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Details

Stereochemistry ACHIRAL
Molecular Formula C13H19NO2
Molecular Weight 221.2955
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EXALAMIDE

SMILES

CCCCCCOC1=CC=CC=C1C(N)=O

InChI

InChIKey=CKSJXOVLXUMMFF-UHFFFAOYSA-N
InChI=1S/C13H19NO2/c1-2-3-4-7-10-16-12-9-6-5-8-11(12)13(14)15/h5-6,8-9H,2-4,7,10H2,1H3,(H2,14,15)

HIDE SMILES / InChI

Molecular Formula C13H19NO2
Molecular Weight 221.2955
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Exalamide is an antifungal agent developed in Japan.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Comparison of the in vitro antifungal activities of clotrimazole, miconazole, econazole and exalamide against clinical isolates of dermatophytes.
1984 Jun

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:20:11 GMT 2023
Edited
by admin
on Fri Dec 15 16:20:11 GMT 2023
Record UNII
7JEC65JCG2
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EXALAMIDE
INN   JAN   MI   WHO-DD  
INN  
Official Name English
EXALAMIDE [JAN]
Common Name English
NSC-758449
Code English
Exalamide [WHO-DD]
Common Name English
EXALAMIDE [MI]
Common Name English
exalamide [INN]
Common Name English
O-(HEXYLOXY)BENZAMIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C514
Created by admin on Fri Dec 15 16:20:12 GMT 2023 , Edited by admin on Fri Dec 15 16:20:12 GMT 2023
Code System Code Type Description
DRUG CENTRAL
1119
Created by admin on Fri Dec 15 16:20:11 GMT 2023 , Edited by admin on Fri Dec 15 16:20:11 GMT 2023
PRIMARY
CAS
53370-90-4
Created by admin on Fri Dec 15 16:20:11 GMT 2023 , Edited by admin on Fri Dec 15 16:20:11 GMT 2023
PRIMARY
INN
4257
Created by admin on Fri Dec 15 16:20:12 GMT 2023 , Edited by admin on Fri Dec 15 16:20:12 GMT 2023
PRIMARY
FDA UNII
7JEC65JCG2
Created by admin on Fri Dec 15 16:20:12 GMT 2023 , Edited by admin on Fri Dec 15 16:20:12 GMT 2023
PRIMARY
NCI_THESAURUS
C65607
Created by admin on Fri Dec 15 16:20:12 GMT 2023 , Edited by admin on Fri Dec 15 16:20:12 GMT 2023
PRIMARY
NSC
758449
Created by admin on Fri Dec 15 16:20:12 GMT 2023 , Edited by admin on Fri Dec 15 16:20:12 GMT 2023
PRIMARY
MESH
C010979
Created by admin on Fri Dec 15 16:20:12 GMT 2023 , Edited by admin on Fri Dec 15 16:20:12 GMT 2023
PRIMARY
SMS_ID
100000082341
Created by admin on Fri Dec 15 16:20:12 GMT 2023 , Edited by admin on Fri Dec 15 16:20:12 GMT 2023
PRIMARY
ChEMBL
CHEMBL1405973
Created by admin on Fri Dec 15 16:20:11 GMT 2023 , Edited by admin on Fri Dec 15 16:20:11 GMT 2023
PRIMARY
PUBCHEM
3316
Created by admin on Fri Dec 15 16:20:12 GMT 2023 , Edited by admin on Fri Dec 15 16:20:12 GMT 2023
PRIMARY
ECHA (EC/EINECS)
258-504-3
Created by admin on Fri Dec 15 16:20:11 GMT 2023 , Edited by admin on Fri Dec 15 16:20:11 GMT 2023
PRIMARY
CHEBI
31585
Created by admin on Fri Dec 15 16:20:11 GMT 2023 , Edited by admin on Fri Dec 15 16:20:11 GMT 2023
PRIMARY
MERCK INDEX
m1147
Created by admin on Fri Dec 15 16:20:12 GMT 2023 , Edited by admin on Fri Dec 15 16:20:12 GMT 2023
PRIMARY Merck Index
EVMPD
SUB07354MIG
Created by admin on Fri Dec 15 16:20:11 GMT 2023 , Edited by admin on Fri Dec 15 16:20:11 GMT 2023
PRIMARY
EPA CompTox
DTXSID9045899
Created by admin on Fri Dec 15 16:20:11 GMT 2023 , Edited by admin on Fri Dec 15 16:20:11 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY