NMS-P715
- Product Name
- NMS-P715
- CAS No.
- 1202055-32-0
- Chemical Name
- NMS-P715
- Synonyms
- NMS-P715 (NMS P715;NMS P715; NMS-P 715; NMS P715; NMS-P 715;Monopolar spindle 1,Mps1,NMS P715,NMS-P715,inhibit,NMSP715,Inhibitor,NMS-P-715;1H-Pyrazolo[4,3-h]quinazoline-3-carboxamide, N-(2,6-diethylphenyl)-4,5-dihydro-1-methyl-8-[[4-[[(1-methyl-4-piperidinyl)amino]carbonyl]-2-(trifluoromethoxy)phenyl]amino]-
- CBNumber
- CB52725630
- Molecular Formula
- C35H39F3N8O3
- Formula Weight
- 676.73
- MOL File
- 1202055-32-0.mol
NMS-P715 Property
- Density
- 1.39±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMSO: soluble
- form
- A solid
- pka
- 11.75±0.70(Predicted)
- color
- White to off-white
- InChIKey
- JFOAJUGFHDCBJJ-UHFFFAOYSA-N
- SMILES
- CN(N=C1C(NC2=C(CC)C=CC=C2CC)=O)C3=C1CCC4=C3N=C(NC5=CC=C(C(NC6CCN(C)CC6)=O)C=C5OC(F)(F)F)N=C4
Safety
- WGK Germany
- WGK 2
- Storage Class
- 11 - Combustible Solids
N-Bromosuccinimide Price
- Product number
- 475949
- Product name
- MPS1 Inhibitor, NMS-P715
- Purity
- The MPS1 Inhibitor, NMS-P715 controls the biological activity of MPS1. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.
- Packaging
- 5 mg
- Price
- $270
- Updated
- 2026/03/19
- Product number
- CS-3396
- Product name
- NMS-P715
- Purity
- >99.0%
- Packaging
- 10mg
- Price
- $300
- Updated
- 2021/12/16
- Product number
- CS-3396
- Product name
- NMS-P715
- Purity
- >99.0%
- Packaging
- 50mg
- Price
- $1008
- Updated
- 2021/12/16
- Product number
- CS-3396
- Product name
- NMS-P715
- Purity
- >99.0%
- Packaging
- 100mg
- Price
- $1680
- Updated
- 2021/12/16
- Product number
- CS-3396
- Product name
- NMS-P715
- Purity
- >99.0%
- Packaging
- 5mg
- Price
- $190
- Updated
- 2021/12/16
NMS-P715 Chemical Properties,Usage,Production
Uses
NMS-P715 is a selective, ATP-competitive inhibitor of MPS1, with an IC50 of 182 nM.
in vivo
NMS-P715 (10 mg/kg) exhibits an oral bioavailability of 37% and good pharmacokinetic properties in nude mice bearing subcutaneous implanted human tumor cell xenografts. NMS-P715 (90 mg/kg, p.o.) is well tolerated and cuases no signs of body weight loss or other overt toxicities in an A2780 ovary carcinoma xenograft model. NMS-P715 (100 mg/kg, p.o.) inhibits the tumor growth by appr 43% in the A375 melanoma xenograft model[1].
IC 50
Mps1: 182 nM (IC50); CK2: 5.7 μM (IC50); MELK: 6.01 μM (IC50); NEK6: 6.02 μM (IC50)
References
[1] Colombo R, et al. Targeting the mitotic checkpoint for cancer therapy with NMS-P715, an inhibitor of MPS1 kinase. Cancer Res. 2010 Dec 15;70(24):10255-64. DOI:10.1158/0008-5472.CAN-10-2101
[2] Slee RB, et al. Selective inhibition of pancreatic ductal adenocarcinoma cell growth by the mitotic MPS1 kinase inhibitor NMS-P715. Mol Cancer Ther. 2014 Feb;13(2):307-315. DOI:10.1158/1535-7163.MCT-13-0324
NMS-P715 Preparation Products And Raw materials
Raw materials
Preparation Products
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