BindingDB logo
myBDB logout

PubMed code 10090780

Compile data set for download or QSAR
Found 28 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074715
PNG
(CHEMBL433805 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)NC(C)=S
Show InChI InChI=1S/C36H55N8O11PS/c1-19(2)29-35(50)41-26(18-28(37)45)33(48)43-30(20(3)4)36(51)44-16-8-10-27(44)34(49)38-15-7-6-9-24(39-21(5)57)31(46)40-25(32(47)42-29)17-22-11-13-23(14-12-22)55-56(52,53)54/h11-14,19-20,24-27,29-30H,6-10,15-18H2,1-5H3,(H2,37,45)(H,38,49)(H,39,57)(H,40,46)(H,41,50)(H,42,47)(H,43,48)(H2,52,53,54)/t24-,25+,26+,27+,29-,30-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 60n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074710
PNG
(CHEMBL435910 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)NC(C)=O
Show InChI InChI=1S/C36H55N8O12P/c1-19(2)29-35(51)41-26(18-28(37)46)33(49)43-30(20(3)4)36(52)44-16-8-10-27(44)34(50)38-15-7-6-9-24(39-21(5)45)31(47)40-25(32(48)42-29)17-22-11-13-23(14-12-22)56-57(53,54)55/h11-14,19-20,24-27,29-30H,6-10,15-18H2,1-5H3,(H2,37,46)(H,38,50)(H,39,45)(H,40,47)(H,41,51)(H,42,48)(H,43,49)(H2,53,54,55)/t24-,25+,26+,27+,29-,30-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 70n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074711
PNG
(CHEMBL355759 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@H](CC2CCCCC2)NC(=O)[C@@H](CC(N)=O)NC1=O)NC(C)=O
Show InChI InChI=1S/C40H61N8O12P/c1-23(2)34-39(55)45-30(22-33(41)50)36(52)46-31(21-25-10-5-4-6-11-25)40(56)48-19-9-13-32(48)38(54)42-18-8-7-12-28(43-24(3)49)35(51)44-29(37(53)47-34)20-26-14-16-27(17-15-26)60-61(57,58)59/h14-17,23,25,28-32,34H,4-13,18-22H2,1-3H3,(H2,41,50)(H,42,54)(H,43,49)(H,44,51)(H,45,55)(H,46,52)(H,47,53)(H2,57,58,59)/t28-,29+,30+,31-,32+,34-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 110n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074706
PNG
(CHEMBL366543 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)NC(C)=S
Show InChI InChI=1S/C36H55N8O11PS/c1-19(2)29-35(50)41-26(18-28(37)45)33(48)43-30(20(3)4)36(51)44-16-8-10-27(44)34(49)38-15-7-6-9-24(39-21(5)57)31(46)40-25(32(47)42-29)17-22-11-13-23(14-12-22)55-56(52,53)54/h11-14,19-20,24-27,29-30H,6-10,15-18H2,1-5H3,(H2,37,45)(H,38,49)(H,39,57)(H,40,46)(H,41,50)(H,42,47)(H,43,48)(H2,52,53,54)/t24-,25-,26-,27-,29+,30+/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 110n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074716
PNG
(CHEMBL438943 | Lys-Pro-Phe-pTyr-Val-Asn-Val-Glu-Ph...)
Show SMILES CC(C)[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(OP(O)(O)=O)cc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCCN)C(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](Cc1ccccc1)C(O)=O
Show InChI InChI=1S/C57H80N11O17P/c1-32(2)47(54(77)61-39(24-25-46(70)71)49(72)65-43(57(80)81)30-35-16-9-6-10-17-35)67-52(75)42(31-45(60)69)64-55(78)48(33(3)4)66-51(74)41(29-36-20-22-37(23-21-36)85-86(82,83)84)62-50(73)40(28-34-14-7-5-8-15-34)63-53(76)44-19-13-27-68(44)56(79)38(59)18-11-12-26-58/h5-10,14-17,20-23,32-33,38-44,47-48H,11-13,18-19,24-31,58-59H2,1-4H3,(H2,60,69)(H,61,77)(H,62,73)(H,63,76)(H,64,78)(H,65,72)(H,66,74)(H,67,75)(H,70,71)(H,80,81)(H2,82,83,84)/t38-,39-,40-,41-,42-,43-,44-,47-,48-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
KEGG
MMDB
PC cid
PC sid
UniChem

