Alkaloids isolated from natural herbs as the anticancer agents. - sprookjes - yvandenbroek - TriplyDB

Alkaloids isolated from natural herbs as the anticancer agents.

Alkaloids isolated from natural herbs as the anticancer agents.

http://www.wikidata.org/entity/Q42324855

about

Phytochemicals and Biogenic Metallic Nanoparticles as Anticancer Agents Sanguinaria canadensis: Traditional Medicine, Phytochemical Composition, Biological Activities and Current Uses Saponins from Chinese Medicines as Anticancer Agents Chalepin: isolated from Ruta angustifolia L. Pers induces mitochondrial mediated apoptosis in lung carcinoma cells RANDOMIZED ANTICANCER AND CYTOTOXICITY ACTIVITIES OF GUIBOURTIA COLEOSPERMA AND DIOSPYROS CHAMAETHAMNUS Tetrandrine Suppresses Cancer Angiogenesis and Metastasis in 4T1 Tumor Bearing Mice.In vitro anti-proliferative activity of Argemone gracilenta and identification of some active components.Differential control of growth, apoptotic activity and gene expression in human colon cancer cells by extracts derived from medicinal herbs, Rhazya stricta and Zingiber officinale and their combination Hormetic Effect of Berberine Attenuates the Anticancer Activity of Chemotherapeutic Agents.Platycodin D induces apoptosis and triggers ERK- and JNK-mediated autophagy in human hepatocellular carcinoma BEL-7402 cells.Cell cycle arrest and apoptosis induction by methanolic leaves extracts of four Annonaceae plants In vitro cytotoxic and in silico activity of piperine isolated from Piper nigrum fruits Linn.Herbal medicine and acupuncture for breast cancer palliative care and adjuvant therapy.Low-cytotoxic synthetic bromorutaecarpine exhibits anti-inflammation and activation of transient receptor potential vanilloid type 1 activities.Anticancer activities of alkaloids extracted from the Ba lotus seed in human nasopharyngeal carcinoma CNE-1 cells.Anti-melanoma activity of Forsythiae Fructus aqueous extract in mice involves regulation of glycerophospholipid metabolisms by UPLC/Q-TOF MS-based metabolomics study.Understanding the Effectiveness of Natural Compound Mixtures in Cancer through Their Molecular Mode of Action.Prediction of pharmacokinetic parameters using a genetic algorithm combined with an artificial neural network for a series of alkaloid drugs.Tetrandrine Induces Apoptosis of Human Nasopharyngeal Carcinoma NPC-TW 076 Cells through Reactive Oxygen Species Accompanied by an Endoplasmic Reticulum Stress Signaling Pathway.The Interference of Selected Cytotoxic Alkaloids with the Cytoskeleton: An Insight into Their Modes of Action.Natural isoquinoline alkaloids: binding aspects to functional proteins, serum albumins, hemoglobin, and lysozyme.Effects of crude extracts from medicinal herbs Rhazya stricta and Zingiber officinale on growth and proliferation of human brain cancer cell line in vitro.Emerging Cytotoxic Alkaloids in the Battle against Cancer: Overview of Molecular Mechanisms.Effect of chirality and lipophilicity in the functional activity of evodiamine and its analogues at TRPV1 channels.Gamma irradiation of medicinally important plants and the enhancement of secondary metabolite production.The use of natural products to target cancer stem cells.Natural small-molecule enhancers of autophagy induce autophagic cell death in apoptosis-defective cells.UPLC-MS/MS Profile of Alkaloids with Cytotoxic Properties of Selected Medicinal Plants of the Berberidaceae and Papaveraceae Families.Recent developments on potential new applications of emetine as anti-cancer agent.Multiple effects of berberine derivatives on colon cancer cells.Anticancer mechanisms of Strobilanthes crispa Blume hexane extract on liver and breast cancer cell lines.Apoptosis sensitization by Euphorbia factor L1 in ABCB1-mediated multidrug resistant K562/ADR cells.Differential modes of photosensitisation in cancer cells by berberine and coralyne.Screening of Natural Bioactive Metabolites and Investigation of Antioxidant, Antimicrobial, Antihyperglycemic, Neuropharmacological, and Cytotoxicity Potentials of Litsea polyantha Juss. Ethanolic Root Extract.Exploring β-Tubulin Inhibitors from Plant Origin using Computational Approach.Cancer Chemoprevention and Piperine: Molecular Mechanisms and Therapeutic Opportunities.Preparation, Characterization and Anti-Ulcer Efficacy of Sanguinarine Loaded Solid Lipid Nanoparticles.Synthetic Fluororutaecarpine Inhibits Inflammatory Stimuli and Activates Endothelial Transient Receptor Potential Vanilloid-Type 1.Effects of curine in HL-60 leukemic cells: cell cycle arrest and apoptosis induction.Anticancer drug discovery from Chinese medicinal herbs.

P2860

Q26750806-E3BDBC87-72CF-4577-98EC-EE396034B18C Q28077612-7E835A1D-8100-427B-81FF-DEC6BF58E476 Q28079313-9FB92F41-F55F-40B0-9157-320E5AF6D78D Q28822187-EFCFCE22-1C4D-4580-A05C-7E5EBF08DE05 Q33800283-6AE04524-A982-4CCE-A2C0-49C1FB3F1040 Q34769302-F7F34C2C-50B6-427E-AA80-A34CB3081B16 Q35063884-F119D157-EE49-425A-915F-BB5EB3409B25 Q35409119-EF61DF60-578B-4E47-A725-E8A101C5633F Q35793110-A17D6FE1-6448-4D50-A4F0-1789FBF672E1 Q35848147-CE383322-64D3-4CD6-A584-BCC4CF25063F Q36393340-07D8553A-8CD1-49FD-B131-2B602040F550 Q36515808-45B16AC8-19D8-45D3-9F55-B292FE2D824E Q36959971-D4141960-ACBD-4FF2-950F-25F1A6C0ABE3 Q37392935-E5323EB9-DF17-4B0B-B7CA-B35B87456B0B Q37406501-87B8235F-CB3F-4E3C-89A7-499A696ADCAA Q37519196-BB44A212-C731-43A5-A937-0B8EAEB4D192 Q37729331-D7C4ECBD-485F-4851-9CCE-EC56F311D48F Q38258986-B9721B97-B51D-4470-91F6-E361D54470D8 Q38740290-B593908A-0DFC-4786-9A98-662DE0EEE75E Q38758021-103000D9-FB4B-423A-AEDA-8E3E3E21AAE1 Q38783090-629E397E-02BD-4704-8AB7-EEE2F80C5903 Q38964722-0205FD36-C87F-421A-A58A-C4BFD2A992FD Q39139241-434399EE-80DC-42B8-BDF5-2B438D8C78EE Q39189093-F764EC20-B9BD-4575-9454-D6625F66B61F Q39438719-9D7F604A-62DA-4637-9B4D-E7ADF1A53668 Q39458512-A1AA9101-B8E0-4CD8-81BF-20EFECA7D359 Q41552829-2AA59890-47DE-411B-B3AF-2382B3C0CA03 Q41689951-BAA3B9CD-050B-48FB-8980-AB1A2AD041BC Q41781729-26D94F5D-7DA8-4172-960C-ED1ACC1E246F Q42151449-1FD74362-CA58-48F6-9A5D-19FFFB9EA091 Q45195757-C7B66093-4EB2-4721-9E7C-4FC12D1CB6DA Q45404446-26B0E84F-6260-40C3-9C3F-1EF4D11EF2D4 Q46312377-D9F15F54-61D4-46F4-ADCD-82398644A1F1 Q47106061-D66B9E16-BAB0-4C81-B651-00A4F32542E8 Q48032873-0B75E893-B348-4271-A647-D9B43DC0DB59 Q50333246-982A1E49-2C59-49D1-A21C-C4AC61A8D024 Q50778983-8AA083BE-E685-447D-A4C8-017E3BEE115A Q50910868-A6E57537-5C18-4A21-B400-4102936C1C5E Q52973137-8E6C070A-A296-4A5F-990C-902A6FD7B09F Q55533017-DE5C5D69-A119-4272-BBD2-993C9F8A662E

P2860

Alkaloids isolated from natural herbs as the anticancer agents.

http://www.wikidata.org/entity/Q42324855

description

2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

2012年论文

@zh

2012年论文

@zh-cn

name

Alkaloids isolated from natural herbs as the anticancer agents.

@en

Alkaloids isolated from natural herbs as the anticancer agents.

@nl

type

label

Alkaloids isolated from natural herbs as the anticancer agents.

@en

Alkaloids isolated from natural herbs as the anticancer agents.

