Welcome to LookChem.com Sign In|Join Free

CAS

  • or
NMS-P715 is a chemical compound characterized by its inhibitory action on the protein kinase MPS1, a key player in cell division, particularly during mitosis. It functions by inhibiting MPS1 activity, which in turn disrupts spindle assembly checkpoints and leads to erroneous chromosomal segregation. The interference with the division process of tumor cells by NMS-P715 can result in cell death, making it a promising candidate for targeted cancer therapy.

1202055-34-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1202055-34-2 Structure
  • Basic information

    1. Product Name: NMS-P715
    2. Synonyms: NMS-P715;N-(2,6-diethylphenyl)-1-Methyl-8-({4-[(1-Methylpiperidin-4-yl)carbaMoyl]-2-(trifluoroMethoxy)phenyl}aMino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxaMide;NMS P715 analog;NMS-P 715 analog;NMS-P715 analog;N-(2,6-diethylphenyl)-1-methyl-8-((4-((1-methylpiperidin-4-yl)carbamoyl)-2-(trifluoromethoxy)phenyl)amino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide NMS-P715
    3. CAS NO:1202055-34-2
    4. Molecular Formula: C35H42N8O3
    5. Molecular Weight: 676.7311696
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1202055-34-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.32±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 11.75±0.70(Predicted)
    10. CAS DataBase Reference: NMS-P715(CAS DataBase Reference)
    11. NIST Chemistry Reference: NMS-P715(1202055-34-2)
    12. EPA Substance Registry System: NMS-P715(1202055-34-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1202055-34-2(Hazardous Substances Data)

1202055-34-2 Usage

Uses

Used in Pharmaceutical Industry:
NMS-P715 is used as a targeted therapy agent for cancer treatment. It is employed to inhibit the activity of the protein kinase MPS1, which is crucial for accurate cell division. By preventing MPS1 activity, NMS-P715 disrupts spindle assembly checkpoints and causes inaccurate chromosomal segregation, leading to the death of tumor cells. This targeted approach can be particularly effective in treating cancers where traditional chemotherapy and radiotherapy may have limited efficacy or cause severe side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 1202055-34-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,0,5 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1202055-34:
(9*1)+(8*2)+(7*0)+(6*2)+(5*0)+(4*5)+(3*5)+(2*3)+(1*4)=82
82 % 10 = 2
So 1202055-34-2 is a valid CAS Registry Number.

1202055-34-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,6-diethylphenyl)-8-({2-methoxy-4-[(1-methylpiperidin-4-yl)carbamoyl]phenyl}amino)-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide

1.2 Other means of identification

Product number -
Other names NMS-P715 analog

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1202055-34-2 SDS

1202055-34-2Downstream Products

1202055-34-2Relevant articles and documents

Synthesis and SAR of new pyrazolo[4,3-h]quinazoline-3-carboxamide derivatives as potent and selective MPS1 kinase inhibitors

Caldarelli, Marina,Angiolini, Mauro,Disingrini, Teresa,Donati, Daniele,Guanci, Marco,Nuvoloni, Stefano,Posteri, Helena,Quartieri, Francesca,Silvagni, Marco,Colombo, Riccardo

, p. 4507 - 4511 (2011/09/12)

The synthesis and SAR of a series of novel pyrazolo-quinazolines as potent and selective MPS1 inhibitors are reported. We describe the optimization of the initial hit, identified by screening the internal library collection, into an orally available, potent and selective MPS1 inhibitor.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1202055-34-2