13 Results for "

CDK12/13

" in MedChemExpress (MCE) Product Catalog:
Products (13)

13 Results for "CDK12/13" in MCE Product Catalog:

  • Targets Recommended:
Cat. No.: HY-151110
CAS No.: 3025994-75-3
Purity:  98.01%
Target:  

PROTACs CDK

Research Areas:  

Cancer

PROTAC CDK12/13 Degrader-1 (7f) is a highly selective cell cycle protein-dependent kinase CDK12/CDK13 dual degrader with the DC50 values of 2.2 nM and 2.1 nM, respectively. PROTAC CDK12/13 Degrader-1 has anti-proliferative activity and can be used in breast cancer research .
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Cat. No.: HY-151110A
Purity:  99.12%
Target:  

PROTACs CDK

Research Areas:  

Cancer

PROTAC CDK12/13 Degrader-1 (7f) TFA is a highly selective cell cycle protein-dependent kinase CDK12/CDK13 dual degrader with the DC50 values of 2.2 nM and 2.1 nM, respectively. PROTAC CDK12/13 Degrader-1 TFA has anti-proliferative activity and can be used in breast cancer research .
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Cat. No.: HY-145072
CAS No.: 2227392-55-2
Purity:  99.45%
Target:  

CDK

Research Areas:  

Cancer

BSJ-01-175 is a potent and selective CDK12/13 covalent inhibitor. BSJ-01-175 demonstrates exquisite selectivity, potent inhibition of RNA polymerase II phosphorylation, and downregulation of CDK12-targeted genes in cancer cells .
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Cat. No.: HY-173059
CAS No.: 3029608-57-6
Target:  

CDK

Research Areas:  

Cancer

CDK12/13-IN-3 (Compound 12b) is the orally active inhibitor for CDK that inhibits CDK12 and CDK13 with IC50 of 107.4 nM and 79.4 nM. CDK12/13-IN-3 inhibits the phosphorylation of Ser2 on the CTD of RNA polymerase II, induces DNA damage, and downregulates the gene expression of DNA damage response (DDR). CDK12/13-IN-3 exhibits antiproliferative activity against multiple cancer cells with IC50 of nanomolar levels. CDK12/13-IN-3 exhibits antitumor effect in mouse models, exhibits good pharmacokinetic properties with an oral bioavailability of 53.6% .
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Cat. No.: HY-173042
CAS No.: 3076450-41-1
Target:  

CDK

Research Areas:  

Cancer

CDK12/13-IN-2 (Compound 24) is a covalent inhibitor of CDK12/13, with IC50 values of 15.5 nM and 12.2 nM for CDK12 and CDK13, respectively. CDK12/13-IN-2 can inhibit the proliferation of breast cancer cells and can be used in the research of triple-negative breast cancer .
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Cat. No.: HY-168658
Research Areas:  

Cancer

CDK12/13 ligand 2 is a potent CDK12 and CDK13 ligand. CDK12/13 ligand 2 can be used to synthesize YJ1206 (HY-168555) .
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Cat. No.: HY-160284
CAS No.: 2407774-31-4
Target:  

CDK

Research Areas:  

Cancer

CDK12/13-IN-1 (Compound 4) is a CDK12/13 inhibitor. CDK12/13-IN-1 has antitumor activity .
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Cat. No.: HY-181036
Research Areas:  

Cancer

CDK12/13 ligand 3 is a CDK12/13 PROTAC ligand. CDK12/13 ligand 3 can be conjugated with E3 ligase ligand (HY-W093272) and linker to synthesize CDK12/13 PROTAC degrader DN1679 (HY-181035). CDK12/13 ligand 3 can be used for cancer research .
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Cat. No.: HY-48507
Research Areas:  

Others

CDK12/13 ligand 4 is a CDK12/13 ligand that can be used for the synthesis of PROTACs, such as PROTAC CDK12/13 Degrader-1 (HY-151110) .
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Cat. No.: HY-168197
Target:  

PROTACs

Research Areas:  

Cancer

Thalidomide-F-piperidine-piperazine-Cbz Conjugate 110 is a conjugate of E3 ligase and linker for the synthesis of CDK12/13 PROTAC degrader (HY-168162) .
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Cat. No.: HY-168163
CAS No.: 2244986-40-9
Target:  

CDK

Research Areas:  

Cancer

ALK-IN-29 (compound 4c) has a certain inhibitory effect on tyrosine protein kinases ALK, CDK2/CyclinE1 and FAK, among which the strongest inhibitory effect on ALK kinase is 40.63% at a concentration of 10 μM. ALK-IN-29 can be used for anti-cancer research .
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Cat. No.: HY-181035
Target:  

PROTACs CDK

Research Areas:  

Cancer

DN1679 is a potent, selective and orally active CRBN-dependent CDK12/13 PROTAC dual degrader. DN1679 shows DC50 of 8.8/9.8 nM (MDA-MB-231), 5.1/6.4 nM (MDA-MB-157) and 17.2/15.8 nM (MDA-MB-468) for CDK12/13. DN1679 can downregulate DNA damage response gene mRNA levels, such as ATM, ATR, BRCA1 and RAD51. DN1679 demonstrates a potent synergistic anti-tumor effect companied with Olaparib (HY-10162). DN1679 can be used for research of triple-negative breast cance .
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Cat. No.: HY-181645
CAS No.: 3024723-74-5
Target:  

CDK

Research Areas:  

Cancer

CDK12-IN-9 is a potent and selective CDK12 inhibitor with an IC50 of 2.2 nM. CDK12-IN-9 inhibits pSER2 (a downstream marker of CDK12/13 activity). CDK12-IN-9 can be used for the research of cancer .
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