Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Yoganjaneyulu Kasetti"'
Enhanced noscapine delivery using estrogen-receptor-targeted nanoparticles for breast cancer therapy
Autor:
Jitender Madan, Upendra Kumar Jain, Prasad V. Bharatam, Sushma R. Gundala, Anju Katyal, Yoganjaneyulu Kasetti, Ritu Aneja
Publikováno v:
Anti-Cancer Drugs. 25:704-716
Noscapine (Nos), an orally available plant-derived antitussive alkaloid, is in phase II clinical trials for cancer chemotherapy. It has extensively been shown to inhibit tumor growth in nude mice bearing human xenografts of hematopoietic, breast, lun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3313e90ff8fce76777da00d1f1338ebc
https://doi.org/10.1097/cad.0000000000000098
https://doi.org/10.1097/cad.0000000000000098
Publikováno v:
European Journal of Organic Chemistry. 2012:1746-1752
The regioselective ring lithiation of BF3-complexed 3-picoline (1a), 3,4-lutidine (1b), and 3,5-lutidine (1c) was studied. The dilithiation of 1a, 1b, and 1c was also investigated to experimentally explore the relative preference of the sites on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5add46ed9f661cf3e4e35ccb04b084c
https://doi.org/10.1002/ejoc.201101592
https://doi.org/10.1002/ejoc.201101592
Publikováno v:
Journal of Physical Organic Chemistry. 25:649-657
Ab initio and semi-empirical calculations were performed on the monomers, dimers and tetramers of the antidiabetic drug nateglinide to understand the conformational preferences and to explore their possible relation with polymorphism. The reported cr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb6ee0df05fcd91303819bf8d69ab0a9
https://doi.org/10.1002/poc.1956
https://doi.org/10.1002/poc.1956
Publikováno v:
Talanta. 83:644-650
Reaction of N-methylpyrrole and 7,7,8,8-tetracyanoquinodimethane (TCNQ) furnishes an intense blue unsymmetrical charge-transfer compound through regioselective attachment of tricyanoquinodimethane at the 2-position of N-methylpyrrole which was found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2be6c8cb29e8987d0174bc370cd4f576
https://doi.org/10.1016/j.talanta.2010.10.019
https://doi.org/10.1016/j.talanta.2010.10.019
Publikováno v:
The Journal of Physical Chemistry B. 114:11603-11611
Quantum chemical calculations have been performed using HF, B3LYP, and MP2 methods on the model sulfonylurea PhSO(2)NHC(=O)NHMe to understand the conformational and tautomeric preferences. The results indicate that a conformer with intramolecular hyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8c8872e0ddc4b1778e2e43b8fc5af8a
https://doi.org/10.1021/jp101327k
https://doi.org/10.1021/jp101327k
Autor:
Vítor Félix, Paula Brandão, Sonam Bhatia, Jaspreet S. Dhau, Amritpal Singh, Kamal N. Singh, Parsad V. Bharatam, Yoganjaneyulu Kasetti
Publikováno v:
ChemInform. 45
Complexation of pyridines (I) with BF3 allows the regioselective 2,6-dilithiation or 2-lithiation with LDA.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10a4cbb504e446c5582815eebd63a377
https://doi.org/10.1002/chin.201417160
https://doi.org/10.1002/chin.201417160
Autor:
Vítor Félix, Yoganjaneyulu Kasetti, Amritpal Singh, Kamal Nain Singh, Jaspreet S. Dhau, Paula Brandão, Sonam Bhatia, Parsad V. Bharatam
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
The BF3-directed lithiation of 3-chloro- and 3-bromopyridine (1a and 1b, espectively) has been investigated. The reactions of 3-chloro- or 3-bromopyridine-BF3 adduct with LDA (1.3/1.1 equiv) followed by quenching with benzaldehyde or iodine exclusive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3e63a2955f33c1255fd2ccd334255c5
http://hdl.handle.net/10773/20938
http://hdl.handle.net/10773/20938
Publikováno v:
Journal of molecular modeling. 19(4)
Several therapeutically important compounds contain guanylurea (GU) moiety. The appropriate tautomeric state of these species has not been explored, preliminary studies indicated that the traditional representation of this class of compounds use a hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a9d6aa9ce66fe2fd2b39d691190b7bb
https://pubmed.ncbi.nlm.nih.gov/23325568
https://pubmed.ncbi.nlm.nih.gov/23325568
Publikováno v:
The journal of physical chemistry. A. 116(36)
Several medicinally important compounds carry a 2-(thiazol-2-yl)guanidine unit. These species are generally (erroneously) represented as 1-(thiazol-2-yl)guanidine species. Quantum chemical studies were performed to identify the appropriate tautomeric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7bec7d47eb77590779d58ba794239d0
https://pubmed.ncbi.nlm.nih.gov/22920939
https://pubmed.ncbi.nlm.nih.gov/22920939
Publikováno v:
ChemInform. 43
Monolithiation—electrophilic substitution of BF3-complexed methylpyridines (I) proceeds exclusively at position 6 of the pyridine ring, leaving the methyl groups unsubstituted.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdff945e7024469e65372aec2625dc34
https://doi.org/10.1002/chin.201233161
https://doi.org/10.1002/chin.201233161