(Q104987776)

English

D-pinitol

chemical compound

In more languages

Statements

type of chemical entity

0 references

1 reference

based on heuristic

inferred from SMILES

(2R)-6-methoxycyclohexane-1,2,3,4,5-pentol

1 reference

based on heuristic

inferred from SMILES

1D-1-O-Methyl-myo-inositol

1 reference

based on heuristic

inferred from SMILES

1 reference

based on heuristic

inferred from SMILES

1 reference

based on heuristic

inferred from SMILES

1 reference

based on heuristic

inferred from SMILES

1D-3-O-Methyl-myo-inositol

1 reference

based on heuristic

inferred from SMILES

D-pinitol dehydrogenase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

194.079038168 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

1D-6-O-methyl-myo-inositol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(1R,2S,3R,4S,5R,6S)-6-methoxycyclohexane-1,2,3,4,5-pentol

1 reference

based on heuristic

inferred from InChIKey

1D-3-O-methyl-myo-inositol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChIKey

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

(1R,2R,3S,4S,5R,6R)-6-methoxycyclohexane-1,2,3,4,5-pentol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

1D-1-O-methyl-myo-inositol

2 references

based on heuristic

inferred from InChIKey

based on heuristic

inferred from InChI

L-(-)-quebrachitol

1 reference

based on heuristic

inferred from InChI

1 reference

based on heuristic

inferred from InChI

(1S,2R,3R,4S,5S,6S)-6-methoxycyclohexane-1,2,3,4,5-pentol

1 reference

based on heuristic

inferred from InChI

(1R,2S,3S,4S,5S,6R)-6-methoxycyclohexane-1,2,3,4,5-pentol

1 reference

based on heuristic

inferred from InChI

(1S,2R,3S,4R,5S,6R)-6-methoxycyclohexane-1,2,3,4,5-pentol

1 reference

based on heuristic

inferred from InChI

1D-5-O-methyl-chiro-inositol

1 reference

based on heuristic

inferred from InChI

chemical formula

C₇H₁₄O₆

0 references

canonical SMILES

OC1C(O)C(O)C(OC)C(O)C1O

0 references

isomeric SMILES

CO[C@@H]1[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@H]1O

0 references

Genista ephedroides

1 reference

Flavonoids fromGenista ephedroides

1 reference

Zanhasaponins A and B, antiphospholipase A2 saponins from an antiinflammatory extract of Zanha africana root bark.

Apuleia leiocarpa

1 reference

The flavones of Apuleia leiocarpa

1 reference

Ethyl brevifolin carboxylate and other constituents from Acer oblongum leaves

Ammopiptanthus mongolicus

1 reference

(+)-3α-Hydroxylupanine, a new alkaloid from Ammopiptanthus mongolicus (MAXIM.) CHENG F.

Astragalus macropus

1 reference

Triterpene glycosides from Astragalus and their genins. LXXVII. Cyclomacrogenin B, a new cycloartane triterpenoid

Astragalus mucidus

1 reference

Triterpene glycosides from Astragalus and their genins. LXXXVIII. Cycloascidoside A, a new bisdesmoside of cycloasgenin C

Astragalus pterocephalus

1 reference

Triterpene glycosides ofAstragalus and their genins. LVI. Cyclopycnanthoside— A new cycloartane glycoside

Astragalus sieversianus

1 reference

Triterpene glycosides from Astragalus and their genins. LXXVI. Glycosides from A. sieversianus

Astragalus tomentosus

1 reference

Cycloartane triterpene glycosides from EgyptianAstragalus species

Cordia boissieri

1 reference

Dimethyl-3,4′-kaempferol de Cordia boissieri

Cyclopia falcata

1 reference

Phenolic metabolites from honeybush tea (Cyclopia subternata).

Cyclopia subternata

1 reference

Phenolic metabolites from honeybush tea (Cyclopia subternata).

Detarium microcarpum

1 reference

Carbohydrates from Detarium microcarpum bark extract.

Dorycnium hirsutum

1 reference

Antioxidant flavonol glycosides from Dorycnium hirsutum

Erythrophleum fordii

1 reference

New diterpenoids and the bioactivity of Erythrophleum fordii

Eysenhardtia subcoriacea

1 reference

Antioxidant aryl-prenylcoumarin, flavan-3-ols and flavonoids from Eysenhardtia subcoriacea.

