BDBM50238580 CHEMBL4099451

SMILES: CSCCC[C@@H]1NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@@H]2CSSC[C@H](NC(=O)CN)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](Cc3ccc(O)cc3)NC(=O)[C@@H]3CCCN3C(=O)[C@H](CO)NC1=O)C(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)N2

InChI Key: InChIKey=UMRUMCFCWHJXSF-MUJNREOGSA-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 = 50238580   

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
Nicotinic acetylcholine receptor alpha6/alpha3/beta4 (Rattus norvegicus-Rattus norvegicus (Rat))	BDBM50238580 (CHEMBL4099451) Show SMILES CSCCC[C@@H]1NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@@H]2CSSC[C@H](NC(=O)CN)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](Cc3ccc(O)cc3)NC(=O)[C@@H]3CCCN3C(=O)[C@H](CO)NC1=O)C(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)N2 |r| Show InChI InChI=1S/C62H92N18O19S5/c1-30(2)48-60(97)77-44-28-104-102-26-42(68-47(85)20-63)55(92)76-43(56(93)73-39(23-82)54(91)71-37(19-33-21-65-29-66-33)61(98)79-15-6-10-46(79)59(96)78-48)27-103-101-25-41(49(64)86)75-52(89)36(18-32-11-13-34(84)14-12-32)70-58(95)45-9-5-16-80(45)62(99)40(24-83)74-51(88)35(8-7-17-100-4)69-50(87)31(3)67-53(90)38(22-81)72-57(44)94/h11-14,21,29-31,35-46,48,81-84H,5-10,15-20,22-28,63H2,1-4H3,(H2,64,86)(H,65,66)(H,67,90)(H,68,85)(H,69,87)(H,70,95)(H,71,91)(H,72,94)(H,73,93)(H,74,88)(H,75,89)(H,76,92)(H,77,97)(H,78,96)/t31-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,48-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	39	n/a	n/a	n/a	n/a	n/a	n/a
Hainan University Curated by ChEMBL					Assay Description Antagonist activity at rat alpha6/alpha3beta4 nACHR expressed in xenopous laevis oocyte assessed as inhibition of ACh induced channel current after 5...				J Med Chem 60: 5826-5833 (2017) Article DOI: 10.1021/acs.jmedchem.7b00546 BindingDB Entry DOI: 10.7270/Q28C9ZHM
					More data for this Ligand-Target Pair
Neuronal acetylcholine receptor Alpha-3/Beta-4 (Rattus norvegicus (Rat))	BDBM50238580 (CHEMBL4099451) Show SMILES CSCCC[C@@H]1NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@@H]2CSSC[C@H](NC(=O)CN)C(=O)N[C@@H](CSSC[C@H](NC(=O)[C@H](Cc3ccc(O)cc3)NC(=O)[C@@H]3CCCN3C(=O)[C@H](CO)NC1=O)C(N)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)N2 |r| Show InChI InChI=1S/C62H92N18O19S5/c1-30(2)48-60(97)77-44-28-104-102-26-42(68-47(85)20-63)55(92)76-43(56(93)73-39(23-82)54(91)71-37(19-33-21-65-29-66-33)61(98)79-15-6-10-46(79)59(96)78-48)27-103-101-25-41(49(64)86)75-52(89)36(18-32-11-13-34(84)14-12-32)70-58(95)45-9-5-16-80(45)62(99)40(24-83)74-51(88)35(8-7-17-100-4)69-50(87)31(3)67-53(90)38(22-81)72-57(44)94/h11-14,21,29-31,35-46,48,81-84H,5-10,15-20,22-28,63H2,1-4H3,(H2,64,86)(H,65,66)(H,67,90)(H,68,85)(H,69,87)(H,70,95)(H,71,91)(H,72,94)(H,73,93)(H,74,88)(H,75,89)(H,76,92)(H,77,97)(H,78,96)/t31-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,48-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Hainan University Curated by ChEMBL					Assay Description Antagonist activity at rat alpha3beta4 nACHR expressed in xenopous laevis oocyte assessed as inhibition of ACh induced channel current after 5 mins a...				J Med Chem 60: 5826-5833 (2017) Article DOI: 10.1021/acs.jmedchem.7b00546 BindingDB Entry DOI: 10.7270/Q28C9ZHM
					More data for this Ligand-Target Pair