(Q420367)

Foundational Model of Anatomy

1 August 2019

1 reference

galactitol metabolic process

participant

1 reference

galactitol biosynthetic process

product

1 reference

galactitol catabolic process

reactant

1 reference

galactitol transmembrane transporter activity

cargo

1 reference

1 reference

galactitol 2-dehydrogenase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

chemical structure

Dulcitol.svg
1,132 × 509; 1 KB

1 reference

imported from Wikimedia project

German Wikipedia

mass

182.079038 dalton

1 reference

galactitol (English)

5 October 2016

C₆H₁₄O₆

1 reference

galactitol (English)

5 October 2016

C(C(C(C(C(CO)O)O)O)O)O

1 reference

galactitol (English)

5 October 2016

C([C@H]([C@@H]([C@@H]([C@H](CO)O)O)O)O)O

1 reference

galactitol (English)

5 October 2016

189 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

found in taxon

Homo sapiens

3 references

Recon 2.2: from reconstruction to model of human metabolism

The human saliva metabolome

A community-driven global reconstruction of human metabolism.

Astragalus brachycarpus

1 reference

Phenolic compounds ofAstragalus brachycarpus. I

Bostrychia bispora

1 reference

Polyol Content of Bostrychia and Stictosiphonia (Rhodomelaceae, Rhodophyta) from Field and Culture

Bostrychia calliptera

1 reference

Polyol Content of Bostrychia and Stictosiphonia (Rhodomelaceae, Rhodophyta) from Field and Culture

Bostrychia montagnei

1 reference

Polyol Content of Bostrychia and Stictosiphonia (Rhodomelaceae, Rhodophyta) from Field and Culture

Bostrychia moritziana

1 reference

Polyol Content of Bostrychia and Stictosiphonia (Rhodomelaceae, Rhodophyta) from Field and Culture

Bostrychia radicans

1 reference

Polyol Content of Bostrychia and Stictosiphonia (Rhodomelaceae, Rhodophyta) from Field and Culture

Bostrychia simpliciuscula

1 reference

Polyol Content of Bostrychia and Stictosiphonia (Rhodomelaceae, Rhodophyta) from Field and Culture

Bostrychia tenella

1 reference

Polyol Content of Bostrychia and Stictosiphonia (Rhodomelaceae, Rhodophyta) from Field and Culture

Buddleja officinalis

1 reference

Sulfated Triterpenes from Melissa officinalis L.

Cajanus cajan

1 reference

Analysis of phenolic acids and carbohydrates in pigeon pea (Cajanus cajan) plant

Carum carvi

1 reference

Water-soluble constituents of caraway: aromatic compound, aromatic compound glucoside and glucides

Elaeodendron croceum

1 reference

Flavanoids and triterpenoids from Cassine papillosa and the absolute configuration of 11,11-dimethyl-1,3,8,10-tetra-hydroxy-9-methoxypeltogynan

Elaeodendron transvaalense

1 reference

11,11-dimethyl-1,3,8,10-tetrahydroxy-9-methoxypeltogynan and three pentacyclic triterpenes from Cassine transvaalensis

Celastrus angulatus

1 reference

Alkaloids from Celastrus angulatus

Celastrus orbiculatus

1 reference

Glycosidic Constituents of Celastrus orbiculatus

Cocos nucifera

1 reference

Generation of Mannitol from Copra Meal

Euonymus europaeus

1 reference

Sorbitol and dulcitol in some celastraceous and rosaceous plants, hosts of Yponomeuta spp.

Globba racemosa

1 reference

Chemical constituents from Exochorda racemosa

Gymnopilus spectabilis

1 reference

Minor Constituents of Gymnopilus spectabilis

Lagotis brevituba

1 reference

Glucosides from Lagotis brevituba

Melampyrum chlorostachyum

1 reference

Dulcitol, aucubin, and melampyroside fromMelampyrum chlorostachium

Nectandra amazonum

1 reference

Lignoids from Nectandra amazonum and N. glabrescens

Pachyrhizus erosus

1 reference

Studies on the constituents of seeds of Pachyrrhizus erosus and their anti herpes simplex virus (HSV) activities

Padina antillarum

1 reference

ChemInform Abstract: Constituents of the Brown Alga Padina tetrastromatica (Hauck)-II

Padina tetrastromatica

1 reference

ChemInform Abstract: Constituents of the Brown Alga Padina tetrastromatica (Hauck)-II

Plenckia populnea

1 reference

Friedelane and oleanane triterpenoids from bark wood ofAustroplenckia populnea

Pleurostylia opposita

1 reference

Triterpenes from the leaves of Pleurostylia opposita

Prunus padus

1 reference

Sorbitol and dulcitol in some celastraceous and rosaceous plants, hosts of Yponomeuta spp.

Prunus spinosa

1 reference

Sorbitol and dulcitol in some celastraceous and rosaceous plants, hosts of Yponomeuta spp.

