8 Results for "

Mps1-IN-1

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

8 Results for "Mps1-IN-1" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-13298
CAS No.: 1125593-20-5
Purity:  99.77%
Target:  

Mps1

Research Areas:  

Cancer

Mps1-IN-1 is a potent, selective and ATP-competitive Mps1 kinase inhibitor, with an IC50 and a Kd of 367 nM and 27 nM .
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Cat. No.: HY-13994
CAS No.: 1228817-38-6
Purity:  98.04%
Research Areas:  

Cancer

Mps1-IN-2 is a potent, selective and ATP-competitive dual Mps1/Plk1 inhibitor, with an IC50 and a Kd of 145 nM and 12 nM for Mps1 and a Kd of 61 nM for Plk1.
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Cat. No.: HY-110347
CAS No.: 1883548-93-3
Target:  

Mps1

Research Areas:  

Cancer

Mps1-IN-1 dihydrochloride is a potent and ATP-competitive Mps1 kinase inhibitor with an IC50 of 367 nM. Mps1-IN-1 dihydrochloride inhibit Mps1 mitotic kinase activity and abrogates spindle assembly checkpoint (SAC) function. Mps1-IN-1 dihydrochloride decreases the viability of both cancer and ‘normal’ cells .
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Cat. No.: HY-168540
Research Areas:  

Cancer

PROTAC MPS1 degrader 1 is a selective monopolar spindle 1 (Mps1/TTK) PROTAC degrader, with DC50 values of 17.7, 108.67 and 570.25 nM against TTK, AURKA and AURKB, respectively. PROTAC MPS1 degrader 1 exhibits cytotoxicity against acute myeloid leukemia cells. PROTAC MPS1 degrader 1 can be used in research related to acute myeloid leukemia .
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Cat. No.: HY-144308
CAS No.: 2645409-78-3
Target:  

Mps1

Research Areas:  

Others

RMS-07 is a covalent Monopolar Spindle Kinase 1 (MPS1/TTK) inhibitor, with an apparent IC50 of 13.1 nM. RMS-07 targets a poorly conserved cysteine in the kinase's hinge region .
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Cat. No.: HY-116470
CAS No.: 1202055-39-7
Target:  

Mps1

Research Areas:  

Cancer

Mps1/TTK-IN-1 (Compound cpd-5), a derivative of NMS-P715 (HY-12382), is a Mps1 kinase inhibitor with an IC50 of 9.2 nM and a Kd of 1.6 nM. Mps1/TTK-IN-1 specifically targets the ATP-binding pocket of the Mps1 kinase. Mps1/TTK-IN-1 maintains inhibitory activity against Mps1 drug-resistant mutants (C604Y, C604W) with IC50 values of 170 and 19 nM and Kd values of 471 and 349 nM. Mps1/TTK-IN-1 can block the phosphorylation of kinetochore protein KNL1 mediated by Mps1, interfere with the spindle assembly checkpoint function, prevent the correct separation of chromosomes, and thereby inhibit the mitosis and proliferation of tumor cells .
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Cat. No.: HY-W141926
CAS No.: 17686-38-3
Target:  

PROTAC Linkers

Research Areas:  

Others

N-Glutarylglycine is a PROTAC linker that can be used to synthesize PROTACs, such as PROTAC MPS1 degrader 1 (HY-168540) .
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Cat. No.: HY-168155
Target:  

Fungal

Research Areas:  

Cancer

Mps1-IN-9 (compound M-12) is an Mps1-targeted inhibitor discovered for broad-spectrum antifungal agents. .
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