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squalene

Structure via PubChem · Public domain (PubChem)

EntityQ407560· pop 37· linked from 231 articles

Also known as all-trans-squalene, spinacene, trans-squalene, (all-E)-2,6,10,15,19,23-hexamethyl-2,6,10,14,18,22-tetracosahexaene, (14E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene, (E,E,E,E)-Squalene, (6Z,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene, 2,6,10,15,19,23-Hexamethyl-2,6,10,14,18,22-tetracosahexaene

composto chimico

OverviewAI-generated

Squalene is a chemical compound with the formula C₃₀H₅₀. Its IUPAC name is (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene. The substance has a mass of 410.391 and a melting point of -75. It possesses a charge of 0, a topological polar surface area of 0, and no hydrogen bond donors or acceptors. The calculated xlogp value is 11.6.

The compound is associated with 6,558 entries in the PubMed database. It is referenced by 231 other encyclopedia articles.

Synthesized by Vinony from 20 facts across 4 sources: Wikidata, PubMed, PubChem, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.

Chemical data

Formula
C30H50
Molecular weight
410.7 g/mol
IUPAC name
(6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene
SMILES
CC(=CCC/C(=C/CC/C(=C/CC/C=C(/CC/C=C(/CCC=C(C)C)\C)\C)/C)/C)C
InChIKey
YYGNTYWPHWGJRM-AAJYLUCBSA-N
XLogP
11.6
Polar surface area
0 Ų
H-bond donors
0
H-bond acceptors
0
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Research

6,558 papers

via PubMed

Wikidata facts

Has part
hydrogen
Mass
410.391
Show 6 more facts
chemical formula
C₃₀H₅₀
canonical SMILES
CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C
isomeric SMILES
CC(=CCC/C(=C/CC/C(=C/CC/C=C(/CC/C=C(/CCC=C(C)C)\C)\C)/C)/C)C
melting point
-75
Commons category
Squalene
subject has role
primary metabolite
Sources (6)

via Wikidata · CC0

Article · Italiano

Lo squalene è un idrocarburo e un triterpene presente nell'olio di fegato degli squali (elasmobranchii) ma anche nei vegetali come i semi di amaranto, crusca di riso, germe di grano e nelle olive. Tutti gli organismi superiori producono squalene, inclusi gli esseri umani. Grazie alla sua natura chimica lo squalene è meno denso dell'acqua, e contribuisce pertanto a sostenere la notevole massa degli squali, contribuendo all'ottima spinta idrostatica di questa specie animale. Tramite ciclizzazione dello squalene abbiamo la formazione dello lanosterolo che è il biochimico degli steroidi e dei triterpeni. Viene generalmente utilizzato come adiuvante nei vaccini.

Abstract from DBpedia / Wikipedia · CC BY-SA

Gallery (3)