fucoxanthin (Q96385)

inferred from SMILES

all-trans-Fucoxanthin

1 reference

imported from Wikimedia project

inferred from SMILES

chemical structure

Fucoxanthin.svg
620 × 125; 30 KB

1 reference

German Wikipedia

mass

658.423339576 dalton

1 reference

inferred from isomeric SMILES

stereoisomer of

9'Z-Fucoxanthin

2 references

inferred from InChIKey

1 reference

C₄₂H₅₈O₆

1 reference

PubChem

canonical SMILES

CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=C=C3C(CC(CC3(C)O)OC(=O)C)(C)C

1 reference

RCSB protein data bank

PDB ligand ID

A86

language of work or name

English

retrieved

16 February 2021

isomeric SMILES

CC(=O)O[C@H]1CC(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@@]23O[C@]2(C)C[C@@H](O)CC3(C)C)\C)\C)[C@](C)(O)C1

0 references

found in taxon

Laminaria saccharina

3 references

Naturally occurring stereoisomers of fucoxanthin

Algal carotenoids 54. Carotenoids of brown algae (Phaeophyceae)

Algal Carotenoids. XII. Chemical Reactions of Carotenoids with 2-Hydroxylated beta-Rings.

Cyclotella meneghiniana

1 reference

Chlorophyll triplet quenching by fucoxanthin in the fucoxanthin-chlorophyll protein from the diatom Cyclotella meneghiniana

Chlamys opercularis

1 reference

High-performance liquid chromatography of carotenoids from some marine shellfish

Gracilaria vermiculophylla

1 reference

Screening for bioactive compounds from algae.

has part(s)

carbon

0 references

different from

(1S,3R)-3-hydroxy-4-[(3Z,5E,7Z,9E,11Z,13E,15Z)-18-{(1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl}-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15-octaen-1-ylidene]-3,5,5-trimethylcyclohexyl acetate

criterion used

chemical structure differs in the spatial configuration of at least one stereogenic center

0 references

Identifiers

InChI

InChI=1S/C42H58O6/c1-29(18-14-19-31(3)22-23-37-38(6,7)26-35(47-33(5)43)27-40(37,10)46)16-12-13-17-30(2)20-15-21-32(4)36(45)28-42-39(8,9)24-34(44)25-41(42,11)48-42/h12-22,34-35,44,46H,24-28H2,1-11H3/b13-12+,18-14+,20-15+,29-16+,30-17+,31-19+,32-21+/t23-,34-,35-,40+,41+,42-/m0/s1

0 references

1 reference

ChEBI release 2020-09-01

CAS Registry Number

3351-86-8

1 reference

https://commonchemistry.cas.org/detail?cas_rn=3351-86-8

10 April 2021

ChemSpider ID

21864745

1 reference

imported from Wikimedia project

English Wikipedia

PubChem CID

5281239

reason for deprecated rank

applies to other chemical entity

intended subject of deprecated statement

0 references

Reaxys registry number

6580822

0 references

ChEBI ID

5186

mapping relation type

exact match

1 reference

International Chemical Identifier

2 references

inferred from InChIKey

SJWWTRQNNRNTPU-ABBNZJFMSA-N

1 reference

MassBank accession ID

MSBNK-Kyoto_Univ-CA000057

0 references

SPLASH

splash10-0007-0078985000-8cac20e609c088478474

0 references

splash10-0007-0077984000-70a052b3f8190dfe006a

0 references

NMRShiftDB structure ID

20173184

1 reference

SJWWTRQNNRNTPU-ABBNZJFMSA-N

DSSTox substance ID

DTXSID901031617

1 reference

SJWWTRQNNRNTPU-ABBNZJFMSA-N

EC number

686-524-6

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.212.315

retrieved

27 December 2018

title

Fucoxanthin (English)

quotation

CAS no.: 3351-86-8 (English)

ECHA Substance Infocard ID

100.212.315

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.212.315

retrieved

27 December 2018

title

Fucoxanthin (English)

quotation

CAS no.: 3351-86-8 (English)

0 references

0 references

fucoxanthin

0 references

DrugBank ID

DB15462

1 reference

Human Metabolome Database ID

0 references

0 references

1 reference