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Y0000485

myo-inositol

European Pharmacopoeia (EP) Reference Standard

Synonyme(s) :

1,2,3,4,5,6-hexahydroxycyclohexane, i-inositol, méso-inositol

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About This Item

Formule empirique (notation de Hill):
C6H12O6
Numéro CAS:
87-89-8
Poids moléculaire :
180.16
Numéro Beilstein :
1907329
Numéro MDL:
MFCD00077932
Code UNSPSC :
41116107
ID de substance PubChem :
329830977
Nomenclature NACRES :
NA.24

Qualité

pharmaceutical primary standard

Densité de vapeur

6.2 (vs air)

Famille d'API

inositol

Fabricant/nom de marque

EDQM

Pf

222-227 °C (lit.)

Application(s)

pharmaceutical (small molecule)

Format

neat

Chaîne SMILES 

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

InChI

1S/C6H12O6/c7-1-2(8)4(10)6(12)5(11)3(1)9/h1-12H/t1-,2-,3-,4+,5-,6-

Clé InChI

CDAISMWEOUEBRE-GPIVLXJGSA-N

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Catégories apparentées

Description générale

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Application

myo-Inositol EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Actions biochimiques/physiologiques

Constituant des phospholipides membranaires, ancres glycosylphosphatidylinositol qui accrochent des glycoprotéines à la surface des cellules, et seconds messagers inositol-phosphate.

Conditionnement

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Autres remarques

Sales restrictions may apply.

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number

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Aleksey Porollo et al.
mBio, 5(6), e01834-e01834 (2014-11-06)
In the context of deciphering the metabolic strategies of the obligate pathogenic fungi in the genus Pneumocystis, the genomes of three species (P. carinii, P. murina, and P. jirovecii) were compared among themselves and with the free-living, phylogenetically related fission
Ethan S Patterson et al.
Developmental biology, 393(1), 44-56 (2014-07-06)
Geminin is a nucleoprotein that can directly bind chromatin regulatory complexes to modulate gene expression during development. Geminin knockout mouse embryos are preimplantation lethal by the 32-cell stage, precluding in vivo study of Geminin's role in neural development. Therefore, here
Alan Winston et al.
PloS one, 10(2), e0118608-e0118608 (2015-02-28)
Changes in cerebral metabolite ratios (CMR) measured on 1H-MRS and changes in cognitive function (CF) are described in subjects commencing combination antiretroviral therapy (cART), although the dynamics of such changes are poorly understood. Neuroasymptomatic, HIV-infected subjects electively commencing cART were
Ming Huang et al.
Journal of plant physiology, 171(14), 1205-1216 (2014-07-16)
Chestnut rose (Rosa roxburghii Tratt) is a fruit crop that contains unusually high levels of l-ascorbic acid (AsA; ∼1300 mg 100g(-1) FW). To explore the mechanisms underlying AsA metabolism, we investigated the distribution and abundance of AsA during fruit development.
Jennifer J Donegan et al.
Molecular pharmacology, 87(3), 492-500 (2015-01-01)
The serotonin 2A (5-HT2A) receptor and the proinflammatory cytokine, interleukin-6 (IL-6), have both been implicated in psychiatric disorders. Previously, we demonstrated that these molecules both facilitate cognitive flexibility, a prefrontal cortex-mediated executive function impaired in multiple mental illnesses. In this
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