Similars

MMDB
Article
PubMed
n/an/a 140n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074705
PNG
(CHEMBL359934 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)NC(C)=O
Show InChI InChI=1S/C36H55N8O12P/c1-19(2)29-35(51)41-26(18-28(37)46)33(49)43-30(20(3)4)36(52)44-16-8-10-27(44)34(50)38-15-7-6-9-24(39-21(5)45)31(47)40-25(32(48)42-29)17-22-11-13-23(14-12-22)56-57(53,54)55/h11-14,19-20,24-27,29-30H,6-10,15-18H2,1-5H3,(H2,37,46)(H,38,50)(H,39,45)(H,40,47)(H,41,51)(H,42,48)(H,43,49)(H2,53,54,55)/t24-,25-,26-,27-,29+,30+/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 180n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074703
PNG
(CHEMBL172299 | Phosphoric acid mono-[4-((5R,8S,11R...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC1=O)C(C)C
Show InChI InChI=1S/C30H44N7O11P/c1-15(2)24-29(43)34-20(13-22(31)38)27(41)36-25(16(3)4)30(44)37-11-5-6-21(37)28(42)32-14-23(39)33-19(26(40)35-24)12-17-7-9-18(10-8-17)48-49(45,46)47/h7-10,15-16,19-21,24-25H,5-6,11-14H2,1-4H3,(H2,31,38)(H,32,42)(H,33,39)(H,34,43)(H,35,40)(H,36,41)(H2,45,46,47)/t19-,20-,21-,24+,25+/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 520n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074712
PNG
(CHEMBL177372 | Phosphoric acid mono-[4-((5R,8S,11R...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)CCCCCCNC(=O)[C@@H]2CCCN2C(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC1=O)C(C)C
Show InChI InChI=1S/C35H54N7O11P/c1-20(2)29-34(48)39-25(19-27(36)43)32(46)41-30(21(3)4)35(49)42-17-9-10-26(42)33(47)37-16-8-6-5-7-11-28(44)38-24(31(45)40-29)18-22-12-14-23(15-13-22)53-54(50,51)52/h12-15,20-21,24-26,29-30H,5-11,16-19H2,1-4H3,(H2,36,43)(H,37,47)(H,38,44)(H,39,48)(H,40,45)(H,41,46)(H2,50,51,52)/t24-,25-,26-,29+,30+/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 600n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074709
PNG
((5S,8R,11S,14R,17R,22R,24aR)-17-Acetylamino-8-carb...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CSSC[C@H](NC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)C(O)=O)NC(C)=O
Show InChI InChI=1S/C36H53N8O14PS2/c1-17(2)28-34(51)40-23(14-27(37)46)31(48)43-29(18(3)4)35(52)44-12-6-7-26(44)33(50)41-25(36(53)54)16-61-60-15-24(38-19(5)45)32(49)39-22(30(47)42-28)13-20-8-10-21(11-9-20)58-59(55,56)57/h8-11,17-18,22-26,28-29H,6-7,12-16H2,1-5H3,(H2,37,46)(H,38,45)(H,39,49)(H,40,51)(H,41,50)(H,42,47)(H,43,48)(H,53,54)(H2,55,56,57)/t22-,23-,24+,25+,26-,28+,29+/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 630n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074704
PNG
(CHEMBL435738 | Phosphoric acid mono-[4-((5R,8S,11R...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)OCCCCCNC(=O)[C@@H]2CCCN2C(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC1=O)C(C)C
