B19800
S-苄基-L-半胱氨酸
97%
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关于此项目
线性分子式:
C6H5CH2SCH2CH(NH2)CO2H
化学文摘社编号:
分子量:
211.28
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
221-273-4
MDL number:
Beilstein/REAXYS Number:
1879358
产品名称
S-苄基-L-半胱氨酸, 97%
InChI key
GHBAYRBVXCRIHT-VIFPVBQESA-N
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
SMILES string
N[C@@H](CSCc1ccccc1)C(O)=O
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
Quality Level
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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
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)
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
[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
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