Structure Database (LMSD)

Common Name
Roretziaxanthin
Systematic Name
3-hydroxy-1',16'-didehydro-1',2'-dihydro-2',6'-cyclo-β-psi-carotene-4,4'-dione
Synonyms
LM ID
LMPR01071055
Formula
C40H50O3
Exact Mass
Calculate m/z
578.375995
Status
Active
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
Halocynthia roretzi (#7729)
Ascidiacea (#7713)
A Novel Carotenoid with a Unique 2,6-Cyclo-ψ-End Group, Roretziaxanthin, from the Sea Squirt Halocynthia roretzi.,
Mar Drugs, 2022
Pubmed ID: 36547879

String Representations

InChiKey (Click to copy)
SIQRNAGQDOFSGC-ROKXECAJSA-N
InChi (Click to copy)
InChI=1S/C40H50O3/c1-27(2)35-25-37(41)32(7)34(35)23-21-30(5)19-13-17-28(3)15-11-12-16-29(4)18-14-20-31(6)22-24-36-33(8)39(43)38(42)26-40(36,9)10/h11-24,35,38,42H,1,25-26H2,2-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,28-15+,29-16+,30-19+,31-20+
SMILES (Click to copy)
C1[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/C2=C(C)C(=O)CC2C(=C)C)=C(C)C(=O)C1O

Calculated Physicochemical Properties

Heavy Atoms 43
Rings 2
Aromatic Rings
Rotatable Bonds 11
Van der Waals Molecular Volume 665.25
Topological Polar Surface Area 54.37
Hydrogen Bond Donors 1
Hydrogen Bond Acceptors 3
logP 10.00
Molar Refractivity 183.98

Admin

Created at
30th Sep 2024
Updated at
30th Sep 2024