6 Results for "

MKN1

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "MKN1" in MCE Product Catalog:

Cat. No.: HY-175842
CAS No.: 3030279-55-8
Target:  

PROTACs CDK

Research Areas:  

Cancer

PROTAC CDK2 Degrader-2 is an orally active CDK2 PROTAC degrader, with DC50 values of 13 nM (MKN1cells) and 17 nM (TOV21G cells). PROTAC CDK2 Degrader-2 induces G1 phase arrest in MKN1 cells. PROTAC CDK2 Degrader-2 achieves tumor stasis in HCC1569 (CCNE1-amplified) xenograft models. PROTAC CDK2 Degrader-2 can be used for the study of CCNE1-amplified cancers [1].
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Cat. No.: HY-163815
CAS No.: 3030271-16-7
Target:  

PROTACs CDK

Research Areas:  

Cancer

CDK2 degrader 2 (Compound I-10) is a PROTAC degrader for CDK2 that degrades CDK2 in MKN1 cell with a DC50 <100 nM [1].
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Cat. No.: HY-156792
CAS No.: 1088216-72-1
Target:  

RIO Kinase

Research Areas:  

Cancer

RIOK2-IN-1 (com 4) is a potent and selective RIOK2 inhibitor (Kd=150 nM), but has low cellular activity (IC50=14,600 nM). RIOK2 is an atypical kinase associated with a variety of human cancers and is involved in ribosome maturation and cell cycle progression. The small molecule inhibitor CQ211 (HY-147655), an improvement of RIOK2-IN-1 as the lead compound, has good in vivo and in vitro activity, inhibits the proliferation of MKN-1 and HT-29 cancer cells, and can xenograft MKN in mice -1 model inhibits tumor progression [1].
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Cat. No.: HY-156465
CAS No.: 2648987-17-9
Target:  

RIO Kinase

Research Areas:  

Cancer

RIOK2-IN-2 (8) is a RIOK2 inhibitor, with IC50 values of 3.02 μM and 5.34 μM in MKN-1 and MOLT4 cells, respectively [1].
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Cat. No.: HY-161463
CAS No.: 3025006-64-5
Target:  

CDK

Research Areas:  

Cancer

CDK2-IN-28 (compound 22) is a CDK2 inhibitor with good selectivity and cellular effects against other CDKs. CDK2-IN-28 has anti-proliferative effects on MKN1 cells (EC50: 0.31 μM) [1].
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Cat. No.: HY-179430
Target:  

Mps1

Research Areas:  

Cancer

TTK-IN-5 is an orally active covalent threonine tyrosine kinase (TTK) inhibitor with selectivity (IC50 = 8.918 nM). TTK-IN-5 exhibits anti-proliferative potencies against MDA-MB-231, A2780, HCT116, HCC1569 and MKN1 cell lines (IC50 values of 0.113 μM, 0.476 μM, 3.136 μM, 3.649 μM, and 1.856 μM, respectively). TTK-IN-5 potently suppresses tumor growth without notable toxicity in A2780 and MDA-MB-231 xenograft mouse models. TTK-IN-5 can be used for the research of cancer such as breast cancer and ovarian cancer [1].
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