Details
Stereochemistry | ACHIRAL |
Molecular Formula | C30H38N4.2C2H4O2 |
Molecular Weight | 574.7534 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(O)=O.CC(O)=O.CC1=CC(NCCCCCCCCCCNC2=CC(C)=NC3=C2C=CC=C3)=C4C=CC=CC4=N1
InChI
InChIKey=KJLDLEIBEQIBFL-UHFFFAOYSA-N
InChI=1S/C30H38N4.2C2H4O2/c1-23-21-29(25-15-9-11-17-27(25)33-23)31-19-13-7-5-3-4-6-8-14-20-32-30-22-24(2)34-28-18-12-10-16-26(28)30;2*1-2(3)4/h9-12,15-18,21-22H,3-8,13-14,19-20H2,1-2H3,(H,31,33)(H,32,34);2*1H3,(H,3,4)
Molecular Formula | C2H4O2 |
Molecular Weight | 60.052 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C30H38N4 |
Molecular Weight | 454.6495 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Quindecamine (also known as UCL-1407) is quinaldine derivative with antibiotic and fungicidal activity. Treatment of rats and mice with Quindecamine (250 mg/kg/ day) each day for 4 weeks followed by 500 mg/kg/day for 2 more weeks reduced spontaneous motility and body weight but produced no pathological abnormalities of the various organs studied. In vitro, the drug showed very good activity against Staphylococcus aureus, Streptococcus hemolyticus, Candida albicans, Trichophyton mentagrophytes, and T. vaginalis. The drug had very good activity in 180 human subjects with various bacterial and mycotic diseases of the skin and mucosa when applied as a 1% salve.
Originator
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:28:32 GMT 2023
by
admin
on
Fri Dec 15 16:28:32 GMT 2023
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Record UNII |
J3Y36BPX1R
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Record Status |
Validated (UNII)
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Record Version |
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-
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64739
Created by
admin on Fri Dec 15 16:28:32 GMT 2023 , Edited by admin on Fri Dec 15 16:28:32 GMT 2023
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19146-62-4
Created by
admin on Fri Dec 15 16:28:32 GMT 2023 , Edited by admin on Fri Dec 15 16:28:32 GMT 2023
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DTXSID80940778
Created by
admin on Fri Dec 15 16:28:32 GMT 2023 , Edited by admin on Fri Dec 15 16:28:32 GMT 2023
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J3Y36BPX1R
Created by
admin on Fri Dec 15 16:28:32 GMT 2023 , Edited by admin on Fri Dec 15 16:28:32 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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SOLVATE->ANHYDROUS |
Related Record | Type | Details | ||
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ACTIVE MOIETY |