跳转至内容
Merck

W381829

Sigma-Aldrich

L-丙氨酸

≥99%

别名:

(S)-2-氨基丙酸, L-α-氨基丙酸

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C3H7NO2
CAS号:
分子量:
89.09
FEMA號碼:
3818
Beilstein:
1720248
EC號碼:
MDL號碼:
分類程式碼代碼:
12164502
eCl@ss:
32160406
PubChem物質ID:
Flavis號碼:
17.002
NACRES:
NA.21

生物源

synthetic

化驗

≥99%

形狀

chunks
crystalline powder
powder

光學活性

[α]20/D +13.5 to +15.5°, c = 10 in 6 M HCl

溶解度

H2O: soluble 89.1 g/L at 20 °C (completely)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

感官的

sweet

SMILES 字串

C[C@H](N)C(O)=O

InChI

1S/C3H7NO2/c1-2(4)3(5)6/h2H,4H2,1H3,(H,5,6)/t2-/m0/s1

InChI 密鑰

QNAYBMKLOCPYGJ-REOHCLBHSA-N

基因資訊

human ... CA1(759) , CA2(760)

正在寻找类似产品? 访问 产品对比指南

應用


  • Exposure to synthesized tribromobisphenol A and critical effects: Metabolic pathways, disease signature, and benchmark dose derivation.: This study provides insight into the metabolic pathways and disease signatures associated with exposure to synthesized tribromobisphenol A, emphasizing the critical role of L-alanine in mediating these effects (Kuang et al., 2024).

  • Prenylated indole diketopiperazine alkaloids as phosphatase inhibitors from the marine-derived fungus Talaromyces purpureogenus.: Identifies new prenylated indole diketopiperazine alkaloids from Talaromyces purpureogenus that act as potent phosphatase inhibitors, with L-alanine being key to their structure and bioactivity, offering potential for drug development (Liang et al., 2024).


免責聲明

用于研发&或非欧盟(EU)食品用途。不用于零售。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

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

其他客户在看

Mom Das et al.
Nucleic acids research, 42(6), 3943-3953 (2013-12-29)
Errors in protein synthesis due to mispairing of amino acids with tRNAs jeopardize cell viability. Several checkpoints to prevent formation of Ala- and Cys-tRNA(Pro) have been described, including the Ala-specific editing domain (INS) of most bacterial prolyl-tRNA synthetases (ProRSs) and
Florian Madura et al.
The Journal of biological chemistry, 288(26), 18766-18775 (2013-05-24)
The T-cell receptor (TCR) recognizes peptides bound to major histocompatibility molecules (MHC) and allows T-cells to interrogate the cellular proteome for internal anomalies from the cell surface. The TCR contacts both MHC and peptide in an interaction characterized by weak
J M Rhoads et al.
Journal of pediatric gastroenterology and nutrition, 9(2), 225-231 (1989-08-01)
We studied sodium-dependent uptake of L-alanine into small intestinal brush border membrane vesicles (BBMV) isolated from piglets 40 h after infection with transmissible gastroenteritis (TGE) virus. Vesicles from TGE-infected pigs and uninfected litter-mate controls showed comparable degrees of enrichment and
Lillian L Siu et al.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 31(19), 2477-2484 (2013-05-22)
The antiepidermal growth factor receptor monoclonal antibody cetuximab has improved survival in patients with metastatic, chemotherapy-refractory, wild-type K-RAS colorectal cancer. The addition of brivanib, a tyrosine kinase inhibitor targeting vascular endothelial growth factor receptor and fibroblast growth factor receptor, to
Rachelle S Doody et al.
The New England journal of medicine, 369(4), 341-350 (2013-07-26)
Alzheimer's disease is characterized by the presence of cortical amyloid-beta (Aβ) protein plaques, which result from the sequential action of β-secretase and γ-secretase on amyloid precursor protein. Semagacestat is a small-molecule γ-secretase inhibitor that was developed as a potential 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