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M0950000

DL-Methionine

European Pharmacopoeia (EP) Reference Standard

Synonyme(s) :

(±)-2-Amino-4-(methylmercapto)butyric acid, DL-2-Amino-4-(methylthio)butanoic acid

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About This Item

Formule linéaire :
CH3SCH2CH2CH(NH2)COOH
Numéro CAS:
59-51-8
Poids moléculaire :
149.21
Numéro Beilstein :
636185
Numéro MDL:
MFCD00063096
Code UNSPSC :
41116107
ID de substance PubChem :
329817841
Nomenclature NACRES :
NA.24

Qualité

pharmaceutical primary standard

Famille d'API

methionine & derivatives

Fabricant/nom de marque

EDQM

Pf

280 °C (dec.) (lit.)

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

CSCCC(N)C(O)=O

InChI

1S/C5H11NO2S/c1-9-3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)

Clé InChI

FFEARJCKVFRZRR-UHFFFAOYSA-N

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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

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

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

PHR1241

L-Méthionine, Pharmaceutical Secondary Standard; Certified Reference Material

M0960000

L-Méthionine, European Pharmacopoeia (EP) Reference Standard

1411504

L-Méthionine, United States Pharmacopeia (USP) Reference Standard

1611955

Selenomethionine, United States Pharmacopeia (USP) Reference Standard

1643292

Racemethionine, United States Pharmacopeia (USP) Reference Standard

1009978

N-Acetyl-D,L-Methionine, United States Pharmacopeia (USP) Reference Standard

PHR2636

N-Acetyl-D,L-Methionine, Pharmaceutical Secondary Standard; Certified Reference Material

PHR2613

Selenomethionine

1012316

S-Adenosyl-L-methionine 1,4-butanedisulfonate, United States Pharmacopeia (USP) Reference Standard

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number

Désolés, nous n'avons pas de COA pour ce produit disponible en ligne pour le moment.

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Consulter la Bibliothèque de documents

Pilar Lloris-Garcerá et al.
Journal of molecular biology, 426(11), 2246-2254 (2014-04-03)
The increasing number of solved membrane protein structures has led to the recognition of a common feature in a large fraction of the small-molecule transporters: inverted repeat structures, formed by two fused homologous membrane domains with opposite orientation in the
Shawn Flanagan et al.
Antimicrobial agents and chemotherapy, 59(1), 178-185 (2014-10-22)
Prolonged treatment with the oxazolidinone linezolid is associated with myelosuppression, lactic acidosis, and neuropathies, toxicities likely caused by impairment of mitochondrial protein synthesis (MPS). To evaluate the potential of the novel oxazolidinone tedizolid to cause similar side effects, nonclinical and
Leen Mathys et al.
PloS one, 9(6), e101181-e101181 (2014-06-27)
N-linked glycans covering the surface of the HIV-1 glycoprotein gp120 are of major importance for the correct folding of this glycoprotein. Of the, on average, 24 N-linked glycans present on gp120, the glycan at Asn260 was reported to be essential
Ole E Sørensen et al.
The Journal of clinical investigation, 124(10), 4539-4548 (2014-09-23)
Papillon-Lefèvre syndrome (PLS) results from mutations that inactivate cysteine protease cathepsin C (CTSC), which processes a variety of serine proteases considered essential for antimicrobial defense. Despite serine protease-deficient immune cell populations, PLS patients do not exhibit marked immunodeficiency. Here, we
Dylan Thomas et al.
Chembiochem : a European journal of chemical biology, 15(11), 1607-1613 (2014-07-22)
Protein arginine N-methyltransferases (PRMTs) catalyze methyl-group transfer from S-adenosyl-L-methionine onto arginine residues in proteins. In this study, modifications were introduced at the guanidine moiety of a peptidyl arginine residue to investigate how changes to the PRMT substrate can modulate enzyme
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