null

SMILES: CC[C@H]1NC(=O)[C@H]([C@H](O)[C@H](C)CCCC(=O)OC)N(C)C(=O)[C@@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C)NC(=O)[C@@H](C)NC(=O)[C@@H](CC(C)C)N(C)C(=O)[C@@H](NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O)C(C)C

InChI Key: InChIKey=SHCGDZWYXUVNNK-LHCCYJQJSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50123743   

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
Protein phosphatase 3 catalytic subunit alpha (Homo sapiens (Human))	BDBM50123743 (6-(5-Ethyl-11,17,26,29-tetraisobutyl-14,32-diisopr...) Show SMILES CC[C@H]1NC(=O)[C@H]([C@H](O)[C@H](C)CCCC(=O)OC)N(C)C(=O)[C@@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C)NC(=O)[C@@H](C)NC(=O)[C@@H](CC(C)C)N(C)C(=O)[C@@H](NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O)C(C)C Show InChI InChI=1S/C63H113N11O14/c1-25-43-59(83)68(17)33-48(75)69(18)44(29-34(2)3)56(80)67-50(38(10)11)62(86)70(19)45(30-35(4)5)55(79)64-41(15)54(78)65-42(16)58(82)71(20)46(31-36(6)7)60(84)72(21)47(32-37(8)9)61(85)73(22)51(39(12)13)63(87)74(23)52(57(81)66-43)53(77)40(14)27-26-28-49(76)88-24/h34-47,50-53,77H,25-33H2,1-24H3,(H,64,79)(H,65,78)(H,66,81)(H,67,80)/t40-,41-,42+,43-,44+,45-,46+,47+,50+,51-,52+,53-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	890	n/a	n/a	n/a	n/a	n/a	n/a
Enanta Pharmaceuticals Curated by ChEMBL					Assay Description Compound was evaluated for its inhibitory activity in a calcineurin inhibition assay				J Med Chem 46: 674-6 (2003) Article DOI: 10.1021/jm025595i BindingDB Entry DOI: 10.7270/Q2QJ7GNM
					More data for this Ligand-Target Pair