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crocin (Q424767)

From Wikidata

chemical compound

trans-crocetin bis(beta-D-gentiobiosyl) ester
crocetin di-beta-D-gentiobiose ester
crocine
crocetin di-gentiobiose ester
alpha-crocin
crocetin digentiobioside
Natural yellow 6
Natural yellow 19
C.I. 75100
Natural red 1
Crocin

Language	Label	Description	Also known as
default for all languages	No label defined
English	crocin	chemical compound	trans-crocetin bis(beta-D-gentiobiosyl) ester crocetin di-beta-D-gentiobiose ester crocine crocetin di-gentiobiose ester alpha-crocin crocetin digentiobioside Natural yellow 6 Natural yellow 19 C.I. 75100 Natural red 1 Crocin

Statements

type of chemical entity

0 references

Crocetin digentiobiosyl ester

1 reference

based on heuristic

inferred from SMILES

0 references

chemical structure

Crocin.png
1,799 × 1,090; 22 KB

1 reference

imported from Wikimedia project

German Wikipedia

stereoisomer of

bis[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (2E,4E,6E,8E,10E,12E,14E)-2,6,11,15-tetramethylhexadeca-2,4,6,8,10,12,14-heptaenedioate

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

SEBIKDIMAPSUBY-OQHQQNNESA-N

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

bis[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (2E,4E,6E,8E,10Z,12E,14Z)-2,6,11,15-tetramethylhexadeca-2,4,6,8,10,12,14-heptaenedioate

1 reference

based on heuristic

inferred from InChI

chemical formula

C₄₄H₆₄O₂₄

1 reference

language of work or name

Crocin (English)

20 November 2016

canonical SMILES

CC(=CC=CC=C(C)C=CC=C(C)C(=O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)C=CC=C(C)C(=O)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O

1 reference

language of work or name

Crocin (English)

20 November 2016

isomeric SMILES

C/C(=C\C=C\C=C(\C=C\C=C(\C(=O)O[C@@H]1O[C@@H]([C@H]([C@@H]([C@H]1O)O)O)CO[C@@H]2O[C@@H]([C@H]([C@@H]([C@H]2O)O)O)CO)/C)/C)/C=C/C=C(/C(=O)O[C@@H]3O[C@@H]([C@H]([C@@H]([C@H]3O)O)O)CO[C@@H]4O[C@@H]([C@H]([C@@H]([C@H]4O)O)O)CO)\C

1 reference

language of work or name

Crocin (English)

20 November 2016

28 references

Effects of crocin analogs on ocular blood flow and retinal function

Uses of saffron

Crocin and crocetin derivatives inhibit skin tumour promotion in mice

Effects of saffron extract and its constituent crocin on learning behaviour and long-term potentiation

Methods for the analysis of the saffron metabolites crocin, crocetins, picrocrocin and safranal for the determination of the quality of the spice using thin-layer chromatography, high-performance liquid chromatography and gas chromatography

Preparative high-performance liquid chromatographic purification of saffron secondary metabolites

Crocin, safranal and picrocrocin from saffron (Crocus sativus L.) inhibit the growth of human cancer cells in vitro

Economic analysis of saffron production

Effects of the active constituents of Crocus sativus L., crocins, in an animal model of anxiety

A quantitative high-performance liquid chromatographic method to analyse commercial saffron (Crocus sativus L.) products.

Simultaneous quantification of five major biologically active ingredients of saffron by high-performance liquid chromatography

Constituents of the stigmas of Crocus sativus and their tyrosinase inhibitory activity

In vitro formation of crocetin glucosyl esters by Crocus sativus callus extract

Post-harvest degradation of carotenoid glucose esters in saffron

Formation of Stigma-Like Structures and Pigment in Cultured Tissues of Crocus sativus

Quality and functionality of saffron: quality control, species assortment and affinity of extract and isolated saffron compounds to NMDA and sigma-1 receptors

TLC Preparative Purification of Picrocrocin, HTCC and Crocin from Saffron

Synthesis of crocin, picrocrocin and safranal by saffron stigma-like structures proliferated in vitro.

