Target
Peptidyl-prolyl cis-trans isomerase F, mitochondrial
Ligand
BDBM50030493
Substrate
n/a
Meas. Tech.
ChEMBL_1436364 (CHEMBL3389567)
Kd
0.900000±n/a nM
Citation
 Fu, JTjandra, MBecker, CBednarczyk, DCapparelli, MElling, RHanna, IFujimoto, RFuregati, MKarur, SKasprzyk, TKnapp, MLeung, KLi, XLu, PMergo, WMiault, CNg, SParker, DPeng, YRoggo, SRivkin, ASimmons, RLWang, MWiedmann, BWeiss, AHXiao, LXie, LXu, WYifru, AYang, SZhou, BSweeney, ZK Potent nonimmunosuppressive cyclophilin inhibitors with improved pharmaceutical properties and decreased transporter inhibition. J Med Chem 57:8503-16 (2014) [PubMed]  Article 
Target
Name:
Peptidyl-prolyl cis-trans isomerase F, mitochondrial
Synonyms:
CYP3 | CyP-D | CyP-M | Cyclophilin D | Cyclophilin F | CypD | Mitochondrial cyclophilin | PPIF | PPIF_HUMAN | PPIase F | Rotamase F
Type:
PROTEIN
Mol. Mass.:
22052.60
Organism:
Homo sapiens (Human)
Description:
ChEMBL_109465
Residue:
207
Sequence:
MLALRCGSRWLGLLSVPRSVPLRLPAARACSKGSGDPSSSSSSGNPLVYLDVDANGKPLGRVVLELKADVVPKTAENFRALCTGEKGFGYKGSTFHRVIPSFMCQAGDFTNHNGTGGKSIYGSRFPDENFTLKHVGPGVLSMANAGPNTNGSQFFICTIKTDWLDGKHVVFGHVKEGMDVVKKIESFGSKSGRTSKKIVITDCGQLS
  
Inhibitor
Name:
BDBM50030493
Synonyms:
CHEMBL3344501 | US9566312, Compound 2.17.4
Type:
Small organic molecule
Emp. Form.:
C69H125N13O13
Mol. Mass.:
1344.8101
SMILES:
[H][C@@]1([C@@H](C)CN2CCN(CCOC)CC2)N(C)C(=O)[C@@H](C)N(C)C(=O)[C@H](CC)NC(=O)[C@]([H])([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](NC1=O)C(C)C |r|
Structure:
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