Alternate Text DC Chemicals' products qualify for U.S. tariff exemptions. We guarantee no price increases due to customs duties and maintain stable supply, continuing to deliver reliable research solutions to our American clients.

Mps1-IN-1

  Cat. No.:  DC5087  
Chemical Structure
1125593-20-5
For research use only. We do not sell to patients.
We match the best price and quality on market.
Email:order@dcchemicals.com  sales@dcchemicals.com
Tel:+86-021-58447131
We are official vendor of:
  • 20
  • 19
  • 18
  • 17
  • 16
  • 15
  • 14
  • 12
  • 11
  • 10
  • 9
  • 8
  • 13
  • 6
  • 5
  • 4
  • 3
  • 2
  • 1
More than 5000 active chemicals with high quality for research!
Field of application
Mps1-IN-1 is a highly potent and selectibe Mpsl inhibitor with IC50 of 367 nM; >1000-fold selectivity relative to the 352 member kinase panel with the major exceptions of Alk and Ltk.
Cas No.: 1125593-20-5
SMILES: O=S(C(C=CC=C1)=C1NC2=CC(NC3=C(OC)C=C(N4CCC(O)CC4)C=C3)=NC5=C2C=CN5)(C(C)C)=O
Formula: C28H33N5O4S
M.Wt: 535.66
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: For the detailed information of 1Mps1-IN-1, the solubility of 1Mps1-IN-1 in water, the solubility of 1Mps1-IN-1 in DMSO, the solubility of 1Mps1-IN-1 in PBS buffer, the animal experiment (test) of 1Mps1-IN-1, the cell expriment (test) of 1Mps1-IN-1, the in vivo, in vitro and clinical trial test of 1Mps1-IN-1, the EC50, IC50,and Affinity of 1Mps1-IN-1, Please contact DC Chemicals.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
DC28264 TC-Mps1-12 TC-Mps1-12 is a potent and selective monopolar spindle 1 (Mps1) inhibitor, with an IC50 of 6.4 nM.
DC5087 Mps1-IN-1 Mps1-IN-1 is a highly potent and selectibe Mpsl inhibitor with IC50 of 367 nM; >1000-fold selectivity relative to the 352 member kinase panel with the major exceptions of Alk and Ltk.
DC11677 CCT-271850 A potent, selective, orally bioavailable Mps1 kinase inhibitor with IC50 of 11 nM.
DC11704 CFI-401870 A potent, selective, orally active Mps1 (TTK) inhibitor with IC50 of 3.1 nM.
X