99853-28-8 Usage
Description
p-Bromophenacyl Lactate is a derivative of Lactic Acid, a compound produced from pyruvate via the enzyme lactate dehydrogenase in the process of fermentation during metabolism and exercise.
Uses
Used in Pharmaceutical Industry:
p-Bromophenacyl Lactate is used as a pharmaceutical agent for its potential applications in treating various medical conditions. Its chemical structure allows it to interact with specific biological targets, making it a candidate for drug development.
Used in Chemical Synthesis:
p-Bromophenacyl Lactate serves as an important intermediate in the synthesis of various organic compounds and pharmaceuticals. Its unique functional groups enable it to participate in a range of chemical reactions, facilitating the production of desired molecules.
Used in Research Applications:
p-Bromophenacyl Lactate is utilized as a research tool in biological and chemical studies. Its properties and reactivity make it valuable for investigating enzyme mechanisms, metabolic pathways, and the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 99853-28-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,8,5 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 99853-28:
(7*9)+(6*9)+(5*8)+(4*5)+(3*3)+(2*2)+(1*8)=198
198 % 10 = 8
So 99853-28-8 is a valid CAS Registry Number.
99853-28-8Relevant articles and documents
Miuramides A and B, Trisoxazole Macrolides from a Mycale sp. Marine Sponge That Induce a Protrusion Phenotype in Cultured Mammalian Cells
Suo, Rei,Takada, Kentaro,Kohtsuka, Hisanori,Ise, Yuji,Okada, Shigeru,Matsunaga, Shigeki
, p. 1108 - 1112 (2018/05/01)
Morphology-guided cell-based screening of the extract of a Mycale sp. marine sponge led to the isolation of two trisoxazole macrolides, miuramides A (1) and B (2), which induced characteristic morphological changes in 3Y1 cells. The structure of 1 including absolute configuration was elucidated by a combination of the analysis of spectroscopic data, derivatization, and degradation. Both compounds exhibit potent cytotoxicity against 3Y1 cells.
