Relevant bibliographies by topics / Curcumine – Analogues

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Curcumine – Analogues'

Author: Grafiati
Published: 8 June 2024
Last updated: 31 July 2025

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Journal articles on the topic "Curcumine – Analogues"

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Al-Asadi, Ali M., Salah S. Al-Luaibi, Basil A. Saleh, Mohammed A. Baashen, and Gamal A. El-Hiti. "Antioxidant Properties of Curcumin Analogues to Inhibit Thermal Degradation of Low-Density Polyethylene: Experimental and DFT Study." Journal of Chemistry 2022 (June 20, 2022): 1–6. http://dx.doi.org/10.1155/2022/5391296.

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Curcumin can be isolated from plants (Curcuma longa) and it belongs to the ginger family. It exhibits many useful properties and acts as an antioxidant. The aim of the current study was to prepare eight curcumin analogues and investigate their antioxidant activities to inhibit the thermal degradation of low-density polyethylene (LDPE). The carbonyl index (CI) was measured to test the effectiveness of the curcumin analogues. Various doses (0.5, 1, 2, 4, and 6% wt/wt) of a mixture containing LDPE and curcumin analogues were prepared, and the CI was measured. The eight curcumin analogues were fou
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Shanmugasundaram, P., D. Easwaramoorthy, J. Herbert Mabel, Srikanth Jeyabalan, and Chetan Ashok. "Synthesis, Characterization, in Silico and in vitro Screening of Anticancer Activity of Novel Curcumin Analogues." Asian Journal of Chemistry 36, no. 11 (2024): 2666–74. http://dx.doi.org/10.14233/ajchem.2024.32700.

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Global problem of cancer associated side effects with current chemotherapeutics and promising anticancer activity of curcumins, intended present study to carry out the synthesis of some new curcumin analogues using chromone aldehydes and cyclic ketones. The study involved in silico screening and in vitro anticancer evaluation of new synthesized compounds against the breast cancer cell line MDA-MB-231 using the MTT assay. All synthesized compounds exhibited significant cytotoxicity, with IC50 values ranging from 34.04 ± 0.05 µg to 43.96 ± 0.05 µg, comparable to the standard drug cisplatin (IC50
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Nocito, Marta Claudia, Arianna De Luca, Francesca Prestia, et al. "Antitumoral Activities of Curcumin and Recent Advances to ImProve Its Oral Bioavailability." Biomedicines 9, no. 10 (2021): 1476. http://dx.doi.org/10.3390/biomedicines9101476.

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Curcumin, a main bioactive component of the Curcuma longa L. rhizome, is a phenolic compound that exerts a wide range of beneficial effects, acting as an antimicrobial, antioxidant, anti-inflammatory and anticancer agent. This review summarizes recent data on curcumin’s ability to interfere with the multiple cell signaling pathways involved in cell cycle regulation, apoptosis and the migration of several cancer cell types. However, although curcumin displays anticancer potential, its clinical application is limited by its low absorption, rapid metabolism and poor bioavailability. To overcome t
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Yi, Yau Xin, Anand Gaurav, and Gabriel A. Akowuah. "Docking Studies of Curcumin and Analogues with Various Phosphodiesterase 4 Subtypes." Current Drug Discovery Technologies 17, no. 2 (2020): 248–60. http://dx.doi.org/10.2174/1570163815666181017091655.

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Introduction: The primary aim of this study is to understand the binding of curcumin and its analogues to different PDE4 subtypes and identify the role of PDE4 subtype inhibition in the anti-inflammatory property of curcumin. Docking analysis has been used to acquire the above mentioned structural information and this has been further used for designing of curcumin derivatives with better anti-inflammatory activity. Materials and Methods: Curcumin and its analogues were subjected to docking using PDE4A, PDE4B, PDE4C and PDE4D as the targets. A data set comprising 18 analogues of curcumin, was
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Cheng, Yatian, Jian Zhang, Yan Shao, et al. "Enzyme-Catalyzed Glycosylation of Curcumin and Its Analogues by Glycosyltransferases from Bacillus subtilis ATCC 6633." Catalysts 9, no. 9 (2019): 734. http://dx.doi.org/10.3390/catal9090734.

