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Details

Stereochemistry ACHIRAL
Molecular Formula C20H27F3N6OS.C4H4O4.2H2O
Molecular Weight 608.631
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of ABT-925

SMILES

O.O.OC(=O)\C=C\C(O)=O.CC(C)(C)C1=NC(=CC(=N1)N2CCN(CCCSC3=NC=CC(=O)N3)CC2)C(F)(F)F

InChI

InChIKey=GFTJDVASDZQGCG-WFNHHOHWSA-N
InChI=1S/C20H27F3N6OS.C4H4O4.2H2O/c1-19(2,3)17-25-14(20(21,22)23)13-15(26-17)29-10-8-28(9-11-29)7-4-12-31-18-24-6-5-16(30)27-18;5-3(6)1-2-4(7)8;;/h5-6,13H,4,7-12H2,1-3H3,(H,24,27,30);1-2H,(H,5,6)(H,7,8);2*1H2/b;2-1+;;

HIDE SMILES / InChI

Molecular Formula H2O
Molecular Weight 18.0153
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C20H27F3N6OS
Molecular Weight 456.528
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C4H4O4
Molecular Weight 116.0722
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Abbott Laboratories was developing the selective dopamine D3 receptor antagonist, ABT-925 (formerly A 437203), for the treatment of schizophrenia. ABT-925 is a selective dopamine D₃ receptor antagonist with an approximately 100-fold higher in vitro affinity for dopamine D₃ versus D₂ receptors. ABT 925 was undergoing phase II clinical development for the treatment of schizophrenia. However, development was discontinued in December 2007.

Approval Year

PubMed

PubMed

TitleDatePubMed
A double-blind, randomized, placebo-controlled study of the dopamine D₃ receptor antagonist ABT-925 in patients with acute schizophrenia.
2011 Apr
Dopamine D₃ receptor antagonism--still a therapeutic option for the treatment of schizophrenia.
2013 Feb
Pharmacological targeting of dopamine D3 receptors: Possible clinical applications of selective drugs.
2015 Sep

Sample Use Guides

Schizophrenia: One hundred fifty-five patients were assessed over a 6-week double-blind treatment period (placebo: n = 48; ABT-925 50 mg once daily [QD]: n = 53; ABT-925 150 mg QD: n = 54). No statistically significant treatment effect was observed with ABT-925 50 mg QD or 150 mg QD compared with placebo on primary or secondary efficacy end points. Pharmacokinetic parameter estimates increased with dose in a linear fashion. ABT-925 50 mg QD and 150 mg QD were generally well tolerated, with adverse event profiles similar to that of placebo.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:49:12 UTC 2023
Edited
by admin
on Fri Dec 15 15:49:12 UTC 2023
Record UNII
XXV4WFG08S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ABT-925
Common Name English
4(3H)-PYRIMIDINONE, 2-((3-(4-(2-(1,1-DIMETHYLETHYL)-6-(TRIFLUOROMETHYL)-4-PYRIMIDINYL)-1-PIPERAZINYL)PROPYL)THIO)-, (2E)-2-BUTENEDIOATE, HYDRATE (1:1:2)
Systematic Name English
Code System Code Type Description
RXCUI
1661017
Created by admin on Fri Dec 15 15:49:12 UTC 2023 , Edited by admin on Fri Dec 15 15:49:12 UTC 2023
PRIMARY RxNorm
CAS
1160247-85-7
Created by admin on Fri Dec 15 15:49:12 UTC 2023 , Edited by admin on Fri Dec 15 15:49:12 UTC 2023
PRIMARY
PUBCHEM
71301278
Created by admin on Fri Dec 15 15:49:12 UTC 2023 , Edited by admin on Fri Dec 15 15:49:12 UTC 2023
PRIMARY
FDA UNII
XXV4WFG08S
Created by admin on Fri Dec 15 15:49:12 UTC 2023 , Edited by admin on Fri Dec 15 15:49:12 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ANHYDROUS->SOLVATE
Related Record Type Details
ACTIVE MOIETY