Target
Nuclear receptor ROR-gamma
Ligand
BDBM352782
Substrate
n/a
Meas. Tech.
Biological Assay
IC50
3.04±n/a nM
Citation
 Aicher, TDVanHuis, CAThomas, WDMacLean, JKAndresen, BMBarr, KJBienstock, CEAnthony, NJDaniels, MLiu, KLiu, YWhite, CMLapointe, BTSciammetta, NSimov, V Tetrahydronaphthyridine, benzoxazine, aza-benzoxazine and related bicyclic compounds for inhibition of RORgamma activity and the treatment of disease US Patent  US9809561 Publication Date 11/7/2017 
Target
Name:
Nuclear receptor ROR-gamma
Synonyms:
NR1F3 | Nuclear receptor ROR-gamma | Nuclear receptor ROR-gamma (RORC) | Nuclear receptor subfamily 1 group F member 3 | RAR-related orphan receptor C (RORc) | RORC | RORG | RORG_HUMAN | RZRG | Retinoid-related orphan receptor-gamma | Retinoid-related orphan receptor-gamma (RORc)
Type:
Enzyme Catalytic Domain
Mol. Mass.:
58218.40
Organism:
Homo sapiens (Human)
Description:
P51449
Residue:
518
Sequence:
MDRAPQRQHRASRELLAAKKTHTSQIEVIPCKICGDKSSGIHYGVITCEGCKGFFRRSQRCNAAYSCTRQQNCPIDRTSRNRCQHCRLQKCLALGMSRDAVKFGRMSKKQRDSLHAEVQKQLQQRQQQQQEPVVKTPPAGAQGADTLTYTLGLPDGQLPLGSSPDLPEASACPPGLLKASGSGPSYSNNLAKAGLNGASCHLEYSPERGKAEGRESFYSTGSQLTPDRCGLRFEEHRHPGLGELGQGPDSYGSPSFRSTPEAPYASLTEIEHLVQSVCKSYRETCQLRLEDLLRQRSNIFSREEVTGYQRKSMWEMWERCAHHLTEAIQYVVEFAKRLSGFMELCQNDQIVLLKAGAMEVVLVRMCRAYNADNRTVFFEGKYGGMELFRALGCSELISSIFDFSHSLSALHFSEDEIALYTALVLINAHRPGLQEKRKVEQLQYNLELAFHHHLCKTHRQSILAKLPPKGKLRSLCSQHVERLQIFQHLHPIVVQAAFPPLYKELFSTETESPVGLSK
  
Inhibitor
Name:
BDBM352782
Synonyms:
(S)-tert-butyl (2-((1H-1,2,4-triazol-1- yl)methyl)-4-((3- (trifluoromethyl)phenyl)sulfonyl)-3,4- dihydro-2H-benzo[b][1,4]oxazin-6- yl)carbamate | US10745364, Example 63C | US9809561, 63C
Type:
Small organic molecule
Emp. Form.:
C23H24F3N5O5S
Mol. Mass.:
539.527
SMILES:
CC(C)(C)OC(=O)Nc1ccc2O[C@@H](Cn3cncn3)CN(c2c1)S(=O)(=O)c1cccc(c1)C(F)(F)F |r|
Structure:
Search PDB for entries with ligand similarity: