المؤلفون: Gowda, Darshini, Vinay Kumar, D.C., Gowda, Byresh, Chethan, B.S., Harsha, K.B., Shalini, V., Sudhanva, M.S., Shobith, R., Rangappa, K.S.

المصدر: Journal of Molecular Structure ; volume 1330, page 141489 ; ISSN 0022-2860

الاتاحة: https://doi.org/10.1016/j.molstruc.2025.141489
https://api.elsevier.com/content/article/PII:S0022286025001784?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0022286025001784?httpAccept=text/plain

المؤلفون: Dogga, Bhushanarao, Reddy, Eeda Koti, Sharanya, C.S., Abhithaj, J., Arun, K.G., Ananda Kumar, C.S., Rangappa, K.S.

المساهمون: Vignan's Foundation for Science Technology and Research University

المصدر: European Journal of Medicinal Chemistry Reports ; volume 6, page 100094 ; ISSN 2772-4174

الاتاحة: http://dx.doi.org/10.1016/j.ejmcr.2022.100094
https://api.elsevier.com/content/article/PII:S2772417422000668?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S2772417422000668?httpAccept=text/plain

المؤلفون: Vinay Kumar, D.C., Chethan, B.S., V．, Shalini, Rangappa, K.S., Lokanath, N.K.

المصدر: Journal of Molecular Structure ; volume 1297, page 136976 ; ISSN 0022-2860

الاتاحة: http://dx.doi.org/10.1016/j.molstruc.2023.136976
https://api.elsevier.com/content/article/PII:S0022286023020665?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0022286023020665?httpAccept=text/plain

المؤلفون: Malojirao, V.H., Girimanchanaika, S.S., Shanmugam, Muthu K., Sherapura, A., Dukanya, Metri, P.K., Vigneshwaran, V., Chinnathambi, A., Alharbi, S.A., Rangappa, S., Mohan, C.D., Basappa, Prabhakar, B.T., Rangappa, K.S.

المساهمون: PHARMACOLOGY

المصدر: Scopus OA2020

مصطلحات موضوعية: Antitumor, Apoptosis, Lung cancer, STAT3

Relation: Malojirao, V.H., Girimanchanaika, S.S., Shanmugam, Muthu K., Sherapura, A., Dukanya, Metri, P.K., Vigneshwaran, V., Chinnathambi, A., Alharbi, S.A., Rangappa, S., Mohan, C.D., Basappa, Prabhakar, B.T., Rangappa, K.S. (2020). Novel 1,3,4-oxadiazole targets STAT3 signaling to induce antitumor effect in lung cancer. Biomedicines 8 (9) : 368. ScholarBank@NUS Repository. https://doi.org/10.3390/BIOMEDICINES8090368; https://scholarbank.nus.edu.sg/handle/10635/197503

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/197503

المؤلفون: Somu, C., Mohan, C.D., Ambekar, S., Dukanya, Rangappa, S., Baburajeev, C.P., Sukhorukov, A., Mishra, S., Shanmugam, M.K., Chinnathambi, A., Awad Alahmadi, T., Alharbi, S.A., Basappa, Rangappa, K.S.

المساهمون: DEPT OF PHARMACOLOGY

المصدر: Scopus OA2020

مصطلحات موضوعية: Anticancer, DNA fragmentation, NF-?B, Oxazine

Relation: Somu, C., Mohan, C.D., Ambekar, S., Dukanya, Rangappa, S., Baburajeev, C.P., Sukhorukov, A., Mishra, S., Shanmugam, M.K., Chinnathambi, A., Awad Alahmadi, T., Alharbi, S.A., Basappa, Rangappa, K.S. (2020). Identification of a novel 1,2 oxazine that can induce apoptosis by targeting NF-κB in hepatocellular carcinoma cells. Biotechnology Reports 25 : e00438. ScholarBank@NUS Repository. https://doi.org/10.1016/j.btre.2020.e00438; https://scholarbank.nus.edu.sg/handle/10635/198937

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/198937

المؤلفون: Lee, J.H., Mohan, C.D., Deivasigamani, A., Jung, Y.Y., Rangappa, S., Basappa, S., Chinnathambi, A., Alahmadi, T.A., Alharbi, S.A., Garg, M., Lin, Z.-X., Rangappa, K.S., Sethi, G., Hui, K.M., Ahn, K.S.