Über Pflanzenfarbstoffe III. Zur Kenntnis der Safranfarbstoffe I

Effects of long-term treatment of colon adenocarcinoma with crocin, a carotenoid from saffron (Crocus sativus L.): an experimental study in the rat

Antidepressant properties of bioactive fractions from the extract of Crocus sativus L.

HPLC quantification of major active components from 11 different saffron (Crocus sativus L.) sources

UV-Vis, FT-Raman, and 1H NMR Spectroscopies of cis-trans Carotenoids from Saffron (Crocus sativus L.)

Analytical and functional aspects on Saffron from Crocus sativus L.: development of quality control methods, species assortment and affinity to sigma-1 and NMDA receptors

Two Kaempferol Sophorosides fromCrocus Sativus

Spectroscopic Characterization of Crocetin Derivatives fromCrocus sativusandGardeniajasminoides

Constituents of the Pollen of Crocus sativus L. and Their Tyrosinase Inhibitory Activity.

Use of in vitro assays to assess the potential antigenotoxic and cytotoxic effects of saffron (Crocus sativus L.).

Gardenia jasminoides

9 references

HPLC Separation of the Major Constituents of Gardeniae Fructus

Isolation and Structure Elucidation of Carotenoid−Glycosyl Esters in Gardenia Fruits (Gardenia jasminoidesEllis) and Saffron (CrocussativusLinne)

Antioxidant properties of crocin from Gardenia jasminoides Ellis and study of the reactions of crocin with linoleic acid and crocin with oxygen

Isolation and structural elucidation of a new lipoxygenase inhibitor from gardeniae fructus

Induction of Callus from Flesh ofGardenia jasminoidesELLIS Fruit and Formation of Yellow Pigment in the Callus

Chemical constituents from the fruit of Gardenia jasminoides and their inhibitory effects on nitric oxide production

Antihyperlipidemic effect of crocin isolated from the fructus of Gardenia jasminoides and its metabolite Crocetin

Neocrocin A: a novel crocetin glycoside with a unique system for binding sugars isolated from gardenia yellow

Spectroscopic Characterization of Crocetin Derivatives fromCrocus sativusandGardeniajasminoides

2 references

UGT75L6 and UGT94E5 mediate sequential glucosylation of crocetin to crocin in Gardenia jasminoides

Profiling of components and validated determination of iridoids in Gardenia Jasminoides Ellis fruit by a high-performance-thin-layer- chromatography/mass spectrometry approach

Buddleja officinalis

1 reference

Marrying structure and genomics

Crocus albiflorus

1 reference

HPLC quantification of major active components from 11 different saffron (Crocus sativus L.) sources

1 reference

HPLC quantification of major active components from 11 different saffron (Crocus sativus L.) sources

Crocus tommasinianus

1 reference

HPLC quantification of major active components from 11 different saffron (Crocus sativus L.) sources

Crocus caeruleus

1 reference

HPLC quantification of major active components from 11 different saffron (Crocus sativus L.) sources

2 references

UGT75L6 and UGT94E5 mediate sequential glucosylation of crocetin to crocin in Gardenia jasminoides

Profiling of components and validated determination of iridoids in Gardenia Jasminoides Ellis fruit by a high-performance-thin-layer- chromatography/mass spectrometry approach

976.378753 dalton

1 reference

language of work or name

Crocin (English)

5 October 2016

described by source

Otto's encyclopedia

statement is subject of

1 reference

Commons category

Crocin

0 references

Identifiers

InChI=1S/C44H64O24/c1-19(11-7-13-21(3)39(59)67-43-37(57)33(53)29(49)25(65-43)17-61-41-35(55)31(51)27(47)23(15-45)63-41)9-5-6-10-20(2)12-8-14-22(4)40(60)68-44-38(58)34(54)30(50)26(66-44)18-62-42-36(56)32(52)28(48)24(16-46)64-42/h5-14,23-38,41-58H,15-18H2,1-4H3/b6-5+,11-7+,12-8+,19-9+,20-10+,21-13+,22-14+/t23-,24-,25-,26-,27-,28-,29-,30-,31+,32+,33+,34+,35-,36-,37-,38-,41-,42-,43+,44+/m1/s1