Show InChI InChI=1S/C34H52N7O12P/c1-19(2)27-32(46)37-24(18-26(35)42)30(44)40-28(20(3)4)33(47)41-15-8-9-25(41)31(45)36-14-6-5-7-16-52-34(48)38-23(29(43)39-27)17-21-10-12-22(13-11-21)53-54(49,50)51/h10-13,19-20,23-25,27-28H,5-9,14-18H2,1-4H3,(H2,35,42)(H,36,45)(H,37,46)(H,38,48)(H,39,43)(H,40,44)(H2,49,50,51)/t23-,24-,25-,27+,28+/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 710n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074708
PNG
(CHEMBL177616 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)NC(C)=O
Show InChI InChI=1S/C37H57N8O12P/c1-20(2)17-26-33(49)43-28(19-30(38)47)35(51)44-31(21(3)4)37(53)45-16-8-10-29(45)36(52)39-15-7-6-9-25(40-22(5)46)32(48)42-27(34(50)41-26)18-23-11-13-24(14-12-23)57-58(54,55)56/h11-14,20-21,25-29,31H,6-10,15-19H2,1-5H3,(H2,38,47)(H,39,52)(H,40,46)(H,41,50)(H,42,48)(H,43,49)(H,44,51)(H2,54,55,56)/t25-,26-,27+,28+,29+,31-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.34E+3n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074717
PNG
(CHEMBL451250 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](CC(N)=O)NC(=O)[C@H](CC2CCCCC2)NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CCCCNC(=O)[C@H]2CCCN2C1=O)NC(C)=O
Show InChI InChI=1S/C40H61N8O12P/c1-23(2)34-40(56)48-19-9-13-32(48)39(55)42-18-8-7-12-28(43-24(3)49)35(51)44-30(21-26-14-16-27(17-15-26)60-61(57,58)59)36(52)45-29(20-25-10-5-4-6-11-25)37(53)46-31(22-33(41)50)38(54)47-34/h14-17,23,25,28-32,34H,4-13,18-22H2,1-3H3,(H2,41,50)(H,42,55)(H,43,49)(H,44,51)(H,45,52)(H,46,53)(H,47,54)(H2,57,58,59)/t28-,29-,30+,31+,32+,34-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.61E+3n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074713
PNG
(CHEMBL367276 | Phosphoric acid mono-{4-[(S)-2-((S)...)
Show SMILES CCCCNC(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(OP(O)(O)=O)cc1)NC(=O)CC)C(C)C)C(C)C
Show InChI InChI=1S/C35H56N7O11P/c1-7-9-16-37-33(47)26-11-10-17-42(26)35(49)30(21(5)6)41-32(46)25(19-27(36)43)39-34(48)29(20(3)4)40-31(45)24(38-28(44)8-2)18-22-12-14-23(15-13-22)53-54(50,51)52/h12-15,20-21,24-26,29-30H,7-11,16-19H2,1-6H3,(H2,36,43)(H,37,47)(H,38,44)(H,39,48)(H,40,45)(H,41,46)(H2,50,51,52)/t24-,25-,26-,29-,30-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.63E+3n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074714
PNG
(CHEMBL263347 | Glu-Pro-Gln-pTyr-Glu-Glu-Ile-Pro-Il...)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](Cc1ccc(OP(O)(O)=O)cc1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCC(O)=O)[C@@H](C)CC)C(O)=O
Show InChI InChI=1S/C51H77N10O21P/c1-5-26(3)41(50(76)61-24-8-10-36(61)48(74)59-42(51(77)78)27(4)6-2)58-45(71)33(18-22-40(67)68)54-43(69)32(17-21-39(65)66)55-46(72)34(25-28-11-13-29(14-12-28)82-83(79,80)81)57-44(70)31(16-19-37(53)62)56-47(73)35-9-7-23-60(35)49(75)30(52)15-20-38(63)64/h11-14,26-27,30-36,41-42H,5-10,15-25,52H2,1-4H3,(H2,53,62)(H,54,69)(H,55,72)(H,56,73)(H,57,70)(H,58,71)(H,59,74)(H,63,64)(H,65,66)(H,67,68)(H,77,78)(H2,79,80,81)/t26-,27-,30-,31-,32-,33-,34-,35-,36-,41-,42-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 6.30E+3n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Growth factor receptor-bound protein 2


