13 Results for "

Mps1 kinase inhibitor

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

13 Results for "Mps1 kinase inhibitor" in MCE Product Catalog:

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11
11 Publications Verification
Cat. No.: HY-12859
CAS No.: 1554458-53-5
Purity:  99.39%
Target:  

Mps1

Research Areas:  

Cancer

BAY 1217389 is a potent, and selective inhibitor of the monopolar spindle 1 (MPS1) kinase with an IC50 value less than 10 nM.
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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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1
1 Cited Publications
Cat. No.: HY-12401
CAS No.: 1609584-72-6
Purity:  99.73%
Target:  

Mps1

Research Areas:  

Cancer

Mps1-IN-3 is a potent and selective MPS1 kinase inhibitor, with an IC50 of 50 nM.
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1
1 Cited Publications
Cat. No.: HY-12603
CAS No.: 1400284-80-1
Purity:  99.10%
Target:  

Mps1

Research Areas:  

Cancer

CCT251455 is a potent and selective mitotic kinase monopolar spindle 1 (MPS1) inhibitor with an IC50 of 3 nM.
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Cat. No.: HY-I0314
CAS No.: 269410-08-4
1H-Pyrazole-4-boronic acid pinacol ester is a drug intermediate that can be used for the synthesis of Mps1 kinase inhibitors .
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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-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-164518
CAS No.: 2772910-13-9
Target:  

Mps1 Apoptosis

Research Areas:  

Cancer

PF-3837 is an Mps1 kinase inhibitor with a Ki value of 0.33 nM and an IC50 value of 5.5 nM. PF-3837 interferes with the cell cycle checkpoint by inhibiting Mps1 catalytic activity, reducing genomic stability, thereby inducing cancer cell apoptosis (Apoptosis). PF-3837 can be used in research on breast cancer .
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Cat. No.: HY-164519
CAS No.: 2771955-09-8
Target:  

Apoptosis Mps1 Mitosis

Research Areas:  

Cancer

PF-7006 is an Mps1 kinase inhibitor with a Ki value of 0.27 nM and an IC50 value of 2.5 nM. PF-7006 interferes with cell cycle checkpoints by inhibiting the catalytic activity of Mps1, reducing histone H3 levels, and shortening the duration of mitosis, leading to apoptosis in cancer cells. Combined use of PF-7006 with Palbociclib (HY-50767) increases cancer cell tolerance to PF-7006. PF-7006 can be used for breast cancer research .
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Cat. No.: HY-W100186
CAS No.: 80047-24-1
Target:  

Aurora Kinase

Research Areas:  

Others

Win 47338 (compound 14) is a control compound of inhibitors of the mitotic kinase monopolar spindle MPS1 and Aurora kinases (AurA/AurB) (Ki>100 μM) .
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Cat. No.: HY-120032
CAS No.: 1610676-27-1
Target:  

Mps1

Research Areas:  

Cancer

CFI-401980 is a selective tyrosine threonine kinase MPS1 inhibitor with a Ki of 0.8 nM. CFI-401980 inhibits the proliferation of HCT116 cell lines. CFI-401980 can be studied in anti-cancer research .
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Cat. No.: HY-116190
CAS No.: 1430741-35-7
Target:  

Mps1 DNA/RNA Synthesis

Research Areas:  

Cancer

CFI-401870 is an orally active threonine tyrosine kinase (TTK (Mps1)) inhibitor with an IC50 of 3.1 nM. CFI-401870 exhibits IC50s against PLK4, KDR, AURKA and other kinases such as AURKB/INCENP were all greater than 1 μM.CFI-401870 inhibits the growth of various cancer cells, causing chromosome lag, an increase in aneuploidy and cell cycle arrest. CFI-401870 can be used for the study of cancers such as colon cancer .
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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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