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TargetTyrosine-protein phosphatase non-receptor type 11
LigandBDBM608516
Substrate/Competitorn/a
Meas. Tech.SHP2 Biochemical Assay
IC50 2.00±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:
BDBM608516
n/a
NameBDBM608516
Synonyms:6-amino-2-[(4S)-4-amino-4,6- dihydrospiro[cyclopenta[d][1,3]thiazole- 5,4'-piperidin]-1'-yl]-5-(2,3- dichlorophenyl)pyrimidine-4- carboxamide | US11696916, Compound 121
TypeSmall organic molecule
Emp. Form.C22H22Cl2N6OS
Mol. Mass.489.421
SMILESCc1nc(nc(C(N)=O)c1-c1cccc(Cl)c1Cl)N1CCC2(Cc3scnc3[C@H]2N)CC1 |r,wD:28.32,(-1.92,3.56,;-1.92,2.02,;-.58,1.25,;-.58,-.29,;-1.92,-1.06,;-3.25,-.29,;-4.58,-1.06,;-4.58,-2.6,;-5.92,-.29,;-3.25,1.25,;-4.58,2.02,;-5.92,1.25,;-7.25,2.02,;-7.25,3.56,;-5.92,4.33,;-5.92,5.87,;-4.58,3.56,;-3.25,4.33,;.75,-1.06,;.75,-2.6,;2.08,-3.37,;3.42,-2.6,;3.42,-4.14,;4.88,-4.62,;5.79,-5.87,;7.25,-5.39,;7.25,-3.85,;5.79,-3.37,;4.88,-2.13,;5.65,-.79,;3.42,-1.06,;2.08,-.29,)|
Structure
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