Structure Database (LMSD)

Common Name
gamma-Carotene
Systematic Name
Synonyms
LM ID
LMPR01070260
Status
Active
Exact Mass
Calculate m/z
536.4382
Formula
C40H56
Show lipids differing only in stereochemistry/bond geometry
View MoNA MS spectra
Download as...
MDLMOL SDF CSV TSV
MDLMOL files can be opened in various drawing programs. In ChemDraw, open as filetype "MDL Molfile".

Main

Classification

Category
Main Class
Sub Class
Prenol Lipids [PR]
Isoprenoids [PR01]
C40 isoprenoids (tetraterpenes) [PR0107]

String Representations

InChiKey (Click to copy)
HRQKOYFGHJYEFS-BXOLYSJBSA-N
InChi (Click to copy)
InChI=1S/C40H56/c1-32(2)18-13-21-35(5)24-15-26-36(6)25-14-22-33(3)19-11-12-20-34(4)23-16-27-37(7)29-30-39-38(8)28-17-31-40(39,9)10/h11-12,14-16,18-20,22-27,29-30H,13,17,21,28,31H2,1-10H3/b12-11+,22-14+,23-16+,26-15+,30-29+,33-19+,34-20+,35-24+,36-25+,37-27+
SMILES (Click to copy)
C1(=C(C)CCCC1(C)C)/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C=C(\C)/CC/C=C(\C)/C

References

Other Databases

Wikipedia
gamma-Carotene
KEGG ID
C05435
HMDB ID
HMDB0112262
CHEBI ID
27740
LIPIDBANK ID
VCA1007
PubChem CID
5280791
Carotenoid ID
CA00191

Calculated Physicochemical Properties

Heavy Atoms 40
Rings 1
Aromatic Rings 0
Rotatable Bonds 13
Van der Waals Molecular Volume 656.52
Topological Polar Surface Area 0.00
Hydrogen Bond Donors 0
Hydrogen Bond Acceptors 0
logP 12.77
Molar Refractivity 183.48

Admin

Created at
-
Updated at
-