Saltar al contenido
Merck

B19800

Sigma-Aldrich

S-Benzyl-L-cysteine

97%

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Fórmula lineal:
C6H5CH2SCH2CH(NH2)CO2H
Número de CAS:
Peso molecular:
211.28
Beilstein/REAXYS Number:
1879358
EC Number:
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

powder

optical activity

[α]20/D +23°, c = 2 in 1 M NaOH

reaction suitability

reaction type: solution phase peptide synthesis

color

white to off-white

mp

214 °C (dec.) (lit.)

application(s)

detection
peptide synthesis

SMILES string

N[C@@H](CSCc1ccccc1)C(O)=O

InChI

1S/C10H13NO2S/c11-9(10(12)13)7-14-6-8-4-2-1-3-5-8/h1-5,9H,6-7,11H2,(H,12,13)/t9-/m0/s1

InChI key

GHBAYRBVXCRIHT-VIFPVBQESA-N

¿Está buscando productos similares? Visita Guía de comparación de productos

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

Los clientes también vieron

Slide 1 of 1

1 of 1

Michelle Rudden et al.
Scientific reports, 10(1), 12500-12500 (2020-07-29)
Body odour is a characteristic trait of Homo sapiens, however its role in human behaviour and evolution is poorly understood. Remarkably, body odour is linked to the presence of a few species of commensal microbes. Herein we discover a bacterial
M Rooseboom et al.
Chemical research in toxicology, 14(1), 127-134 (2001-02-15)
Previously, it was shown that beta-elimination of selenocysteine Se-conjugates by rat renal cytosol leading to pyruvate formation was not solely catalyzed by pyridoxal phosphate-dependent enzymes. It was hypothesized that selenoxidation of the selenocysteine Se-conjugates, followed by syn-elimination, may be an
M Inoue et al.
Journal of biochemistry, 95(1), 247-254 (1984-01-01)
Biosynthesis of N-acetylcysteine S-conjugates of xenobiotics, mercapturic acids, occurs via inter-organ metabolism of the corresponding glutathione derivatives (Inoue, M., Okajima, K., & Morino, Y. (1982) Hepatology 2, 311-316). To elucidate the mechanism of mercapturate biosynthesis and its urinary elimination, hepato-renal
A potent pyridoxal model capable of promoting transamination and beta-elimination of amino acids.
H Kondo et al.
Progress in clinical and biological research, 144A, 101-108 (1984-01-01)
K Okajima et al.
European journal of biochemistry, 142(2), 281-286 (1984-07-16)
Acetylation of cysteine S-conjugates of xenobiotics by microsomal N-acetyltransferase is the final step of detoxicative metabolism leading to mercapturic acid biosynthesis. To elucidate the subcellular site of N-acetylation and the effective mechanism by which the final metabolites are eliminated from

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico