Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Richa Kaur Bhatia"'
Autor:
Ruchika Garg, Richa Kaur Bhatia, Manmohan Yadav, Satyavathi Kancherla, Lakhwinder Singh, Jitender Madan, Maninder Kaur, Evans C. Coutinho, Raghuvir R. S. Pissurlenkar
Publikováno v:
Medicinal Chemistry. 16:212-228
Background: Novel 4-[3-(6/7/8-Substituted 4-Oxo-4H-chromen-3-yl)acryloyl]phenylboronic acid derivatives (5a-h) as well as other 6/7/8-substituted-3-(3-oxo-3-(4-substitutedphenyl) prop-1-enyl)-4H-chromen-4-one derivatives (3a-u) have been designed as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f8dab3e08f34ba778000d323ca2c515
https://doi.org/10.2174/1573406415666190531123751
https://doi.org/10.2174/1573406415666190531123751
Autor:
Richa Kaur Bhatia
Publikováno v:
Current Bioactive Compounds. 15:280-288
The aim of this literature review is to compile data of heterocyclic antigiardial agents. The importance is to analyze the structural requirements for improved antigiardial activity, to overcome resistance and enhance the bioavailability of the compo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::406b695c7335cc647a29e8d93db4e343
https://doi.org/10.2174/1573407214666180201154009
https://doi.org/10.2174/1573407214666180201154009
Autor:
Kiran Jyoti, Evans C. Coutinho, Upendra Kumar Jain, Ramesh Chandra, Elvis A. F. Martis, Richa Kaur Bhatia, Jitender Madan
Publikováno v:
Colloids and Surfaces B: Biointerfaces. 148:674-683
In present investigation, initially curcumin was complexed with 2-HP-β-CD (curcumin-2-HP-β-CD-complex) in 1:1 ratio and later amalgamated with chitosan microspheres (curcumin-2-HP-β-CD-CMs) for selective delivery in colon only through oral route o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abf231af563b9dc9048a418fbb9ae858
https://doi.org/10.1016/j.colsurfb.2016.09.044
https://doi.org/10.1016/j.colsurfb.2016.09.044
Autor:
Richa Kaur Bhatia
Publikováno v:
Current Topics in Medicinal Chemistry. 17:189-207
Isoindole derivatives constitute an important class of biologically active heterocyclic compounds and continue to attract considerable attention due to their diverse pharmacological profile such as, antimicrobial, anthelmintic, insecticidal, cyclooxy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a42477190019ebd57128d219cabf5025
https://doi.org/10.2174/1568026616666160530154100
https://doi.org/10.2174/1568026616666160530154100
Autor:
Jitender, Madan, Richa Kaur, Bhatia
Publikováno v:
Current topics in medicinal chemistry. 17(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85bf8d7dc3df6fe101b9d21a69c20a90
https://pubmed.ncbi.nlm.nih.gov/28093979
https://pubmed.ncbi.nlm.nih.gov/28093979
Autor:
Manveet Kaur, Ramesh Chandra, Evans C. Coutinho, Richa Kaur Bhatia, Jitender Madan, Upendra Kumar Jain, Om Prakash Katare, Raghuvir R. S. Pissurlenkar
Publikováno v:
Carbohydrate Polymers. 101:614-622
Telmisartan (TEL) requires superior bioavailability in cancer cell compartments. To meet these challenges, we have synthesized a 2-HP-β-CD-TEL complex with stability constant (Kc) of 2.39 × 10(-3)mM. The absence in the FTIR spectrum of 2-HP-β-CD-T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1accd76f61176e37deced14a2f521630
https://doi.org/10.1016/j.carbpol.2013.09.077
https://doi.org/10.1016/j.carbpol.2013.09.077
Autor:
Richa Kaur Bhatia, Richa Puri, Jitender Madan, Om Prakash Katare, Upendra Kumar Jain, Ravi Shankar Pandey
Publikováno v:
Drug development and industrial pharmacy. 42(12)
Recently, the anticancer activity of telmisartan (TEL) has been discovered against prostate cancer. Nevertheless, despite favorable therapeutic profile, poor aqueous solubility and suboptimal oral bioavailability hamper the anticancer efficacy of TEL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e5cef306b96f593b490a4858a08b560
https://pubmed.ncbi.nlm.nih.gov/27184705
https://pubmed.ncbi.nlm.nih.gov/27184705
Autor:
Sanjiv Kumar, Ramanjot Kaur, Richa Kaur Bhatia, Harinder Singh, Sandeep Batra, Aakash Deep, Pran Kishore Deb, Dinesh Kaushik, Upendra Kumar Jain
Publikováno v:
Current topics in medicinal chemistry. 17(2)
Imidazo[1,2-a]pyridine is one of the most potential bicyclic 5-6 heterocyclic rings that is recognized as a "drug prejudice" scaffold due to its broad range of applications in medicinal chemistry such as anticancer, antimycobacterial, antileishmanial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6aaad4c8661914ba6fadf616cd71259f
https://pubmed.ncbi.nlm.nih.gov/27237332
https://pubmed.ncbi.nlm.nih.gov/27237332
Autor:
Ajit Kumar Saxena, Mohan Paul S. Ishar, Ashish Kapur, Tilak Raj, Richa Kaur Bhatia, Madhunika Sharma
Publikováno v:
European Journal of Medicinal Chemistry. 45:790-794
6/6,7-Substituted-3-formylchromones (8a-g) were reacted with 2 equivalents thiobenzamide (9) in refluxing toluene to furnish substituted-3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones (10a-g) in high yields. Similarly, when substituted-2-anilino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a95993b728b86a3d34817980ffeaee7c
https://doi.org/10.1016/j.ejmech.2009.11.001
https://doi.org/10.1016/j.ejmech.2009.11.001
Autor:
Richa Kaur Bhatia, Vivek K. Gupta, Tilak Raj, Rakesh Kumar Sharma, Deepak Sharma, Mohan Paul S. Ishar
Publikováno v:
European Journal of Medicinal Chemistry. 44:3209-3216
6/6,7-Substituted 3-formylchromones (9a-e) react with 2 equivalents of 2-phenyl-4-dimethylamino-1-thia-3-azabuta-1,3-diene (10) or thiobenzamide (11) in refluxing toluene to furnish novel substituted 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24dc2cc80cce883c8f54b3988de52301
https://doi.org/10.1016/j.ejmech.2009.03.030
https://doi.org/10.1016/j.ejmech.2009.03.030