المساهمون: DEPT OF PHARMACOLOGY, DUKE-NUS MEDICAL SCHOOL

المصدر: Scopus OA2020

مصطلحات موضوعية: Brusatol, EMT, HCC, Metastasis, Orthotopic mouse model

Relation: Lee, J.H., Mohan, C.D., Deivasigamani, A., Jung, Y.Y., Rangappa, S., Basappa, S., Chinnathambi, A., Alahmadi, T.A., Alharbi, S.A., Garg, M., Lin, Z.-X., Rangappa, K.S., Sethi, G., Hui, K.M., Ahn, K.S. (2020). Brusatol suppresses STAT3-driven metastasis by downregulating epithelial-mesenchymal transition in hepatocellular carcinoma. Journal of Advanced Research 26 : 83-94. ScholarBank@NUS Repository. https://doi.org/10.1016/j.jare.2020.07.004; https://scholarbank.nus.edu.sg/handle/10635/197971

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/197971

المؤلفون: Poh, H.M., Chiou, Y.S., Chong, Q.Y., Chen, R.-M., Rangappa, K.S., Ma, L., Zhu, T., Kumar, A.P., Pandey, V., Basappa, Department of Studies in Organic Chemistry, University of Mysore, Mysore, 570005, India., Lee, S.-C., Lobie, P.E.

المساهمون: CANCER SCIENCE INSTITUTE OF SINGAPORE, MEDICINE, INST OF MOLECULAR & CELL BIOLOGY

المصدر: Scopus OA2019

مصطلحات موضوعية: Acquired resistance, Apoptosis, Dose-dependent toxicity, Doxorubicin, Mammary carcinoma, PI3K/AKT, Trefoil factor 3 (TFF3)

Relation: Poh, H.M., Chiou, Y.S., Chong, Q.Y., Chen, R.-M., Rangappa, K.S., Ma, L., Zhu, T., Kumar, A.P., Pandey, V., Basappa, Department of Studies in Organic Chemistry, University of Mysore, Mysore, 570005, India., Lee, S.-C., Lobie, P.E. (2019). Inhibition of TFF3 enhances sensitivity—and overcomes acquired resistance—to doxorubicin in estrogen receptor-positive mammary carcinoma. Cancers 11 (10) : 1528. ScholarBank@NUS Repository. https://doi.org/10.3390/cancers11101528; https://scholarbank.nus.edu.sg/handle/10635/209544

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/209544

المؤلفون: Rangappa, K.S., Lee, J.H., Rangappa, S., Mohan, C.D., Basappa, Laboratory of Chemical Biology, Department of Studies in Organic Chemistry, University of Mysore, Manasagangotri, Mysore, 570006, India., Sethi, G., Lin, Z.-X., Ahn, K.S.

المساهمون: PHARMACOLOGY

المصدر: Scopus OA2019

مصطلحات موضوعية: Apoptosis, Brusatol, HNSCC, STAT3 inhibitor

Relation: Rangappa, K.S., Lee, J.H., Rangappa, S., Mohan, C.D., Basappa, Laboratory of Chemical Biology, Department of Studies in Organic Chemistry, University of Mysore, Manasagangotri, Mysore, 570006, India., Sethi, G., Lin, Z.-X., Ahn, K.S. (2019). Brusatol, a nrf2 inhibitor targets stat3 signaling cascade in head and neck squamous cell carcinoma. Biomolecules 9 (10) : 550. ScholarBank@NUS Repository. https://doi.org/10.3390/biom9100550; https://scholarbank.nus.edu.sg/handle/10635/209547

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/209547

المؤلفون: Lee, J.H., Mohan, C.D., Basappa, S., Rangappa, S., Chinnathambi, A., Alahmadi, T.A., Alharbi, S.A., Kumar, A.P., Sethi, G., Ahn, K.S., Rangappa, K.S.

