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Details

Stereochemistry ABSOLUTE
Molecular Formula C25H26N4O4.ClH
Molecular Weight 482.959
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OTAMIXABAN HYDROCHLORIDE

SMILES

Cl.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=ROKCPUOLRIBSQQ-BYYQELCVSA-N
InChI=1S/C25H26N4O4.ClH/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);1H/t16-,22-;/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 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
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
Small molecule coagulation cascade inhibitors in the clinic.
2005
Pharmacokinetics of otamixaban, a direct factor Xa inhibitor, in healthy male subjects: pharmacokinetic model development for phase 2/3 simulation of exposure.
2006 Jan
[Factor Xa-inhibition in interventional cardiology].
2007 Dec
Gateways to clinical trials.
2007 Sep
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
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:38:48 GMT 2023
Edited
by admin
on Fri Dec 15 15:38:48 GMT 2023
Record UNII
WL9J31M2HI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OTAMIXABAN HYDROCHLORIDE
WHO-DD  
Common Name English
Otamixaban Hydrochloride [WHO-DD]
Common Name English
METHYL (2R,3R)-2-(3-AMIDINOBENZYL)-3-((4-(1-OXIDO-4-PYRIDINYL)BENZOYL)AMINO)BUTANOATE HYDROCHLORIDE
Systematic Name English
RPR-130673 HCL
Code English
Code System Code Type Description
PUBCHEM
50899073
Created by admin on Fri Dec 15 15:38:48 GMT 2023 , Edited by admin on Fri Dec 15 15:38:48 GMT 2023
PRIMARY
FDA UNII
WL9J31M2HI
Created by admin on Fri Dec 15 15:38:48 GMT 2023 , Edited by admin on Fri Dec 15 15:38:48 GMT 2023
PRIMARY
CAS
409081-12-5
Created by admin on Fri Dec 15 15:38:48 GMT 2023 , Edited by admin on Fri Dec 15 15:38:48 GMT 2023
PRIMARY
EPA CompTox
DTXSID00193901
Created by admin on Fri Dec 15 15:38:48 GMT 2023 , Edited by admin on Fri Dec 15 15:38:48 GMT 2023
PRIMARY
DRUG BANK
DBSALT002029
Created by admin on Fri Dec 15 15:38:48 GMT 2023 , Edited by admin on Fri Dec 15 15:38:48 GMT 2023
PRIMARY
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