(Q413888)

imported from Wikimedia project

inferred from SMILES

chemical structure

Barbaloin2.svg
365 × 284; 11 KB

1 reference

German Wikipedia

Aloin A structure.svg
512 × 459; 51 KB

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mass

418.126382 dalton

1 reference

aloin (English)

5 October 2016

2 references

inferred from InChIKey

(10R)-1,8-dihydroxy-3-(hydroxymethyl)-10-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-anthracen-9-one

1 reference

(10R)-1,8-dihydroxy-3-(hydroxymethyl)-10-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-anthracen-9-one

1 reference

(10R)-1,8-dihydroxy-3-(hydroxymethyl)-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-anthracen-9-one

1 reference

chemical formula

C₂₁H₂₂O₉

1 reference

aloin (English)

19 November 2016

C1=CC2=C(C(=C1)O)C(=O)C3=C(C=C(C=C3C2C4C(C(C(C(O4)CO)O)O)O)CO)O

1 reference

aloin (English)

19 November 2016

C1=CC2=C(C(=C1)O)C(=O)C3=C(C=C(C=C3[C@H]2[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)CO)O

1 reference

Phytochemistry and antiglycation activity of Aloe sinkatana Reynolds

aloin (English)

19 November 2016

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3 references

6′-O-Coumaroylaloesin from Aloe castanea — a taxonomic marker for Aloe section Anguialoe

A reversed-phase high-performance liquid chromatographic method for the determination of aloesin, aloeresin A and anthraquinone in Aloe ferox

2 references

The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

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The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

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The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

Aloe dichotoma

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2′-p-Methoxycoumaroylaloeresin, A C-glucoside from Aloe excelsa

Aloidendron dichotomum

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5 references

Tetrahydroanthracenes as Markers for Subterranean Anthranoid Metabolism in Aloe Species

High-performance liquid chromatographic separation and determination of diastereomeric anthrone-C-glucosyls in Cape aloes

5-Hydroxyaloin A in the Genus Aloe Thin Layer Chromatographic Screening and High Performance Liquid Chromatographic Determination

Geographical variation in the major compounds of Aloe ferox leaf exudate

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The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

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The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

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Leaf Compounds in Potential Plantation Species of Aloe in Kenya

Aloe secundiflora var. secundiflora

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Microdontin A and B: Two New Aloin Derivatives from Aloe microdonta

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2 references

The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

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Aloidendron pillansii

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2 references

Anthracene and chromone derivatives in the exudate of Aloe rabaiensis

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4 references

Simultaneous determination of 18 polyketides typical ofAloe by high performance liquid chromatography and photodiode array detection

Tetrahydroanthracenes as Markers for Subterranean Anthranoid Metabolism in Aloe Species

First proof of anthrone aglycones and diastereomeric anthrone-C-glycosyls in flowers and bracts of Aloe species

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The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

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High-performance liquid chromatographic determination of phenolic compounds in Aloe species

Aloe striatula

1 reference

The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

Aloiampelos striatula

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Aloe secundiflora var. tweediae

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3 references

Tetrahydroanthracenes as Markers for Subterranean Anthranoid Metabolism in Aloe Species

5-Hydroxyaloin A in the Genus Aloe Thin Layer Chromatographic Screening and High Performance Liquid Chromatographic Determination

Chromone and aloin derivatives from Aloe broomii, A. Africana and A. speciosa

Aloe nyeriensis

1 reference

Tetrahydroanthracenes as Markers for Subterranean Anthranoid Metabolism in Aloe Species

Aloe aculeata

1 reference

5-Hydroxyaloin A in the Genus Aloe Thin Layer Chromatographic Screening and High Performance Liquid Chromatographic Determination

Aloe marlothii

1 reference

5-Hydroxyaloin A in the Genus Aloe Thin Layer Chromatographic Screening and High Performance Liquid Chromatographic Determination

Aloe brachystachys

1 reference

The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

aloe brandhamii

1 reference

The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

Aloe dorotheae

1 reference

The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

Aloe leachii

1 reference

The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

Aloe sobolifera

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The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

Aloe monticola

1 reference

The chemotaxonomic significance of the phenyl pyrone aloenin in the genus Aloe

Aloe verecunda

1 reference

First proof of anthrone aglycones and diastereomeric anthrone-C-glycosyls in flowers and bracts of Aloe species

Aloe rubroviolacea

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Constituents of Aloe rubroviolacea

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Chromone and aloin derivatives from Aloe broomii, A. Africana and A. speciosa

Aloe arborescens

7 references

Anti-inflammatory Active Constituents of Aloe arborescens Miller.

