Structure Database (LMSD)
Common Name
Torularhodinaldehyde
Systematic Name
3',4'-Didehydro-β,psi-caroten-16'-al
Synonyms
3D model of Torularhodinaldehyde
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
Buckleyzyma aurantiaca
(#91979)
Cystobasidiomycetes
(#432005)
Imported from Carotenoids DB http://carotenoiddb.jp/
Cystofilobasidium infirmominiatum
(#89913)
Tremellomycetes
(#155616)
Intermediates in the oxidative pathway from torulene to torularhodin in the red yeasts Cystofilobasidium infirmominiatum and C. capitatum (Heterobasidiomycetes, Fungi).,
Phytochemistry, 2007
Phytochemistry, 2007
Pubmed ID:
17597170
String Representations
InChiKey (Click to copy)
IAEFJGPZEPGPGJ-HMHVFHPLSA-N
InChi (Click to copy)
InChI=1S/C40H52O/c1-32(19-12-21-34(3)22-13-23-35(4)24-15-26-37(6)31-41)17-10-11-18-33(2)20-14-25-36(5)28-29-39-38(7)27-16-30-40(39,8)9/h10-15,17-26,28-29,31H,16,27,30H2,1-9H3/b11-10+,19-12+,20-14+,22-13+,24-15+,29-28+,32-17+,33-18+,34-21+,35-23+,36-25+,37-26+
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/C=C(\C)/C=C/C=C(\C)/C=O)=C(C)CC1
Other Databases
Calculated Physicochemical Properties
Heavy Atoms
41
Rings
1
Aromatic Rings
Rotatable Bonds
13
Van der Waals Molecular Volume
660.03
Topological Polar Surface Area
17.07
Hydrogen Bond Donors
Hydrogen Bond Acceptors
1
logP
11.73
Molar Refractivity
183.78
Admin
Created at
17th Nov 2021
Updated at
29th Nov 2021