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Curcumin is a naturally occurring polyphenolic compound that is commonly used in both medicine and food additives, but its low aqueous solubility and poor bioavailability hinder further clinical applications. For assessing the effect of the glycosylation of curcumin on its aqueous solubility, two glycosyltransferase genes (BsGT1 and BsGT2) were cloned from the genome of the strain Bacillus subtilis ATCC 6633 and over-expressed in Escherichia coli. Then, the two glycosyltransferases were purified, and their glycosylation capacity toward curcumin and its two analogues was verified. The results s
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Athipornchai, Anan, Nattisa Niyomtham, Wachirachai Pabuprapap, et al. "Potent Tyrosinase Inhibitory Activity of Curcuminoid Analogues and Inhibition Kinetics Studies." Cosmetics 8, no. 2 (2021): 35. http://dx.doi.org/10.3390/cosmetics8020035.

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Natural tyrosinase inhibitors from herbal plants are promising therapeutic agents for skincare and cosmetic products. Natural curcuminoids exhibit weak antityrosinase properties. The structural modification of curcumin, the major curcuminoid from Curcuma longa, gave 14 analogues. The tyrosinase inhibitory activity of the natural curcuminoids and the modified analogues on both L-tyrosine and DOPA substrates were evaluated. The inhibition kinetics were also undertaken. For analogues with potent activity on the L-tyrosine substrate, the isoxazole analogue 12 and two reduced analogues, hexahydrocu
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Muhammad, Imran, Nadeem Muhammad, Khan Muhammad Asif, et al. "Curcumin and its allied analogues: epigenetic and health perspectives – a review." Czech Journal of Food Sciences 35, No. 4 (2017): 285–310. http://dx.doi.org/10.17221/584/2015-cjfs.

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Curcumin (diferuoyl methane) is a yellow active ingredient present in turmeric. It is a homodimer of feruloylmethane that comprises a hydroxyl and methoxy group (heptadiene with two Michael acceptors), and α-, β-diketone. It contains various metabolites, i.e. hexahydrocurcumin (HHC), tetrahydrocurcumin (THC), octahydrocurcumin (OHC), dihydrocurcumin (DHC), curcumin sulphate, and curcumin glucuronide. Curcumin has been proven the most effective histone deacetylase (HDAC) inhibitor in HeLa nuclear extracts. It has the ability to affect the Akt, growth factors, NF-kB, and metastatic and angiogeni
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Morais de Lima, Ednilza, Gabriel Antônio dos Santos, Khaled Hayek, José Jardes Da Gama Bitencourt, and Carolina Passarelli Gonçalves. "Biossíntese Dirigida pelo Precursor de Curcumina pela Curcuma longa L." Ensaios e Ciência C Biológicas Agrárias e da Saúde 25, no. 3 (2021): 357–60. http://dx.doi.org/10.17921/1415-6938.2021v25n3p357-360.

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O composto (E,E)-1,7-bis(4-hidroxi-3-metoxifenil)-1,6-heptadieno-3,5-diona, conhecido popularmente como curcumina, é um composto fitoquímico encontrado nos rizomas da Curcuma longa L. Esta substância já demonstrou diversas atividades terapêuticas importantes, como anti-inflamatória, antioxidante, antibacteriana, antiviral e antitumoral, por exemplo. Entretanto, apesar de ser o composto majoritário da via biossintética da Curcuma longa L. é descrito que apenas de 2 a 8% do peso total do rizoma, corresponde à quantidade de curcumina que pode ser extraída. Com o objetivo de estimular a biossíntes
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R, Thirumalaisamy. "Comparative Anti–Alzheimer’s Potential Evaluation of Curcumin and Curcumin Analogues obtained from ZINC Database: An in-Silico Validation." TEXILA INTERNATIONAL JOURNAL OF PUBLIC HEALTH 9, no. 4 (2021): 269–83. http://dx.doi.org/10.21522/tijph.2013.09.04.art023.

