benzophenone/स्तन कैन्सर

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पृष्ठ 1 से 36 परिणाम

Benzophenone-1 and nonylphenol stimulated MCF-7 breast cancer growth by regulating cell cycle and metastasis-related genes via an estrogen receptor α-dependent pathway.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

Endocrine-disrupting chemicals (EDC) are defined as environmental compounds that produce adverse health manifestations in mammals by disrupting the endocrine system. Benzophenone-1 (2,4-dihydroxybenzophenone, BP1) and nonylphenol (NP), which are discharged from numerous industrial products, are

A tetraprenylated benzophenone 7-epiclusianone induces cell cycle arrest at G1/S transition by modulating critical regulators of cell cycle in breast cancer cell lines

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

Breast cancer is a complex disease and encompassing different types of tumor. Although advances in understanding of the molecular bases of breast cancer biology, the therapeutic proposals available still are not effective. In this scenario, the present study aimed to evaluate the mechanisms

Estrogenic potency of benzophenone UV filters in breast cancer cells: proliferative and transcriptional activity substantiated by docking analysis.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

The results from recent studies show that some benzophenones (BPs) and their hydroxylated metabolites can function as weak estrogens (E2) in the environment. However, little is known about the structure-activity relationship of these molecules. We have examined the effects of exposure to ten

Garcinol, an acetyltransferase inhibitor, suppresses proliferation of breast cancer cell line MCF-7 promoted by 17β-estradiol.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

The acetyltransferase inhibitor garcinol, a polyisoprenylated benzophenone, is extracted from the rind of the fruit of Garcinia indica, a plant found extensively in tropical regions. Anti-cancer activity has been suggested but there is no report on its action via inhibiting acetylation against cell

Phenolic metabolites of clomiphene: [(E,Z)-2-[4-(1,2-diphenyl-2-chlorovinyl)phenoxy]ethyl]diethylamine. Preparation, electrophilicity, and effects in MCF 7 breast cancer cells.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

The triarylethylene antiestrogen clomiphene was previously shown to undergo biotransformation to an active metabolite, 4-hydroxyclomiphene, and to 3-methoxy-4-hydroxyclomiphene plus the respective regioisomers of these, 4 and 5. We now report the synthesis and further chemical and biochemical

Metabolism and toxicity of benzophenone in isolated rat hepatocytes and estrogenic activity of its metabolites in MCF-7 cells.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

The metabolism and cytotoxicity of benzophenone and estrogenic activity of its metabolites have been studied in freshly isolated rat hepatocytes and cultured MCF-7 human breast cancer cells, respectively. The incubation of hepatocytes with benzophenone (0.25-1.0 mM) elicited a concentration- and

Rapid assessment of estrogenic compounds by CXCL-test illustrated by the screening of the UV-filter derivative benzophenones.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

CXCL-test is a method that uses the estrogen-dependent secretion of the natural endogenous chemokine CXCL12 to evaluate the estrogenic activity of molecules. CXCL12 chemokine is involved in the estrogen dependent proliferation of breast cancer cells. Its measure is an indicator of cell proliferation

Effects of exposure to six chemical ultraviolet filters commonly used in personal care products on motility of MCF-7 and MDA-MB-231 human breast cancer cells in vitro.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

Benzophenone (BP)-1, BP-2, BP-3, octylmethoxycinnamate (OMC), 4-methylbenzilidenecamphor and homosalate are added to personal care products to absorb ultraviolet light. Their presence in human milk and their oestrogenic activity suggests a potential to influence breast cancer development. As

Synthesis, in vitro and in vivo activity of benzophenone-based inhibitors of steroid sulfatase.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

Steroid sulfatase (STS) is an important new therapeutic target in oncology. Attempts to design nonsteroidal STS inhibitors, because of the oestrogenicity of the original lead oestrone 3-O-sulfamate in rodents, have led to the discovery of benzophenone-4,4'-O,O-bis-sulfamate (BENZOMATE, 3). The

UPLC-QTOFMS(E)-Guided Dereplication of the Endangered Chinese Species Garcinia paucinervis to Identify Additional Benzophenone Derivatives.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

A number of Garcinia species accumulate benzophenone derivatives that may be useful for the treatment of breast cancer. The dereplication of new benzophenone derivatives from Garcinia species is challenging due to the occurrence of multiple isomers and the known compounds found in their extracts. In

Synthesis of Benzophenones and in vitro Evaluation of Their Anticancer Potential in Breast and Prostate Cancer Cells.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

Breast and prostate cancers are frequently treated with chemotherapy. Several novel chemicals are being reported for this purpose, particularly synthetic and natural benzophenones. This work reports the synthesis of substituted 2-hydroxybenzophenones through 1,4-conjugate addition/intramolecular

Enhanced antitumor potential induced by chloroacetate-loaded benzophenones acting as fused tubulin-pyruvate dehydrogenase kinase 1 (PDHK1) ligands.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

The majority of cancers detected every year are treated with anti-cancer compounds. Unfortunately, many tumors become resistant to antineoplastic drugs. One option is to use cocktails of compounds acting on different targets to try to overcome the resistant cells. This type of approach can produce

Effects of nemorosone, isolated from the plant Clusia rosea, on the cell cycle and gene expression in MCF-7 BUS breast cancer cell lines.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

BACKGROUND Breast cancer is the cause of considerable morbidity and mortality in women. While estrogen receptor antagonists have been widely used in breast cancer treatment, patients have increasingly shown resistance to these agents and the identification of novel targeted therapies is therefore

Cytotoxic activity of nemorosone in human MCF-7 breast cancer cells.

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

Estrogen receptor (ER) antagonists have been widely used for breast cancer treatment; however, patients have increasingly shown resistance and sensitivity to the high toxicity of these drugs, and identification of novel targeted therapies is therefore required. To determine whether nemorosone, a

Design, synthesis, and anticancer evaluation of benzophenone derivatives bearing naphthalene moiety as novel tubulin polymerization inhibitors

केवल पंजीकृत उपयोगकर्ता ही लेखों का अनुवाद कर सकते हैं

साइन अप करने के लिए लॉग इन करें

A series of benzophenone derivatives bearing naphthalene moiety were designed, synthesized, characterized by ¹H NMR, ¹³C NMR, and HRMS and evaluated for their antiproliferative activity against human breast cancer cell line (MCF-7). Most of the tested derivatives showed good to

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