Structure Database (LMSD)
Common Name
Tunaxanthin A
Systematic Name
(3S,6S,3'S,6'S)-ε,ε-Carotene-3,3'-diol
Synonyms
3D model of Tunaxanthin A
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Category
Main Class
Sub Class
References
Comments
Imported from http://carotenoiddb.jp/
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Acanthochitona rubrolineata
(#761904)
Polyplacophora
(#6650)
Comparative biochemical studies of carotenoids in marine invertebrates - the first positive identification of ε,ε-carotene derivatives and isolation of two new carotenoids from chitons".,
Comparative Biochemistry and Physiology, 1989
Comparative Biochemistry and Physiology, 1989
Thunnus obesus
(#8241)
Actinopteri
(#186623)
Carotenoids and their metabolism in big-eye tuna Thunnus obesus,
NIPPON SUISAN GAKKAISHI, 1987
NIPPON SUISAN GAKKAISHI, 1987
String Representations
InChiKey (Click to copy)
BIPAHAFBQLWRMC-FBZONVGVSA-N
InChi (Click to copy)
InChI=1S/C40H56O2/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/h11-26,35-38,41-42H,27-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+/t35-,36-,37-,38-/m1/s1
SMILES (Click to copy)
C1C(C)(C)[C@H](/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)=C[C@H]1O
Other Databases
Calculated Physicochemical Properties
Heavy Atoms
42
Rings
2
Aromatic Rings
Rotatable Bonds
10
Van der Waals Molecular Volume
664.38
Topological Polar Surface Area
40.46
Hydrogen Bond Donors
2
Hydrogen Bond Acceptors
2
logP
10.83
Molar Refractivity
185.06
Admin
Created at
17th Nov 2021
Updated at
6th Jan 2022