Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C21H29N5O6 |
Molecular Weight | 447.4849 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCOC(=O)N[C@@H](CNC(=O)C[C@H]1CC(=NO1)C2=CC=C(C=C2)C(N)=N)C(=O)OC
InChI
InChIKey=IRAXRQFCCSHQDX-WBVHZDCISA-N
InChI=1S/C21H29N5O6/c1-3-4-9-31-21(29)25-17(20(28)30-2)12-24-18(27)11-15-10-16(26-32-15)13-5-7-14(8-6-13)19(22)23/h5-8,15,17H,3-4,9-12H2,1-2H3,(H3,22,23)(H,24,27)(H,25,29)/t15-,17+/m1/s1
Roxifiban (also known as DMP754), a potent antiplatelet agent in inhibiting platelet aggregation, and has a high specificity and affinity for human platelet glycoprotein IIb/IIIa complex (GPIIb/IIIa) receptors. Roxifiban participated in clinical trials phase III for the treatment of peripheral arterial disorders. This drug was also well tolerated in patients with chronic stable angina pectoris and was studied in the treatment of heparin-induced thrombocytopenia, and thrombosis. However, the development of this drug appears to have been discontinued.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Oral antiplatelet efficacy of the platelet GPIIb/IIIa antagonist, DMP754 in non-human primates. | 1998 Mar 1 |
|
Comparative efficacy between the glycoprotein IIb/IIIa antagonists roxifiban and orbofiban in inhibiting platelet responses in flow models of thrombosis. | 2002 Apr |
|
The use of roxifiban (DMP754), a novel oral platelet glycoprotein IIb/IIIa receptor inhibitor, in patients with stable coronary artery disease. | 2003 |
|
[Long-lasting thrombocytopenia induced by glycoprotein IIb/IIIa inhibitor]. | 2017 Nov |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/14727937
Ninety-eight patients were randomized to receive either a placebo or 1 of 8 oral dosages of roxifiban. Twenty-two patients were enrolled in multiple-dose regimens, bringing the total study population to 120. The oral dosages were 0.25, 0.5, 0.75, 1, 1.25, 1.5, 2, or 2.5 mg/day for up to 30 days.
Route of Administration:
Oral
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C1327
Created by
admin on Fri Dec 15 18:36:48 GMT 2023 , Edited by admin on Fri Dec 15 18:36:48 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
Q476FMZ72G
Created by
admin on Fri Dec 15 18:36:48 GMT 2023 , Edited by admin on Fri Dec 15 18:36:48 GMT 2023
|
PRIMARY | |||
|
170902-47-3
Created by
admin on Fri Dec 15 18:36:48 GMT 2023 , Edited by admin on Fri Dec 15 18:36:48 GMT 2023
|
PRIMARY | |||
|
177230
Created by
admin on Fri Dec 15 18:36:48 GMT 2023 , Edited by admin on Fri Dec 15 18:36:48 GMT 2023
|
PRIMARY | |||
|
7619
Created by
admin on Fri Dec 15 18:36:48 GMT 2023 , Edited by admin on Fri Dec 15 18:36:48 GMT 2023
|
PRIMARY | |||
|
100000084386
Created by
admin on Fri Dec 15 18:36:48 GMT 2023 , Edited by admin on Fri Dec 15 18:36:48 GMT 2023
|
PRIMARY | |||
|
C152267
Created by
admin on Fri Dec 15 18:36:48 GMT 2023 , Edited by admin on Fri Dec 15 18:36:48 GMT 2023
|
PRIMARY | |||
|
CHEMBL18301
Created by
admin on Fri Dec 15 18:36:48 GMT 2023 , Edited by admin on Fri Dec 15 18:36:48 GMT 2023
|
PRIMARY | |||
|
DTXSID70168969
Created by
admin on Fri Dec 15 18:36:48 GMT 2023 , Edited by admin on Fri Dec 15 18:36:48 GMT 2023
|
PRIMARY | |||
|
C118235
Created by
admin on Fri Dec 15 18:36:48 GMT 2023 , Edited by admin on Fri Dec 15 18:36:48 GMT 2023
|
PRIMARY | |||
|
SUB10398MIG
Created by
admin on Fri Dec 15 18:36:48 GMT 2023 , Edited by admin on Fri Dec 15 18:36:48 GMT 2023
|
PRIMARY |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)
SUBSTANCE RECORD