Structure Database (LMSD)

OH HO OH OH
Common Name
(3R,4R,3'S,4'R)-Crustaxanthin
Systematic Name
(3R,4R,3'S,4'R)-β,β-Carotene-3,4,3',4'-tetrol
Synonyms
LM ID
LMPR01070666
Formula
Exact Mass
Calculate m/z
600.41786
Status
Active

Main

Classification

String Representations

InChiKey (Click to copy)
BHCRLQHBUDRLQM-JBOPIHFUSA-N
InChi (Click to copy)
InChI=1S/C40H56O4/c1-27(17-13-19-29(3)21-23-33-31(5)37(43)35(41)25-39(33,7)8)15-11-12-16-28(2)18-14-20-30(4)22-24-34-32(6)38(44)36(42)26-40(34,9)10/h11-24,35-38,41-44H,25-26H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,27-15+,28-16+,29-19+,30-20+/t35-,36+,37-,38-/m1/s1
SMILES (Click to copy)
C1C(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@@H](O)[C@@H](O)CC2(C)C)=C(C)[C@@H](O)[C@@H]1O

References

Comments
Imported from http://carotenoiddb.jp/

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Salvelinus alpinus (#8036)
Actinopteri (#186623)
Astaxanthin and its metabolites idoxanthin and crustaxanthin in flesh, skin, and gonads of sexually immature and maturing Arctic charr (Salvelinus alpinus (L.)).,
Comp Biochem Physiol B Biochem Mol Biol, 2000
Pubmed ID: 10818273

Other Databases

PubChem CID
Carotenoid ID

Calculated Physicochemical Properties

Heavy Atoms 44
Rings 2
Aromatic Rings
Rotatable Bonds 10
Van der Waals Molecular Volume 681.96
Topological Polar Surface Area 80.92
Hydrogen Bond Donors 4
Hydrogen Bond Acceptors 4
logP 9.63
Molar Refractivity 189.00

Admin

Created at
17th Nov 2021
Updated at
2nd Dec 2021