Structure Database (LMSD)

Common Name
3'-Hydroxy-epsilon,epsilon-caroten-3-one
Systematic Name
(6R,3'R,6'R)-3'-Hydroxy-ε,ε-caroten-3-one
Synonyms
  • 3'-OH-epsilon,epsilon-Caroten-3-one
  • 3-Hydroxy-epsilon,epsilon-caroten-3'-one
  • (6R,3'R,6'R)-3-Dehydrolactucaxanthin
LM ID
LMPR01070196
Formula
C40H54O2
Exact Mass
Calculate m/z
566.41238
Status
Curated
Show lipids differing only in stereochemistry/bond geometry

Classification

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

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Gallus gallus (#9031)
Aves (#8782)
Isolation of three new carotenoids and proposed metabolic payhways of carotenoids in hen's egg yolk,
Comp. Biochem. Physiol., 1986
Thunnus obesus (#8241)
Actinopteri (#186623)
Carotenoids and their metabolism in big-eye tuna Thunnus obesus,
NIPPON SUISAN GAKKAISHI, 1987

String Representations

InChiKey (Click to copy)
OTHWKRBAHPOBSP-HXMUPQSBSA-N
InChi (Click to copy)
InChI=1S/C40H54O2/c1-29(17-13-19-31(3)21-23-37-33(5)25-35(41)27-39(37,7)8)15-11-12-16-30(2)18-14-20-32(4)22-24-38-34(6)26-36(42)28-40(38,9)10/h11-26,35,37-38,41H,27-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+/t35-,37-,38-/m0/s1
SMILES (Click to copy)
[C@H]1(/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/[C@H]2C(C)=C[C@H](O)CC2(C)C)C(C)=CC(=O)CC1(C)C

Other Databases

HMDB ID
HMDB02020
LIPIDBANK ID
VCA1114
PubChem CID
14409080
Carotenoid ID
CA00696

Calculated Physicochemical Properties

Heavy Atoms 42
Rings 2
Aromatic Rings 0
Rotatable Bonds 10
Van der Waals Molecular Volume 661.74
Topological Polar Surface Area 37.30
Hydrogen Bond Donors 1
Hydrogen Bond Acceptors 2
logP 10.75
Molar Refractivity 183.54

Admin

Created at
-
Updated at
30th Nov 2021