52340-48-4 Usage
Description
Undecylprodigiosin, also known as prodigiosin, is a red-colored secondary metabolite produced by certain bacteria, such as Serratia marcescens. It is a prodigiosin-like pigment with unique chemical properties and biological activities, making it a potential candidate for various applications in different industries.
Uses
Used in Pharmaceutical Applications:
Undecylprodigiosin is used as an antimalarial agent for its ability to combat malaria-causing parasites. Its potent antimalarial properties make it a promising candidate for the development of new drugs to treat this life-threatening disease.
Used in Gastrointestinal Applications:
Undecylprodigiosin is used as an antiulcer agent, helping to alleviate the symptoms of ulcers and promote healing in the gastrointestinal tract. Its antiulcer activity contributes to its potential use in the development of medications for treating ulcer-related conditions.
Used in Cancer Research:
Undecylprodigiosin is used as an apoptotic agent in cancer research, due to its ability to induce programmed cell death in cancer cells. This characteristic makes it a valuable tool for studying the mechanisms of apoptosis and for the development of novel anticancer therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 52340-48-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,4 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52340-48:
(7*5)+(6*2)+(5*3)+(4*4)+(3*0)+(2*4)+(1*8)=94
94 % 10 = 4
So 52340-48-4 is a valid CAS Registry Number.
52340-48-4Relevant articles and documents
Pyrrole-singlet oxygen reactions leading to α,α'-bipyrroles. Synthesis of prodigiosin and analogs
Wasserman, Harry H.,Petersen, Anders K.,Xia, Mingde,Wang, Jianji
, p. 7587 - 7589 (1999)
Reaction of the tert-butyl ester of 3-methoxy-2-pyrrolecarboxylic acid with singlet oxygen yields a hydroperoxide intermediate which undergoes coupling with pyrroles to yield precursors of prodigiosin and ring A analogs, readily convertible to the corresponding tripyrromethenes.