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Details

Stereochemistry RACEMIC
Molecular Formula C16H35NO.C3H6O3
Molecular Weight 347.5331
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MYRALACT

SMILES

CC(O)C(O)=O.CCCCCCCCCCCCCCNCCO

InChI

InChIKey=HLFJBIVEMZFFOG-UHFFFAOYSA-N
InChI=1S/C16H35NO.C3H6O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17-15-16-18;1-2(4)3(5)6/h17-18H,2-16H2,1H3;2,4H,1H3,(H,5,6)

HIDE SMILES / InChI

Molecular Formula C16H35NO
Molecular Weight 257.4552
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C3H6O3
Molecular Weight 90.0779
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Myralact is an antiseptic included in multi-ingredient preparations, e.g. vaginal tablets Ginetris, intended for the topical treatment of vaginal infections.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Ginetris

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Trichomonal vaginitis treated with one dose of metronidazole.
1971 Dec

Sample Use Guides

re-treated with a course of Ginetris vaginal tablets (chloramphenicol 250 mg.; myralact 10 mg.; cloponone 2.5 mg.); one tablet was inserted twice daily for 5 days and this was followed by a single dose of 2 g. metronidazole.
Route of Administration: Vaginal
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:48:56 UTC 2023
Edited
by admin
on Fri Dec 15 18:48:56 UTC 2023
Record UNII
8V316C2371
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MYRALACT
INN   MART.   WHO-DD  
INN  
Official Name English
2-(TETRADECYLAMINO)ETHANOL LACTATE
Systematic Name English
Myralact [WHO-DD]
Common Name English
myralact [INN]
Common Name English
MYRALACT [MART.]
Common Name English
Code System Code Type Description
INN
1767
Created by admin on Fri Dec 15 18:48:57 UTC 2023 , Edited by admin on Fri Dec 15 18:48:57 UTC 2023
PRIMARY
ECHA (EC/EINECS)
239-552-4
Created by admin on Fri Dec 15 18:48:57 UTC 2023 , Edited by admin on Fri Dec 15 18:48:57 UTC 2023
PRIMARY
ChEMBL
CHEMBL395447
Created by admin on Fri Dec 15 18:48:57 UTC 2023 , Edited by admin on Fri Dec 15 18:48:57 UTC 2023
PRIMARY
CAS
15518-87-3
Created by admin on Fri Dec 15 18:48:57 UTC 2023 , Edited by admin on Fri Dec 15 18:48:57 UTC 2023
PRIMARY
PUBCHEM
71873
Created by admin on Fri Dec 15 18:48:57 UTC 2023 , Edited by admin on Fri Dec 15 18:48:57 UTC 2023
PRIMARY
NCI_THESAURUS
C175152
Created by admin on Fri Dec 15 18:48:57 UTC 2023 , Edited by admin on Fri Dec 15 18:48:57 UTC 2023
PRIMARY
SMS_ID
100000084423
Created by admin on Fri Dec 15 18:48:57 UTC 2023 , Edited by admin on Fri Dec 15 18:48:57 UTC 2023
PRIMARY
EPA CompTox
DTXSID8046400
Created by admin on Fri Dec 15 18:48:57 UTC 2023 , Edited by admin on Fri Dec 15 18:48:57 UTC 2023
PRIMARY
EVMPD
SUB09100MIG
Created by admin on Fri Dec 15 18:48:57 UTC 2023 , Edited by admin on Fri Dec 15 18:48:57 UTC 2023
PRIMARY
FDA UNII
8V316C2371
Created by admin on Fri Dec 15 18:48:57 UTC 2023 , Edited by admin on Fri Dec 15 18:48:57 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE