13C, 15N CP-MAS as well as FT-IR studies of gossypol derivatives with aromatic substituents in solid 13C, 15N CP-MAS, FT–IR and PM5 studies of some Schiff bases of gossypol in solid 13C, 15N NMR and CP-MAS as well as FT-IR and PM5 studies of Schiff base of gossypol with l-phenylalanine methyl ester in solution and solid 145 Inhibitory effects of gossypol on bovine in vitro embryo production 1H and 13C NMR Experiments and Chemical Shifts Calculations on gossypol: a Compound Extracted from Cottonseeds 1H AND 13C NMR Studies of Tetrabutylammonium Salts of gossypol in Chloroform Solution 1H‐ and 13C‐NMR, FTIR, UV‐VIS, ESI‐MS, and PM5 studies as well as emission properties of a new Schiff base of gossypol with 5‐methoxytryptamine and a new hydrazone of gossypol with dansylhydrazine 1H and13C NMR spectra of transformation products of gossypol in solutions 1H NMR studies of gossypol and its complexes with some organic compounds 1H NMR study on the solvent effect on imine-enamine tautomerism of the condensation product of gossypol with 4-aminoantipyrine 1H NMR, FT‐IR and MS studies and PM5 semiempirical calculations of complexes between the Schiff base of gossypol with 2‐(aminomethyl)‐15‐crown‐5 and Ca2+, Pb2+ … 1H, 13C and 15N NMR, FT-IR as well as PM5 studies of a new Schiff base of gossypol with 3, 6-dioxadecylamine in solution 1H, 13C NMR, FT-IR as well as PM5 semiempirical studies of new hydrazone of gossypol with 2, 2′-diethoxyethyl hydrazine 3‐amino‐1‐propanol as a complexing agent in the determination of total gossypol A beam of dawn light of study on gossypol as a safe, effective, and reversible male antifertility contraceptive--evaluation of the studies by using low dose gossypol combined with steroid hormone for male contraception A bioenergetic model of gossypol action: effects of gossypol on adult rat spermatogenic cells A circular dichroism study of (+) gossypol binding to proteins A combined regimen of gossypol plus methyltestosterone and ethinylestradiol as a contraceptive induces germ cell apoptosis and expression of its related genes in … A Comparative Study on Rapid and Slow Loading of gossypol in Treatment of Gynecological Diseases [J] A COMPARATIVE STUDY ON THE INHIBITORY EFFECT OF gossypol ON SPERM ATPASE IN DIFFERENT ANIMAL SPECIES [J] A comparison between the cytotoxicity induced by gossypol in two testicular cell lines A developmental toxicity evaluation of gossypol A gossypol biosynthetic intermediate disturbs plant defence response A HISTOLOGICAL STUDY OF THE EFFECT OF gossypol ON THE ANTERIOR LOBE OF PITUITARY OF CASTRATED HOGS. A histopathologic study of the effects of gossypol on the female rat A liposomal delivery vehicle for the anticancer agent gossypol A method for the preparation of labelled gossypol by the incorporation of 14C acetate A method for the preparation of labelled gossypol by the incorporation of sup 14 C acetate A Microbial Fermentation of Soybean and Cottonseed Meal Increases Antioxidant Activity and gossypol Detoxification in Diets for Nile tilapia, Oreochromis niloticus A mixture of cottonseed meal, soybean meal and animal byproduct mixture as a fish meal substitute: growth and tissue gossypol enantiomer in juvenile rainbow
Adipose tissue, often referred to as fat, plays a crucial role in our health by storing energy, regulating hormones, and insulating our bodies. However, as we age or experience obesity, adipose tissue undergoes a complex change known as senescence. This process creates senescent cells that release a harmful cocktail of molecules called the Senescence-Associated Secretory Phenotype (SASP). SASP disrupts the healthy functioning of adipose tissue. It promotes inflammation, hinders the formation of new fat cells,and disrupts the body's ability to regulate blood sugar. This dysfunction contributes to a cascade of age-related diseases including type 2 diabetes, heart disease, and even Alzheimer's. Understanding how SASP and adipose tissue senescence interact is a promising avenue for researchers seeking to develop interventions to promote healthy aging and combat chronic diseases. Exercise prevents diet-induced cellular senescence in adipose tissue Physiological aging: links among adipose tissue dysfunction, diabetes, and frailty Unbiased analysis of senescence associated secretory phenotype (SASP) to identify common components following different genotoxic stresses Aging and adipose tissue: potential interventions for diabetes and regenerative medicine Roles of chemokine ligand-2 (CXCL2) and neutrophils in influencing endothelial cell function and inflammation of human adipose tissue Ablation of XP-V gene causes adipose tissue senescence and metabolic abnormalities The emerging role of senescent cells in tissue homeostasis and pathophysiology Cellular senescence and the senescent secretory phenotype in age-related chronic diseases JAK inhibition alleviates the cellular senescence-associated secretory phenotype and frailty in old age Growth hormone action predicts age-related white adipose tissue dysfunction and senescent cell burden in mice Aging-related inflammation in osteoarthritis Cellular senescence in type 2 diabetes: a therapeutic opportunity The fat cell senescence hypothesis: a mechanism responsible for abrogating the resolution of inflammation in chronic disease Feast and famine: adipose tissue adaptations for healthy aging Macrophages in age-related chronic inflammatory diseases Proposed metabolic vicious circle in patients with large myocardial infarcts and high plasma-free-fatty-acid concentrations Perspective: targeting the JAK/STAT pathway to fight age-related dysfunction Effect of low-dose rapamycin on senescence markers and physical functioning in older adults with coronary artery disease: results of a pilot study. Systemic DNA damage response and metabolic syndrome as a premalignant state Stem cell senescence and regenerative paradigms Cellular senescence in ageing, age-related disease and longevity Contribution of adipose tissue inflammation to the development of type 2 diabetes mellitus Phytochemicals suppress nuclear factor-κB signaling: impact on health span and the aging process Effect of lipopolysaccharides on adipogenic potential and premature senescence of adipocyte progenitors Developments in our understanding of the effects of growth hormone on white adipose tissue from mice: implications to the clinic Cellular senescence in aging and age-related disease: from mechanisms to therapy Deleted in B reast C ancer 1 regulates cellular senescence during obesity Growth differentiation factor 6 derived from mesenchymal stem/stromal cells reduces age-related functional deterioration in multiple tissues Mitochondrial dysfunction induces senescence with a distinct secretory phenotype Impact of growth hormone on regulation of adipose tissue Senescence-associated secretory phenotype (SASP) involvement in the development of cancer, aging, and age related diseases Clearance of p16Ink4a-positive senescent
The role of matrix metalloproteinases in aging "Proteases are a set of enzymes that have been involved in multiple biological processes throughout evolution. Among them, extracellular matrix (ECM) remodeling has emerged as one of the most relevant functions exerted by these proteins, being essential in the regulation of critical events such as embryonic development or tissue homeostasis. Hence, it is not surprising that dysregulation in any protease function that affects ECM homeostasis may contribute to the aging process. Matrix metalloproteinases (MMPs) are one of the most important families of proteases involved in the tight control of ECM remodeling over time. In this review, we will discuss how MMPs and other proteases alter ECM composition and mechanical properties in aging, thereby affecting stem cell niches and the development of senescent phenotypes. Finally, we will summarize recent findings that associate MMPs with the development of age-related diseases, such as neurodegenerative disorders." SCIENTIFIC STUDIES Role of matrix metalloproteinases (MMPs) in colorectal cancer matrix metalloproteinases (MMPs) in oral diseases matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs): Positive and negative regulators in tumor cell adhesion The role of matrix metalloproteinases (MMPs) in human caries matrix metalloproteinases (MMPs): chemical–biological functions and (Q) SARs matrix metalloproteinases (MMPs) and their physiological inhibitors (TIMPs) are differentially expressed during excisional skin wound repair Imbalance of expression of matrix metalloproteinases (MMPs) and tissue inhibitors of the matrix metalloproteinases (TIMPs) in human pancreatic carcinoma matrix metalloproteinases (MMPs) and tissue inhibitors of MMPs in the respiratory tract: potential implications in asthma and other lung diseases Expression of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) in healthy and diseased human gingiva Proteolytic events of wound-healing—coordinated interactions among matrix metalloproteinases (MMPs), integrins, and extracellular matrix molecules matrix metalloproteinases (MMPs) regulate fibrin-invasive activity via MT1-MMP–dependent and–independent processes UVA irradiation stimulates the synthesis of various matrix‐metalloproteinases (MMPs) in cultured human fibroblasts The matrix metalloproteinases (MMPs) in the decidua and fetal membranes Renal expression of SIBLING proteins and their partner matrix metalloproteinases (MMPs) Immunohistochemical study of matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) in pulmonary lymphangioleiomyomatosis (LAM) The role of matrix metalloproteinases (MMPs) in the pathophysiology of chronic obstructive pulmonary disease (COPD): a therapeutic role for inhibitors of MMPs? Expression profile of matrix metalloproteinases (MMPs) and tissue inhibitors of MMPs in mature human odontoblasts and pulp tissue Assays of matrix metalloproteinases (MMPs) activities: a review matrix metalloproteinases (MMPs) in breast cancer cell lines of different tumorigenicity. Elevation of matrix metalloproteinases (MMPs) in multiple sclerosis and impact of immunomodulators The role of matrix metalloproteinases (MMPs) and their inhibitors (TIMPs) in the development of esophageal cancer Expression of matrix metalloproteinases (MMPs) in primary human breast cancer and breast cancer cell lines: New findings and review of the literature Effects of age on plasma matrix metalloproteinases (MMPs) and tissue inhibitor of metalloproteinases (TIMPs) The effects of selective inhibitors of matrix metalloproteinases (MMPs) on bone resorption and the identification of MMPs and TIMP-1 in isolated osteoclasts matrix metalloproteinases (MMPs), the main extracellular matrix (ECM) enzymes in collagen degradation, as a target for anticancer drugs Screening
The ketogenic diet is a high-fat, adequate-protein, low-carbohydrate diet that in medicine is used primarily to treat difficult-to-control (refractory) epilepsy in children. The diet forces the body to burn fats rather than carbohydrates. Normally, the carbohydrates contained in food are converted into glucose, which is then transported around the body and is particularly important in fueling brain function. However, if little carbohydrate remains in the diet, the liver converts fat into fatty acids and ketone bodies. The ketone bodies pass into the brain and replace glucose as an energy source. An elevated level of ketone bodies in the blood, a state known as ketosis, leads to a reduction in the frequency of epileptic seizures.[1] Around half of children and young people with epilepsy who have tried some form of this diet saw the number of seizures drop by at least half, and the effect persists even after discontinuing the diet.[2] Some evidence indicates that adults with epilepsy may benefit from the diet, and that a less strict regimen, such as a modified Atkins diet, is similarly effective.[1] Potential side effects may include constipation, high cholesterol, growth slowing, acidosis, and kidney stones.[3] The original therapeutic diet for paediatric epilepsy provides just enough protein for body growth and repair, and sufficient calories[Note 1] to maintain the correct weight for age and height. The classic therapeutic ketogenic diet was developed for treatment of paediatric epilepsy in the 1920s and was widely used into the next decade, but its popularity waned with the introduction of effective anticonvulsant medications. This classic ketogenic diet contains a 4:1 ratio by weight of fat to combined protein and carbohydrate. This is achieved by excluding high-carbohydrate foods such as starchy fruits and vegetables, bread, pasta, grains, and sugar, while increasing the consumption of foods high in fat such as nuts, cream, and butter.[1] Most dietary fat is made of molecules called long-chain triglycerides (LCTs). However, medium-chain triglycerides (MCTs)—made from fatty acids with shorter carbon chains than LCTs—are more ketogenic. A variant of the classic diet known as the MCT ketogenic diet uses a form of coconut oil, which is rich in MCTs, to provide around half the calories. As less overall fat is needed in this variant of the diet, a greater proportion of carbohydrate and protein can be consumed, allowing a greater variety of food choices.[4][5] In 1994, Hollywood producer Jim Abrahams, whose son's severe epilepsy was effectively controlled by the diet, created the Charlie Foundation for Ketogenic Therapies to further promote diet therapy. Publicity included an appearance on NBC's Dateline program and ...First Do No Harm (1997), a made-for-television film starring Meryl Streep. The foundation sponsored a research study, the results of which—announced in 1996—marked the beginning of renewed scientific interest in the diet.[1] Possible therapeutic uses for the ketogenic diet have been studied for many additional neurological disorders, some of which include: Alzheimer's disease, amyotrophic lateral sclerosis, headache, neurotrauma, pain, Parkinson's disease, and sleep disorders.[6] - wiki SCIENTIFIC STUDIES 10 Graphs That Show The Power Of A Ketogenic Diet 10 Patients, 10 Years–Long Term Follow-Up Of Cardiovascular Risk Factors In Glut1 Deficiency Treated With Ketogenic Diet Therapies: A Prospective, Multicenter … 10 Questions About The Ketogenic Diet 113 Ketogenic Diet Services At Children'S Hospital Across The United Kingdom 31P-Nmr Study Of Brain Metabolism In The Rat Model Of The Ketogenic Diet 3T
Apoptosis, also known as programmed cell death, is a crucial process for maintaining human health throughout our lives.It acts as a cellular self-destruct mechanism, eliminating damaged or dysfunctional cells that could otherwise become harmful. This controlled elimination prevents the accumulation of cells with mutations or DNA damage, which could lead to cancer. Apoptosis also plays a vital role in shaping our bodies during embryonic development and sculpting our immune system by removing immature or autoreactive lymphocytes. test The intricate dance of apoptosis is tightly regulated, and its proper functioning is essential for healthy aging. In a well-functioning system, apoptosis eliminates old or damaged cells that can no longer function effectively. This cellular renewal helps maintain tissue health and organ function. However, as we age, the balance of apoptosis can become disrupted. Decreased apoptosis can lead to the accumulation of damaged cells, potentially contributing to age-related diseases. Conversely, excessive apoptosis can deplete vital tissues, leading to organ dysfunction. Understanding the regulation of apoptosis is therefore a key area of research in the fight against aging and age-related diseases. SCIENTIFIC STUDIES Mitochondria and Apoptosis Apoptosis Signaling Apoptosis and disease The biochemistry of Apoptosis Mitochondrial control of Apoptosis Apoptosis in cancer Apoptosis by Death Factor Apoptosis in development Apoptosis in AIDS Caspases: the executioners of Apoptosis. Dysregulation of Apoptosis in Cancer Mechanisms of Apoptosis Defining Apoptosis. Apoptosis: Molecular Regulation of Cell Death Neural Apoptosis p53-Dependent Apoptosis pathways Apoptosis in neurodegenerative disorders Calcium orchestrates Apoptosis Apoptosis and carcinogenesis. An evolutionary perspective on Apoptosis Apoptosis - the p53 network Apoptosis in the nervous system JNK signaling in Apoptosis Mitochondria and Apoptosis Apoptosis: an overview Apoptosis-based therapies PI3K: Downstream AKTion Blocks Apoptosis A model for p53-induced Apoptosis Apoptosis regulators. Cell Death: The Significance of Apoptosis Oxidative stress as a mediator of Apoptosis Ceramide: an intracellular signal for Apoptosis Oxidative stress and Apoptosis Apoptosis—an introduction Gonadal cell Apoptosis. Viruses and Apoptosis Mitochondrial dynamics and Apoptosis Mitochondrial control of nuclear Apoptosis Ischemia-induced neuronal Apoptosis Cytochrome C-Mediated Apoptosis Inhibition of Macroautophagy Triggers Apoptosis The molecular biology of Apoptosis Molecular characterization of mitochondrial Apoptosis-inducing factor S-nitrosylation regulates Apoptosis Apoptosis, autophagy, and more Angiogenesis and Apoptosis IAP family proteins—suppressors of Apoptosis Placental Apoptosis in preeclampsia Emerging roles of caspase-3 in Apoptosis Apoptosis in cancer therapy: Crossing the threshold Apoptosis in the Failing Human Heart Phagocyte recognition of cells undergoing Apoptosis Ras signalling and Apoptosis Viruses and Apoptosis Apoptosis. The role of the endonuclease. The morphology of Apoptosis Caspase Family Proteases and Apoptosis Nuclear changes in Apoptosis Immunohistochemical evidence for Apoptosis in Alzheimer's disease. Control of Apoptosis by p53 Mitochondrial fission in Apoptosis Apoptosis and melanoma chemoresistance Apoptosis signaling in lymphocytes. Apoptosis: Molecular Control Point in Toxicity death, and the pursuit of Apoptosis Fas Ligand-Induced Apoptosis Endostatin Induces Endothelial Cell Apoptosis Apoptosis: Mechanisms and Roles in Pathology Induction of Apoptosis by Cancer Chemotherapy Apoptosis: A Review of Programmed Cell Death Apoptosis in resolution of inflammation Mechanisms of p53-dependent Apoptosis The role of DNA fragmentation in Apoptosis Proliferation, cell cycle and Apoptosis
Urolithin A is a natural molecule that has been found to downregulate androgen receptor activation and suppress the growth of prostate cancer. It is a metabolite derived from ellagic acid, which is found in various fruits and nuts. Some of the top foods and herbs that contain ellagic acid and can potentially produce urolithin A include: 1. Pomegranates: Pomegranate juice and seeds are rich sources of ellagic acid, which can be metabolized into urolithin A in the gut. 2. Raspberries: Raspberries are another fruit that contains ellagic acid and can potentially produce urolithin A. 3. Walnuts: Walnuts are a type of nut that contains ellagic acid and can contribute to the production of urolithin A. 4. Strawberries: Strawberries are known to contain ellagic acid, which can be converted into urolithin A. 5. Blackberries: Blackberries are also a good source of ellagic acid and can potentially produce urolithin A. The health benefits of urolithin A include: 1. Anti-cancer properties: Urolithin A has been shown to inhibit cell proliferation and induce apoptosis in various cancer cell lines, including prostate cancer cells. It targets the androgen receptor signaling axis, which is crucial for the growth and progression of prostate cancer. 2. Anti-inflammatory effects: Urolithin A has been found to possess anti-inflammatory properties, which can help reduce inflammation in the body and potentially protect against chronic diseases associated with inflammation. 3. Antioxidant activity: Urolithin A exhibits antioxidant activity, which can help neutralize harmful free radicals and protect cells from oxidative damage. 4. Gut health benefits: Urolithin A is produced by the gut microbiota through the metabolism of ellagic acid. It has been shown to have beneficial effects on gut health by promoting the growth of beneficial bacteria and reducing inflammation in the gut. … emblica L.) Fruits Ameliorate Vascular Smooth Muscle Cell Dysfunction in Hyperglycemia: An Underlying Mechanism Involved in Ellagitannin Metabolite Urolithin A A natural molecule, Urolithin A, downregulates androgen receptor activation and suppresses growth of prostate cancer A Novel Candidate for Prevention and Treatment of Atherosclerosis: Urolithin B Decreases Lipid Plaque Deposition in apoE−/− Mice and Increases Early Stages of … Activation of the miR-34a-Mediated SIRT1/mTOR Signalling Pathway by Urolithin A Attenuates D-Galactose-Induced Brain Aging in Mice An increased autophagic flux contributes to the anti-inflammatory potential of Urolithin A in macrophages Anti-inflammatory properties of a pomegranate extract and its metabolite urolithin-A in a colitis rat model and the effect of colon inflammation on phenolic metabolism Antiaging Effects of Urolithin A on Replicative Senescent Human Skin Fibroblasts Antimelanogenic effect of Urolithin A and urolithin B, the colonic metabolites of ellagic acid, in B16 melanoma cells Antiproliferative activity of the ellagic acid-derived gut microbiota isoUrolithin A and comparison with its Urolithin A isomer: the role of cell metabolism Antiproliferative activity of the ellagic acid-derived gut microbiota isoUrolithin A and comparison with its Urolithin A isomer: the role of cell metabolism Antiproliferative effect of Urolithin A, the ellagic acid-derived colonic metabolite, on hepatocellular carcinoma HepG2. 2.15 cells by targeting Lin28a/let-7a axis Bioactivity screening for xylopic
Honokiol Simple Lignans Of The Cphephec Kind Are Illustrated By The Antibacterials Honokiol And The Protein Kinase A Bisphenolic Honokiol Analog Outcompetes Oral Antimicrobial Agent Cetylpyridinium Chloride Via A Membrane-Associated Mechanism A Cocktail Of Betulinic Acid, Parthenolide, Honokiol And Ginsenoside Rh2 In Liposome Systems For Lung Cancer Treatment A Concise Synthesis Of 4′-O-Methyl Honokiol A Concise Synthesis Of Honokiol A Facile Graphene Nanosheets‐Based Electrochemical Sensor For Sensitive Detection Of Honokiol In Traditional Chinese Medicine A Naturally Occurring Rexinoid, Honokiol, Can Serve As A Regulator Of Various Retinoid X Receptor Heterodimers A Novel Composite Drug Delivery System: Honokiol Nanoparticles In Thermosensitive Hydrogel Based On Chitosan A Novel Gsh Responsive Poly (Alpha-Lipoic Acid) Nanocarrier Bonding With The Honokiol-Dmxaa Conjugate For Combination Therapy A Novel Honokiol Liposome: Formulation, Pharmacokinetics, And Antitumor Studies A Novel Sensing Platform Based On Ionic Liquid Integrated Carboxylic-Functionalized Graphene Oxide Nanosheets For Honokiol Determination A Novel Transdermal Honokiol Formulation Based On Pluronic F127 Copolymer A Short And Efficient Synthesis Of Honokiol Via Claisen Rearrangement A Simultaneous Determination Of Honokiol And Magnolol In Oriental Pharmaceutical Decoctions Containing Magnolia Bark By Ion-Pair High-Performance Liquid … A Study On Extracting And Determining Magnolol And Honokiol In Huoxiang Zhengqi Troche A Study On The Extracting And Determining Method For Magnolol And Honokiol In Muxiang Shunqi Pills [J] A Study On The Ultrasonic Extraction For Magnolol And Honokiol In Leaves Of Magnolia Offcinalis Rend Et Wils A Validated Ultra-Hplc–Ms/Ms Method For Determination Of Honokiol In Human Plasma And Its Application To A Clinical Pharmacokinetic Study Abrogation Of Established Inflammatory Arthritis By The Gabaa Agonist Honokiol.(50.18) Absorptive Feature Of Honokiol And Magnolol In The Rat′ S Intestines [J] Abstract A134: Honokiol Targets Stat3 In Head And Neck Squamous Cell Carcinoma Abstract B02: Honokiol Attenuates Stemness, Growth And Metastasis Of Pancreatic Tumor Cells: A Novel Natural Agent For Therapy And Prevention Abstract C46: The Pharmacokinetics And Pharmacodynamics Study Of Honokiol In Sprague-Dawley Rats And Colorectal Tumor-Bearing Mice Abstract Lb-187: Novel Mechanistic Insights Into The Bioactive Compound Honokiol-Mediated Inhibition Of Epithelial To Mesenchymal Transition In Breast Cancer … Abstract Lb-61: Inhibiting “Dedifferentiation” In Breast Cancer Cells Using Honokiol-A Plant Derived Polyphenol Abstract# 2975: Honokiol, A Natural Product, Induces G1-Phase Cell Cycle Arrest And Caspase-3-Dependent Apoptosis In Human Non-Small Cell Lung Cancer Cells Abstract# 925: Chemopreventive Effects Of Honokiol On Uv-B Induced Skin Cancer Development Activation Of Tumor Suppressor Lkb1 By Honokiol Abrogates Cancer Stem-Like Phenotype In Breast Cancer Via Inhibition Of Oncogenic Stat3 Acute And Subchronic Toxicities In Dogs And Genotoxicity Of Honokiol Microemulsion Acute And Sub-Chronic Toxicity Studies Of Honokiol Microemulsion Advances On Semisynthesis, Total Synthesis, And Structure-Activity Relationships Of Honokiol And Magnolol Derivatives An Electrochemical Sensor For Honokiol Based On A Glassy Carbon Electrode Modified With Mos 2/Graphene Nanohybrid Film An Expedient Synthesis Of Honokiol And Its Analogues As Potential Neuropreventive Agents Analysis Of Magnolol And Honokiol In Biological Fluids By Capillary Zone Electrophoresis Analysis Of Magnolol And Honokiol In Traditional Chinese Drug Hoe-Po Analysis Of Β-Eudesmolmagnolol And Honokiol In Magnolia Officinalis By Ptgc
Zerumbone Zerumbone, a tropical ginger sesquiterpene, activates phase II drug metabolizing enzymes Zerumbone, a tropical ginger sesquiterpene, inhibits colon and lung carcinogenesis in mice Zerumbone induced apoptosis in liver cancer cells via modulation of Bax/Bcl-2 ratio Antitumor activity of extract of Zingiber aromaticum and its bioactive sesquiterpenoid Zerumbone Studies in sesquiterpenes—XVI: Zerumbone, a monocyclic sesquiterpene ketone Zerumbone, a sesquiterpene in subtropical ginger, suppresses skin tumor initiation and promotion stages in ICR mice Anti-inflammatory effect of Zerumbone on acute and chronic inflammation models in mice Chemoprevention of azoxymethane-induced rat aberrant crypt foci by dietary Zerumbone isolated from Zingiber zerumbet Zerumbone induces apoptosis in T-acute lymphoblastic leukemia cells In vitro ultramorphological assessment of apoptosis induced by Zerumbone on (HeLa) Zerumbone-loaded nanostructured lipid carriers: preparation, characterization, and antileukemic effect Zerumbone, an HIV-inhibitory and cytotoxic sesquiterpene of Zingiber aromaticum and Z. zerumbet Anticancer and antimicrobial activities of Zerumbone from Characterization of the inclusion complex of Zerumbone with hydroxypropyl-β-cyclodextrin Chemistry of Zerumbone. 2. Regulation of ring bond cleavage and unique antibacterial activities of Zerumbone derivatives Preliminary analysis of the antinociceptive activity of Zerumbone Zerumbone abolishes NF-κB and IκBα kinase activation leading to suppression of antiapoptotic and metastatic gene expression, upregulation of apoptosis … Antitumor effects of Zerumbone from Zingiber zerumbet in P-388D1 cells in vitro and in vivo Attractive reactivity of a natural product, Zerumbone Zerumbone, a Southeast Asian ginger sesquiterpene, markedly suppresses free radical generation, proinflammatory protein production, and cancer cell proliferation … Zerumbone down-regulates chemokine receptor CXCR4 expression leading to inhibition of CXCL12-induced invasion of breast and pancreatic tumor cells Suppression of dextran sodium