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
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
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 |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/17139573Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/17979700
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17139573
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.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL244 Sources: https://www.ncbi.nlm.nih.gov/pubmed/17979700 |
0.5 nM [Ki] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
252 ng/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17178269 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17178269 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17178269 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17178269 |
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
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
6476 ng × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17178269 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17178269 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17178269 |
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 EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17178269 |
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
Dose | Population | Adverse 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
AE | Significance | Dose | Population |
---|---|---|---|
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: |
Substance Class |
Chemical
Created
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Edited
Mon Mar 31 18:04:05 GMT 2025
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Record UNII |
WL9J31M2HI
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