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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H21F3N2O2
Molecular Weight 378.3881
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TILAPERTIN

SMILES

OC(=O)CN1CCN(CC1)[C@H](C2=CC=CC=C2)C3=CC=CC(=C3)C(F)(F)F

InChI

InChIKey=MDLQJNCGZVDZFV-LJQANCHMSA-N
InChI=1S/C20H21F3N2O2/c21-20(22,23)17-8-4-7-16(13-17)19(15-5-2-1-3-6-15)25-11-9-24(10-12-25)14-18(26)27/h1-8,13,19H,9-12,14H2,(H,26,27)/t19-/m1/s1

HIDE SMILES / InChI

Molecular Formula C20H21F3N2O2
Molecular Weight 378.3881
Charge 0
Count
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Description

Tilapertin (also known as AMG 747) is a piperazineacetic acid derivative patented by Amgen Inc as glycine transporter-1 inhibitor useful for the treatment of negative symptoms of schizophrenia. Oral administration of AMG 747 dose-dependently increases cerebrospinal fluid(CSF) glycine concentration in rats. In humans, Tilapertin has linear pharmacokinetics, prolonged half-life, and acceptable safety and tolerability at multiple doses up to 60 mg daily dosing. Unfortunately, in clinical trials, Tilapertin failed to demonstrate superior efficacy compare antipsychotic therapy in clinically stable people with schizophrenia.

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency

PubMed

Sample Use Guides

In Vivo Use Guide
5 mg, 15 mg, or 40 mg once-daily
Route of Administration: Oral
Substance Class Chemical
Record UNII
A2SV488G98
Record Status Validated (UNII)
Record Version