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Curcumin and its eleven analogues obtained from the ZINC database were screened for its anti-Alzheimer’s potential validated through in silico approach. Curcumin, eleven curcumin analogues from the ZINC database, and six standard anti-Alzheimer’s drugs were obtained from SWISS ADME and Pub chem database. All obtained molecules were subjected to drug-likeness, molecular docking, and ADMET analysis. Curcumin and eleven curcumin analogues show no violations against five drug-likeness rules, whereas 2 standard drugs (CID¬_11269353, CID_46883536) out of 5 screened standard drug molecules shows viol
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Ahsan, Mohamed Jawed, Kavita Choudhary, Amena Ali, et al. "Synthesis, DFT Analyses, Antiproliferative Activity, and Molecular Docking Studies of Curcumin Analogues." Plants 11, no. 21 (2022): 2835. http://dx.doi.org/10.3390/plants11212835.

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With 19.3 million new cases and almost 10 million deaths in 2020, cancer has become a leading cause of death today. Curcumin and its analogues were found to have promising anticancer activity. Inspired by curcumin’s promising anticancer activity, we prepared three semi-synthetic analogues by chemically modifying the diketone function of curcumin to its pyrazole counterpart. The curcumin analogues (3a–c) were synthesized by two different methods, followed by their DFT analyses to study the HOMO/LUMO configuration to access the stability of compounds (∆E = 3.55 to 3.35 eV). The curcumin analogue
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Dissertations / Theses on the topic "Curcumine – Analogues"

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Jourdan, Jean-Pierre. "Conception, synthèse et évaluation biologique de nouveaux analogues de la curcumine : potentiels agents pléiotropes d'intérêt thérapeutique dans la maladie d'Alzheimer." Caen, 2015. http://www.theses.fr/2015CAEN4012.

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La maladie d’Alzheimer, forme la plus commune des démences séniles, est une maladie progressive, chronique, neurodégénérative et irréversible. Les causes physiopathologiques de cette démence sont nombreuses. Parmi elles on peut citer l’agrégation de peptides β-amyloïdes, l’hyperphosphorylation de la protéine Tau, l’inflammation neuronale et le stress oxydatif. Une des approches thérapeutiques récemment développées pour modifier l’évolution de cette maladie multifactorielle est la conception de ligands multicibles. On trouve dans la nature des molécules douées de telles fonctions, dont la curcu
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Pecourneau, Jérémy. "Réponses photoinduites d'analogue biomimétique de la cyclocurcumine : vers des thérapies assistées par la lumière." Electronic Thesis or Diss., Université de Lorraine, 2022. http://www.theses.fr/2022LORR0205.

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Au-delà de la thérapie photodynamique (PDT), il existe plusieurs alternatives thérapeutiques assistées par la lumière parmi lesquelles la thérapie photothermique (PTT) ou encore la photoisomérisation dont l’action mécanique induirait des dommages cellulaires au sein des membranes. De plus, les molécules capables d’absorber simultanément deux photons permettraient de surmonter la nécessité d’une excitation à haute énergie par photon tout en gardant une pénétration suffisante des tissus. Dans ce contexte, nous nous sommes intéressés à la conception et à l’étude d’analogues biomimétiques de la cy
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Schmitt, Bonell. "Curcumin analogues as ligands for Re (I) and (V)." Thesis, Nelson Mandela Metropolitan University, 2012. http://hdl.handle.net/10948/d1020975.

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Coordination properties of 4-bromo-N-(diethylcarbamothioyl)benzamide (Hbeb) and 4-bromo-N-(diphenylcarbamothioyl)benzamide (Hbpb) with oxorhenium(V) and rhenium(I) are reported and discussed. Transition metal complexes of these ligands were studied due to the wide range of applications of thiourea derivatives in biological fields. N-[Di(alkyl/aryl)carbamothioyl]benzamide derivatives readily coordinate to metal ions as O,S-donors and the catalytic property of the complexes can be altered by these ligands, due to steric and electronic properties provided by various substituents. The coordination
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Souza, Nayane de. "Efeitos citotóxicos do DM-1 em células de melanoma resistentes a um inibidor de BRAF e na expressão de metaloproteinases." Universidade de São Paulo, 2017. http://www.teses.usp.br/teses/disponiveis/9/9143/tde-06122017-105135/.