Genista cadasonensis

1 reference

Endemic Sardinian plants: the case of Genista cadasonensis Valsecchi

Genista corsica

1 reference

A new isoflavone from Genista corsica

1 reference

Dihydrostilbene derivatives from Glycyrrhiza glabra leaves

Heterobasidion annosum

1 reference

Adhesion and development of the root rot fungus (Heterobasidion annosum) on conifer tissues: effects of spore and host surface constituents

Onobrychis viciifolia

1 reference

Polyphenols, condensed tannins, and other natural products in Onobrychis viciifolia (Sainfoin).

Sarcophyte sanguinea

1 reference

Exocarpic acid and other compounds from tubers and inflorescences of Sarcophyte sanguinea

Simmondsia chinensis

2 references

Identification of 4,5-didemethyl-4-O-alpha-D-glucopyranosylsimmondsin and pinitol alpha-D-galactosides in jojoba seed meal (Simmondsia chinensis).

Novel biosynthesis of d-pinitol in simmondsia chinensis

Tribulus cistoides

1 reference

Cholestane- and pregnane-type glycosides from the roots of Tribulus cistoides

Chesneya mongolica

1 reference

(+)-3α-Hydroxylupanine, a new alkaloid from Ammopiptanthus mongolicus (MAXIM.) CHENG F.

1 reference

Antioxidant flavonol glycosides from Dorycnium hirsutum

Astragalus fruticosus

1 reference

Cycloartane triterpene glycosides from EgyptianAstragalus species

Astragalus syriacus

1 reference

Cycloartane triterpene glycosides from EgyptianAstragalus species

1 reference

Secondary metabolites from Glycine soja and their growth inhibitory effect against Spodoptera litura

1 reference

Antioxidant flavonol glycosides from Dorycnium hirsutum

Identifiers

InChI=1S/C7H14O6/c1-13-7-5(11)3(9)2(8)4(10)6(7)12/h2-12H,1H3/t2-,3-,4-,5-,6+,7+/m0/s1

0 references

DSCFFEYYQKSRSV-KLJZZCKASA-N

0 references

CAS Registry Number

2 references

imported from Wikimedia project

English Wikipedia

DSCFFEYYQKSRSV-KLJZZCKASA-N

CAS Common Chemistry

9 April 2021

https://commonchemistry.cas.org/detail?cas_rn=10284-63-6

1 reference

imported from Wikimedia project

English Wikipedia

Reaxys registry number

2043789

0 references

mapping relation type

2 references

ChEBI release 2021-03-01

matched by identifier from

International Chemical Identifier

InChI=1S/C7H14O6/c1-13-7-5(11)3(9)2(8)4(10)6(7)12/h2-12H,1H3/t2-,3-,4-,5-,6+,7+/m0/s1

1 reference

imported from Wikimedia project

English Wikipedia

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

DSCFFEYYQKSRSV-KLJZZCKASA-N

DSSTox substance ID

1 reference

matched by identifier from

DSCFFEYYQKSRSV-KLJZZCKASA-N

DSSTOX compound identifier

DTXCID101022684

0 references

0 references

0 references

1 reference

matched by identifier from

DSCFFEYYQKSRSV-KLJZZCKASA-N

Human Metabolome Database ID

2 references

based on heuristic

inferred from InChIKey

matched by identifier from

DSCFFEYYQKSRSV-KLJZZCKASA-N

1 reference

matched by identifier from

DSCFFEYYQKSRSV-KLJZZCKASA-N

1 reference

matched by identifier from

DSCFFEYYQKSRSV-KLJZZCKASA-N

Probes And Drugs ID

0 references

0 references

1 reference

Freebase Data Dumps

publication date

28 October 2013

Microsoft Academic ID

0 references

Sitelinks

Wikipedia(8 entries)

azbwiki پینیتول
enwiki Pinitol
eswiki Pinitol
fawiki پینیتول
frwiki Pinnitol
jawiki ピニトール
shwiki Pinitol
srwiki Pinitol

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)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q104987776&oldid=2186473514"