主要文件

查看所有文档

B19800

S-苄基-L-半胱氨酸

Name: <I>S</I>-苄基-<SC>L</SC>-半胱氨酸
Brand: ALDRICH

97%

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

线性分子式:

C₆H₅CH₂SCH₂CH(NH₂)CO₂H

化学文摘社编号:

3054-01-1

分子量:

211.28

NACRES:

NA.22

PubChem Substance ID:

24891622

eCl@ss:

32160406

UNSPSC Code:

12352209

EC Number:

221-273-4

MDL number:

MFCD00002613

Beilstein/REAXYS Number:

1879358

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

Quality Level

100

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

说明

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)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本？

如果您需要特殊版本，可通过批号或批次号查找具体证书。

搜索COA

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

The molecular basis of thioalcohol production in human body odour.

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

Cysteine conjugate S-oxidase. Characterization of a novel enzymatic activity in rat hepatic and renal microsomes.

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

Cysteine, a chelating moiety for synthesis of technetium-99m radiopharmaceuticals--Part IV. Benzyl cysteine and derivatives.

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

查看所有相关文献

全球贸易项目编号

货号	GTIN
B19800-10G	04061833426517