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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
Structure of QUINDECAMINE ACETATE

SMILES

O.O.CC(O)=O.CC(O)=O.CC1=CC(NCCCCCCCCCCNC2=CC(C)=NC3=C2C=CC=C3)=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

HIDE SMILES / InChI
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

Sources: JP40028465

Approval Year

PubMed

PubMed

TitleDatePubMed
Compounds that block both intermediate-conductance (IK(Ca)) and small-conductance (SK(Ca)) calcium-activated potassium channels.
2000 Apr
Patents

Patents

Name Type Language
QUINDECAMINE ACETATE
USAN  
USAN  
Official Name English
1,10-DECANEDIAMINE, N,N'-BIS(2-METHYL-4-QUINOLINYL)-, DIACETATE DIHYDRATE
Systematic Name English
4,4'-(DECAMETHYLENEDIIMINO)DIQUINALDINE DIACETATE DIHYDRATE
Systematic Name English
RMI 8090DJ
Code English
RMI-8090DJ
Code English
QUINDECAMINE ACETATE [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C258
Created by admin on Fri Dec 15 15:10:37 GMT 2023 , Edited by admin on Fri Dec 15 15:10:37 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL125375
Created by admin on Fri Dec 15 15:10:37 GMT 2023 , Edited by admin on Fri Dec 15 15:10:37 GMT 2023
PRIMARY
PUBCHEM
20055313
Created by admin on Fri Dec 15 15:10:37 GMT 2023 , Edited by admin on Fri Dec 15 15:10:37 GMT 2023
PRIMARY
NCI_THESAURUS
C152119
Created by admin on Fri Dec 15 15:10:37 GMT 2023 , Edited by admin on Fri Dec 15 15:10:37 GMT 2023
PRIMARY
CAS
5714-05-6
Created by admin on Fri Dec 15 15:10:37 GMT 2023 , Edited by admin on Fri Dec 15 15:10:37 GMT 2023
PRIMARY
FDA UNII
5JH93XA08W
Created by admin on Fri Dec 15 15:10:37 GMT 2023 , Edited by admin on Fri Dec 15 15:10:37 GMT 2023
PRIMARY