BDBM50032771 (4aR,6aR,10S)-7-(1,5-Dimethyl-hexyl)-1,4a,6a,10-tetramethyl-hexadecahydro-indeno[5,4-f]quinolin-2-one::(4aR,6aR,7R,10S)-7-(1,5-Dimethyl-hexyl)-1,4a,6a,10-tetramethyl-hexadecahydro-indeno[5,4-f]quinolin-2-one::CHEMBL25448::MK-386
SMILES: CC(C)CCCC(C)C1CCC2C3[C@@H](C)CC4N(C)C(=O)CC[C@]4(C)C3CC[C@]12C
InChI Key: InChIKey=XUTZDXHKQDPUMA-WOCATEOUSA-N
Data: 2 IC50
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5α-Reductase 1 (5α-R1) (Homo sapiens (Human)) | BDBM50032771 ((4aR,6aR,10S)-7-(1,5-Dimethyl-hexyl)-1,4a,6a,10-te...) | UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 0.5 | n/a | n/a | n/a | n/a | n/a | n/a |
Università di Firenze Curated by ChEMBL | Assay Description Inhibition of human Steroid 5-alpha-reductase type I | Bioorg Med Chem Lett 10: 353-6 (2000) BindingDB Entry DOI: 10.7270/Q2K35SVJ | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
Steroid 5-alpha-reductase (Homo sapiens (Human)) | BDBM50032771 ((4aR,6aR,10S)-7-(1,5-Dimethyl-hexyl)-1,4a,6a,10-te...) | PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 154 | n/a | n/a | n/a | n/a | n/a | n/a |
Università di Firenze Curated by ChEMBL | Assay Description Compound was tested for inhibition against human Steroid 5-alpha-reductase type 2 | Bioorg Med Chem Lett 10: 353-6 (2000) BindingDB Entry DOI: 10.7270/Q2K35SVJ | |||||||||||
More data for this Ligand-Target Pair |