null

SMILES: [#7]-[#6](=O)-[#6]-[#6]-[#6@@H]-1-[#7]-[#6](=O)-[#6@H](-[#6]-c2ccccc2)-[#7]-[#6](=O)-[#6@H](-[#7]-[#6](=O)-[#6]-[#6]-[#16]-[#16]-[#6]-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#7])=O)-[#7]-[#6]-1=O)-[#6](=O)-[#7]-1-[#6]-[#6]-[#6]-[#6@H]-1-[#6](=O)-[#7]-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6]-[#6](-[#7])=O)-[#6](-c1ccccc1)-c1ccccc1

InChI Key: InChIKey=HGNJZHKQNIASIY-AWKBIXBLSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50414484   

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
Vasopressin V1a receptor (RAT)	BDBM50414484 (CHEMBL541246) Show SMILES [#7]-[#6](=O)-[#6]-[#6]-[#6@@H]-1-[#7]-[#6](=O)-[#6@H](-[#6]-c2ccccc2)-[#7]-[#6](=O)-[#6@H](-[#7]-[#6](=O)-[#6]-[#6]-[#16]-[#16]-[#6]-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#7])=O)-[#7]-[#6]-1=O)-[#6](=O)-[#7]-1-[#6]-[#6]-[#6]-[#6@H]-1-[#6](=O)-[#7]-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6]-[#6](-[#7])=O)-[#6](-c1ccccc1)-c1ccccc1 |r| Show InChI InChI=1S/C52H68N14O11S2/c53-39(67)21-20-34-46(72)62-36(27-40(54)68)48(74)64-37(51(77)66-24-11-19-38(66)49(75)61-33(18-10-23-58-52(56)57)45(71)59-28-41(55)69)29-79-78-25-22-42(70)65-44(43(31-14-6-2-7-15-31)32-16-8-3-9-17-32)50(76)63-35(47(73)60-34)26-30-12-4-1-5-13-30/h1-9,12-17,33-38,43-44H,10-11,18-29H2,(H2,53,67)(H2,54,68)(H2,55,69)(H,59,71)(H,60,73)(H,61,75)(H,62,72)(H,63,76)(H,64,74)(H,65,70)(H4,56,57,58)/t33-,34+,35+,36+,37+,38+,44-/m1/s1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	1.58E+3	n/a	n/a	n/a	n/a	n/a
University of Gdansk Curated by ChEMBL					Assay Description Antagonist activity at vasopressin V1a receptor in phenoxybenzamine-treated Wistar rat uterus assessed as inhibition of vasopressin-induced arteial v...				Eur J Med Chem 44: 2862-67 (2009) BindingDB Entry DOI: 10.7270/Q28P61RJ
					More data for this Ligand-Target Pair
Oxytocin receptor (RAT)	BDBM50414484 (CHEMBL541246) Show SMILES [#7]-[#6](=O)-[#6]-[#6]-[#6@@H]-1-[#7]-[#6](=O)-[#6@H](-[#6]-c2ccccc2)-[#7]-[#6](=O)-[#6@H](-[#7]-[#6](=O)-[#6]-[#6]-[#16]-[#16]-[#6]-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-[#6](-[#7])=O)-[#7]-[#6]-1=O)-[#6](=O)-[#7]-1-[#6]-[#6]-[#6]-[#6@H]-1-[#6](=O)-[#7]-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-[#6]-[#6](-[#7])=O)-[#6](-c1ccccc1)-c1ccccc1 |r| Show InChI InChI=1S/C52H68N14O11S2/c53-39(67)21-20-34-46(72)62-36(27-40(54)68)48(74)64-37(51(77)66-24-11-19-38(66)49(75)61-33(18-10-23-58-52(56)57)45(71)59-28-41(55)69)29-79-78-25-22-42(70)65-44(43(31-14-6-2-7-15-31)32-16-8-3-9-17-32)50(76)63-35(47(73)60-34)26-30-12-4-1-5-13-30/h1-9,12-17,33-38,43-44H,10-11,18-29H2,(H2,53,67)(H2,54,68)(H2,55,69)(H,59,71)(H,60,73)(H,61,75)(H,62,72)(H,63,76)(H,64,74)(H,65,70)(H4,56,57,58)/t33-,34+,35+,36+,37+,38+,44-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	16.2	n/a	n/a	n/a	n/a	n/a
University of Gdansk Curated by ChEMBL					Assay Description Antagonist activity at oxytocin receptor in Wistar rat uterus assessed as inhibition of oxytocin-induced uterotonic activity treated 1 min prior to o...				Eur J Med Chem 44: 2862-67 (2009) BindingDB Entry DOI: 10.7270/Q28P61RJ
					More data for this Ligand-Target Pair