13310
S-Benzyl-L-cysteine
purum, ≥98.0% (NT)
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About This Item
Linear Formula:
C6H5CH2SCH2CH(NH2)CO2H
CAS Number:
Molecular Weight:
211.28
EC Number:
221-273-4
UNSPSC Code:
12352200
MDL number:
Beilstein/REAXYS Number:
1879358
eCl@ss:
32160406
grade
purum
assay
≥98.0% (NT)
optical activity
[α]20/D +28.5±1°, c = 1.5% in 1 M NaOH
mp
214 °C (dec.) (lit.), ~220 °C (dec.)
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
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
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
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 919772-250MG | 04065265451550 |
| 919772-1G | 04065265451543 |
| 683345-500MG | 04061832755618 |
| 683345-5G | 04061832755625 |
| 328774-1G | 04061826717776 |
| 328774-500MG | 04061826717790 |
| 328774-100G | 04061833546635 |
| 328774-500G | 04061833498965 |
| 328774-25G | 04061826717783 |
| 328774-5G | 04061826717813 |
| 683345-50G | 04061833411582 |
| 328774-50G | 04061826717806 |
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