المساهمون: CANCER SCIENCE INSTITUTE OF SINGAPORE, PHARMACOLOGY

المصدر: Scopus OA2019

مصطلحات موضوعية: ACHP, Cytotoxicity, NSCLC, STAT3 signaling inhibitor

Relation: Lee, J.H., Mohan, C.D., Basappa, S., Rangappa, S., Chinnathambi, A., Alahmadi, T.A., Alharbi, S.A., Kumar, A.P., Sethi, G., Ahn, K.S., Rangappa, K.S. (2019). The IκB kinase inhibitor ACHP targets the STAT3 signaling pathway in human non-small cell lung carcinoma cells. Biomolecules 9 (12) : 875. ScholarBank@NUS Repository. https://doi.org/10.3390/biom9120875; https://scholarbank.nus.edu.sg/handle/10635/206248

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/206248

المؤلفون: Mohan, C.D, Bharathkumar, H, Dukanya, Department of Studies in Organic Chemistry, University of Mysore, Mysore, India, Rangappa, S, Shanmugam, M.K, Chinnathambi, A, Alharbi, S.A, Alahmadi, T.A, Bhattacharjee, A, Lobie, P.E, Deivasigamani, A, Hui, K.M, Sethi, G, Basappa, Laboratory of Chemical Biology, Department of Chemistry, Bangalore University, Bangalore, India, Department of Studies in Organic Chemistry, University of Mysore, Mysore, India, Rangappa, K.S, Kumar, A.P

المساهمون: DEPT OF PHARMACOLOGY

المصدر: Unpaywall 20201031

مصطلحات موضوعية: 2 [3 (3 oxo 2h pyrido[3,2 b][1,4]oxazin 4(3h) yl)propyl]isoindoline 1,3 dione, 4 (2,6 dichlorobenzyl) 2h pyrido[3,2 b][1,4]oxazin 3(4h) one, 4 (4 isopropylbenzyl) 2h pyrido[3,2 b][1,4]oxazin 3(4h) one, 4 (4 nitrobenzyl) 2h pyrido [3,2 b][1,4]oxazin 3(4h) one, 4 (cyclohexylmethyl) 2h pyrido[3,2 b][1,4]oxazin 3(4h) one, 4 [(3 oxo 2h pyrido[3,2 b][1,4]oxazin 4(3h) yl)methyl]benzonitrile, 4 [(6,6 dimethyl 4 phenyl 5,6 dihydro 4h 1,2 oxazin 3 yl)methyl] 2h pyrido[3,2 b][1,4]oxazin 3(4h) one, 4 [4 (tert butyl)benzyl] 2h pyrido[3,2 b][1,4]oxazin 3(4h) one, 4 [[4 (4 chlorophenyl) 6,6 dimethyl 5,6 dihydro 4h 1,2 oxazin 3 yl]methyl] 2h pyrido[3,2 b][1,4]oxazin 3(4h) one, 4' [(3 oxo 2h pyrido[3,2 b][1,4]oxazin 4(3H) yl)methyl] [1,10 biphenyl] 2 carbonitrile, antineoplastic agent, DNA, immunoglobulin enhancer binding protein, liver protective agent, luciferase, transcription factor RelA, unclassified drug, animal experiment, animal model, animal tissue, antiproliferative activity, apoptosis, Article, cancer inhibition, cell viability, computer model, controlled study, dose response, down regulation, drug effect

Relation: Mohan, C.D, Bharathkumar, H, Dukanya, Department of Studies in Organic Chemistry, University of Mysore, Mysore, India, Rangappa, S, Shanmugam, M.K, Chinnathambi, A, Alharbi, S.A, Alahmadi, T.A, Bhattacharjee, A, Lobie, P.E, Deivasigamani, A, Hui, K.M, Sethi, G, Basappa, Laboratory of Chemical Biology, Department of Chemistry, Bangalore University, Bangalore, India, Department of Studies in Organic Chemistry, University of Mysore, Mysore, India, Rangappa, K.S, Kumar, A.P (2018). N-substituted pyrido-1,4-Oxazin-3-ones induce apoptosis of hepatocellular carcinoma cells by targeting NF-?B signaling pathway. Frontiers in Pharmacology 9 (NOV) : 1125. ScholarBank@NUS Repository. https://doi.org/10.3389/fphar.2018.01125; https://scholarbank.nus.edu.sg/handle/10635/181171

