Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C22H23N5O5 |
| Molecular Weight | 437.4485 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@]1(NC(=O)N(CC(=O)N[C@@H](CC(O)=O)C2=CC=CC=C2)C1=O)C3=CC=C(C=C3)C(N)=N
InChI
InChIKey=BQTUWUXJPAYSPB-AOMKIAJQSA-N
InChI=1S/C22H23N5O5/c1-22(15-9-7-14(8-10-15)19(23)24)20(31)27(21(32)26-22)12-17(28)25-16(11-18(29)30)13-5-3-2-4-6-13/h2-10,16H,11-12H2,1H3,(H3,23,24)(H,25,28)(H,26,32)(H,29,30)/t16-,22-/m0/s1
| Molecular Formula | C22H23N5O5 |
| Molecular Weight | 437.4485 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Carafiban is orally active heterocyclic peptide mimetics fibrinogen IIb/IIIa receptor antagonist with antithrombotic activity. Carafiban is a prodrug, that underwent metabolic transformation to active metabolite des-ethyl- Carafiban, that inhibited dose-dependently and reversibly human platelet aggregation. In conscious dogs, Carafiban showed a high plasma availability of the active moiety of 42±8% and a plasma half-life of 9.9 h after oral administration as measured by bioassay. Carafiban may potentially be used for chronic treatment and prophylaxis of thrombotic diseases in humans.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 17:22:19 GMT 2025
by
admin
on
Wed Apr 02 17:22:19 GMT 2025
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| Record UNII |
Q9GG3H64D2
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| Record Status |
Validated (UNII)
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| Record Version |
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Systematic Name | English |
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9912737
Created by
admin on Wed Apr 02 17:22:19 GMT 2025 , Edited by admin on Wed Apr 02 17:22:19 GMT 2025
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170565-45-4
Created by
admin on Wed Apr 02 17:22:19 GMT 2025 , Edited by admin on Wed Apr 02 17:22:19 GMT 2025
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Q9GG3H64D2
Created by
admin on Wed Apr 02 17:22:19 GMT 2025 , Edited by admin on Wed Apr 02 17:22:19 GMT 2025
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PRIMARY |
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TARGET -> INHIBITOR |
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PRODRUG -> METABOLITE ACTIVE |
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ACTIVE MOIETY |
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