Structure Database (LMSD)

O O HO HO O O O
Common Name
Nor-peridinin2
Systematic Name
(3S,5R,6S,8S,3'S,5'R,6'S)-5,8-Epoxy-3'-ethanoyloxy-3,5'-dihydroxy-5,6,5',6'-tetrahydro-6',7'-didehydro-12',13',20'-trinor-β,β-caroten-19,11-olide
Synonyms
LM ID
LMPR01070861
Formula
C39H50O7
Exact Mass
Calculate m/z
630.355655
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)
KQQRQKINDGGYIE-SCGZQCCASA-N
InChi (Click to copy)
InChI=1S/C39H50O7/c1-25(16-17-33-37(6,7)23-30(44-27(3)40)24-38(33,8)43)14-12-10-11-13-15-26(2)18-29-19-31(35(42)45-29)32-20-34-36(4,5)21-28(41)22-39(34,9)46-32/h10-16,18-20,28,30,32,41,43H,21-24H2,1-9H3/b12-10+,13-11+,25-14+,26-15+,29-18-/t17-,28-,30-,32-,38+,39+/m0/s1
SMILES (Click to copy)

References

Comments
Imported from http://carotenoiddb.jp/

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Symbiodinium sp. (#2950)
Dinophyceae (#2864)
Isolation and characterization of dinochrome A and B, anti-carcinogenic active carotenoids from the fresh Water red tide Peridinium bipes.,
Chem Pharm Bull (Tokyo), 2002
Pubmed ID: 12499607

Other Databases

PubChem CID
101243266
Carotenoid ID
CA01088

Calculated Physicochemical Properties

Heavy Atoms 46
Rings 4
Aromatic Rings
Rotatable Bonds 8
Van der Waals Molecular Volume 666.31
Topological Polar Surface Area 106.43
Hydrogen Bond Donors 2
Hydrogen Bond Acceptors 7
logP 8.64
Molar Refractivity 181.78

Admin

Created at
17th Nov 2021
Updated at
18th Dec 2021