Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C25H32O4 |
Molecular Weight | 396.5192 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 2 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@]12C[C@@H](O)[C@H](\C=C\[C@@H](O)C3CCCCC3)[C@@]1([H])C\C(C2)=C\C4=CC(=CC=C4)C(O)=O
InChI
InChIKey=OINUMRGCICIETD-CGKNXJIZSA-N
InChI=1S/C25H32O4/c26-23(18-6-2-1-3-7-18)10-9-21-22-14-17(13-20(22)15-24(21)27)11-16-5-4-8-19(12-16)25(28)29/h4-5,8-12,18,20-24,26-27H,1-3,6-7,13-15H2,(H,28,29)/b10-9+,17-11+/t20-,21+,22-,23+,24+/m0/s1
Molecular Formula | C25H32O4 |
Molecular Weight | 396.5192 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 2 |
Optical Activity | UNSPECIFIED |
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/1632291
The antithrombotic efficacy of naxaprostene has been tested in rabbits with copper coil-induced carotid artery thrombosis. With oral pretreatment, 10 mg/kg naxaprostene prevented thrombotic arterial occlusion; with intraduodenal pretreatment the efficacy of naxaprostene was enhanced and 1 mg/kg was sufficient to exert an antithrombotic effect.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3096342
ADP-induced aggregation is inhibited 25% by 50 nmol/l CG 4305 (naxaprostene).
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:08:45 GMT 2023
by
admin
on
Fri Dec 15 16:08:45 GMT 2023
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Record UNII |
6QS1XD4508
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Record Status |
Validated (UNII)
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Record Version |
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-
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NCI_THESAURUS |
C78568
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6QS1XD4508
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SUB09172MIG
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100000080344
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C87383
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6446653
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DTXSID301024705
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CHEMBL2105172
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87269-59-8
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6189
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C050548
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Related Record | Type | Details | ||
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