D-pinitol (Q104987776)

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

inferred from SMILES

1 reference

1 reference

1 reference

1 reference

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

1 reference

D-pinitol dehydrogenase activity

inferred from SMILES

part of

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

mass

194.079038168 dalton

1 reference

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

inferred from SMILES

stereoisomer of

2 references

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

1 reference

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

2 references

1 reference

L-pinitol

2 references

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

2 references

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

2 references

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

1 reference

1 reference

1 reference

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

1 reference

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

1 reference

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

1 reference

chemical formula

C₇H₁₄O₆

0 references

canonical SMILES

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

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isomeric SMILES

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

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found in taxon

Genista ephedroides

1 reference

Flavonoids fromGenista ephedroides

Zanha africana

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

Acer oblongum

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

liquorice

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.

Lotus hirsutus

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

Glycine soja

1 reference

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

Lotus tenuis

1 reference

Antioxidant flavonol glycosides from Dorycnium hirsutum

Identifiers

InChI

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

imported from Wikimedia project

0 references

CAS Registry Number

10284-63-6

2 references

English Wikipedia

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

9 April 2021

ChemSpider ID

10369209

1 reference

imported from Wikimedia project

English Wikipedia

Reaxys registry number

2043789

0 references

ChEBI ID

28548

mapping relation type

exact match

1 reference

imported from Wikimedia project

ChEBI release 2021-03-01

ChEMBL ID

CHEMBL493737

1 reference

2 references

matched by identifier from

DSSTOX compound identifier

DSSTox substance ID

DTXSID50883108

0 references

0 references

0 references

0 references

1 reference

6 July 2021

CAS no.: 10284-63-6 (English)

title

Methylinositol (English)

Human Metabolome Database ID

HMDB0034219

2 references

matched by identifier from