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TargetTyrosine-protein phosphatase non-receptor type 11
LigandBDBM503356
Substrate/Competitorn/a
Meas. Tech.SHP2 Biochemical Assay
IC50 960±n/a nM
Citation Jorand-Lebrun, CBoivin, RMochalkin, IJohnson, TLinde, NMusch, DKumar, D Carboxamide-pyrimidine derivatives as SHP2 antagonists US Patent US11696916 Publication Date 7/11/2023
More Info.:Get all data from this article,  Assay Method
 
Tyrosine-protein phosphatase non-receptor type 11
Name:Tyrosine-protein phosphatase non-receptor type 11
Synonyms:3.1.3.48 | PTN11_HUMAN | PTP-1D | PTP-2C | PTP2C | PTPN11 | Protein Tyrosine Phosphatase PPN11/Shp2 | Protein tyrosine phosphatase (PTP) Shp2 | Protein-Tyrosine Phosphatase SHP-2 | Protein-tyrosine phosphatase 1D | Protein-tyrosine phosphatase 2C | SH-PTP2 | SH-PTP3 | SHP-2 | SHP2 | SHPTP2 | Src homology phosphatase 2 (SHP-2) | Tyrosine-protein phosphatase non-receptor type 11 (PTPN11) | Tyrosine-protein phosphatase non-receptor type 11 (SHP-2) | Tyrosine-protein phosphatase non-receptor type 11 (SHP2)
Type:Protein phosphatase
Mol. Mass.:68443.59
Organism:Homo sapiens (Human)
Description:Q06124
Residue:593
Sequence:
MTSRRWFHPNITGVEAENLLLTRGVDGSFLARPSKSNPGDFTLSVRRNGAVTHIKIQNTG
DYYDLYGGEKFATLAELVQYYMEHHGQLKEKNGDVIELKYPLNCADPTSERWFHGHLSGK
EAEKLLTEKGKHGSFLVRESQSHPGDFVLSVRTGDDKGESNDGKSKVTHVMIRCQELKYD
VGGGERFDSLTDLVEHYKKNPMVETLGTVLQLKQPLNTTRINAAEIESRVRELSKLAETT
DKVKQGFWEEFETLQQQECKLLYSRKEGQRQENKNKNRYKNILPFDHTRVVLHDGDPNEP
VSDYINANIIMPEFETKCNNSKPKKSYIATQGCLQNTVNDFWRMVFQENSRVIVMTTKEV
ERGKSKCVKYWPDEYALKEYGVMRVRNVKESAAHDYTLRELKLSKVGQGNTERTVWQYHF
RTWPDHGVPSDPGGVLDFLEEVHHKQESIMDAGPVVVHCSAGIGRTGTFIVIDILIDIIR
EKGVDCDIDVPKTIQMVRSQRSGMVQTEAQYRFIYMAVQHYIETLQRRIEEEQKSKRKGH
EYTNIKYSLADQTSGDQSPLPPCTPTPPCAEMREDSARVYENVGLMQQQKSFR
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  Blast E-value cutoff:
BDBM503356
n/a
NameBDBM503356
Synonyms:5-(2,3-Dichloro-phenyl)-6-methyl-2- (5-methyl-hexahydro-pyrrolo[3,4- c]pyrrol-2-yl)-pyrimidine-4- carboxylic acid amide | US11033547, Compound 56 | US11696916, Compound 56
TypeSmall organic molecule
Emp. Form.C19H21Cl2N5O
Mol. Mass.406.309
SMILESCN1CC2CN(CC2C1)c1nc(C)c(-c2cccc(Cl)c2Cl)c(n1)C(N)=O |(7.76,.54,;6.22,.54,;5.31,-.7,;3.85,-.23,;2.39,-.7,;1.48,.54,;2.39,1.79,;3.85,1.31,;5.31,1.79,;-.06,.54,;-.83,1.88,;-2.37,1.88,;-3.14,3.21,;-3.14,.54,;-4.68,.54,;-5.45,-.79,;-6.99,-.79,;-7.76,.54,;-6.99,1.88,;-7.76,3.21,;-5.45,1.88,;-4.68,3.21,;-2.37,-.79,;-.83,-.79,;-3.14,-2.12,;-2.05,-3.21,;-4.68,-2.12,)|
Structure
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