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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H21F3N4O2
Molecular Weight 418.4122
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of JBI-778

SMILES

O[C@@H](CNC(=O)C1=CN2C=C(C=CC2=N1)C(F)(F)F)CN3CCC4=C(C3)C=CC=C4

InChI

InChIKey=BBWOALSAXDLCTK-KRWDZBQOSA-N
InChI=1S/C21H21F3N4O2/c22-21(23,24)16-5-6-19-26-18(13-28(19)11-16)20(30)25-9-17(29)12-27-8-7-14-3-1-2-4-15(14)10-27/h1-6,11,13,17,29H,7-10,12H2,(H,25,30)/t17-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H21F3N4O2
Molecular Weight 418.4122
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 19:29:21 GMT 2023
Edited
by admin
on Sat Dec 16 19:29:21 GMT 2023
Record UNII
B4P2B52Y6S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
JBI-778
Code English
Imidazo[1,2-a]pyridine-2-carboxamide, N-[(2S)-3-(3,4-dihydro-2(1H)-isoquinolinyl)-2-hydroxypropyl]-6-(trifluoromethyl)-
Common Name English
N-[(2S)-3-(3,4-Dihydro-2(1H)-isoquinolinyl)-2-hydroxypropyl]-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxamide
Systematic Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 923622
Created by admin on Sat Dec 16 19:29:21 GMT 2023 , Edited by admin on Sat Dec 16 19:29:21 GMT 2023
Code System Code Type Description
PUBCHEM
138634367
Created by admin on Sat Dec 16 19:29:21 GMT 2023 , Edited by admin on Sat Dec 16 19:29:21 GMT 2023
PRIMARY
FDA UNII
B4P2B52Y6S
Created by admin on Sat Dec 16 19:29:21 GMT 2023 , Edited by admin on Sat Dec 16 19:29:21 GMT 2023
PRIMARY
CAS
2334452-88-7
Created by admin on Sat Dec 16 19:29:21 GMT 2023 , Edited by admin on Sat Dec 16 19:29:21 GMT 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
Collectively, pre-clinical pharmacology studies indicate that JBI-778 is a potent and selective, substrate competitive-SAM cooperative, brain penetrant protein arginine methyl transferase 5 (PRMT5) inhibitor. JBI-778 shows higher selectivity against other PRMTs. The compound shows an IC50 of ~3 nM against PRMT5:MEP50 in the biochemical assay
COMPETITIVE INHIBITOR
IC50
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
BRAIN/PLASMA RATIO PHARMACOKINETIC Route of Administration
PHARMACOKINETIC