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Details

Stereochemistry RACEMIC
Molecular Formula C21H44O3
Molecular Weight 344.5723
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BATILOL

SMILES

CCCCCCCCCCCCCCCCCCOCC(O)CO

InChI

InChIKey=OGBUMNBNEWYMNJ-UHFFFAOYSA-N
InChI=1S/C21H44O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-24-20-21(23)19-22/h21-23H,2-20H2,1H3

HIDE SMILES / InChI

Molecular Formula C21H44O3
Molecular Weight 344.5723
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: description was created based on several sources, including: http://lekarstwo.ru/en/preparati/batilolum.html http://en.medico-online.com/ovr7_batilol.html

The drug stimulates erythrocytes and leucopoiesis. Applied for the prevention of radiation sickness with X-ray and radiotherapy. For a better intake to take batilol together with a small amount of vegetable oil or butter. Side-effects are neuralgia and allergic reactions.

Originator

Sources: DOI: 10.1039/JR9340001232

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
Batilol

Approved Use

Prevention and treatment of radiation sickness

Launch Date

1970
Curative
Batilol

Approved Use

Curative effect of the drug is also observed in cases of poisoning by benzene.

Launch Date

1970
PubMed

PubMed

TitleDatePubMed
[Chemical constituents from the south China sea gorgonian coral Subergorgia reticulata].
2006 Jun
[Chemical constituents of a new species of Spongia sponge].
2010 Apr
An update on the therapeutic role of alkylglycerols.
2010 Aug 5
Multiple beneficial health effects of natural alkylglycerols from shark liver oil.
2010 Jul 19
[Study on the chemical constituents of Antipathes dichotoma].
2010 Sep
Patents

Patents

Sample Use Guides

0.02 g 2 times a day for prevention and 3 to 4 times a day in the treatment of radiation sickness
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:41:55 GMT 2025
Edited
by admin
on Mon Mar 31 18:41:55 GMT 2025
Record UNII
39YR661C4U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BATILOL
INN   WHO-DD  
INN  
Official Name English
BATYL ALCOHOL
INCI   MI  
INCI  
Preferred Name English
BATYL ALCOHOL [MI]
Common Name English
Batilol [WHO-DD]
Common Name English
batilol [INN]
Common Name English
NSC-284200
Code English
(±)-3-(OCTADECYLOXY)-1,2-PROPANEDIOL
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID0047799
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
ChEMBL
CHEMBL1482516
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
FDA UNII
39YR661C4U
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
INN
1454
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
MESH
C033433
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
RXCUI
1306190
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY RxNorm
SMS_ID
100000081314
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-874-7
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
CHEBI
74001
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
DAILYMED
39YR661C4U
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
PUBCHEM
3681
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
NCI_THESAURUS
C166663
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
CAS
544-62-7
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
CHEBI
34117
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
NSC
284200
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
EVMPD
SUB06111MIG
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY
MERCK INDEX
m2279
Created by admin on Mon Mar 31 18:41:55 GMT 2025 , Edited by admin on Mon Mar 31 18:41:55 GMT 2025
PRIMARY Merck Index
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY