跳转至内容
Merck

P5125

Sigma-Aldrich

DL-青霉胺

别名:

β,β-二甲基-DL-半胱氨酸, DL-2-氨基-3-巯基-3-甲基丁酸

登录查看公司和协议定价


About This Item

线性分子式:
(CH3)2C(SH)CH(NH2)COOH
CAS号:
分子量:
149.21
Beilstein:
2039817
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:

mp

204-208 °C (lit.)

储存温度

2-8°C

SMILES字符串

CC(C)(S)C(N)C(O)=O

InChI

1S/C5H11NO2S/c1-5(2,9)3(6)4(7)8/h3,9H,6H2,1-2H3,(H,7,8)

InChI key

VVNCNSJFMMFHPL-UHFFFAOYSA-N

正在寻找类似产品? 访问 产品对比指南

象形图

Exclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

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

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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。

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

Youngmi Jo et al.
Journal of natural products, 69(10), 1399-1403 (2006-10-28)
Six new phenylethanoid glucosides, ternstrosides A-F (1-6), a new kaempferol derivative (7), and eight known compounds were isolated from the fresh leaves of Ternstroemia japonica. The structures were elucidated by 1D and 2D NMR spectroscopic analyses. Compounds 1-7 showed potent
Yanxia Xu et al.
Bioorganic & medicinal chemistry letters, 21(6), 1754-1757 (2011-02-15)
By linking the mercapto groups with isopropyl and introducing L-amino acid into the 5-carboxyl of DMSA a class of novel 5-(1-carbonyl-L-amino-acid)-2,2- dimethyl-[1,3]dithiolane-4-carboxylic acids were prepared. Their in vivo activities were evaluated on lead loaded mice at the dose of 0.4
J I Levin et al.
Bioorganic & medicinal chemistry letters, 15(19), 4345-4349 (2005-08-09)
The SAR of a series of potent sulfonamide hydroxamate TACE inhibitors bearing a butynyloxy P1' group was explored. In particular, compound 5k has excellent in vitro potency against TACE enzyme and in cells, and oral activity in an in vivo
N André Sasaki et al.
Bioorganic & medicinal chemistry, 17(6), 2310-2320 (2009-03-06)
2,3-Diaminopropionic acid (Dap) and N-terminal Dap peptides have been found to inhibit in vitro protein-modifications by methylglyoxal (MG), one of the highly reactive alpha-dicarbonyl compounds. MG scavenging potency of the newly synthesized N-terminal Dap peptides is demonstrated by RP-HPLC, SDS-PAGE
Clara Rosso-Fernández et al.
Trials, 16, 102-102 (2015-04-16)
Ventilator-associated pneumonia (VAP) is one of the most common and severe hospital-adquired infections, and multidrugresistant gram-negative bacilli (MDR-GNB) constitute the main etiology in many countries. Inappropriate empiric antimicrobial treatment is associated with increased mortality. In this context, the empirical treatment

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门