(Q27107901)

English

(all-E)-phytoene

chemical compound

all-trans-phytoene
7,7',8,8',11,11',12,12'-octahydro-psi,psi-carotene
(6E,10E,14E,16E,18E,22E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,10,14,16,18,22,26,30-nonaene
(all-E)-Phytoene
All-trans-7,7',8,8',11,11',12,12'-octahydro-Lycopene
trans-Phytoene

In more languages

Statements

type of chemical entity

0 references

biogenic aliphatic hydrocarbon

0 references

0 references

544.500802±0 dalton

1 reference

language of work or name

Phytoene (English)

5 October 2016

chemical formula

C₄₀H₆₄

1 reference

language of work or name

Phytoene (English)

18 November 2016

canonical SMILES

CC(=CCCC(=CCCC(=CCCC(=CC=CC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C)C

1 reference

language of work or name

Phytoene (English)

18 November 2016

isomeric SMILES

CC(=CCC/C(=C/CC/C(=C/CC/C(=C/C=C/C=C(/CC/C=C(/CC/C=C(/CCC=C(C)C)\C)\C)\C)/C)/C)/C)C

1 reference

language of work or name

Phytoene (English)

18 November 2016

2 references

Olive (Olea Europea)

Pigments of Olea europea

Aspergillus giganteus

1 reference

Carotene biosynthesis by a cell extract of Aspergillus giganteus mut alba

Capsicum annuum

2 references

Color quality in paprika

Biosynthesis of terpenoids: YchB protein of Escherichia coli phosphorylates the 2-hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol

Celastrus orbiculatus

1 reference

Sterically hindered carotenoids with 3Z, 5Z configuration from the seeds of oriental bitter sweet, Celastrus orbiculatus.

1 reference

Separation, identification, and quantification of the major carotenoids in extracts of apricots, peaches, cantaloupe, and pink grapefruit by liquid chromatography

Hibiscus syriacus

1 reference

Identification of carotenoid constituents in Hibiscus syriacus

1 reference

Plant Pigments identified in the common blue butterfly.

Phycomyces blakesleeanus

3 references

Carotenoid biosynthesis by Aphanocapsa homogenates coupled to a phytoene-generating system from Phycomyces blakesleeanus

Correlation between in vivo and in vitro carotenogenesis in Phycomyces

Chemical bioregulation of carotenogenesis in Phycomyces blakesleeanus

1 reference

Biosynthesis of kaurene, squalene and phytoene from mevalonate-2-14C in a cell-free system from pea fruits

Prunus armeniaca

1 reference

Separation, identification, and quantification of the major carotenoids in extracts of apricots, peaches, cantaloupe, and pink grapefruit by liquid chromatography

1 reference

Separation, identification, and quantification of the major carotenoids in extracts of apricots, peaches, cantaloupe, and pink grapefruit by liquid chromatography

1 reference

Carotenoids of the grape

1 reference

Carotenoid biosynthesis in some maize mutants

1 reference

Biosynthesis of C20-carotenoids in Crocus sativus

Rhodomicrobium vannielii

1 reference

The carotenoids of Rhodomicrobium vannielii (rhodospirillaceae) and the effect of diphenylamine on the carotenoid composition

Rhodospirillum rubrum

1 reference

Alternative pathways of spirilloxanthin biosynthesis in Rhodospirillum rubrum

Gibberella fujikuroi

1 reference

Terpenoid biosynthesis in cell extracts of wild-type and mutant strains of Gibberella fujikuroi

1 reference

HPLC-PDA-MS/MS of anthocyanins and carotenoids from dovyalis and tamarillo fruits

Citrus × paradisi

2 references

Separation, identification, and quantification of the major carotenoids in extracts of apricots, peaches, cantaloupe, and pink grapefruit by liquid chromatography

Determination of .beta.-carotene and other hydrocarbon carotenoids in red grapefruit cultivars

Fusarium fujikuroi

1 reference

Terpenoid biosynthesis in cell extracts of wild-type and mutant strains of Gibberella fujikuroi

subject has role

primary metabolite

1 reference

https://plantreactome.gramene.org/PathwayBrowser/#/R-OSA-2744345&DTAB=MT

Identifiers

InChI=1S/C40H64/c1-33(2)19-13-23-37(7)27-17-31-39(9)29-15-25-35(5)21-11-12-22-36(6)26-16-30-40(10)32-18-28-38(8)24-14-20-34(3)4/h11-12,19-22,27-30H,13-18,23-26,31-32H2,1-10H3/b12-11+,35-21+,36-22+,37-27+,38-28+,39-29+,40-30+

1 reference

language of work or name

Phytoene (English)

18 November 2016

YVLPJIGOMTXXLP-KEKOKYSKSA-N

2 references

language of work or name

Phytoene (English)

18 November 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

Global Substance Registration System

language of work or name

(all-E)-phytoene (English)

18 November 2016

CAS Common Chemistry

5 April 2021

https://commonchemistry.cas.org/detail?cas_rn=540-04-5

YVLPJIGOMTXXLP-KEKOKYSKSA-N

1 reference

language of work or name

(all-E)-Phytoene (English)

18 November 2016

1 reference

language of work or name

Phytoene (English)

18 November 2016

Reaxys registry number

1845455

1 reference

language of work or name

all-trans-phytoene (English)

5 October 2016

mapping relation type

2 references

language of work or name

CHEMBL1988265 (English)

18 November 2016

matched by identifier from

International Chemical Identifier

InChI=1S/C40H64/c1-33(2)19-13-23-37(7)27-17-31-39(9)29-15-25-35(5)21-11-12-22-36(6)26-16-30-40(10)32-18-28-38(8)24-14-20-34(3)4/h11-12,19-22,27-30H,13-18,23-26,31-32H2,1-10H3/b12-11+,35-21+,36-22+,37-27+,38-28+,39-29+,40-30+

1 reference

language of work or name

CHEMBL1988265 (English)

18 November 2016

UniChem compound ID

1 reference

MassBank accession ID

MSBNK-Kyoto_Univ-CA000094

0 references

splash10-000i-0009000000-8c33bce1347d6ac39543

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DSSTox substance ID

2 references

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

matched by identifier from

YVLPJIGOMTXXLP-KEKOKYSKSA-N

DSSTOX compound identifier

0 references

Human Metabolome Database ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

YVLPJIGOMTXXLP-KEKOKYSKSA-N

2 references

Global Substance Registration System

language of work or name

(all-E)-phytoene (English)

18 November 2016

matched by identifier from

YVLPJIGOMTXXLP-KEKOKYSKSA-N

Probes And Drugs ID

0 references

1 reference

language of work or name

all-trans-phytoene (English)

5 October 2016

0 references

1 reference

6 April 2020

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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