BDBM50074705 CHEMBL359934::Phosphoric acid mono-[4-((5S,8R,11S,14R,17R,23aR)-17-acetylamino-8-carbamoylmethyl-5,11-diisopropyl-4,7,10,13,16,23-hexaoxo-docosahydro-3a,6,9,12,15,22-hexaaza-cyclopentacyclodocosen-14-ylmethyl)-phenyl] ester

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

InChI Key: InChIKey=ZFXYMDBTOLQWLR-WOMNCXHOSA-N

Data: 2 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50074705   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Grb2-SH2 (Homo sapiens (Human))	BDBM50074705 (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 UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a	n/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))	BDBM50074705 (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/a	n/a	7.30E+4	n/a	n/a	n/a	n/a	n/a	n/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