sulfate-induced colitis in mice by Zerumbone, a subtropical ginger sesquiterpene, and nimesulide: separately and in combination Zerumbone enhances TRAIL-induced apoptosis through the induction of death receptors in human colon cancer cells: Evidence for an essential role of reactive … Zerumbone, a bioactive sesquiterpene, induces G2/M cell cycle arrest and apoptosis in leukemia cells via a Fas‐and mitochondria‐mediated pathway Key cell signaling pathways modulated by Zerumbone: role in the prevention and treatment of cancer Nuclear magnetic resonance spectroscopy. The conformational mobility of humulene and Zerumbone In vitro covalent binding proteins of Zerumbone, a chemopreventive food factor Zerumbone inhibits tumor angiogenesis via NF-κB in gastric cancer Chemistry of Zerumbone. 1. Simplified isolation, conjugate addition reactions, and a unique ring contracting transannular reaction of its dibromide Zerumbone inhibits interleukin-6 and induces apoptosis and cell cycle arrest in ovarian and cervical cancer cells Zerumbone abolishes RANKL-induced NF-κB activation, inhibits osteoclastogenesis, and suppresses human breast cancer–induced bone loss in athymic nude mice Potential chemoprevention of diethylnitrosamine-initiated and 2-acetylaminofluorene-promoted hepatocarcinogenesis by Zerumbone from the rhizomes of the … Zerumbone, a Southeast Asian ginger sesquiterpene, induced apoptosis of pancreatic carcinoma cells through p53 signaling pathway Anticancer activity of natural compound (Zerumbone) extracted from Zingiber zerumbet in human HeLa cervical cancer cells The chemistry of Zerumbone. Part 5: Structural transformation of the dimethylamine derivatives Antibacterial and antimutagenic activities of novel Zerumbone analogues Zerumbone, an anti‐inflammatory phytochemical, induces expression of proinflammatory cytokine genes in human colon adenocarcinoma cell
Withaferin A (Ashwaganda) 2, 3-Dihydro-3β-methoxy Withaferin-A Protects Normal Cells against Stress: Molecular Evidence of Its Potent Cytoprotective Activity 2, 3-Dihydrowithaferin A-3β-O-sulfate, a new potential prodrug of withaferin A from aeroponically grown Withania somnifera 3beta-methoxy derivation of Withaferin-a Attenuates its Anticancer potency: Bioinformatics and molecular evidences 5,6-De-epoxy-5-en-7-one-17-hydroxy withaferin A, a new cytotoxic steroid from Withania somnifera L. Dunal leaves A novel combination of withaferin A and sorafenib shows synergistic efficacy against both papillary and anaplastic thyroid cancers A novel combination of withaferin A and sulforaphane inhibits epigenetic machinery, cellular viability and induces apoptosis of breast cancer cells A rapid and simple high performance thin layer chromatographic method for simultaneous analysis of β-sitosterol-D-glucoside, gallic acid, withaferin A and withanolide A in Ashvagandharishta A Study on the efficacy of Withaferin-A in reducing oxidative stress against DEN induced hepatocellular carcinoma A validated and densitometric HPTLC method for the quantification of Withaferin-A and Withanolide-A in different plant parts of two morphotypes of Withania somnifera A110 THORACIC CANCERS: PATHOGENESIS AND NOVEL TARGETS: The Use Of Withaferin-A As An Anti-Metastatic Agent In Non-Small Cell Lung Cancer Abstract A10: Withaferin-A, a natural compound inhibits AKT-induced metastatic colorectal cancer Abstract A115: withaferin A downregulates her-2/neu protein expression in human breast cancer cells. Abstract A2-32: Identification of withaferin A as a novel cancer stem cell inhibitor to overcome drug resistance in non-small cell lung carcinoma Abstract A29: Targeting adenylate kinase-4 modulation of HIF-1α: Stability identifies Withaferin-A suppresses lung cancer metastasis Abstract A4: withaferin A induces apoptosis in imatinib-resistant CML cells by repressing the Akt signaling pathway Abstract A48: Ovarian tumor-induced immunosuppression of NK cells and its prevention by dietary supplementation of herbal withaferin A (Ashwagandha). Abstract B41: withaferin A promotes ROS-mediated differentiation of neuroblastoma Abstract B57: A natural plant-derived compound, withaferin A, exploits the stress pathway to induce antitumor immunity. Abstract B84: Withaferin‐A is a novel HSF‐1 inhibitor with potent antitumor effects in melanoma in vivo Abstract C218: Novel therapeutic potential in targeting micro tubules by naturally occurring anti cancer agent withaferin A in human cancers. Abstract LB-113: A novel role of withaferin A as an effective pro-apoptotic receptor agonist (PARA) and insights into the underlying