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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

Molecular Formula C25H26N4O4
Molecular Weight 446.4983
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

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
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
252 ng/mL
100 μg/kg/h 1 times / day other, intravenous
dose: 100 μg/kg/h
route of administration: Intravenous
experiment type: OTHER
co-administered:
OTAMIXABAN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
458 ng/mL
125 μg/kg/h 1 times / day other, intravenous
dose: 125 μg/kg/h
route of administration: Intravenous
experiment type: OTHER
co-administered:
OTAMIXABAN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
635 ng/mL
150 μg/kg/h 1 times / day other, intravenous
dose: 150 μg/kg/h
route of administration: Intravenous
experiment type: OTHER
co-administered:
OTAMIXABAN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
85 ng/mL
50 μg/kg/h 1 times / day other, intravenous
dose: 50 μg/kg/h
route of administration: Intravenous
experiment type: OTHER
co-administered:
OTAMIXABAN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
6476 ng × h/mL
100 μg/kg/h 1 times / day other, intravenous
dose: 100 μg/kg/h
route of administration: Intravenous
experiment type: OTHER
co-administered:
OTAMIXABAN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
12007 ng × h/mL
125 μg/kg/h 1 times / day other, intravenous
dose: 125 μg/kg/h
route of administration: Intravenous
experiment type: OTHER
co-administered:
OTAMIXABAN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
15674 ng × h/mL
150 μg/kg/h 1 times / day other, intravenous
dose: 150 μg/kg/h
route of administration: Intravenous
experiment type: OTHER
co-administered:
OTAMIXABAN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: UNKNOWN
2437 ng × h/mL
50 μg/kg/h 1 times / day other, intravenous
dose: 50 μg/kg/h
route of administration: Intravenous
experiment type: OTHER
co-administered:
OTAMIXABAN plasma
Homo sapiens
population: UNHEALTHY
age: ADULT
sex: FEMALE / MALE
food status: 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:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Disc. AE: Bleeding...
AEs leading to
discontinuation/dose reduction:
Bleeding (4.7%)
Sources:
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:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
Small molecule coagulation cascade inhibitors in the clinic.
2005
Drug evaluation: the directly activated Factor Xa inhibitor otamixaban.
2006 Dec
Asymmetric synthesis of intermediates for otamixaban and premafloxacin by the chiral ligand-controlled asymmetric conjugate addition of a lithium amide.
2006 Jun 9
The discovery of the Factor Xa inhibitor otamixaban: from lead identification to clinical development.
2007
[Factor Xa-inhibition in interventional cardiology].
2007 Dec
Gateways to clinical trials.
2007 Sep
[What's new on antithrombotics?].
2009 Aug
Otamixaban in acute coronary syndromes.
2009 Sep 5
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
New drugs for the treatment of coronary artery syndromes: otamixaban and ticagrelor.
2010 Feb
Recent research on antithrombotics. News on the treatment of patients with acute coronary syndromes.
2010 May
Post-operative thromboprophylaxis: new oral thrombin and factor X inhibitors and their place in clinical practice.
2010 May 24
Clinical pharmacology of direct and indirect factor Xa inhibitors.
2010 Nov 12
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
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:21:07 GMT 2025
Edited
by admin
on Mon Mar 31 18:21:07 GMT 2025
Record UNII
S173RED00L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FXV-673
Preferred Name English
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
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 Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID40172917
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY
FDA UNII
S173RED00L
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY
MERCK INDEX
m8266
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY Merck Index
PUBCHEM
5496659
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY
ChEMBL
CHEMBL46618
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY
NCI_THESAURUS
C90704
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY
WIKIPEDIA
OTAMIXABAN
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY
DRUG BANK
DB06635
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY
SMS_ID
300000034257
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY
INN
8096
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY
CAS
193153-04-7
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY
MESH
C435830
Created by admin on Mon Mar 31 18:21:07 GMT 2025 , Edited by admin on Mon Mar 31 18:21:07 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY