Structure Database (LMSD)

O OH HO
Common Name
Diadinochrome A
Systematic Name
(8'S)-5,8-Epoxy-7',8'-didehydro-5,8-dihydro-β,β-carotene-3,3'-diol
Synonyms
LM ID
LMPR01070716
Formula
Exact Mass
Calculate m/z
582.407295
Status
Active

Main

Classification

String Representations

InChiKey (Click to copy)
USOIUYXBYYVLLZ-CUWMNBMNSA-N
InChi (Click to copy)
InChI=1S/C40H54O3/c1-28(17-13-18-30(3)21-22-35-32(5)23-33(41)25-38(35,6)7)15-11-12-16-29(2)19-14-20-31(4)36-24-37-39(8,9)26-34(42)27-40(37,10)43-36/h11-20,24,33-34,36,41-42H,23,25-27H2,1-10H3/b12-11+,17-13+,19-14+,28-15+,29-16+,30-18+,31-20+/t33-,34+,36-,40-/m1/s1
SMILES (Click to copy)
C1C(C)(C)C2=C[C@@H](O[C@]2(C)C[C@H]1O)/C(/C)=C/C=C/C(/C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C#CC1=C(C)C[C@@H](O)CC1(C)C

References

Comments
Imported from http://carotenoiddb.jp/

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Peridinium bipes (#2868)
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
Carotenoid ID

Calculated Physicochemical Properties

Heavy Atoms 43
Rings 3
Aromatic Rings
Rotatable Bonds 7
Van der Waals Molecular Volume 660.81
Topological Polar Surface Area 51.76
Hydrogen Bond Donors 2
Hydrogen Bond Acceptors 3
logP 10.35
Molar Refractivity 184.38

Admin

Created at
17th Nov 2021
Updated at
3rd Dec 2021