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Camptothecin mw

WebCamptothecin traps an important cellular enzyme, topoisomerase I, in complexes with DNA. This prevents cancer cell DNA replication and results in the death of the cancer cell. This unique mode of action rekindled interest in developing analogs of camptothecin that were both water soluble and retained anticancer activity. WebMolecular Weight (MW) 348.35 Formula C20H16N2O4 CAS No. 7689-03-4 Synonyms N/A 2 years -20°C Powder 2 weeks4°C in DMSO 6 months-80°C in DMSO Solubility (25°C) …

In-silico prediction of highly promising natural ... - ScienceDirect

WebCamptothecin; 9-Nitro-20 (S) Camptothecin (Rubitecan) 10-Hydroxy Camptothecin; 9-Amino Camptothecin; Topo II. Doxorubicin (Adriacin) Daunomycin; Etoposide (VP16) Amsacrine (m-AMSA) Genistein; Ellipticine; HU-331; Gyrase & Topo IV. Ciprofloxacin; Cell Context DNA Repair. Homologous Recombination Reporter Cells. Human: HeLa … WebJan 14, 2024 · Camptothecin the third most in demand alkaloid, is commercially extracted in India from the endangered plant, Nothapodytes nimmoniana. Endophytes, the microorganisms that reside within plants,... shanolina flower shop https://value-betting-strategy.com

Sustainable production of camptothecin from an - Nature

WebCamptothecin (CPT), a proven anticancer drug, is distributed across several families and genera and is still extracted from Nothapoytes foetida and Camptotheca acuminata, due to their initial discovery in these two plants. The study of biogenesis and chemistry of CPT is imperative, as this paves a way for semisynthesis or total synthesis of CPT. WebMW 348.35. Cell-permeable DNA topoisomerase inhibitor. Potent antitumour and antibiotic agent. Achieve your results faster with highly validated, pure and trusted compounds. ... The cells were incubated at 37°C for 3h in media containing different concentrations of ab120115 (camptothecin) in DMSO, fixed with 4% formaldehyde for 10 minutes at ... WebCamptothecin, Camptotheca acuminata A cell-permeable DNA topoisomerase I inhibitor.; CAS Number: 7689-03-4; Synonyms: Camptothecin, Camptotheca acuminata,4-Ethyl-4-hydroxy-1H-pyrano[3ʹ,4ʹ:6,7]indolizino[1,2-b]quinoline-3,14(4H,12H)dione; find Sigma-Aldrich-208925 MSDS, related peer-reviewed papers, technical documents, similar … poms elizabeth city nc

Camptothecin, 98%, Thermo Scientific Chemicals - Fisher Sci

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Camptothecin mw

Camptothecin, Camptotheca acuminata - Sigma-Aldrich

WebCamptothecin showed best apoptosis at 12uM concentration which is equal to 4ug/ml of your working concentration. I calculated it as follows: Camptothecin MW= 348.36 4ug/ml= 4mg/L 4mg/L/348.35... WebIt is a synthetic, water-soluble analog of the natural chemical compound camptothecin. It is used in the form of its hydrochloride salt to treat ovarian cancer, lung cancer and other …

Camptothecin mw

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WebCamptothecin is a natural product extracted from the bark of the tree Camptotheca acuminata. Topoisomerase-I is a nuclear enzyme that relieves torsional strain in DNA by opening single strand breaks. [16] Once topoisomerase-I creates a single strand break, the DNA can rotate in front of the advancing replication fork. WebDescription: Camptothecin (CPT) is a cytotoxic quinoline alkaloid which inhibits the DNA enzyme topoisomerase I (topo I). It was discovered in 1966 by M. E. Wall and M. C. …

Web位置:首页 > 产品库 > 7-Ethyl-d3-camptothecin. 7-Ethyl-d3-camptothecin. ... 分子量 Molecular Weight: 379: 闪点 FP: 409.1±32.9 ℃ ... WebDownload scientific diagram Structures of Camptothecin (1, MW 348) and its analogues (2, MW 365; 3, MW 378). from publication: The Anti-HIV Actions of 7- and 10-Substituted Camptothecins ...

WebCamptothecin is a topo I poison that both inhibits enzyme activity and stabilizes formation of topo I cleavage complexes (Hsiang et al J. Biol. Chem. 260:14873-14878, 1985). TopoGEN provides this reagent as a control inhibitor/poison of topoisomerase I. For in vitro cleavage detection, we recommend that the drug be tested in the range 100 uM ... WebJan 4, 2005 · Camptothecin- and etoposide-induced apoptosis in human leukemia cells is independent of cell death receptor-3 and -4 aggregation but accelerates tumor necrosis factor–related apoptosis-inducing ligand–mediated cell death Molecular Cancer Therapeutics American Association for Cancer Research Article ARTICLE January 04 …

WebCamptothecin is an alkaloid first isolated from the stem wood of the tree Camptotheca acuminata (Nyssaceae), and has potent antitumor activity. 31 Camptothecin acts by inhibiting the enzyme topoisomerase-I, which is responsible for relaxing supercoils that are generated during transcription and DNA replication. 32 A number of reports have ...

Web(S)-(+)-Camptothecin binds irreversibly to the DNA-topoisomerase I complex, inhibiting the reassociation of DNA after cleavage by topoisomerase I and traps the enzyme in a covalent linkage with DNA. … shan oliverWebCamptothecin, an quinolone alkaloid, is used as a chemotherapeutic agent in the treatment of leukemia (Jones et al., 1997). Camptothecin complexes with type I DNA … poms englishWebApr 13, 2024 · The fabrication of pH-sensitive lignin-based materials has received considerable attention in various fields, such as biomass refining, pharmaceuticals, and detecting techniques. However, the pH-sensitive mechanism of these materials is usually depending on the hydroxyl or carboxyl content in the lignin structure, which hinders the … poms erosion of the occupational baseWebJan 14, 2024 · An m/z of 349.12 corresponds to that of camptothecin with all unlabelled carbon atoms and the presence of one 13 C labeled carbon would increase the … shan onWebApr 10, 2024 · The virtual screening revealed that two alkaloidal metabolites, camptothecin and GKK1032A2 showed excellent binding energy with any target proteins compared to reference commercial fungicides, Azoxystrobin and Strobilurin. ... The molecular weight of the selected compounds was more or less than 500 g/mol (348.35 g/mol and 503.67 … shanon beninihttp://www.cnreagent.com/s/sv245399.html shanon applegarth springfield moWebHerein, we fabricated a novel amphiphilic lactose-camptothecin prodrug molecular Lac-SS-CPT which can self-assemble into Lac-SS-CPT glyco-nano prodrug system for GSH responsive and targeted drug co-delivery due to the existence of disulfide bond and lactose. 41–44 Then, the CPT-based glyco-nano prodrug system further provides a suitable ... shanon argenta