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11.
Srinivasa Rao Dasari Subbaiah Tondepu Lakshmana Rao Vadali Mutyala Naidu Ganivada Nareshvarma Seelam 《Journal of heterocyclic chemistry》2019,56(1):195-208
In this research article, a highly efficient, cost‐effective synthesis of various hybrid molecules possessing 1,2,3‐triazolyltetrazoles and evaluation of their biological activity have been addressed. The structure elucidation of these new library hybrid molecules has been carried out by IR, 1H NMR, 13C NMR, and mass spectral analysis. The compounds have been screened for their anticancer activity against human colon cancer cell line Colo‐205 and human lung cancer cell line HOP‐205, and the results attest that most of the compounds have shown very good therapeutic nature. In particular, compounds 3d , 3j , 6a , and 6e were more cytotoxic than Adriamycin against all tested human cancer cell lines with 68%, 101.8%, 94%, and 104.5% growth, respectively. In the present investigation, a series of 3a – j and 6a – h were subjected to molecular properties prediction, drug likeness by Molinspiration, and toxicity risks by Molsoft software programs. All the 18 analogues were chosen on the basis of Lipinski “Rule of five” for the synthesis, screening their antibacterial and anticancer as oral bioavailable drugs/leads. 相似文献
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Endoori Srinivas anna Venkateswara Rao Gulipalli Kali Charan Bodige Srinu Pommidi Anil Kumar Surapureddi Sri Ramakrishna Seelam Nareshvarma 《Russian Journal of General Chemistry》2022,92(9):1775-1784
Russian Journal of General Chemistry - A novel series of imidazo[1,2-a]pyridine linked 1,2,3-triazole derivatives has been designed, synthesized and the structures have been confirmed by 1H and 13C... 相似文献
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Selective Synthesis of Single‐ and Multi‐Walled Supramolecular Nanotubes by Using Solvophobic/Solvophilic Controls: Stepwise Radial Growth via “Coil‐on‐Tube” Intermediates
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Dr. Seelam Prasanthkumar Dr. Wei Zhang Prof. Dr. Wusong Jin Prof. Dr. Takanori Fukushima Prof. Dr. Takuzo Aida 《Angewandte Chemie (International ed. in English)》2015,54(38):11168-11172
Novel hexa‐peri‐hexabenzocoronene (HBC) derivatives, FHBC and FHBC*, which carry perfluoroalkyl segments on one side of the HBC core and long alkyl tails on the other, were synthesized. Their perfluoroalkyl segments are highly solvated in C6F6 (solvophilic effect) and do not assemble, whereas in CH2Cl2, they are excluded (solvophobic effect) and assemble together consequently. For example, the use of C6F6 and CH2Cl2 as assembling media for FHBC leads to the selective formation of single‐ and multi‐walled nanotubes, respectively. When a higher monomer concentration is applied in CH2Cl2, multi‐walled nanotubes with a larger number of walls result. FHBC in CH2Cl2 self‐assembles rather slowly, thereby allowing for the observation of coil‐on‐tube structures, which are possible intermediates for the stepwise radial growth of the nanotubular wall. Casting of the multi‐walled nanotubes onto a quartz plate yields a superhydrophobic thin film with a water contact angle of 161±2°. 相似文献
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Thipanni Anitha Madoori Mrinalini Damera Vani Seelam Prasanthkumar Kallu Rajender Reddy Lingamallu Giribabu 《Photochemistry and photobiology》2020,96(6):1182-1190
Herein, we report the versatile synthetic strategy and opto-electronic properties for the phosphorylation of BODIPY derivatives 5aa - 5ak by substituting with an electron-donating/withdrawing group at the ortho position. Nevertheless, this new methodology relatively promotes the tolerance of the aldehyde moiety and the high yield for the synthesis of BODIPY o-OPhos derivatives. The photophysical studies suggest improved optical properties due to the inductive effect of various electron-donating/withdrawing groups. The UV-visible and the emission data suggest that BODIPY o-OPhos derivatives emphasize the property of the excited states with an increase in fluorescence intensity and high quantum yields due to the presence of bulky phospsho-triester at the meso- position which hinders the free rotation around the C-Ar bond and facilitates the development of OLEDs and various organophosphorus warfare agents. Electrochemical studies reveal 5ak depicts the ease of redox activity amongst the 5aa - 5ak derivatives. The density functional theory indicates the highest occupied molecular orbital on the BODIPY moiety whereas the lowest unoccupied molecular orbital delocalized on BODIPY and the phospho-triester moieties. Thus, the unique development of the novel BODIPY derivatives with improved optical and redox properties pave the way for fluorescent probes and bioimaging techniques. 相似文献
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Gulipalli K. C. Ravula P. Bodige S. Endoori S. Cherukumalli P. K. R. Narendra Sharath Chandra J. N. Seelam N. 《Russian Journal of General Chemistry》2019,89(7):1502-1512
Russian Journal of General Chemistry - A novel series of thiophene-2-carboxamide derivatives are designed and synthesized, and their structures are confirmed by 1H and 13C NMR, and mass spectra.... 相似文献
16.