(Homo sapiens (Human))
BDBM50074707
PNG
(CHEMBL174819 | Phosphoric acid mono-[4-((5R,8S,11R...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)CNC(=O)[C@H]2CCCN2C(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC1=O)C(C)C
Show InChI InChI=1S/C30H44N7O11P/c1-15(2)24-29(43)34-20(13-22(31)38)27(41)36-25(16(3)4)30(44)37-11-5-6-21(37)28(42)32-14-23(39)33-19(26(40)35-24)12-17-7-9-18(10-8-17)48-49(45,46)47/h7-10,15-16,19-21,24-25H,5-6,11-14H2,1-4H3,(H2,31,38)(H,32,42)(H,33,39)(H,34,43)(H,35,40)(H,36,41)(H2,45,46,47)/t19-,20-,21+,24+,25+/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.08E+4n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Growth factor receptor bound protein 2 to biotinylated KPFY*VNVEF Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074709
PNG
((5S,8R,11S,14R,17R,22R,24aR)-17-Acetylamino-8-carb...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CSSC[C@H](NC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)C(O)=O)NC(C)=O
Show InChI InChI=1S/C36H53N8O14PS2/c1-17(2)28-34(51)40-23(14-27(37)46)31(48)43-29(18(3)4)35(52)44-12-6-7-26(44)33(50)41-25(36(53)54)16-61-60-15-24(38-19(5)45)32(49)39-22(30(47)42-28)13-20-8-10-21(11-9-20)58-59(55,56)57/h8-11,17-18,22-26,28-29H,6-7,12-16H2,1-5H3,(H2,37,46)(H,38,45)(H,39,49)(H,40,51)(H,41,50)(H,42,47)(H,43,48)(H,53,54)(H2,55,56,57)/t22-,23-,24+,25+,26-,28+,29+/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 3.80E+4n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074715
PNG
(CHEMBL433805 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)NC(C)=S
Show InChI InChI=1S/C36H55N8O11PS/c1-19(2)29-35(50)41-26(18-28(37)45)33(48)43-30(20(3)4)36(51)44-16-8-10-27(44)34(49)38-15-7-6-9-24(39-21(5)57)31(46)40-25(32(47)42-29)17-22-11-13-23(14-12-22)55-56(52,53)54/h11-14,19-20,24-27,29-30H,6-10,15-18H2,1-5H3,(H2,37,45)(H,38,49)(H,39,57)(H,40,46)(H,41,50)(H,42,47)(H,43,48)(H2,52,53,54)/t24-,25+,26+,27+,29-,30-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 5.50E+4n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074705
PNG
(CHEMBL359934 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)NC(C)=O
Show InChI InChI=1S/C36H55N8O12P/c1-19(2)29-35(51)41-26(18-28(37)46)33(49)43-30(20(3)4)36(52)44-16-8-10-27(44)34(50)38-15-7-6-9-24(39-21(5)45)31(47)40-25(32(48)42-29)17-22-11-13-23(14-12-22)56-57(53,54)55/h11-14,19-20,24-27,29-30H,6-10,15-18H2,1-5H3,(H2,37,46)(H,38,50)(H,39,45)(H,40,47)(H,41,51)(H,42,48)(H,43,49)(H2,53,54,55)/t24-,25-,26-,27-,29+,30+/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 7.30E+4n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074706
PNG
(CHEMBL366543 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)NC(C)=S
Show InChI InChI=1S/C36H55N8O11PS/c1-19(2)29-35(50)41-26(18-28(37)45)33(48)43-30(20(3)4)36(51)44-16-8-10-27(44)34(49)38-15-7-6-9-24(39-21(5)57)31(46)40-25(32(47)42-29)17-22-11-13-23(14-12-22)55-56(52,53)54/h11-14,19-20,24-27,29-30H,6-10,15-18H2,1-5H3,(H2,37,45)(H,38,49)(H,39,57)(H,40,46)(H,41,50)(H,42,47)(H,43,48)(H2,52,53,54)/t24-,25-,26-,27-,29+,30+/m1/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 8.80E+4n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074707
PNG
(CHEMBL174819 | Phosphoric acid mono-[4-((5R,8S,11R...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)CNC(=O)[C@H]2CCCN2C(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC1=O)C(C)C
Show InChI InChI=1S/C30H44N7O11P/c1-15(2)24-29(43)34-20(13-22(31)38)27(41)36-25(16(3)4)30(44)37-11-5-6-21(37)28(42)32-14-23(39)33-19(26(40)35-24)12-17-7-9-18(10-8-17)48-49(45,46)47/h7-10,15-16,19-21,24-25H,5-6,11-14H2,1-4H3,(H2,31,38)(H,32,42)(H,33,39)(H,34,43)(H,35,40)(H,36,41)(H2,45,46,47)/t19-,20-,21+,24+,25+/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074704
PNG
(CHEMBL435738 | Phosphoric acid mono-[4-((5R,8S,11R...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)OCCCCCNC(=O)[C@@H]2CCCN2C(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC1=O)C(C)C
