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质量水平
方案
97%
表单
powder
旋光性
[α]20/D +23°, c = 2 in 1 M NaOH
反应适用性
reaction type: solution phase peptide synthesis
颜色
white to off-white
mp
214 °C (dec.) (lit.)
应用
detection
peptide synthesis
SMILES字符串
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 key
GHBAYRBVXCRIHT-VIFPVBQESA-N
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储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
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
[Synthesis and antifibrinolytic activity of dipeptides of E-aminocaproic acid and sulfur-containing amino acids].
K Midura-Nowaczek et al.
Acta poloniae pharmaceutica, 45(1), 35-41 (1988-01-01)
A A Elfarra
Chemico-biological interactions, 96(1), 47-55 (1995-04-28)
Several xenobiotics and their corresponding cysteine S-conjugates are metabolized in vivo to cysteine S-conjugate sulfoxides and/or N-acetylcysteine S-conjugate sulfoxides. Homocysteine S-conjugates, such as methionine and ethionine, are also metabolized in vivo to sulfoxides. The enzymatic basis for these metabolic reactions
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
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
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