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Melanoma é o câncer mais agressivo e a mutação BRAF V600E é a mais frequente entre os pacientes. O vemurafenibe foi o primeiro inibidor específico desta mutação aprovado pela Food and Drug Administration. Entretanto, após cerca de seis meses há recidiva e superar os mecanismos de resistência responsáveis por este fenômeno ainda é um desafio. A curcumina é um tumérico com características antitumorais e anti-inflamatórias, entretanto sua baixa biodisponibilidade e estabilidade limitam seu uso e por isso impulsionaram a busca por análogos capazes de serem eficientes e comercializados. O DM-1, é u
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Al-shdifat, Laith Mohammad Hilal. "Approaches to Enhancing the Properties of a Promising Curcumin Analogue." Thesis, The University of Sydney, 2021. https://hdl.handle.net/2123/25786.

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A range of derivatives has previously been synthesized in order to overcome the stability and pharmacokinetic hurdles that hinder the in vivo investigation of the natural product, curcumin. One such derivative, pyrazole 15, has been demonstrated to inhibit the proliferation of a highly metastatic androgen-independent prostate cancer cell line (PC3). In this work, pyrazole analogues, 15 and 32 and the corresponding curcumin analogues, 30 and 31 were synthesized using a microwave-assisted technique. A stability study, and in silico assessment, of curcumin 1 and thirteen pyrazole analogues (15,1
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Abdelhamid, Dalia. "Natural Products as Lead Compounds for Drug Development. Part I: Synthesis and Biological Activity of a Structurally Diverse Library of Curcumin Analogues. Part II: Synthesis of Novel Sterol Natural Products and Related Analogues as Antileishmanial Ag." The Ohio State University, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=osu1299685922.

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Tedesco, Serena. "Activation phenotypes of human monocyte-derived macrophages: methodological approaches and pharmacological modulation by curcumin analogues." Doctoral thesis, Università degli studi di Padova, 2016. http://hdl.handle.net/11577/3427229.

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Under normal conditions macrophages provide immune surveillance and host defense in tissues to maintain homeostasis. However, upon sensing changes in the microenvironment, macrophages become activated, undergoing a morphological and functional switch. Activation of these cells is not an “all-or-none” process, but rather a continuum characterized by a wide spectrum of molecular and functional phenotypes ranging from the “classical” M1 activated phenotype, with a highly pro-inflammatory profile, to the “alternative” M2 phenotype, associated with a beneficial, less inflammatory, protective profil
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SINGH, REETIKA. "COMPARATIVE ANALYSIS OF DIFFERENT CURCUMIN ANALOGUES TO INHIBIT TLR4 EXPRESSION IN BREAST CANCER- AN IN-SILICO STUDY." Thesis, DELHI TECHNOLOGICAL UNIVERSITY, 2021. http://dspace.dtu.ac.in:8080/jspui/handle/repository/18459.

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Chronic inflammation is closely related to the emergence of a number of cancers, including Breast cancer. Inflammation causes damage to the cell’s DNA which leads to its abnormal growth and formation of tumor mass. One of the most commonly known receptor responsible for inflammatory reactions is Toll-like receptor 4 (TLR4). It is activated majorly by bacterial LPS. Its activation further activates Cyclooxygenase enzyme that catalyzes the conversion of arachidonic acid into prostaglandins that lead to inflammation-like conditions. COX2 has also been correlated to the promotion of tumor g
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"INVESTIGATING THE MASS SPECTROMETRIC BEHAVIOR OF NOVEL ANTINEOPLASTIC CURCUMIN ANALOGUES." Thesis, 2015. http://hdl.handle.net/10388/ETD-2015-01-1911.

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Curcumin analogues are novel antineoplastic agents designed by structural modifications of the natural product curcumin to enhance its therapeutic effects. Various curcumin analogues displayed a significant cytotoxic effect towards different cancer cell lines including leukemia, melanoma, and colon cancer. In order to evaluate the safety, efficiency and metabolism of the new anticancer candidates, sensitive and high throughput analytical methods are needed. Thirteen curcumin analogues with the backbone structure of 3,5-bis(benzylidene)-4-piperidone were tested. The ionization behavior of curcu
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Ze, Chen Chu, та 陳楚澤. "Xanthine Oxidase and α-Glucosidase Inhibition of Curcumin and Curcumin Analogs". Thesis, 2015. http://ndltd.ncl.edu.tw/handle/y83s8x.

