KUMAR, S Pranush, Tarang JADAV, Amit Kumar SAHU, Moumita Ghosh CHOWDHARY, Ankit SIWACH, Harit PATEL, Sagarkumar PATEL, Niraj RAJPUT, Amit SHARD, Amit Suresh KHAIRNAR a Pinaki SENGUPTA. Assessment of metabolic stability and pharmacokinetics by LC-MS/MS and establishment of the safe dose of IMID-2, a novel anticancer molecule under drug discovery. BIOMEDICAL CHROMATOGRAPHY. HOBOKEN: WILEY, 2023, roč. 37, č. 6, s. 1-8. ISSN 0269-3879. Dostupné z: https://dx.doi.org/10.1002/bmc.5618.
Další formáty:   BibTeX LaTeX RIS
Základní údaje
Originální název Assessment of metabolic stability and pharmacokinetics by LC-MS/MS and establishment of the safe dose of IMID-2, a novel anticancer molecule under drug discovery
Autoři KUMAR, S Pranush, Tarang JADAV, Amit Kumar SAHU, Moumita Ghosh CHOWDHARY, Ankit SIWACH, Harit PATEL, Sagarkumar PATEL, Niraj RAJPUT, Amit SHARD, Amit Suresh KHAIRNAR (356 Indie, domácí) a Pinaki SENGUPTA (garant).
Vydání BIOMEDICAL CHROMATOGRAPHY, HOBOKEN, WILEY, 2023, 0269-3879.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30104 Pharmacology and pharmacy
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 1.800 v roce 2022
Kód RIV RIV/00216224:14110/23:00130692
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1002/bmc.5618
UT WoS 000955749900001
Klíčová slova anglicky acute oral toxicity; IMID-2; LC-MS; MS; metabolic stability; pharmacokinetics
Štítky 14110515, rivok
Příznaky Mezinárodní význam, Recenzováno
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 2. 2. 2024 11:45.
Anotace
Pyruvate kinase (PK) M2 activators ramp up glycolysis in cancer cells, leading to a reversal of the Warburg effect in cancer cells. A promising PKM2 activator molecule, IMID-2, developed by the National Institute of Pharmaceutical Education and Research-Ahmedabad showed promising anticancer activity against MCF-7 and COLO-205 cell lines, which represent breast and colon cancer. Its physicochemical properties, like solubility, ionization constant, partition coefficient and distribution constant, have already been established. Its metabolic pathway is also well established through in vitro and in vivo metabolite profiling and reported previously. In this study, we have evaluated the metabolic stability of IMID-2 using LC-MS/MS and investigated the safety aspect of the molecule through an acute oral toxicity study. In vivo studies in rats confirmed that the molecule is safe even at a dose level of 175 mg/kg. Furthermore, a pharmacokinetic study of IMID-2 was also carried out using LC-MS/MS to understand its absorption, distribution, metabolism, and excretion profile. The molecule was found to have promising bioavailability through the oral route. This research work is thus another step in the drug testing of this promising anticancer molecule. The molecule can be considered to be a potential anticancer lead based on the earlier report substantiated by current findings.
VytisknoutZobrazeno: 9. 7. 2024 10:58