Show InChI InChI=1S/C34H52N7O12P/c1-19(2)27-32(46)37-24(18-26(35)42)30(44)40-28(20(3)4)33(47)41-15-8-9-25(41)31(45)36-14-6-5-7-16-52-34(48)38-23(29(43)39-27)17-21-10-12-22(13-11-21)53-54(49,50)51/h10-13,19-20,23-25,27-28H,5-9,14-18H2,1-4H3,(H2,35,42)(H,36,45)(H,37,46)(H,38,48)(H,39,43)(H,40,44)(H2,49,50,51)/t23-,24-,25-,27+,28+/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074712
PNG
(CHEMBL177372 | Phosphoric acid mono-[4-((5R,8S,11R...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)CCCCCCNC(=O)[C@@H]2CCCN2C(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC1=O)C(C)C
Show InChI InChI=1S/C35H54N7O11P/c1-20(2)29-34(48)39-25(19-27(36)43)32(46)41-30(21(3)4)35(49)42-17-9-10-26(42)33(47)37-16-8-6-5-7-11-28(44)38-24(31(45)40-29)18-22-12-14-23(15-13-22)53-54(50,51)52/h12-15,20-21,24-26,29-30H,5-11,16-19H2,1-4H3,(H2,36,43)(H,37,47)(H,38,44)(H,39,48)(H,40,45)(H,41,46)(H2,50,51,52)/t24-,25-,26-,29+,30+/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074703
PNG
(CHEMBL172299 | Phosphoric acid mono-[4-((5R,8S,11R...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC1=O)C(C)C
Show InChI InChI=1S/C30H44N7O11P/c1-15(2)24-29(43)34-20(13-22(31)38)27(41)36-25(16(3)4)30(44)37-11-5-6-21(37)28(42)32-14-23(39)33-19(26(40)35-24)12-17-7-9-18(10-8-17)48-49(45,46)47/h7-10,15-16,19-21,24-25H,5-6,11-14H2,1-4H3,(H2,31,38)(H,32,42)(H,33,39)(H,34,43)(H,35,40)(H,36,41)(H2,45,46,47)/t19-,20-,21-,24+,25+/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074713
PNG
(CHEMBL367276 | Phosphoric acid mono-{4-[(S)-2-((S)...)
Show SMILES CCCCNC(=O)[C@@H]1CCCN1C(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccc(OP(O)(O)=O)cc1)NC(=O)CC)C(C)C)C(C)C
Show InChI InChI=1S/C35H56N7O11P/c1-7-9-16-37-33(47)26-11-10-17-42(26)35(49)30(21(5)6)41-32(46)25(19-27(36)43)39-34(48)29(20(3)4)40-31(45)24(38-28(44)8-2)18-22-12-14-23(15-13-22)53-54(50,51)52/h12-15,20-21,24-26,29-30H,7-11,16-19H2,1-6H3,(H2,36,43)(H,37,47)(H,38,44)(H,39,48)(H,40,45)(H,41,46)(H2,50,51,52)/t24-,25-,26-,29-,30-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074711
PNG
(CHEMBL355759 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@H](CC2CCCCC2)NC(=O)[C@@H](CC(N)=O)NC1=O)NC(C)=O
Show InChI InChI=1S/C40H61N8O12P/c1-23(2)34-39(55)45-30(22-33(41)50)36(52)46-31(21-25-10-5-4-6-11-25)40(56)48-19-9-13-32(48)38(54)42-18-8-7-12-28(43-24(3)49)35(51)44-29(37(53)47-34)20-26-14-16-27(17-15-26)60-61(57,58)59/h14-17,23,25,28-32,34H,4-13,18-22H2,1-3H3,(H2,41,50)(H,42,54)(H,43,49)(H,44,51)(H,45,55)(H,46,52)(H,47,53)(H2,57,58,59)/t28-,29+,30+,31-,32+,34-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.50E+5n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074710
PNG
(CHEMBL435910 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)NC(C)=O
Show InChI InChI=1S/C36H55N8O12P/c1-19(2)29-35(51)41-26(18-28(37)46)33(49)43-30(20(3)4)36(52)44-16-8-10-27(44)34(50)38-15-7-6-9-24(39-21(5)45)31(47)40-25(32(48)42-29)17-22-11-13-23(14-12-22)56-57(53,54)55/h11-14,19-20,24-27,29-30H,6-10,15-18H2,1-5H3,(H2,37,46)(H,38,50)(H,39,45)(H,40,47)(H,41,51)(H,42,48)(H,43,49)(H2,53,54,55)/t24-,25+,26+,27+,29-,30-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.50E+5n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074717
PNG
(CHEMBL451250 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](CC(N)=O)NC(=O)[C@H](CC2CCCCC2)NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CCCCNC(=O)[C@H]2CCCN2C1=O)NC(C)=O
Show InChI InChI=1S/C40H61N8O12P/c1-23(2)34-40(56)48-19-9-13-32(48)39(55)42-18-8-7-12-28(43-24(3)49)35(51)44-30(21-26-14-16-27(17-15-26)60-61(57,58)59)36(52)45-29(20-25-10-5-4-6-11-25)37(53)46-31(22-33(41)50)38(54)47-34/h14-17,23,25,28-32,34H,4-13,18-22H2,1-3H3,(H2,41,50)(H,42,55)(H,43,49)(H,44,51)(H,45,52)(H,46,53)(H,47,54)(H2,57,58,59)/t28-,29-,30+,31+,32+,34-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.50E+5n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src


