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Details

Stereochemistry ACHIRAL
Molecular Formula C30H50
Molecular Weight 410.718
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 4
Charge 0

SHOW SMILES / InChI
Structure of SQUALENE

SMILES

CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C=C(/C)CC\C=C(/C)CCC=C(C)C

InChI

InChIKey=YYGNTYWPHWGJRM-AAJYLUCBSA-N
InChI=1S/C30H50/c1-25(2)15-11-19-29(7)23-13-21-27(5)17-9-10-18-28(6)22-14-24-30(8)20-12-16-26(3)4/h15-18,23-24H,9-14,19-22H2,1-8H3/b27-17+,28-18+,29-23+,30-24+

HIDE SMILES / InChI
Squalene is a naturally occurring polyprenyl compound primarily known for its key role as an intermediate in cholesterol synthesis. It received its name because of its occurrence in shark liver oil (Squalus spp.), which contains large quantities and is considered the richest source of squalene. However, it is widely distributed in nature, with reasonable amounts found in olive oil, palm oil, wheat-germ oil, amaranth oil, and rice bran oil. The primary therapeutic use of squalene currently is as an adjunctive therapy in a variety of cancers. Although epidemiological, experimental and animal evidence suggests anti-cancer properties, to date no human trials have been conducted to verify the role this nutrient might have in cancer therapy regimens.

Approval Year

Doses

Doses

DosePopulationAdverse events​
27 g 1 times / day multiple, oral
Highest studied dose
Dose: 27 g, 1 times / day
Route: oral
Route: multiple
Dose: 27 g, 1 times / day
Sources: Page: p.503
healthy, ADULT
n = 20
Health Status: healthy
Age Group: ADULT
Sex: F
Food Status: FED
Population Size: 20
Sources: Page: p.503
Other AEs: Loose stools...
Other AEs:
Loose stools (55%)
Sources: Page: p.503
AEs

AEs

AESignificanceDosePopulation
Loose stools 55%
27 g 1 times / day multiple, oral
Highest studied dose
Dose: 27 g, 1 times / day
Route: oral
Route: multiple
Dose: 27 g, 1 times / day
Sources: Page: p.503
healthy, ADULT
n = 20
Health Status: healthy
Age Group: ADULT
Sex: F
Food Status: FED
Population Size: 20
Sources: Page: p.503
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Simvastatin modulates expression of the PON1 gene and increases serum paraoxonase: a role for sterol regulatory element-binding protein-2.
2003 Nov 1
Effect of squalene on tissue defense system in isoproterenol-induced myocardial infarction in rats.
2004 Sep
Two new sesquiterpenoids and anti-HIV principles from the root bark of Zanthoxylum ailanthoides.
2005 Nov 1
Benzopyrans, biphenyls and xanthones from the root of Garcinia linii and their activity against Mycobacterium tuberculosis.
2006 Apr
The adjuvants aluminum hydroxide and MF59 induce monocyte and granulocyte chemoattractants and enhance monocyte differentiation toward dendritic cells.
2008 Apr 15
Patents

Sample Use Guides

The efficacy of diets with different contents of squalene (100, 200, 400, 600 mg per day) was compared. It was shown that antiatherosclerotic diet with inclusion 600 mg squalene has promoted the most positive changes of immune status. The consumption of 200-400 mg of squalene per day produced the more significant antioxidant effect.
Route of Administration: Oral
Squalene (12.5-25 uM) treatment significantly protected the CFUs (human bone marrow (BM) derived colony-forming unit) from cisplatin-induced toxicity
Name Type Language
SQUALENE
GREEN BOOK   INCI   MI   WHO-DD  
INCI  
Official Name English
Squalene [WHO-DD]
Common Name English
2,6,10,14,18,22-TETRACOSAHEXAENE, 2,6,10,15,19,23-HEXAMETHYL-, (6E,10E,14E,18E)-
Systematic Name English
MONTANIDE ISA 720 COMPONENT SQUALENE
Common Name English
SQUALENE [MI]
Common Name English
SQUALENE OIL
Common Name English
SQUALENE [EP MONOGRAPH]
Common Name English
SQUALENE [INCI]
Common Name English
MF59 COMPONENT SQUALENE
Common Name English
SQUALENE [GREEN BOOK]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C860
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LOINC 79326-5
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DSLD 1853 (Number of products:19)
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Code System Code Type Description
MERCK INDEX
m10166
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PRIMARY Merck Index
SMS_ID
100000091876
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PRIMARY
PUBCHEM
638072
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PRIMARY
MESH
D013185
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PRIMARY
NCI_THESAURUS
C77219
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PRIMARY
DAILYMED
7QWM220FJH
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PRIMARY
RXCUI
10014
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ALTERNATIVE
EVMPD
SUB25541
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PRIMARY
CAS
111-02-4
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PRIMARY
WIKIPEDIA
SQUALENE
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PRIMARY
HSDB
8242
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PRIMARY
CHEBI
15440
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PRIMARY
RXCUI
253201
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PRIMARY
FDA UNII
7QWM220FJH
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PRIMARY
EPA CompTox
DTXSID0026044
Created by admin on Sat Dec 16 20:10:29 GMT 2023 , Edited by admin on Sat Dec 16 20:10:29 GMT 2023
PRIMARY
ECHA (EC/EINECS)
203-826-1
Created by admin on Sat Dec 16 20:10:29 GMT 2023 , Edited by admin on Sat Dec 16 20:10:29 GMT 2023
PRIMARY
DRUG BANK
DB11460
Created by admin on Sat Dec 16 20:10:29 GMT 2023 , Edited by admin on Sat Dec 16 20:10:29 GMT 2023
PRIMARY