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Details

Stereochemistry RACEMIC
Molecular Formula C19H40N2O2
Molecular Weight 328.5331
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DAPABUTAN

SMILES

CCCCCCCCCCCCNCCCNC(C)CC(O)=O

InChI

InChIKey=KRGUCURBMCFAOW-UHFFFAOYSA-N
InChI=1S/C19H40N2O2/c1-3-4-5-6-7-8-9-10-11-12-14-20-15-13-16-21-18(2)17-19(22)23/h18,20-21H,3-17H2,1-2H3,(H,22,23)

HIDE SMILES / InChI

Molecular Formula C19H40N2O2
Molecular Weight 328.5331
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Dapabutan an antiseptic bacteriostatic drug, active against Gram-positive bacteria. Dapabutan is a component of a local antiseptic drug Sterlane.

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:38:18 GMT 2023
Edited
by admin
on Fri Dec 15 16:38:18 GMT 2023
Record UNII
1R0Y7O07NF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DAPABUTAN
INN  
INN  
Official Name English
Dapabutan [WHO-DD]
Common Name English
dapabutan [INN]
Common Name English
(±)-3-((3-(DODECYLAMINO)PROPYL)AMINO)BUTYRIC ACID
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C254
Created by admin on Fri Dec 15 16:38:18 GMT 2023 , Edited by admin on Fri Dec 15 16:38:18 GMT 2023
Code System Code Type Description
CAS
6582-31-6
Created by admin on Fri Dec 15 16:38:18 GMT 2023 , Edited by admin on Fri Dec 15 16:38:18 GMT 2023
PRIMARY
FDA UNII
1R0Y7O07NF
Created by admin on Fri Dec 15 16:38:18 GMT 2023 , Edited by admin on Fri Dec 15 16:38:18 GMT 2023
PRIMARY
EVMPD
SUB06905MIG
Created by admin on Fri Dec 15 16:38:18 GMT 2023 , Edited by admin on Fri Dec 15 16:38:18 GMT 2023
PRIMARY
PUBCHEM
65586
Created by admin on Fri Dec 15 16:38:18 GMT 2023 , Edited by admin on Fri Dec 15 16:38:18 GMT 2023
PRIMARY
ECHA (EC/EINECS)
229-510-3
Created by admin on Fri Dec 15 16:38:18 GMT 2023 , Edited by admin on Fri Dec 15 16:38:18 GMT 2023
PRIMARY
INN
7157
Created by admin on Fri Dec 15 16:38:18 GMT 2023 , Edited by admin on Fri Dec 15 16:38:18 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104206
Created by admin on Fri Dec 15 16:38:18 GMT 2023 , Edited by admin on Fri Dec 15 16:38:18 GMT 2023
PRIMARY
EPA CompTox
DTXSID20863912
Created by admin on Fri Dec 15 16:38:18 GMT 2023 , Edited by admin on Fri Dec 15 16:38:18 GMT 2023
PRIMARY
NCI_THESAURUS
C74153
Created by admin on Fri Dec 15 16:38:18 GMT 2023 , Edited by admin on Fri Dec 15 16:38:18 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY