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R0630000

Riboflavin sodium phosphate

European Pharmacopoeia (EP) Reference Standard

Synonim(y):

Riboflavin 5′-monophosphate sodium salt, Riboflavin Sodium phosphate

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About This Item

Wzór empiryczny (zapis Hilla):
C17H20N4NaO9P
Numer CAS:
130-40-5
Masa cząsteczkowa:
478.33
Beilstein:
4106529
Numer WE:
204-988-6
Numer MDL:
MFCD00065362
Kod UNSPSC:
41116107
Identyfikator substancji w PubChem:
329823989
NACRES:
NA.24

pochodzenie biologiczne

synthetic

klasa czystości

pharmaceutical primary standard

agency

EP

rodzina API

riboflavin

Postać

solid

producent / nazwa handlowa

EDQM

metody

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

Zastosowanie

pharmaceutical (small molecule)

format

neat

temp. przechowywania

2-8°C

ciąg SMILES

[Na+].Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)COP(O)([O-])=O)c2cc1C

InChI

1S/C17H21N4O9P.Na/c1-7-3-9-10(4-8(7)2)21(15-13(18-9)16(25)20-17(26)19-15)5-11(22)14(24)12(23)6-30-31(27,28)29;/h3-4,11-12,14,22-24H,5-6H2,1-2H3,(H,20,25,26)(H2,27,28,29);/q;+1/p-1/t11-,12+,14-;/m0./s1

Klucz InChI

OHSHFZJLPYLRIP-BMZHGHOISA-M

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Opis ogólny

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.

Zastosowanie

Riboflavin sodium phosphate EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Opakowanie

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

Inne uwagi

Sales restrictions may apply.
This page may contain text that has been machine translated.

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

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Certyfikaty analizy (CoA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Brian C Smith et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(38), E3577-E3586 (2013-09-05)
Nitric oxide (NO) produced by NO synthase (NOS) participates in diverse physiological processes such as vasodilation, neurotransmission, and the innate immune response. Mammalian NOS isoforms are homodimers composed of two domains connected by an intervening calmodulin-binding region. The N-terminal oxidase
Carlos Marcuello et al.
Biochimica et biophysica acta, 1834(3), 665-676 (2013-01-08)
Biochemical characterization of Corynebacterium ammoniagenes FADS (CaFADS) pointed to certain confusion about the stoichiometry of this bifunctional enzyme involved in the production of FMN and FAD in prokaryotes. Resolution of its crystal structure suggested that it might produce a hexameric
Ruchanok Tinikul et al.
Biochemistry, 52(39), 6834-6843 (2013-09-06)
Bacterial luciferase (LuxAB) is a two-component flavin mononucleotide (FMN)-dependent monooxygenase that catalyzes the oxidation of reduced FMN (FMNH(-)) and a long-chain aliphatic aldehyde by molecular oxygen to generate oxidized FMN, the corresponding aliphatic carboxylic acid, and concomitant emission of light.
Jong-Chin Lin et al.
Biophysical journal, 103(11), 2320-2330 (2013-01-04)
Riboswitches, structured elements in the untranslated regions of messenger RNAs, regulate gene expression by binding specific metabolites. We introduce a kinetic network model that describes the functions of riboswitches at the systems level. Using experimental data for flavin mononucleotide riboswitch
Yulia V Bertsova et al.
The Journal of biological chemistry, 288(20), 14276-14286 (2013-04-06)
Na(+)-translocating NADH:quinone oxidoreductase (Na(+)-NQR) contains two flavin residues as redox-active prosthetic groups attached by a phosphoester bond to threonine residues in subunits NqrB and NqrC. We demonstrate here that flavinylation of truncated Vibrio harveyi NqrC at Thr-229 in Escherichia coli
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