Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C30H38N4.2C2H4O2.2H2O |
| Molecular Weight | 610.784 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.O.CC(O)=O.CC(O)=O.CC1=CC(NCCCCCCCCCCNC2=C3C=CC=CC3=NC(C)=C2)=C4C=CC=CC4=N1
InChI
InChIKey=XHJVGKULSGWYHF-UHFFFAOYSA-N
InChI=1S/C30H38N4.2C2H4O2.2H2O/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);2*1H2
| Molecular Formula | H2O |
| Molecular Weight | 18.0153 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| 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
Mon Mar 31 17:49:04 GMT 2025
by
admin
on
Mon Mar 31 17:49:04 GMT 2025
|
| Record UNII |
5JH93XA08W
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Code | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C258
Created by
admin on Mon Mar 31 17:49:04 GMT 2025 , Edited by admin on Mon Mar 31 17:49:04 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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CHEMBL125375
Created by
admin on Mon Mar 31 17:49:04 GMT 2025 , Edited by admin on Mon Mar 31 17:49:04 GMT 2025
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PRIMARY | |||
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20055313
Created by
admin on Mon Mar 31 17:49:04 GMT 2025 , Edited by admin on Mon Mar 31 17:49:04 GMT 2025
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PRIMARY | |||
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300000055043
Created by
admin on Mon Mar 31 17:49:04 GMT 2025 , Edited by admin on Mon Mar 31 17:49:04 GMT 2025
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PRIMARY | |||
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C152119
Created by
admin on Mon Mar 31 17:49:04 GMT 2025 , Edited by admin on Mon Mar 31 17:49:04 GMT 2025
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PRIMARY | |||
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5714-05-6
Created by
admin on Mon Mar 31 17:49:04 GMT 2025 , Edited by admin on Mon Mar 31 17:49:04 GMT 2025
|
PRIMARY | |||
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5JH93XA08W
Created by
admin on Mon Mar 31 17:49:04 GMT 2025 , Edited by admin on Mon Mar 31 17:49:04 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ANHYDROUS->SOLVATE | |||
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|
PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |