Zobrazeno 1 - 10
of 79
pro vyhledávání: '"Banoth Karan, Kumar"'
Autor:
Raja Rajeswari Rajeshkumar, Banoth Karan Kumar, Pavadai Parasuraman, Theivendren Panneerselvam, Krishnan Sundar, Damodar Nayak Ammunje, Sureshbabu Ram Kumar Pandian, Sankaranarayanan Murugesan, Shanmugampillai Jeyarajaguru Kabilan, Selvaraj Kunjiappan
Publikováno v:
BioImpacts, Vol 12, Iss 6, Pp 487-499 (2022)
Introduction: Parkinson's disease (PD) is a chronic, devastating neurodegenerative disorder marked by the death of dopaminergic neurons in the midbrain's substantia nigra pars compacta (Snpc). In alpha-synuclein (α-Syn) self-aggregation, the existen
Externí odkaz:
https://doaj.org/article/cd505d2b5bcc44ea9ee8d112fea87fac
Autor:
Faheem, Sanchita Dey, Samridhi Johri, M. Abirami, Banoth Karan Kumar, Donatella Taramelli, Nicoletta Basilico, Rafael Balana-Fouce, Kondapalli Venkata Gowri Chandra Sekhar, Sankaranarayanan Murugesan
Publikováno v:
European Journal of Medicinal Chemistry Reports, Vol 4, Iss , Pp 100031- (2022)
Infections caused by protozoan parasites continue to be a significant cause of morbidity and mortality across the globe, with malaria and leishmaniasis forming the fulcrum of these infections. Decreased effectiveness of existing drugs and increasing
Externí odkaz:
https://doaj.org/article/04cea1591d5341f79d36b1e8e9bd65f4
Autor:
Banoth, Karan Kumar, Faheem, ChandraSekhar, Kondapalli Venkata Gowri, Adinarayana, Nandikolla, Murugesan, Sankaranarayanan
Publikováno v:
In Heliyon September 2020 6(9)
Autor:
Vinuta Kamat, Rangappa Santosh, Boja Poojary, Suresh P. Nayak, Banoth Karan Kumar, Murugesan Sankaranarayanan, Faheem, Sheela Khanapure, Delicia Avilla. Barretto, Shyam K. Vootla
Publikováno v:
ACS Omega, Vol 5, Iss 39, Pp 25228-25239 (2020)
Externí odkaz:
https://doaj.org/article/bcdbba759aa5402e91bb01af2f09eea4
Autor:
Joseph Christina Rosy, Ewa Babkiewicz, Piotr Maszczyk, Piotr Mrówka, Banoth Karan Kumar, Sankaranarayanan Murugesan, Selvaraj Kunjiappan, Krishnan Sundar
Publikováno v:
Biomolecules, Vol 12, Iss 7, p 887 (2022)
Pseudomonas aeruginosa is an opportunistic pathogen that can cause acute and severe infections. Increasing resistance to antibiotics has given rise to the urgent need for an alternative antimicrobial agent. A promising strategy is the inhibition of i
Externí odkaz:
https://doaj.org/article/b33bb7134ec34dd488a4225957f68456
Autor:
Kondapalli Venkata Gowri Chandra Sekhar, Sankaranarayan Murugesan, Snehal Rajkumar Jadhav, Banoth Karan Kumar, Renuka Parshuram Joshi, Chougule Kishor Suryakant, Ala Chandu, Mohammed Muzaffar-Ur-Rehman, Yogesh Mahadu Khetmalis, Adinarayana Nandikolla
Publikováno v:
Current Topics in Medicinal Chemistry. 23:713-735
Abstract: Tropical, vector-borne, and neglected diseases with a limited number of medication ther-apies include Leishmaniasis, Malaria, Chagas and Human African Trypanosomiasis (HAT). Chro-mones are a large class of heterocyclic compounds with signif
Autor:
Penta Ashoka, Faheem, Murugesan Sankaranarayanan, Banoth Karan Kumar, Kondapalli Venkata Gowri Chandra Sekhar, Subhash Chander
Publikováno v:
Medicinal Chemistry. 18:629-654
Background: From time immemorial, natural products have been used for the treatment of various diseases. Various natural products, their semisynthetic derivatives, and synthetic analogs have been explored for their anti-infective properties. One such
Publikováno v:
Structural Chemistry. 33:2063-2082
Autor:
M. Abirami, Banoth Karan Kumar, null Faheem, Sanchita Dey, Samridhi Johri, Rosa M. Reguera, Rafael Balaña-Fouce, Kondapalli Venkata Gowri Chandra Sekhar, Murugesan Sankaranarayanan
Publikováno v:
European Journal of Medicinal Chemistry. 257:115471
Autor:
Yogesh Mahadu Khetmalis, Surendar Chitti, Anjani Umarani Wunnava, Banoth Karan Kumar, Muthyala Murali Krishna Kumar, Sankaranarayanan Murugesan, Kondapalli Venkata Gowri Chandra Sekhar
Publikováno v:
RSC Medicinal Chemistry. 13:327-342
34 imidazo[1,2-a]pyridine amides & sulfonamides are synthesized & evaluated for in vitro anti-TB activity against MTB H37Rv. IPA-6 is most potent with MIC 0.05 μg mL−1 & 125 times active than ethambutol & docked to MTB enoyl acyl protein reductase