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Details

Stereochemistry ACHIRAL
Molecular Formula 2C11H19O2.Ca
Molecular Weight 406.6136
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CALCIUM UNDECYLENATE

SMILES

C=CCCCCCCCCC(=O)[O-].C=CCCCCCCCCC(=O)[O-].[Ca+2]

InChI

InChIKey=CLOKKBBIKHZGNX-UHFFFAOYSA-L
InChI=1S/2C11H20O2.Ca/c2*1-2-3-4-5-6-7-8-9-10-11(12)13;/h2*2H,1,3-10H2,(H,12,13);/q;;+2/p-2

HIDE SMILES / InChI
Calcium Undecylenate is the calcium salt of undecylenic acid, an 11 carbon mono-unsaturated fatty acid with broad-spectrum antifungal activity. Undecylenic acid inhibits the morphogenesis of Candida albicans to its invasive fungal form and inhibits the conversion of unicellular yeast to their hyphal form.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
The antimicrobial activities of undecylenic acid and its calcium salt are from 5 to 30 /mkg per ml at pH 6.0 for all dermatophytes studied. The effect of pH on the rate of growth was determined by measurement of colony diameters of Trichophyton mentagrophytes grown on the surface of glucose-tryptose agar plates Ten plates were inoculated for each pH, incubated at 25 C, and read after 10 days.
Name Type Language
CALCIUM UNDECYLENATE
INCI   USAN   USP  
INCI   USAN  
Official Name English
CALCIUM UNDECENOATE
MART.   WHO-DD  
Systematic Name English
UNDECYLENATE CALCIUM
VANDF  
Common Name English
CALCIUM UNDECENOATE [MART.]
Common Name English
CRUEX
Brand Name English
UNDECYLENATE CALCIUM [VANDF]
Common Name English
CALCIUM UNDECYLENATE [INCI]
Common Name English
CALCIUM UNDECYLENATE [USAN]
Common Name English
CALCIUM UNDECENOATE [WHO-DD]
Common Name English
CALCIUM UNDECYLENATE [USP MONOGRAPH]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C514
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
CFR 21 CFR 333.210
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
Code System Code Type Description
DRUG BANK
DB15678
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
PRIMARY
CAS
1322-14-1
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
PRIMARY
PUBCHEM
14865
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
PRIMARY
EPA CompTox
1322-14-1
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
PRIMARY
ECHA (EC/EINECS)
215-331-8
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
PRIMARY
NCI_THESAURUS
C75199
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
PRIMARY
FDA UNII
77YW1RTU8V
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
PRIMARY
ChEMBL
CHEMBL2104130
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
PRIMARY
EVMPD
SUB47776
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
PRIMARY
RXCUI
89746
Created by admin on Fri Jun 25 20:52:58 UTC 2021 , Edited by admin on Fri Jun 25 20:52:58 UTC 2021
PRIMARY RxNorm