1 reference

language of work or name

Crocin (English)

20 November 2016

SEBIKDIMAPSUBY-RTJKDTQDSA-N

2 references

language of work or name

Crocin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

Global Substance Registration System

language of work or name

crocin (English)

20 November 2016

SEBIKDIMAPSUBY-RTJKDTQDSA-N

CAS Common Chemistry

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=42553-65-1

1 reference

language of work or name

a-Crocin (English)

20 November 2016

2 references

language of work or name

Crocin (English)

20 November 2016

matched by identifier from

SEBIKDIMAPSUBY-RTJKDTQDSA-N

Reaxys registry number

78445

1 reference

language of work or name

crocin-1 (English)

5 October 2016

mapping relation type

2 references

language of work or name

CROCIN (English)

20 November 2016

matched by identifier from

International Chemical Identifier

InChI=1S/C44H64O24/c1-19(11-7-13-21(3)39(59)67-43-37(57)33(53)29(49)25(65-43)17-61-41-35(55)31(51)27(47)23(15-45)63-41)9-5-6-10-20(2)12-8-14-22(4)40(60)68-44-38(58)34(54)30(50)26(66-44)18-62-42-36(56)32(52)28(48)24(16-46)64-42/h5-14,23-38,41-58H,15-18H2,1-4H3/b6-5+,11-7+,12-8+,19-9+,20-10+,21-13+,22-14+/t23-,24-,25-,26-,27-,28-,29-,30-,31+,32+,33+,34+,35-,36-,37-,38-,41-,42-,43+,44+/m1/s1

1 reference

language of work or name

CROCIN (English)

20 November 2016

1 reference

matched by identifier from

SEBIKDIMAPSUBY-RTJKDTQDSA-N

UniChem compound ID

1 reference

1 reference

Hazardous Substances Data Bank

publication date

28 October 2019

Crocin (English)

10 May 2021

DSSTox substance ID

2 references

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

matched by identifier from

SEBIKDIMAPSUBY-RTJKDTQDSA-N

DSSTOX compound identifier

0 references

1 reference

Global Substance Registration System

language of work or name

crocin (English)

20 November 2016

ECHA Substance Infocard ID

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Bis(6-O-β-D-glucopyranosyl-β-D-glucopyranosyl) 8,8'-diapo-ψ,ψ-carotenedioate (English)

CAS no.: 42553-65-1 (English)

1 reference

CosIng database

28 December 2019

CROCIN (English)

CAS no.: 42553-65-1 (English)

1 reference

matched by identifier from

SEBIKDIMAPSUBY-RTJKDTQDSA-N

Human Metabolome Database ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

SEBIKDIMAPSUBY-RTJKDTQDSA-N

1 reference

language of work or name

crocin-1 (English)

5 October 2016

2 references

Global Substance Registration System

language of work or name

crocin (English)

20 November 2016

matched by identifier from

SEBIKDIMAPSUBY-RTJKDTQDSA-N

Probes And Drugs ID

0 references

0 references

0 references

2 references

https://www.swisslipids.org/#/downloads

6 November 2021

matched by identifier from

SEBIKDIMAPSUBY-RTJKDTQDSA-N

1 reference

Freebase Data Dumps

publication date

28 October 2013

Microsoft Academic ID (discontinued)

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

Sitelinks

Wikipedia(18 entries)

arwiki كروسين
cawiki Crocina
dewiki Crocin
enwiki Crocin
eowiki Krokino
eswiki Crocin
frwiki Crocine
hiwiki क्रोसिन
itwiki Crocina
jawiki クロシン
kowiki 크로신
nlwiki Crocine
rowiki Crocină
ruwiki Кроцин
shwiki Krocin
simplewiki Crocin
srwiki Krocin
trwiki Krosin

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(1 entry)

commonswiki Category:Crocin

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