Details
Stereochemistry | RACEMIC |
Molecular Formula | C16H12F5N3O2S |
Molecular Weight | 405.342 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NS(=O)(=O)C1=CC=C(C=C1)N2N=C(CC2C3=CC=C(F)C=C3F)C(F)(F)F
InChI
InChIKey=ZZMJXWXXMAAPLI-UHFFFAOYSA-N
InChI=1S/C16H12F5N3O2S/c17-9-1-6-12(13(18)7-9)14-8-15(16(19,20)21)23-24(14)10-2-4-11(5-3-10)27(22,25)26/h1-7,14H,8H2,(H2,22,25,26)
Approval Year
PubMed
Title | Date | PubMed |
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Development and validation of two chromatographic methods for the quantification of E-6087 and one of its metabolites, E-6132, in rat plasma. | 2001 Mar |
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Pharmacokinetics of E-6087, a new anti-inflammatory agent, in rats and dogs. | 2001 Sep |
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Enantioseparation of novel COX-2 anti-inflammatory drugs by capillary electrophoresis using single and dual cyclodextrin systems. | 2002 Jun |
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Determination of enantiomeric purity of a novel COX-2 anti-inflammatory drug by capillary electrophoresis using single and dual cyclodextrin systems. | 2003 May |
Patents
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9953093
Created by
admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023
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VM9PYQ1MQG
Created by
admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023
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300000023685
Created by
admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023
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C174926
Created by
admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023
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11305
Created by
admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023
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251442-94-1
Created by
admin on Sat Dec 16 16:30:43 GMT 2023 , Edited by admin on Sat Dec 16 16:30:43 GMT 2023
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PRIMARY |
ACTIVE MOIETY