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碩士<br>輔仁大學<br>食品科學系碩士班<br>103<br>Curcumin is a constituent from root and stem of family Zingiberaceae and Araceae. It has been used as a natural colorant in food industry. Curcumin has a great value in food and medicine, and it has been reported that curcumin could inhibit the activities of xanthine oxidase (XO) and α-glucosidase that make curcumin can be used for treatment of gout and diabetes. Chemical synthesis, which can change the structure of component, can enhance the activities, even create a new one. Therefore, the objective of this research is to evaluate the characterization of curc
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Book chapters on the topic "Curcumine – Analogues"

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Awad, H., U. Das, J. Dimmock, and A. El-Aneed. "Tandem Mass Spectrometric Analysis of Novel Antineoplastic Curcumin Analogues." In Detection of Chemical, Biological, Radiological and Nuclear Agents for the Prevention of Terrorism. Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9238-7_15.

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Ranjbar, Reza, Hossein Bagheri, Faezeh Ghasemi, Paul C. Guest, and Amirhossein Sahebkar. "Effects of Curcumin and Its Analogues on Infectious Diseases." In Studies on Biomarkers and New Targets in Aging Research in Iran. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-56153-6_5.

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Haldar, Animeshchandra G. M., Kanhaiya M. Dadure, and Debarshi Kar Mahapatra. "Recent Advancements of Curcumin Analogs and Curcumin Formulations in Context to Modern Pharmacotherapeutics Perspectives." In Applied Pharmaceutical Practice and Nutraceuticals. Apple Academic Press, 2021. http://dx.doi.org/10.1201/9781003054894-9.

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Ginnebaugh, Kevin R., Aamir Ahmad, and Fazlul H. Sarkar. "Updates on the Promising Anticancer Activity of CDF, a Synthetic Curcumin Analogue." In Critical Dietary Factors in Cancer Chemoprevention. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-21461-0_1.

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Yang, Jennifer, and Gregory B. Lesinski. "Curcumin Analogs as Inhibitors of the Jak-STAT Signal Transduction Pathway." In Novel Apoptotic Regulators in Carcinogenesis. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-4917-7_10.

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Wei, Dangheng, Yanghui Liu, Xiaoying Jia, Fengxia Guo, and Jiangzhang Wu. "A novel synthetic analogue of curcumin, B7, inhibits inflammatory factors expression in H2O2 induced endothelial cells." In IFMBE Proceedings. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-29305-4_166.

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Badavath, Vishnu Nayak, Siddhartha Maji, Munusamy Saravanabhavan, Saurabh Gupta, M. V. N. L. Chaitanya, and Venkatesan Jayaprakash. "Synthetic Analogues of Curcumin: The Search for Anticancer and Antioxidant Activities." In Science of Spices and Culinary Herbs - Latest Laboratory, Pre-clinical, and Clinical Studies. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815274370124060007.

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Curcumin, a key component of Curcuma longa L.'s rhizome, has a wide range of biological activities, as evidenced by intensive research over the last five decades. Curcumin has recently been utilized as an alternative medical ingredient in Southeast Asia to cure a variety of diseases, including stomach trouble, flatulence, jaundice, arthritis, sprains, wounds, skin infections, etc. Curcumin has also been shown to have antioxidant, anti-inflammatory, antiviral, antibacterial, antifungal, and anticancer properties. Medicinal chemists employ rational structural modifications to improve the pharmac
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Shioorkar, Mahesh G., and Omprakash S. Chavan. "ENVIRONMENTALLY BENIGN MICROWAVE ASSISTED CATALYST FREE SYNTHESIS OF CURCUMIN PYRIMIDINONE AND THIOPYRIMIDINONE ANALOGUES." In Futuristic Trends in Chemical, Material Sciences & Nano Technology Volume 2 Book 12. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2023. http://dx.doi.org/10.58532/v2bs12p2ch4.

