Camptothecin mw
WebCamptothecin, an quinolone alkaloid, is used as a chemotherapeutic agent in the treatment of leukemia (Jones et al., 1997). Camptothecin complexes with type I DNA … WebApr 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 …
Camptothecin mw
Did you know?
WebCamptothecin is an alkaloid compound used as an anti-cancer agent. It is a topoisomerase I inhibitor in DNA synthesis. Camptothecin has been shown to bind and stabilize a topoisomerase I-DNA complex in vitro, preventing … 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) …
WebJan 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 … 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...
WebCamptothecin (NSC-100880, CPT, Campathecin, (S)-(+)-Camptothecin) is a specific inhibitor of DNA topoisomerase I (Topo I) with IC50 of 0.68 μM in a cell-free assay. Camptothecin induces apoptosis in cancer cells via … 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 ...
WebHerein, 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 ...
WebCamptothecin, Camptotheca acuminata. Synonym (s): Camptothecin, Camptotheca acuminata. Empirical Formula (Hill Notation): C20H16N2O4. CAS No.: 7689-03-4. Molecular Weight: 348.35. Compare. Product No. tsw supportWebJan 15, 2024 · As a famous quinoline alkaloid, camptothecin (CPT) presented the significant anti-tumor activity, as well as the interesting insecticidal activities, but the low solubility, poor hydrophobicity and cuticular penetration of CPT have been severely limited the field application. In this study, we conjugated the camptothecin with polyethylene … pho bistreaux food truck menuWebJan 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 … tsw suggestionsWeb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 ℃ ... tsw strategic advisoryWebJan 15, 2024 · As a famous quinoline alkaloid, camptothecin (CPT) presented the significant anti-tumor activity, as well as the interesting insecticidal activities, but the low … tsw syicol cameraWebCamptothecin, an alkaloid isolated from the Chinese tree Camptotheca acuminate, is a potent cytotoxic agent, acting by the inhibition of DNA topoisomerase I [107]. Numerous derivatives of camptothecin have been synthesized in order to improve its pharmacological profile for effective anti‐tumour drugs. tsw switchWebDec 1, 2012 · Camptothecin exists in two distinguishable forms at different pH conditions, an active closed lactone ring and an inactive carboxylate form (Fig. 1).At alkaline and physiological conditions, camptothecin lactone is unstable and rapidly converts to the inactive carboxylate form, leading to the loss of antitumor activity [5].Furthermore, like … tswsyl.gnway.cc:8088