U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
In vitro anti-HIV-1 activity of sn-2-substituted 1-O-octadecyl-sn-glycero-3-phosphonoformate analogues and synergy with zidovudine.
2000 May
Chemical constituents of Pseudopterogorgia species of the Indian ocean.
2001
[Isolation and identification of chemical constituents from Acropora pulchra].
2001 Sep
A new sphingolipid from the gorgonian Junceella juncea of the Indian Ocean.
2004 Dec
The Kemp elimination in membrane mimetic reaction media. Probing catalytic properties of cationic vesicles formed from a double-tailed amphiphile and linear long-tailed alcohols or alkyl pyranosides.
2004 Jun 21
Novel mutual pro-drugs of 2',3'-dideoxyinosine with 3-octadecyloxy-propane-1,2-diol by straightforward enzymatic regioselective synthesis in acetone.
2005 Jan
Two new glycosides from the soft coral Sinularia firma.
2006 Dec
[Chemical constituents from the south China sea gorgonian coral Subergorgia reticulata].
2006 Jun
[Clinical experiment of cytokines induced killer cells for treatment of benzene poisoning].
2007 Sep
Antileukemic effects of Didemnum psammatodes (Tunicata: Ascidiacea) constituents.
2008 Nov
[Chemical constituents of a new species of Spongia sponge].
2010 Apr
A Pex7 hypomorphic mouse model for plasmalogen deficiency affecting the lens and skeleton.
2010 Apr
In vitro study of the effect of diesterified alkoxyglycerols with conjugated linoleic acid on adipocyte inflammatory mediators.
2010 Apr 6
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 Fri Dec 15 17:12:17 GMT 2023
Edited
by admin
on Fri Dec 15 17:12:17 GMT 2023
Record UNII
39YR661C4U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BATILOL
INN   WHO-DD  
INN  
Official Name English
BATYL ALCOHOL [MI]
Common Name English
Batilol [WHO-DD]
Common Name English
batilol [INN]
Common Name English
NSC-284200
Code English
BATYL ALCOHOL
INCI   MI  
INCI  
Official Name English
(±)-3-(OCTADECYLOXY)-1,2-PROPANEDIOL
Systematic Name English
BATYL ALCOHOL [INCI]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID0047799
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
ChEMBL
CHEMBL1482516
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
FDA UNII
39YR661C4U
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
INN
1454
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
MESH
C033433
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
RXCUI
1306190
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY RxNorm
SMS_ID
100000081314
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-874-7
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
CHEBI
74001
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
DAILYMED
39YR661C4U
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
PUBCHEM
3681
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
NCI_THESAURUS
C166663
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
CAS
544-62-7
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
CHEBI
34117
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
NSC
284200
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
EVMPD
SUB06111MIG
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY
MERCK INDEX
m2279
Created by admin on Fri Dec 15 17:12:18 GMT 2023 , Edited by admin on Fri Dec 15 17:12:18 GMT 2023
PRIMARY Merck Index
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY