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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H19N3O.ClH
Molecular Weight 329.824
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FABESETRON HYDROCHLORIDE

SMILES

Cl.CC1=C(C[C@H]2CCC3=C(C)C4=C(C=CC=C4)N3C2=O)N=CN1

InChI

InChIKey=POKFYJWUPWZYQV-BTQNPOSSSA-N
InChI=1S/C18H19N3O.ClH/c1-11-14-5-3-4-6-17(14)21-16(11)8-7-13(18(21)22)9-15-12(2)19-10-20-15;/h3-6,10,13H,7-9H2,1-2H3,(H,19,20);1H/t13-;/m1./s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C18H19N3O
Molecular Weight 293.363
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including, http://www.ncbi.nlm.nih.gov/pubmed/16079468

Fabesetron is a dual 5HT3 and 5HT4 receptors antagonist that was developed in Japan for the treatment of chemotherapy-induced emesis and gastrointestinal disorders. The development of the drug was terminated in phase II.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Q13639|||Q9NY73
Gene ID: 3360.0
Gene Symbol: HTR4
Target Organism: Homo sapiens (Human)
Target ID: P46098
Gene ID: 3359.0
Gene Symbol: HTR3A
Target Organism: Homo sapiens (Human)
8.84 null [pIC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Secondary
Unknown

Approved Use

Unknown
Primary
Unknown

Approved Use

Unknown
Secondary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Antiemetic activity of FK1052, a 5-HT3- and 5-HT4-receptor antagonist, in Suncus murinus and ferrets.
2005-08
Prediction of human hepatic clearance from in vivo animal experiments and in vitro metabolic studies with liver microsomes from animals and humans.
2001-10
Probable involvement of the 5-hydroxytryptamine(4) receptor in methotrexate-induced delayed emesis in dogs.
2000-03
Combined blockade of 5-HT3- and 5-HT4-serotonin receptors inhibits colonic functions in conscious rats and mice.
1997-04
New 5-HT3 (serotonin-3) receptor antagonists. III. An efficient synthesis of carbon 14-labeled (+)-8,9-dihydro-10-methyl-7-[(5-methyl-1H-imidazol-4- yl)methyl]pyrido[1,2-a]indol-6(7H)-one hydrochloride (FK 1052).
1995-08
New 5-HT3 (serotonin-3) receptor antagonists. I. Synthesis and structure-activity relationships of pyrido[1,2-a]indoles.
1994-12
New 5-HT3 (serotonin-3) receptor antagonists, II. Synthesis and structure-activity relationships of pyrimido[1,6-a]indoles.
1994-12
Effect of FK1052, a potent 5-hydroxytryptamine3 and 5-hydroxytryptamine4 receptor dual antagonist, on colonic function in vivo.
1993-07
Pharmacological characterization of FK1052, a dihydropyridoindole derivative, as a new serotonin 3 and 4 dual receptor antagonist.
1993-05
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
The effect of fabesteron on short-circuit current was investigated using submucosa-mucosa sheets of guinea-pig distal colon. The drug at 10(-9) M suppressed the 5-HT-evoked response to 69% of control.
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:30:50 GMT 2025
Edited
by admin
on Mon Mar 31 21:30:50 GMT 2025
Record UNII
DIU098C1O7
Record Status Validated (UNII)
Record Version
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Name Type Language
FABESETRON HYDROCHLORIDE
JAN  
Common Name English
FK-1052
Preferred Name English
PYRIDO(1,2-A)INDOL-6(7H)-ONE, 8,9-DIHYDRO-10-METHYL-7-((5-METHYL-1H-IMIDAZOL-4-YL)METHYL)-, MONOHYDROCHLORIDE, (R)-
Common Name English
FABESETRON HYDROCHLORIDE [JAN]
Common Name English
PYRIDO(1,2-A)INDOL-6(7H)-ONE, 8,9-DIHYDRO-10-METHYL-7-((5-METHYL-1H-IMIDAZOL-4-YL)METHYL)-, MONOHYDROCHLORIDE, (7R)-
Common Name English
FK1052
Code English
FABESETRON MONOHYDROCHLORIDE
Common Name English
Code System Code Type Description
CHEBI
31588
Created by admin on Mon Mar 31 21:30:50 GMT 2025 , Edited by admin on Mon Mar 31 21:30:50 GMT 2025
PRIMARY
FDA UNII
DIU098C1O7
Created by admin on Mon Mar 31 21:30:50 GMT 2025 , Edited by admin on Mon Mar 31 21:30:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID7048168
Created by admin on Mon Mar 31 21:30:50 GMT 2025 , Edited by admin on Mon Mar 31 21:30:50 GMT 2025
PRIMARY
PUBCHEM
180494
Created by admin on Mon Mar 31 21:30:50 GMT 2025 , Edited by admin on Mon Mar 31 21:30:50 GMT 2025
PRIMARY
CAS
129299-90-7
Created by admin on Mon Mar 31 21:30:50 GMT 2025 , Edited by admin on Mon Mar 31 21:30:50 GMT 2025
PRIMARY
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