capsanthin (Q425431)

Gene Ontology release 2019-11-16

capsanthin catabolic process

subject has role

reactant

1 reference

Gene Ontology release 2019-11-16

capsanthin biosynthetic process

subject has role

product

1 reference

Gene Ontology release 2019-11-16

capsanthin synthase activity

1 reference

reference URL

http://geneontology.org/external2go/rhea2go

1 February 2021

0 references

Capsanthin.svg
532 × 154; 14 KB

1 reference

imported from Wikimedia project

German Wikipedia

mass

584.422946 dalton

1 reference

(2E,4Z,6E,8E,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

Capsanthin (English)

5 October 2016

2 references

(2E,4E,6E,8E,10E,12E,14E,16Z,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

2 references

(2E,4E,6E,8Z,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

2 references

(2E,4E,6E,8Z,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

2 references

(2E,4Z,6E,8E,10E,12E,14E,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

2 references

(2E,4E,6E,8E,10E,12Z,14Z,16E,18E)-19-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-1-[(1S,4R)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethylnonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one

1 reference

1 reference

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chemical formula

C₄₀H₅₆O₃

1 reference

Capsanthin (English)

20 November 2016

CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)C2(CC(CC2(C)C)O)C)C)C

1 reference

Capsanthin (English)

20 November 2016

CC1=C(C(C[C@@H](C1)O)(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@@]2(C[C@H](CC2(C)C)O)C)/C)/C

1 reference

Nutritional and Medical Importance of Red Pepper (Capsicum spp.)

Capsanthin (English)

20 November 2016

20 references

Dietary capsanthin, the main carotenoid in paprika (Capsicum annuum), alters plasma high-density lipoprotein-cholesterol levels and hepatic gene expression in rats.

Isolation of Carotenoids with 3,5,6-Trihydroxy-5,6-dihydro-β-end Groups from Red Paprika (Capsicum annuum)

Use of HPLC and multivariate methods for the evaluation of the stability of colour pigments of paprika (Capsicum annuum) powder

Isocratic non-aqueous reversed-phase high-performance liquid chromatographic separation of capsanthin and capsorubin in red peppers (Capsicum annuum L.), paprika and oleoresin

Color quality in paprika

Separation and quantification of the carotenoid pigments in red peppers (Capsicum annuum L.), paprika, and oleoresin by reversed-phase HPLC

Carotenoids and carotenoid esters from new cross-cultivars of paprika

Influence of the Industrial Drying Processes of Pepper Fruits(Capsicum annuum Cv. Bola) for Paprika on the Carotenoid Content

Separation of paprika pigments by HPLC

Carotenoid composition in the fruits of red paprika (Capsicum annuum var. lycopersiciforme rubrum) during ripening; biosynthesis of carotenoids in red paprika

Structure-reactivity relationship in the oxidation of carotenoid pigments of the pepper (Capsicum annuum L.).

Carotenoid Composition in the Fruits ofCapsicumannuumCv. Szentesi Kosszarvú during Ripening

Carotenoid biosynthesis changes in five red pepper (Capsicum annuum L.) cultivars during ripening. Cultivar selection for breeding

Quantitative Analysis of Carotenoids and Carotenoid Esters in Fruits by HPLC: Red Bell Peppers

Free and esterified carotenoids in green and red fruits of Capsicum annuum

Isolation of Carotenoids with 3,5,6-Trihydroxy-5,6-dihydro-β-end Groups from Red Paprika (Capsicum annuum)

ChemInform Abstract: Novel Carotenoid 3,6-Epoxides from Red Paprika, Capsicum annuum.

Analysis of molecular species of glycolipids in fruit pastes of red bell pepper (Capsicum annuum L.) by high-performance liquid chromatography-mass spectrometry

Characterization of carotenoids and carotenoid esters in red pepper pods (Capsicum annuum L.) by high-performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry

Red junglefowl

1 reference

Determination of egg yolk xanthophylls by isocratic high-performance liquid chromatography

Lilium lancifolium

2 references

Isolation and characterization of 3,5,6-trihydroxy-carotenoids from petals ofLilium tigrinum

Das Carotinoidspektrum der Antheren und Petalen vonLilium tigrinum cv.‘Red Night’

Commons category

Capsanthin

0 references

Identifiers

InChI

InChI=1S/C40H56O3/c1-29(17-13-19-31(3)21-23-36-33(5)25-34(41)26-38(36,6)7)15-11-12-16-30(2)18-14-20-32(4)22-24-37(43)40(10)28-35(42)27-39(40,8)9/h11-24,34-35,41-42H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+/t34-,35+,40+/m1/s1

1 reference

Capsanthin (English)

20 November 2016

2 references

Capsanthin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

465-42-9

2 references

Global Substance Registration System

UNII

420NY1J57N

capsanthin (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=465-42-9

9 April 2021

1 reference

capsanthin (English)

20 November 2016

2 references

Capsanthin (English)

20 November 2016

Reaxys registry number

2493991

1 reference

capsanthin (English)

5 October 2016

mapping relation type

2 references

CAPSANTHIN (English)

20 November 2016

International Chemical Identifier

1 reference

CAPSANTHIN (English)

20 November 2016

2 references

MSBNK-Kyoto_Univ-CA000015

1 reference

MassBank accession ID

0 references

SPLASH

splash10-014i-0000190000-e855e3467e0449488dd4

0 references

NMRShiftDB structure ID

40266034

1 reference

HSDB ID

7977

1 reference

Hazardous Substances Data Bank

28 October 2019

Capsanthin (English)

10 May 2021

1 reference

DSSTOX compound identifier

0 references

1 reference

Global Substance Registration System

UNII

420NY1J57N

capsanthin (English)

ECHA Substance Infocard ID

20 November 2016

100.006.696

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.006.696

27 December 2018

Open Food Facts food additive ID

(3R,3'S,5'R)-3,3'-dihydroxy-β,κ-caroten-6'-one (English)

quotation

CAS no.: 465-42-9 (English)

E number

E160c(i)

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E160c

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e160c-paprika-extract

0 references

1 reference

28 December 2019

CAPSANTHIN/CAPSORUBIN (English)

quotation

CAS no.: 465-42-9 (English)

Human Metabolome Database ID

0 references

1 reference

Global Substance Registration System

capsanthin (English)

5 October 2016

2 references

UNII

420NY1J57N

capsanthin (English)

20 November 2016

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

capsanthin (English)

5 October 2016

1 reference

30 June 2018

SwissLipids ID

SLM:000501172

1 reference