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Describe method consist of ecofriendly procedure for the preparation of Curcumin Pyrimidinone and Thiopyrimidinone analogues from Curcumin urea/thiourea With the help of MW irradiation for appropriate time. Green impact of reaction significantly enhanced due to no use of catalyst and under MWI process. Good to excellent yield of products, simple working strategy and easy purification are the advantage of present methodology
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Sivalingam, Nageswaran, Thennavan Ulaganathan, Ganshyam Jayakumar, Siddarth Venkatt, Aadhavan Balakumar, and Sruthi Sritharan. "Unraveling the Chemistry of Curcumin for Colon Cancer Prevention and Treatment." In Multidisciplinary Applications of Natural Science for Drug Discovery and Integrative Medicine. IGI Global, 2023. http://dx.doi.org/10.4018/978-1-6684-9463-9.ch003.

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Colorectal cancer is the leading cause of mortality. Several studies are focused on understanding the molecular mechanism to develop potential therapeutics to enhance patient health standards. Curcumin is a bioactive component derived from Curcuma Longa implicated with a spectrum of anticancer properties such as antioxidants. It has been proposed to possess promising features in suppressing colon cancer proliferation. However, the pharmacokinetics studies denote that curcumin lacks bioavailability at the target site which leads to systemic metabolism and excretion. So, studies were diverted to
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Gokhale, Kunal M., Chaitanya Walekar, and Snehal Manje. "Novel Curcumin Analogues: Synthesis and Therapeutic Applications." In Current Overview on Pharmaceutical Science Vol. 5. B P International (a part of SCIENCEDOMAIN International), 2023. http://dx.doi.org/10.9734/bpi/cops/v5/17813d.

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Conference papers on the topic "Curcumine – Analogues"

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Nagaraju, Ganji Purnachandra, Shijun Zhu, Roberto Diaz, Mamoru Shoji, and Bassel F. El-Rayes. "Abstract 3828: Potent curcumin analogues inhibit pancreatic cancer cell growth and angiogenesis." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-3828.

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Leow, Pay Chin, Choon Pei Boon, Chong Yew Lee, Mei-Lin Go та Pui-Lai Rachel Ee. "Abstract 755: Design and synthesis of curcumin analogues as Wnt/β-catenin antagonists". У Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-755.

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Kasinski, Andrea, Yuhong Du, Shala Thomas та ін. "Abstract B106: Inhibition of IKKb and NFκB signaling by a novel curcumin analogue". У Abstracts: Frontiers in Cancer Prevention Research 2008. American Association for Cancer Research, 2008. http://dx.doi.org/10.1158/1940-6207.prev-08-b106.

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Mardiana, L., B. Ardiansah, A. Septiarti, R. Bakri, and G. Kosamagi. "Ultrasound-assisted synthesis of curcumin analogs promoted by activated chicken eggshells." In INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES 2016 (ISCPMS 2016): Proceedings of the 2nd International Symposium on Current Progress in Mathematics and Sciences 2016. Author(s), 2017. http://dx.doi.org/10.1063/1.4991200.

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Pisano, Marina, Ilaria Sassu, Sara Cossu, et al. "Abstract 3804: Molecular changes induced by the curcumin biphenyl analogue D6 in melanoma cells." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-3804.

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Yadav, Babasaheb D., Sebastien Taurin, Lesley Larsen, and Rhonda J. Rosengren. "Abstract 3556: New curcumin analogues are cytotoxic towards estrogen receptor negative human breast cancer cell lines." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-3556.

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Bao, Bin, Shadan Ali, Dejuan Kong, et al. "Abstract 173: Targeted killing of cancer stem-like cells by a novel analogue of curcumin." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-173.

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Pisano, Marina, Gabriella Pagnan, Maria Antonietta Dettori, et al. "Abstract B202: A new curcumin analogue compound endowed with strong antitumor activity against neuroectoderma‐derived cancers." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics--Nov 15-19, 2009; Boston, MA. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/1535-7163.targ-09-b202.

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Amin, A. R. M. Ruhul, Michelle Lee, Mohammad A. Rahman, James R. Fuchs, Zhuo G. Chen, and Dong M. Shin. "Abstract 5425: Potent curcumin analogue FLLL-22, but not natural curcumin, targets the DNA damage pathway for apoptosis in lung and head and neck cancer cells." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-5425.

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Obara, Megumi, Shinobu Ohnuma, Eduardo E. Chufan, et al. "Abstract 3242: Synthetic analogs of curcumin as modulators of multidrug resistance-linked ABC transporters." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-3242.

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