Salacia oblonga

1 reference

Antidiabetic principles of natural medicines. IV. Aldose reductase and qlpha-glucosidase inhibitors from the roots of Salacia oblonga Wall. (Celastraceae): structure of a new friedelane-type triterpene, kotalagenin 16-acetate

Kothala himbutu

1 reference

Absolute stereostructure of potent alpha-glucosidase inhibitor, Salacinol, with unique thiosugar sulfonium sulfate inner salt structure from Salacia reticulata

Sophora tetraptera

1 reference

Alkaloids of sophora tetraptera sensu reiche

Vahlia capensis

1 reference

Phenolic and antibacterial constituents of Vahlia capensis

Veronica persica

1 reference

Phenylethanoid and iridoid glycosides from Veronica persica

Escherichia coli

2 references

A comprehensive genome-scale reconstruction of Escherichia coli metabolism--2011.

Mutations affecting transport of the hexitols D-mannitol, D-glucitol, and galactitol in Escherichia coli K-12: isolation and mapping

Sporochnus comosus

1 reference

Comosusols A−D and Comosone A: Cytotoxic Compounds from the Brown AlgaSporochnus comosus

Aspergillus ochraceus

1 reference

Polyatomic alcohols from the marine isolate of the fungus Aspergillus ochraceus

Cassytha filiformis

1 reference

Über das Vorhandensein von Dulcit in <I>Cassytha filiformis</I> L

Lophopetalum javanicum

1 reference

Über einige Inhaltsstoffe der Stammrinde von Lophopetalum toxicum

Monteverdia ilioppjfeowneviufheiuwfew fgr

1 reference

Constituents from Maytenus ilicifolia leaves and bioguided fractionation for gastroprotective activity

Melampyrum elatius

1 reference

Chemical study ofMelampyrum elatius

Salacia chinensis

1 reference

Salaprionol and Ponkoranol with Thiosugar Sulfonium Sulfate Structure from Salacia prinoides and a-Glucosidase Inhibitory Activity of Ponkoranol and Kotalanol Desulfate

Tadehagi triquetrum

1 reference

Four new prenylated isoflavonoids in Tadehagi triquetrum.

ivy-leaved speedwell

1 reference

Iridoid glucosides from Veronica hederifolia

Monteverdia guyanensis

1 reference

A sesquiterpene evoninoate alkaloid from Maytenus guianensis

Pristimera celastroides

1 reference

Natural Insecticides from Hippocratea Excelsa and Hippocratea Celastroides

Hippocratea volubilis

1 reference

Natural Insecticides from Hippocratea Excelsa and Hippocratea Celastroides

Gymnosporia nemorosa

1 reference

The chemistry of toxic principles from Maytenus nemerosa

Elaeodendron papillosum

1 reference

Flavanoids and triterpenoids from Cassine papillosa and the absolute configuration of 11,11-dimethyl-1,3,8,10-tetra-hydroxy-9-methoxypeltogynan

Cannabis sativa

1 reference

Constituents of Cannabis sativa L. XVII. A review of the natural constituents

Monteverdia horrida

1 reference

Triterpenes from Maytenus horrida

Commons category

Galactitol

0 references

Identifiers

InChI

InChI=1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4+,5+,6-

1 reference

galactitol (English)

5 October 2016

2 references

galactitol (English)

5 October 2016

ChEBI release 2020-09-01

2 references

galactitol (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=608-66-2

8 April 2021

1 reference

D-Galactitol (English)

5 October 2016

1 reference

galactitol (English)

5 October 2016

Reaxys registry number

1721903

1 reference

galactitol (English)

5 October 2016

83163

0 references

ChEBI ID

16813

mapping relation type

2 references

galactitol (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4+,5+,6-

1 reference

GALACTITOL (English)

5 October 2016

2 references

inferred from InChIKey

InChIKey

MSBNK-Osaka_Univ-OUF00234

1 reference

MassBank accession ID

0 references

SPLASH

splash10-001i-0900000000-d5604b353e57220ab33d

0 references

splash10-001i-0900000000-cf851f66d130211afebc

0 references

splash10-001i-0900000000-3cb52d2c17b8cbc2ba16

0 references

splash10-001i-0900000000-f339f4ab298f287adc8c

0 references

splash10-0f89-4900000000-62a5e50bf5e90f7b3739

0 references

splash10-0f89-4900000000-dd3bcb4967dabd59e1a9

0 references

splash10-0gb9-1983000000-0a0dafcfea843fbb3c72

0 references

splash10-0a4i-9000000000-552b84764ceb9b497a7e

0 references

splash10-052f-9000000000-dfb4eef021d94d514588

0 references

splash10-005a-5900000000-35da0de23de5b9170aed

0 references

DSSTox substance ID

DTXSID1046051

1 reference

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

DSSTOX compound identifier

0 references

0 references

1 reference

Global Substance Registration System

UNII

113ZQ1Y7DD

GALACTITOL (English)

ECHA Substance Infocard ID

5 October 2016

100.009.242

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Galactitol (English)

CAS no.: 608-66-2 (English)

1 reference

1 reference

imported from Wikimedia project

Galactitol

0 references

MeSH tree code

D02.033.800.400

0 references

D09.853.400

0 references

Human Metabolome Database ID

HMDB0000107

2 references

based on heuristic

inferred from InChIKey

InChIKey

1 reference

Global Substance Registration System

galactitol (English)

5 October 2016

2 references

UNII

113ZQ1Y7DD

GALACTITOL (English)

5 October 2016

InChIKey

Immune Epitope Database and Analysis Resource

0 references

0 references

1 reference

1 March 2022

1 reference

6 April 2020

Foundational Model of Anatomy ID

82791

subject named as

Galactitol

1 reference