Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C19H21N3O2S |
| Molecular Weight | 355.454 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C\C=C(/C1=CC=CC=C1)C2=CC3=C(C=C2)N=C(N)N3S(=O)(=O)C(C)C
InChI
InChIKey=BFPYUXIFGJJYHU-AYSLTRBKSA-N
InChI=1S/C19H21N3O2S/c1-4-16(14-8-6-5-7-9-14)15-10-11-17-18(12-15)22(19(20)21-17)25(23,24)13(2)3/h4-13H,1-3H3,(H2,20,21)/b16-4+
| Molecular Formula | C19H21N3O2S |
| Molecular Weight | 355.454 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Inhibition of the enteroviruses that cause acute hemorrhagic conjunctivitis (AHC) by benzimidazoles; enviroxime (LY 122772) and enviradone (LY 127123). | 1995-08 |
|
| Liquid chromatographic analysis of enviradene, a new antiviral agent, in plasma and its application in bioavailability studies in the dog. | 1985-08 |
|
| Prevention of death in mice infected with coxsackievirus A16 using guanidine HCl mixed with substituted benzimidazoles. | 1982-12 |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8540755
The 50% CPE inhibitory dose (ID50) for enviroxime and enviradene (LY 127123) against 11 EV70 and 15 CA24v isolates ranged from 0.01 to 0.3 microgram and 0.01-0.65 microgram/ml, respectively.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:17:48 GMT 2025
by
admin
on
Mon Mar 31 18:17:48 GMT 2025
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| Record UNII |
9Q79A81839
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| Record Status |
Validated (UNII)
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| Record Version |
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NCI_THESAURUS |
C281
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CHEMBL290507
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6435398
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DTXSID00230769
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T-109
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9Q79A81839
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C65514
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SUB06555MIG
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5340
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100000080261
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80883-55-2
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