Target
Orexin/Hypocretin receptor type 1
Ligand
BDBM401792
Substrate
n/a
Meas. Tech.
FLIPR Ca2+ Flux Assay
IC50
30.0±n/a nM
Citation
 Liverton, NKuduk, SDBeshore, DLuo, YMeng, N Pyrazole, triazole and tetrazole orexin receptor antagonists US Patent  US10010539 Publication Date 7/3/2018 
Target
Name:
Orexin/Hypocretin receptor type 1
Synonyms:
Hcrtr1 | Hypocretin receptor type 1 | OX1R_RAT | Orexin receptor type 1 (OX1) | Orexin receptor type 1 (OX1R) | Ox-1-R | Ox1-R | Ox1R
Type:
Protein
Mol. Mass.:
46817.55
Organism:
Rattus norvegicus (Rat)
Description:
P56718
Residue:
416
Sequence:
MEPSATPGAQPGVPTSSGEPFHLPPDYEDEFLRYLWRDYLYPKQYEWVLIAAYVAVFLIALVGNTLVCLAVWRNHHMRTVTNYFIVNLSLADVLVTAICLPASLLVDITESWLFGHALCKVIPYLQAVSVSVAVLTLSFIALDRWYAICHPLLFKSTARRARGSILGIWAVSLAVMVPQAAVMECSSVLPELANRTRLFSVCDERWADELYPKIYHSCFFFVTYLAPLGLMGMAYFQIFRKLWGPQIPGTTSALVRNWKRPSEQLEAQHQGLCTEPQPRARAFLAEVKQMRARRKTAKMLMVVLLVFALCYLPISVLNVLKRVFGMFRQASDREAVYACFTFSHWLVYANSAANPIIYNFLSGKFREQFKAAFSCCLPGLGPSSSARHKSLSLQSRCSVSKVSEHVVLTTVTTVLS
  
Inhibitor
Name:
BDBM401792
Synonyms:
((2R,5R)-5-(4-(2-Hydroxypropan-2- yl)-2H-1,2,3-triazol-2-yl)-2- methylpiperidin-1-yl)(2-(2,2,2- trifluoroethyl)phenyl)methanone | US10010539, 9
Type:
Small organic molecule
Emp. Form.:
C20H25F3N4O2
Mol. Mass.:
410.4333
SMILES:
C[C@@H]1CC[C@H](CN1C(=O)c1ccccc1CC(F)(F)F)n1ncc(n1)C(C)(C)O |r|
Structure:
Search PDB for entries with ligand similarity: