Structure Database (LMSD)

Common Name
Chlorobactene
Systematic Name
Synonyms
LM ID
LMPR01070163
Formula
C40H52
Exact Mass
Calculate m/z
532.4069
Status
Active
Show lipids differing only in stereochemistry/bond geometry

Main

Classification

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

String Representations

InChiKey (Click to copy)
VJASLAGEYVTOGS-IQAIWTHGSA-N
InChi (Click to copy)
InChI=1S/C40H52/c1-31(2)17-13-20-34(5)23-15-25-35(6)24-14-21-32(3)18-11-12-19-33(4)22-16-26-36(7)27-30-40-38(9)29-28-37(8)39(40)10/h11-12,14-19,21-30H,13,20H2,1-10H3/b12-11+,21-14+,22-16+,25-15+,30-27+,32-18+,33-19+,34-23+,35-24+,36-26+
SMILES (Click to copy)
C1(=C(C)C=CC(C)=C1C)/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

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Chlorobaculum tepidum (#1097)
Chlorobiia (#191410)
New carotenoids from the thermophilic green sulfur bacterium Chlorobium tepidum: 1',2'-dihydro-gamma-carotene, 1',2'-dihydrochlorobactene, and OH-chlorobactene glucoside ester, and the carotenoid composition of different strains.,
Arch Microbiol, 1997
Pubmed ID: 9297463

Other Databases

KEGG ID
C15908
CHEBI ID
80167
LIPIDBANK ID
VCA1081
PubChem CID
10098570
Carotenoid ID
CA00704
PDB ID
F26

Calculated Physicochemical Properties

Heavy Atoms 40
Rings 1
Aromatic Rings 1
Rotatable Bonds 13
Van der Waals Molecular Volume 640.34
Topological Polar Surface Area 0.00
Hydrogen Bond Donors 0
Hydrogen Bond Acceptors 0
logP 12.33
Molar Refractivity 183.70

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