MK2a Inhibitor

Base Information

Chemical Name:MK2a Inhibitor
CAS No.:41179-33-3
Molecular Formula:C22H20FNO2
Molecular Weight:349.405
Hs Code.:
ChEMBL ID:CHEMBL235658
DSSTox Substance ID:DTXSID60464220
Nikkaji Number:J3.043.697K
Pharos Ligand ID:4XW84C15RGBS,BJPQQDZMS2W7
Wikidata:Q27086816
Mol file:41179-33-3.mol

Synonyms:CMPD1;41179-33-3;MK2a Inhibitor;CMPD-1;4-(2'-Fluoro-[1,1'-biphenyl]-4-yl)-N-(4-hydroxyphenyl)butanamide;4-[4-(2-fluorophenyl)phenyl]-N-(4-hydroxyphenyl)butanamide;2'-FLUORO-N-(4-HYDROXYPHENYL)-[1,1'-BIPHENYL]-4-BUTANAMIDE;CHEMBL235658;MAPKAPK2a Inhibitor;SCHEMBL169905;GTPL6009;CHEBI:92949;DTXSID60464220;HMS3229K04;HMS3268P13;HMS3413K11;HMS3677K11;EX-A7609;BDBM50411445;AKOS024456977;CCG-206869;NCGC00092325-01;MS-25394;MK2a Inhibitor - CAS 41179-33-3;HY-108643;CS-0029377;F77818;BRD-K54095730-001-01-5;Q27086816

Suppliers and Price of MK2a Inhibitor

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
CMPD-1
10mg
$ 446.00

TRC
CMPD-1
1mg
$ 100.00

Tocris
CMPD-1 ≥99%(HPLC)
50
$ 773.00

Tocris
CMPD-1 ≥99%(HPLC)
10
$ 189.00

Sigma-Aldrich
MK2a Inhibitor - CAS 41179-33-3 - Calbiochem
5mg
$ 238.65

ChemScene
CMPD1 99.45%
5mg
$ 260.00

Cayman Chemical
MK2a Inhibitor
10mg
$ 150.00

Cayman Chemical
MK2a Inhibitor
5mg
$ 94.00

Cayman Chemical
MK2a Inhibitor
1mg
$ 25.00

Cayman Chemical
MK2a Inhibitor
50mg
$ 625.00

Total 9 raw suppliers

Chemical Property of MK2a Inhibitor

Chemical Property:

Melting Point:128-130 °C
Boiling Point:585.0±50.0 °C(Predicted)
PKA:10.11±0.26(Predicted)
Flash Point:307.6oC
PSA：49.33000
Density:1.229±0.06 g/cm3(Predicted)
LogP:5.23270
Storage Temp.:Store at RT
XLogP3:4.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:6
Exact Mass:349.14780704
Heavy Atom Count:26
Complexity:428

Purity/Quality:

97% ^*data from raw suppliers

CMPD-1 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C2=CC=C(C=C2)CCCC(=O)NC3=CC=C(C=C3)O)F
Uses All Prestige Antibodies Powered by Atlas Antibodies are developed and validated by the Human Protein Atlas (HPA) project (www.proteinatlas.org)and as a result, are supported by the most extensive characterization in the industry. The Human Protein Atlas project can be subdivided into three efforts: Human Tissue Atlas, Cancer Atlas, and Human Cell Atlas. The antibodies that have been generated in support of the Tissue and Cancer Atlas projects have been tested by immunohistochemistry against hundreds of normal and disease tissues and through the recent efforts of the Human Cell Atlas project, many have been characterized by immunofluorescence to map the human proteome not only at the tissue level but now at the subcellular level. These images and the collection of this vast data set can be viewed on the Human Protein Atlas (HPA) site by clicking on the Image Gallery link. To view these protocols and other useful information about Prestige Antibodies and the HPA, visit . Monoclonal Anti-SOX9 antibody produced in mouse has been used in immunofluorescence.

Technology Process of MK2a Inhibitor

There total 2 articles about MK2a Inhibitor which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 15.0%

: 40096-53-5
4-[4-(2-Fluorophenyl)phenyl]butanoic acid

: 123-30-8
4-amino-phenol

: 41179-33-3
MK2a Inhibitor

Guidance literature:: 4-[4-(2-Fluorophenyl)phenyl]butanoic acid; In dichloromethane; at 0 ℃;

4-amino-phenol; With triethylamine; In dichloromethane; at 20 ℃; for 24h; Further stages.;
DOI:10.1016/j.bmcl.2007.10.036