(Homo sapiens (Human))
BDBM50074708
PNG
(CHEMBL177616 | Phosphoric acid mono-[4-((5S,8R,11S...)
Show SMILES CC(C)C[C@@H]1NC(=O)[C@@H](Cc2ccc(OP(O)(O)=O)cc2)NC(=O)[C@H](CCCCNC(=O)[C@H]2CCCN2C(=O)[C@@H](NC(=O)[C@@H](CC(N)=O)NC1=O)C(C)C)NC(C)=O
Show InChI InChI=1S/C37H57N8O12P/c1-20(2)17-26-33(49)43-28(19-30(38)47)35(51)44-31(21(3)4)37(53)45-16-8-10-29(45)36(52)39-15-7-6-9-25(40-22(5)46)32(48)42-27(34(50)41-26)18-23-11-13-24(14-12-23)57-58(54,55)56/h11-14,20-21,25-29,31H,6-10,15-19H2,1-5H3,(H2,38,47)(H,39,52)(H,40,46)(H,41,50)(H,42,48)(H,43,49)(H,44,51)(H2,54,55,56)/t25-,26-,27+,28+,29+,31-/m0/s1
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.50E+5n/an/an/an/an/an/a



Novartis Forschungsinstitut

Curated by ChEMBL


Assay Description
Inhibitory activity against binding of Src protein tryrosine kinase SH2 domain to biotinylated EPQY*EEIPI Peptide by ELISA.


J Med Chem 42: 971-80 (1999)


Article DOI: 10.1021/jm9811007
BindingDB Entry DOI: 10.7270/Q28S4P35
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%