Unprecedented Charge‐Transfer Complex of Fused Diporphyrin as Near‐Infrared Absorption‐Induced High‐Aspect‐Ratio Nanorods
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B. Shivaprasad Achary Dr. Sabapathi Gokulnath Samrat Ghosh Madoori Mrinalini Dr. Seelam Prasanthkumar Dr. Lingamallu Giribabu 《化学:亚洲杂志》2016,11(24):3498-3502
Charge‐transfer (CT) complexes of near‐infrared absorbing systems have been unknown until now. Consequently, structural similarities between donor and acceptor are rather important to achieve this phenomenon. Herein, we report electron donors such as non‐fused diporphyrin‐anthracene (DP), zinc diporphyrin‐anthracene (ZnDP) and fused zinc diporphyrin‐anthracene (FZnDP) in which FZnDP absorbs in NIR region and permits a CT complex with the electron acceptor, perylene diimide (PDI ) in CHCl3 exclusively. UV/Vis‐NIR absorption, 1H NMR, NOESY and powder X‐ray diffraction analysis demonstrated that the CT complex formation occurs by π–π stacking between perylene units in FZnDP and PDI upon mixing together in a 1:1 molar concentration in CHCl3, unlike non‐fused ZnDP and DP. TEM and AFM images revealed that the CT complex initially forms nanospheres leading to nanorods by diffusion of CH3OH vapors into the CHCl3 solution of FZnDP/PDI (1:1 molar ratio). Therefore, these CT nanorods could lead to significant advances in optical, biological and ferroelectric applications. 相似文献
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Gulipalli K. Ch. Ravula P. Bodige S. Endoori S. Cherukumalli P. Koteswara Rao Chandra J. N. Narendra Sharath Seelam N. 《Russian Journal of General Chemistry》2020,90(7):1336-1344
Russian Journal of General Chemistry - A new series of urea and thiourea bearing thiophene-2-carboxalate derivatives has been designed against protein tyrosine phosphatase 1B (PTP1B) active site,... 相似文献
18.
LC‐MS/MS assay for the determination of lurasidone and its active metabolite,ID‐14283 in human plasma and its application to a clinical pharmacokinetic study
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Mahitej Yadav Katteboina Nageswara Rao Pilli Ramesh Mullangi Raghunadha Reddy Seelam Shobha Rani Satla 《Biomedical chromatography : BMC》2016,30(7):1065-1074
The authors proposed a sensitive, selective and rapid liquid chromatography–tandem mass spectrometric (LC‐MS/MS) assay procedure for the quantification of lurasidone and its active metabolite, i.e. ID‐14283 in human plasma simultaneously using corresponding isotope labeled compounds as internal standards as per regulatory guidelines. After liquid–liquid extraction with tert‐butyl methyl ether, the analytes were chromatographed on a C18 column using an optimized mobile phase composed of 5 mm ammonium acetate (pH 5.0) and acetonitrile (15:85, v/v) and delivered at a flow rate of 1.00 mL/min. The assay exhibits excellent linearity in the concentration ranges of 0.25–100 and 0.10–14.1 ng/mL for lurasidone and ID‐14283, respectively. The precision and accuracy results over five concentration levels in four different batches were well within the acceptance limits. Lurasidone and ID‐14283 were found to be stable in battery of stability studies. The method was rapid with the chromatographic run time 2.5 min, which made it possible to analyze 300 samples in a single day. Additionally, this method was successfully used to estimate the in vivo plasma concentrations of lurasidone and ID‐14283 obtained from a pharmacokinetic study in south Indian male subjects and the results were authenticated by conducting incurred samples reanalysis. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
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Srinivasa Rao Dasari Subbaiah Tondepu Lakshmana Rao Vadali Nareshvarma Seelam 《Journal of heterocyclic chemistry》2019,56(4):1318-1329
A novel series of 1,4‐disubstituted‐1,2,3‐triazole derivatives 3a – l and 5a – i were one‐pot synthesized via CuAAC‐alkyne click chemistry and evaluated for their antibacterial activity against four organisms and screened for their anticancer activity against human colon cancer cell line HT‐29 and human lung cancer cell line HTB‐29. These hybrid molecules structure elucidation has been performed by IR, 1H‐NMR, 13C‐NMR, and mass spectral analysis. Synthesized nonsteroidal anti‐inflammatory drugs‐triazoles evaluated for their antibacterial activities against bacterial microorganisms Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus, and Klebsiella pneumonia. Final compounds 3i , 3c , and 5b showed magnificent broad spectrum activity against P. aeruginosa, K. pneumonia, E. coli, and S. aureus with zone of inhibition values of 20, 15, 17, and 16 mm, respectively. Among the series of compound, 3j showed the best antibacterial activity against all the strains. Further, the compounds 3i and 5a were more cytotoxic than cisplatin against all tested two human cancer cell lines, with 50.8%, and 52.3% and 73.4% and 75.3% of growth, respectively. The synthesized compounds were tested for kinase inhibitory activity against glycogen synthase kinase‐3 protein kinases, in addition, for cytotoxic activity against two different human cancer cell lines. 相似文献