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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H26N4O4
Molecular Weight 446.4983
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OTAMIXABAN

SMILES

COC(=O)[C@H](CC1=CC=CC(=C1)C(N)=N)[C@@H](C)NC(=O)C2=CC=C(C=C2)C3=CC=[N+]([O-])C=C3

InChI

InChIKey=PFGVNLZDWRZPJW-OPAMFIHVSA-N
InChI=1S/C25H26N4O4/c1-16(22(25(31)33-2)15-17-4-3-5-21(14-17)23(26)27)28-24(30)20-8-6-18(7-9-20)19-10-12-29(32)13-11-19/h3-14,16,22H,15H2,1-2H3,(H3,26,27)(H,28,30)/t16-,22-/m1/s1

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/17979700

Otamixaban is a synthetically derived parenteral fXa inhibitor currently in late stage clinical development at Sanofi-Aventis for the management of acute coronary syndrome. Otamixaban is a potent (Ki = 0.5 nM), selective, rapid acting, competitive and reversible fXa inhibitor that effectively inhibits both free and prothrombinase-bound fXa. Factor Xa (fXa) is a critical serine protease situated at the confluence of the intrinsic and extrinsic pathways of the blood coagulation cascade. FXa catalyzes the conversion of prothrombin to thrombin via the prothrombinase complex. Its singular role in thrombin generation, coupled with its potentiating effects on clot formation render it an attractive target for therapeutic intervention. In vivo experiments have demonstrated that Otamixaban is highly efficacious in rodent, canine and porcine models of thrombosis. In addition, recent clinical findings indicate that Otamixaban is efficacious, safe and well tolerated in humans and therefore has considerable potential for the treatment of acute coronary syndrome. Following the results of the Treatment of non-ST elevation Acute coronary syndrome with otamixaban, Sanofi has decided to discontinue the investigational programme with otamixaban, due to efficacy lower than expected. Otamixaban did not show superior benefit/risk to the combination of unfractionated heparin.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.5 nM [Ki]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Doses

Doses

DosePopulationAdverse events​
0.14 mg/kg 1 times / hour multiple, intravenous
Studied dose
Dose: 0.14 mg/kg, 1 times / hour
Route: intravenous
Route: multiple
Dose: 0.14 mg/kg, 1 times / hour
Sources: Page: p.1150
unhealthy, ADULT
n = 5106
Health Status: unhealthy
Condition: myocardial infarction
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Population Size: 5106
Sources: Page: p.1150
Disc. AE: Bleeding...
AEs leading to
discontinuation/dose reduction:
Bleeding (4.7%)
Sources: Page: p.1150
AEs

AEs

AESignificanceDosePopulation
Bleeding 4.7%
Disc. AE
0.14 mg/kg 1 times / hour multiple, intravenous
Studied dose
Dose: 0.14 mg/kg, 1 times / hour
Route: intravenous
Route: multiple
Dose: 0.14 mg/kg, 1 times / hour
Sources: Page: p.1150
unhealthy, ADULT
n = 5106
Health Status: unhealthy
Condition: myocardial infarction
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Population Size: 5106
Sources: Page: p.1150
PubMed

PubMed

TitleDatePubMed
Anticoagulant and anti-platelet effects are maintained following coadministration of otamixaban, a direct factor Xa inhibitor, and acetylsalicylic acid.
2006 Feb
Asymmetric synthesis of intermediates for otamixaban and premafloxacin by the chiral ligand-controlled asymmetric conjugate addition of a lithium amide.
2006 Jun 9
Otamixaban for the treatment of patients with non-ST-elevation acute coronary syndromes (SEPIA-ACS1 TIMI 42): a randomised, double-blind, active-controlled, phase 2 trial.
2009 Sep 5
Recent research on antithrombotics. News on the treatment of patients with acute coronary syndromes.
2010 May
Patents

Sample Use Guides

0.080 mg/kg bolus followed by continuous 0.100 mg/kg/h infusion
Route of Administration: Intravenous
In Vitro Use Guide
Unknown
Name Type Language
OTAMIXABAN
INN   MI   WHO-DD  
INN  
Official Name English
otamixaban [INN]
Common Name English
METHYL (2R,3R)-2-(3-CARBAMIMIDOYLBENZYL)-3-((4-(1-OXIDOPYRIDIN-4-YL)BENZOYL)AMINO)BUTANOATE
Systematic Name English
FXV673
Code English
OTAMIXABAN [MI]
Common Name English
FXV-673
Code English
RPR130673
Code English
RPR-130673
Code English
XRP0673
Code English
Otamixaban [WHO-DD]
Common Name English
XRP-0673
Code English
Classification Tree Code System Code
NCI_THESAURUS C263
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID40172917
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY
FDA UNII
S173RED00L
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY
MERCK INDEX
m8266
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY Merck Index
PUBCHEM
5496659
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY
ChEMBL
CHEMBL46618
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY
NCI_THESAURUS
C90704
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY
WIKIPEDIA
OTAMIXABAN
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY
DRUG BANK
DB06635
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY
SMS_ID
300000034257
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY
INN
8096
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY
CAS
193153-04-7
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY
MESH
C435830
Created by admin on Fri Dec 15 16:11:04 GMT 2023 , Edited by admin on Fri Dec 15 16:11:04 GMT 2023
PRIMARY