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/181171

المؤلفون: Bhuvanalakshmi, G, Basappa, Laboratory of Chemical Biology, Department of Chemistry, Bangalore University, Bangalore, India, Rangappa, K.S, Dharmarajan, A, Sethi, G, Kumar, A.P, Warrier, S

المساهمون: DEPT OF PHARMACOLOGY

المصدر: Unpaywall 20201031

مصطلحات موضوعية: aldehyde dehydrogenase, beta catenin, caspase 3, caspase 7, diosgenin, glycogen synthase kinase 3beta, Hermes antigen, reactive oxygen metabolite, secreted frizzled related protein 4, Wnt protein, antiangiogenic activity, antineoplastic activity, antiproliferative activity, apoptosis, Article, breast cancer cell line, cancer inhibition, cancer stem cell, cell cycle checkpoint, cell self-renewal, chick, controlled study, drug efficacy, embryo, epithelial mesenchymal transition, G0 phase cell cycle checkpoint, gene expression, loss of function mutation, migration inhibition, nonhuman

Relation: Bhuvanalakshmi, G, Basappa, Laboratory of Chemical Biology, Department of Chemistry, Bangalore University, Bangalore, India, Rangappa, K.S, Dharmarajan, A, Sethi, G, Kumar, A.P, Warrier, S (2017). Breast cancer stem-like cells are inhibited by diosgenin, a steroidal saponin, by the attenuation of the Wnt β-catenin signaling via the Wnt antagonist secreted frizzled related protein-4. Frontiers in Pharmacology 8 (MAR) : 124. ScholarBank@NUS Repository. https://doi.org/10.3389/fphar.2017.00124; https://scholarbank.nus.edu.sg/handle/10635/181291

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/181291

المؤلفون: Mahesha, Udaya Kumar, A.H., Vindya, K.G., Pampa, K.J., Rangappa, K.S., Lokanath, N.K.

المصدر: Journal of Molecular Structure ; volume 1250, page 131746 ; ISSN 0022-2860

الاتاحة: http://dx.doi.org/10.1016/j.molstruc.2021.131746
https://api.elsevier.com/content/article/PII:S0022286021018718?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0022286021018718?httpAccept=text/plain

المؤلفون: Sivaramakrishnan, V., Ilamathi, M., Girish, K.S., Kemparaju, K., Rangappa, K.S., Dhananjaya, Bhadrapura Lakkappa

المساهمون: Indo-European - Marie Curie IRSES -, DST Indo-Srilankan - DST- MTR

المصدر: Journal of Biomolecular Structure and Dynamics ; volume 35, issue 9, page 1979-1989 ; ISSN 0739-1102 1538-0254

الاتاحة: http://dx.doi.org/10.1080/07391102.2016.1203820
https://www.tandfonline.com/doi/pdf/10.1080/07391102.2016.1203820

المؤلفون: Shwetha, B, Sudhanva, M. Srinivasa, Jagadeesha, G.S, Thimmegowda, N.R, Hamse, Vivek K., Sridhar, B.T, Thimmaiah, K.N, Ananda Kumar, C.S, Shobith, Rangappa, Rangappa, K.S

المصدر: Bioorganic Chemistry ; volume 108, page 104586 ; ISSN 0045-2068

الاتاحة: http://dx.doi.org/10.1016/j.bioorg.2020.104586
https://api.elsevier.com/content/article/PII:S0045206820318848?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0045206820318848?httpAccept=text/plain

المؤلفون: Poloju, Sridhar, Cholkar, Kishore, K. Kouassi, Gilles, David Van Horn, J., Rangappa, K.S., M. Made Gowda, Netkal

المصدر: American Journal of Organic Chemistry ; volume 2, issue 3, page 58-62 ; ISSN 2163-1271

الاتاحة: http://dx.doi.org/10.5923/j.ajoc.20120203.04

المؤلفون: Rangappa, K.S.

