Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C24H27N5O5 |
Molecular Weight | 465.5017 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)C[C@H](NC(=O)CN1C(=O)N[C@](C)(C1=O)C2=CC=C(C=C2)C(N)=N)C3=CC=CC=C3
InChI
InChIKey=SSGOEPXWNBXKPQ-UUOWRZLLSA-N
InChI=1S/C24H27N5O5/c1-3-34-20(31)13-18(15-7-5-4-6-8-15)27-19(30)14-29-22(32)24(2,28-23(29)33)17-11-9-16(10-12-17)21(25)26/h4-12,18H,3,13-14H2,1-2H3,(H3,25,26)(H,27,30)(H,28,33)/t18-,24-/m0/s1
Molecular Formula | C24H27N5O5 |
Molecular Weight | 465.5017 |
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
Sat Dec 16 17:07:04 GMT 2023
by
admin
on
Sat Dec 16 17:07:04 GMT 2023
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Record UNII |
39IWK4M2UW
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Record Status |
Validated (UNII)
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Record Version |
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-
Download
Name | Type | Language | ||
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Official Name | English | ||
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Common Name | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29750
Created by
admin on Sat Dec 16 17:07:04 GMT 2023 , Edited by admin on Sat Dec 16 17:07:04 GMT 2023
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Code System | Code | Type | Description | ||
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SUB06084MIG
Created by
admin on Sat Dec 16 17:07:04 GMT 2023 , Edited by admin on Sat Dec 16 17:07:04 GMT 2023
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177563-40-5
Created by
admin on Sat Dec 16 17:07:04 GMT 2023 , Edited by admin on Sat Dec 16 17:07:04 GMT 2023
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193944
Created by
admin on Sat Dec 16 17:07:04 GMT 2023 , Edited by admin on Sat Dec 16 17:07:04 GMT 2023
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CHEMBL17313
Created by
admin on Sat Dec 16 17:07:04 GMT 2023 , Edited by admin on Sat Dec 16 17:07:04 GMT 2023
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C76113
Created by
admin on Sat Dec 16 17:07:04 GMT 2023 , Edited by admin on Sat Dec 16 17:07:04 GMT 2023
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PRIMARY | |||
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100000081607
Created by
admin on Sat Dec 16 17:07:04 GMT 2023 , Edited by admin on Sat Dec 16 17:07:04 GMT 2023
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7665
Created by
admin on Sat Dec 16 17:07:04 GMT 2023 , Edited by admin on Sat Dec 16 17:07:04 GMT 2023
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PRIMARY | |||
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39IWK4M2UW
Created by
admin on Sat Dec 16 17:07:04 GMT 2023 , Edited by admin on Sat Dec 16 17:07:04 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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METABOLITE ACTIVE -> PRODRUG |
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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