC CDK9 degrader-2 is a PROTAC degrader targeting CDK9, with an IC50 of 523 nM. PROTAC CDK9 degrader-2 selectively degrades CDK9 via the cereblon-dependent ubiquitin-proteasome pathway and inhibits the proliferation of cancer cells overexpressing CDK9. PROTAC CDK9 degrader-2 can be used for cancer research .
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Cat. No.: HY-176165
CAS No.: 3081246-18-3
Research Areas:  

Cancer

CDK9/EZH2-IN-1 (Compound D16) is a CDK9/EZH2 dual-target inhibitor (IC50: 83.9/108.6 nM). CDK9/EZH2-IN-1 induces apoptosis and DNA double-strand breaks (DSBs). CDK9/EZH2-IN-1 inhibits the proliferation activity of MKN45, MDA-MB-453 and SW620 cancer cells (IC50 values are 136.3, 171.3 and 315.7 nM, respectively) .
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Cat. No.: HY-147797
CAS No.: 1180924-34-8
Target:  

EGFR CDK

Research Areas:  

Cancer

EGFR/HER2/CDK9-IN-2 (Compound 9) is a potent inhibitor of EGFR/HER2/CDK9 with IC50s of 145.35, 129.07, and 117.13 nM, respectively. EGFR/HER2/CDK9-IN-2 exhibits remarkable antitumor activity .
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Cat. No.: HY-156083
CAS No.: 3020773-81-0
Research Areas:  

Cancer

CDK9 degrader-2 is a bifunctional degrader of ATTEC (Autophagy-Tethering Compound) that degrades the CDK9/cyclin T1 complex. CDK9 degrader-2 forms a ternary complex with CDK9 and LC3B, and achieves degradation through the autophagy-lysosome pathway, a process independent of the ubiquitin-proteasome system. CDK9 degrader-2 downregulates the expression of Mcl-1 and c-Myc proteins, induces apoptosis, and exhibits antitumor activity in in vivo MV4-11 xenograft models. CDK9 degrader-2 can be used for leukemia research .
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Cat. No.: HY-130850
CAS No.: 3542-63-0
Purity:  98.09%
Research Areas:  

Cancer

CDK9-IN-10 is a potent CDK9 inhibitor. CDK9-IN-10 is the ligand for the PROTAC CDK9 degrader-2 (HY-112811) .
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Cat. No.: HY-160235
CAS No.: 2732859-29-7
Research Areas:  

Cancer

Pomalidomide-C2-amide-C5-azidea is an E3 linker conjugate, pomalidomide, that can be used to synthesize highly effective PROTAC molecules towards CDK9. Pomalidomide-C2-amide-C5-azidea has antiproliferative activity .
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Cat. No.: HY-147796
CAS No.: 879730-44-6
Target:  

EGFR CDK

Research Areas:  

Cancer

EGFR/HER2/CDK9-IN-1 (Compound 4) is a potent inhibitor of EGFR/HER2/CDK9 with IC50s of 90.17, 131.39, and 67.04 nM, respectively. EGFR/HER2/CDK9-IN-1 exhibits remarkable antitumor activity .
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Cat. No.: HY-147798
CAS No.: 422276-47-9
Target:  

EGFR CDK

Research Areas:  

Cancer

EGFR/HER2/CDK9-IN-3 (Compound 10) is a potent inhibitor of EGFR/HER2/CDK9 with IC50s of 191.08, 132.65, and 113.98 nM, respectively. EGFR/HER2/CDK9-IN-3 exhibits remarkable antitumor activity .
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Cat. No.: HY-189422
Research Areas:  

Cancer

CDK9/EZH2-IN-2 is a potent dual CDK9 and EZH2 inhibitor with an IC50 of 8.9 nM against EZH2. CDK9/EZH2-IN-2 inhibits anti-apoptotic proteins and induces DNA damage by blocking the activity of CDK9 and EZH2, ultimately leading to tumor cell apoptosis. CDK9/EZH2-IN-2 can be used for research on diffuse large B-cell lymphoma .
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Cat. No.: HY-150946
CAS No.: 1453836-45-7
Research Areas:  

Cancer

CDK9 ligand 2 (compound CDK9 ligand 4) is a CDK9 ligand. CDK9 ligand 2 is used for the synthesis of PROTAC CDK9 degrader-14 (HY-133617) .
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