@nl

prefLabel

Alkaloids isolated from natural herbs as the anticancer agents.

@en

Alkaloids isolated from natural herbs as the anticancer agents.

@nl

P1433

Q42324855-BFD9EA08-EC36-4B6C-AADE-CC8D0EF113B2

P1476

Q42324855-88B7D526-C983-47B8-8B0B-D85121CEBC23

P2093

Q42324855-0A622E1E-4F46-4182-90A8-5AAFECDC14A0

Q42324855-26F8080C-DF8D-4C27-875B-1650E276BDAF

Q42324855-7568BAC2-C4E6-4321-8674-603DD7EFF44B

Q42324855-E16A5C7C-2A84-4EEA-8B96-06D2D9B04ACE

P2860

Q42324855-00137BAE-7810-491B-A6AF-FC00BB433F3C

Q42324855-03558016-6B47-44CC-9224-E546C82BD59F

Q42324855-03A94E65-635C-4882-B98A-3A6E0A40AEE8

Q42324855-0A6A9A58-E9C0-47BE-A532-AD03AEA96302

Q42324855-0AD98AF7-1CBB-4D41-9964-F5D0790B4013

Q42324855-0CDBEB98-8517-4253-AA4A-441B2175CEF9

Q42324855-0E3A4E4D-7542-4F14-8EB3-C08C7EC5CA7C

Q42324855-0E51FA5A-B20D-4E49-9A72-AAA38D8A88F9

Q42324855-112CB747-D5CB-46A3-B4BD-424470018372

Q42324855-115009E5-E90F-42F3-8071-ACDFE72CBACB

P304

Q42324855-AC8A32FD-5369-431A-ABA1-BE534769D34E

P31

Q42324855-D0BBD268-E593-433B-B8CE-653118396B2D

P356

Q42324855-169A0E2B-4CB7-4F9A-9D95-E422E4563662

P478

Q42324855-87D87A1E-E8D8-47B1-95DB-733D65CA5F31

P50

Q42324855-9FF590DA-DDEE-41FD-ACCD-48886E1389A9

P577

Q42324855-41A8B10F-CADB-4D14-A475-3861513A14AA

P5875

Q42324855-F8AE6C01-6CC9-4CFD-8443-8E039CF13ECA

P698

Q42324855-8C203F2A-74CD-4DE0-978A-BEE28D2228D5

P932

Q42324855-C1718602-A700-4092-9C5A-ACCC671455DB

P356

P1433

Evidence-based Complementary and Alternative Medicine

P1476

Alkaloids isolated from natural herbs as the anticancer agents

@en

P2093

Jiao-Lin Bao

http://www.w3.org/2001/XMLSchema#string

Min Huang

http://www.w3.org/2001/XMLSchema#string

Xiu-Ping Chen

http://www.w3.org/2001/XMLSchema#string

Yi-Tao Wang

http://www.w3.org/2001/XMLSchema#string

P2860

Disruption of nucleocytoplasmic trafficking of cyclin D1 and topoisomerase II by sanguinarine

Berberine inhibits metastasis of nasopharyngeal carcinoma 5-8F cells by targeting Rho kinase-mediated Ezrin phosphorylation at threonine 567

Capsaicin-like anti-obese activities of evodiamine from fruits of Evodia rutaecarpa, a vanilloid receptor agonist

Activation of prodeath Bcl-2 family proteins and mitochondrial apoptosis pathway by sanguinarine in immortalized human HaCaT keratinocytes

Antimicrobial activity of berberine alone and in combination with ampicillin or oxacillin against methicillin-resistant Staphylococcus aureus

Multi-target drugs: the trend of drug research and development

Preparation, characterization, pharmacokinetics and tissue distribution of solid lipid nanoparticles loaded with tetrandrine.

Enhancement of radiosensitivity in human glioblastoma U138MG cells by tetrandrine.

Sanguinarine-induced apoptosis is associated with an early and severe cellular glutathione depletion.

Atypical apoptosis in L929 cells induced by evodiamine isolated from Evodia rutaecarpa.

P304

485042

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1155/2012/485042

http://www.w3.org/2001/XMLSchema#string

P478

2012

http://www.w3.org/2001/XMLSchema#string

P50

P577

2012-09-04T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

230872186

http://www.w3.org/2001/XMLSchema#string

P698

22988474

http://www.w3.org/2001/XMLSchema#string

P932

3440018

http://www.w3.org/2001/XMLSchema#string