المصدر: Alzheimer's & Dementia ; volume 5, issue 4S_Part_8 ; ISSN 1552-5260 1552-5279

الاتاحة: http://dx.doi.org/10.1016/j.jalz.2009.04.235
https://api.elsevier.com/content/article/PII:S1552526009003574?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1552526009003574?httpAccept=text/plain
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1016%2Fj.jalz.2009.04.235
https://onlinelibrary.wiley.com/doi/pdf/10.1016/j.jalz.2009.04.235
https://onlinelibrary.wiley.com/doi/full-xml/10.1016/j.jalz.2009.04.235

المؤلفون: Prasad, S.B. Benaka, Kumar, Y.C. Sunil, Kumar, C.S. Ananda, Sadashiva, C.T, Vinaya, K, Rangappa, K.S

المصدر: The Open Medicinal Chemistry Journal ; volume 1, issue 1, page 4-10 ; ISSN 1874-1045

الاتاحة: http://dx.doi.org/10.2174/1874104500701010004

المؤلفون: Dukanya, Shanmugam, Muthu K., Rangappa, S., Metri, P.K., Mohan, S., Basappa, Rangappa, K.S.

المساهمون: DEPT OF PHARMACOLOGY

المصدر: Scopus OA2020

مصطلحات موضوعية: Anti-cancer, Characterization, Indazole, MTT assay

Relation: Dukanya, Shanmugam, Muthu K., Rangappa, S., Metri, P.K., Mohan, S., Basappa, Rangappa, K.S. (2020). Anti-proliferative activity and characterization data on oxadiazole derivatives. Data in Brief 31 : 105979. ScholarBank@NUS Repository. https://doi.org/10.1016/j.dib.2020.105979; https://scholarbank.nus.edu.sg/handle/10635/197656

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/197656

المؤلفون: Narasimhamurthy, K.H., Girish, Y.R., Thimmaraju, N., Rangappa, K.S.

المساهمون: Department of Science and Technology, Ministry of Science and Technology, India, Council of Scientific and Industrial Research, India, University Grants Committee

المصدر: Chemical Data Collections ; volume 21, page 100230 ; ISSN 2405-8300

الاتاحة: http://dx.doi.org/10.1016/j.cdc.2019.100230
https://api.elsevier.com/content/article/PII:S2405830019300515?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S2405830019300515?httpAccept=text/plain

المؤلفون: Mohan, C.D, Anilkumar, N.C, Rangappa, S, Shanmugam, M.K, Mishra, S, Chinnathambi, A, Alharbi, S.A, Bhattacharjee, A, Sethi, G, Kumar, A.P, Basappa, Laboratory of Chemical Biology, Department of Chemistry, Bangalore University, Bangalore, India, Department of Studies in Organic Chemistry, University of Mysore, Mysore, India, Rangappa, K.S

المساهمون: CANCER SCIENCE INSTITUTE OF SINGAPORE, DEPT OF PHARMACOLOGY

المصدر: Unpaywall 20200831

Relation: Mohan, C.D, Anilkumar, N.C, Rangappa, S, Shanmugam, M.K, Mishra, S, Chinnathambi, A, Alharbi, S.A, Bhattacharjee, A, Sethi, G, Kumar, A.P, Basappa, Laboratory of Chemical Biology, Department of Chemistry, Bangalore University, Bangalore, India, Department of Studies in Organic Chemistry, University of Mysore, Mysore, India, Rangappa, K.S (2018). Novel 1,3,4-oxadiazole induces anticancer activity by targeting NF-κB in hepatocellular carcinoma cells. Frontiers in Oncology 8 (MAR) : 42. ScholarBank@NUS Repository. https://doi.org/10.3389/fonc.2018.00042; https://scholarbank.nus.edu.sg/handle/10635/176052

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/176052