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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
MOL RATIO 1 MOL RATIO (average)
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Description

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.

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency
0.5 nM [Ki]

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Cmax

ValueDoseCo-administeredAnalytePopulation
252 ng/mL
100 μg/kg/h 1 times / day other, intravenous
OTAMIXABAN plasma
Homo sapiens
458 ng/mL
125 μg/kg/h 1 times / day other, intravenous
OTAMIXABAN plasma
Homo sapiens
635 ng/mL
150 μg/kg/h 1 times / day other, intravenous
OTAMIXABAN plasma
Homo sapiens
85 ng/mL
50 μg/kg/h 1 times / day other, intravenous
OTAMIXABAN plasma
Homo sapiens

AUC

ValueDoseCo-administeredAnalytePopulation
6476 ng × h/mL
100 μg/kg/h 1 times / day other, intravenous
OTAMIXABAN plasma
Homo sapiens
12007 ng × h/mL
125 μg/kg/h 1 times / day other, intravenous
OTAMIXABAN plasma
Homo sapiens
15674 ng × h/mL
150 μg/kg/h 1 times / day other, intravenous
OTAMIXABAN plasma
Homo sapiens
2437 ng × h/mL
50 μg/kg/h 1 times / day other, intravenous
OTAMIXABAN plasma
Homo sapiens

Doses

AEs

PubMed

Sample Use Guides

In Vivo Use Guide
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
Record UNII
S173RED00L
Record Status Validated (UNII)
Record Version