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Merck

B19800

Sigma-Aldrich

S-苄基-L-半胱氨酸

97%

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About This Item

线性分子式:
C6H5CH2SCH2CH(NH2)CO2H
CAS号:
分子量:
211.28
Beilstein:
1879358
EC號碼:
MDL號碼:
分類程式碼代碼:
12352209
eCl@ss:
32160406
PubChem物質ID:
NACRES:
NA.22

化驗

97%

形狀

powder

光學活性

[α]20/D +23°, c = 2 in 1 M NaOH

反應適用性

reaction type: solution phase peptide synthesis

顏色

white to off-white

mp

214 °C (dec.) (lit.)

應用

detection
peptide synthesis

SMILES 字串

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 密鑰

GHBAYRBVXCRIHT-VIFPVBQESA-N

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儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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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
P J Sausen et al.
The Journal of biological chemistry, 265(11), 6139-6145 (1990-04-15)
Cysteine conjugate S-oxidase activity, with S-benzyl-L-cysteine as substrate, was found mostly in the microsomal fractions of rat liver and kidney. In the presence of oxygen and NADPH, S-benzyl-L-cysteine is converted to S-benzyl-L-cysteine sulfoxide; no S-benzyl-L-cysteine sulfone was detected. The Vmax
S Mukherjee et al.
Nuclear medicine and biology, 20(4), 413-426 (1993-05-01)
To explore the possibility of utilizing cysteine derivatives for technetium-99m radiopharmaceutical preparation with clinical potential, we synthesized two benzyl substituted cysteine compounds, namely, S-benzyl cysteine 1 and cysteine benzyl ester 3. It was expected, from our previous studies on benzoyl
R S Phillips et al.
The Journal of biological chemistry, 266(28), 18642-18648 (1991-10-05)
Lysine 269 in Escherichia coli tryptophan indole-lyase (tryptophanase) has been changed to arginine by site-directed mutagenesis. The resultant K269R mutant enzyme exhibits kcat values about 10% those of the wild-type enzyme with S-(o-nitrophenyl)-L-cysteine, L-tryptophan, and S-benzyl-L-cysteine, while kcat/Km values are
A Heuner et al.
Pflugers Archiv : European journal of physiology, 417(5), 523-527 (1991-01-01)
We investigated the capacity and the localization of N-acetylation of the mercapturic acid precursor S-benzyl-L-cysteine (BC), as well as the tubular reabsorption of this compound in the rat kidney in vivo et situ by renal clearance and continuous microinfusion and

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