molecular mechanisms Abstract LB-154: Epigenetic silencing of triple-negative breast cancer hallmarks by withaferin A Abstract NTOC-100: OVARIAN TUMOR-ASSOCIATED GRP78 INDUCES IMMUNOSUPPRESSION AND withaferin A (ASHWAGANDHA) ENHANCES ANTI … Abstract P2-09-12: withaferin A-mediated inhibition of breast carcinoma involves concomitant activation of CHOP and Elk1 via ERK/ribosomal S6 kinase (RSK) … Abstract# 3903: Inhibition of human cervical cancer cell growth by withaferin A and potential mechanisms Actin microfilament aggregation induced by withaferin A is mediated by annexin II Activation of signal transducer and activator of transcription 3 fails to confer resistance against withaferin A-induced apoptosis in human breast cancer cells Age related differences in stress-induced neurobehavioral patterns in rats modulated by withaferin-A and other antioxidants Agrobacterium rhizogenes mediated hairy root culture system of Withania somnifera L Dunal for withaferin A production Ameliorative effect of withaferin A on ageing-mediated impairment in the dopamine system and its
Ursolic Acid 23-Hydroxy Ursolic acid Protects Atherosclerosis-Prone Mice From Monocyte Dysfunction 27-O-(E)-P-Coumaric Acyl Ursolic acid Via Jnk/Sapk Signal Pathway Regulates Apoptosis Of Human Breast Cancer Mda-Mb-231 Cell Line 27-P-Cumaroxy-Ursolsäure, Ein Neuer Inhaltsstoff Von Ilex Aquifolium L.[1]/27-P-Cumaroxy Ursolic acid-A New Constituent Of Ilex Aquifolium L.[1] 2D Raman Spectroscopy As An Alternative Technique For Distinguishing Oleanoic Acid And Ursolic acid 3D-Qsar And Docking Studies On Ursolic acid Derivatives For Anticancer Activity Based On Bladder Cell Line T24 Targeting Nf-Kb Pathway Inhibition 858. Triterpenoids From New Zealand Plants. Isolation Of Ursolic acid From Gaultheria Subcorymbosa Col. A Bioinformatic And Mechanistic Study Elicits The Antifibrotic Effect Of Ursolic acid Through The Attenuation Of Oxidative Stress With The Involvement Of Erk, Pi3K … A Comparative Study For The Extraction Methods And Solvent Selection For Isolation, Quantitative Estimation And Validation Of Ursolic acid In The Leaves Of … A Comparative Study Of The Separation Of Oleanolic Acid And Ursolic acid In Prunella Vulgaris By High-Performance Liquid Chromatography And Cyclodextrin-Modified … A Comparative Study On The Isolation And Cerium (Iv) Ammonium Nitrate Mediated Oxidative Transformation Of Oleanolic Acid And Ursolic acid A Comparison Of The Effects Of Ursolic acid And L-Leucine Supplementation On Igf-1 Receptor And Akt-Mtor Signaling In Response To Resistance Exercise In Trained … A Convenient Separation Of Ursolic And Oleanolic Acid A functionalized multi-walled carbon nanotube-based composite monolith as a solid-phase extraction adsorbent for on-line purification and enrichment of Ursolic acid in medicinal plants A High Content Drug Screen Identifies Ursolic acid As An Inhibitor Of Amyloid Β Protein Interactions With Its Receptor Cd36 A Hydrophilic Conjugate Approach Toward The Design And Synthesis Of Ursolic acid Derivatives As Potential Antidiabetic Agent A Metal Organic Framework Polymer Monolithic Column As A Novel Adsorbent For On-Line Solid Phase Extraction And Determination Of Ursolic acid In Chinese Herbal … A Myrtus Communis Extract Enriched In Myrtucummulones And Ursolic acid Reduces Resistance Of Propionibacterium Acnes Biofilms To Antibiotics Used In Acne … A New Synthetic Ursolic acid Derivative Iua With Anti-Tumor Efficacy Against Osteosarcoma Cells Via Inhibition Of Jnk Signaling Pathway A Novel Co-Drug Of Aspirin And Ursolic acid Interrupts Adhesion, Invasion And Migration Of Cancer Cells To Vascular Endothelium Via Regulating Emt And Egfr … A Novel Form Of Melanoma Apoptosis Resistance: Melanogenesis Up-Regulation In Apoptotic B16-F0 Cells Delays Ursolic acid-Triggered Cell Death A Novel Synthetic Ursolic acid Derivative Inhibits Growth And Induces Apoptosis In Breast Cancer Cell Lines A Pentacyclic Triterpene Natural Product, Ursolic acid And Its Prodrug Us597 Inhibit Targets Within Cell Adhesion Pathway And Prevent Cancer Metastasis A Phase I Pharmacokinetic Study Of Ursolic acid Nanoliposomes In Healthy Volunteers And Patients With Advanced Solid Tumors A Phase I Trial To Evaluate The Multiple-Dose Safety And Antitumor Activity Of Ursolic acid Liposomes In Subjects With Advanced Solid Tumors A Preliminary Investigation Of Ursolic acid In Cell Suspension Culture Of Salvia Officinalis A Rapid Tandem Mass Spectrometric Assay For Determination Of Ursolic acid–Application To Analysis Of Ursolic acid In Four Species Of Staphylea L. And