The distribution of the phenolic metabolites barbaloin, aloeresin and aloenin as a peripheral defense strategy in the succulent leaf parts of Aloe arborescens

THE BARBALOIN CONTENT AND DISTRIBUTION IN ALOE ARBORESCENS LEAVES ACCORDING TO THE LEAF PART, AGE, POSITION, AND SEASON

High-performance liquid chromatographic determination of phenolic compounds in Aloe species

Inhibition by aloenin and barbaloin of histamine release from rat peritoneal mast cells.

Inhibition of mushroom-tyrosinase by aloe extract

Aloe vera

7 references

Three chromone components from Aloe vera leaves

Leaf Compounds in Potential Plantation Species of Aloe in Kenya

High-performance liquid chromatographic determination of phenolic compounds in Aloe species

Determination of aloenin, barbaloin and isobarbaloin in aloe species by micellar electrokinetic chromatography.

Determination of barbaloin in rat serum.

Anthrones from Aloe barbadensis

physically interacts with

taste receptor type 2

subject has role

agonist

1 reference

The Molecular Receptive Ranges of Human TAS2R Bitter Taste Receptors

described by source

Ottův slovník naučný

statement is subject of

Q47497886

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Commons category

Aloin

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Identifiers

National Library of Israel J9U ID

987007294759505171

1 reference

National Library of Israel Names and Subjects Authority File

Library of Congress authority ID

sh85003793

subject named as

Aloin

1 reference

https://thes.bncf.firenze.sbn.it/termine.php?id=22198

Nuovo soggettario

reference URL

InChI=1S/C21H22O9/c22-6-8-4-10-14(21-20(29)19(28)17(26)13(7-23)30-21)9-2-1-3-11(24)15(9)18(27)16(10)12(25)5-8/h1-5,13-14,17,19-26,28-29H,6-7H2/t13-,14+,17-,19+,20-,21+/m1/s1

14 June 2021

InChI

1 reference

AFHJQYHRLPMKHU-OSYMLPPYSA-N

aloin (English)

19 November 2016

2 references

aloin (English)

19 November 2016

ChEBI release 2020-09-01

CAS Registry Number

1415-73-2

2 references

Global Substance Registration System

UNII

648RW354S9

AFHJQYHRLPMKHU-OSYMLPPYSA-N

aloin a (English)

19 November 2016

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=1415-73-2

1 reference

aloin A (English)

19 November 2016

1 reference

aloin (English)

19 November 2016

Reaxys registry number

6077558

1 reference

aloin A (English)

5 October 2016

mapping relation type

1 reference

CHEMBL2103763 (English)

19 November 2016

1 reference

MSBNK-Univ_Toyama-TY000086

CHEMBL2103763 (English)

19 November 2016

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MassBank accession ID

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SPLASH

splash10-014i-0000900000-84d481d052aa3b62e6f2

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DSSTox substance ID

DTXSID0045967

1 reference

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

DSSTOX compound identifier

DTXCID8025967

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EC number

215-808-0

1 reference

Global Substance Registration System

UNII

648RW354S9

aloin a (English)

ECHA Substance Infocard ID

19 November 2016

100.014.371

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.014.371

27 December 2018

AICS Chemical ID (BEING DELETED)

(R)-10-β-D-glucopyranosyl-1,8-dihydroxy-3-(hydroxymethyl)anthracen-9(10H)-one (English)

quotation

CAS no.: 1415-73-2 (English)

6618

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Human Metabolome Database ID

0 references

1 reference

Global Substance Registration System

aloin A (English)

5 October 2016

1 reference

UNII

648RW354S9

aloin a (English)

19 November 2016

0 references

1 reference