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Camptothecin mw

WebJan 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 … 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 …

Camptothecin CPT CAS#7689-03-4 topoisomerase I inhbitior

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 ... WebMolecular Weight (g/mol) 348.35: MDL Number: MFCD00081076: InChI Key: VSJKWCGYPAHWDS-FQEVSTJZSA-N: Synonym: camptothecin, camptothecine, s-+ … imgtown 3600 https://lancelotsmith.com

Camptothecin, 98%, Thermo Scientific Chemicals - Fisher Sci

WebMin: 1. Step: 1. Add to Cart. TG2011-4. Topoisomerase I Western Blot Marker. The Western blot marker set for topo I is used to unambiguously locate the position of the 100 kDa form of intact topo I. This product is supplied in SDS-PAGE loading buffer and ready to load directly onto an SDS-PAGE. $ 375.00. Max: 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... WebAug 21, 2009 · Human serum was spiked with camptothecin and the sample injected in a mixture of 250 μl each of upper and lower layer. Fig. 8 depicts the chromatogram of this run. As an extracted ion chromatogram at m/z = 349 shows, camptothecin, of MW 348, elutes at 37.9 min, or nearly identical to its elution time from dog bile. In this solvent system, the ... list of popular song lyrics

Protein MW Markers - TopoGEN

Category:Camptothecin, Camptotheca acuminata - Sigma-Aldrich

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Camptothecin mw

Camptothecin - an overview ScienceDirect Topics

WebCamptothecin. Camptothecin is a naturally occurring alkaloid derived from the plant Camptotheca acuminata that was identified in an anticancer drug discovery screen in the 1960s.67 Camptothecin forms a stable ternary complex, preventing normal DNA re-ligation, and causes the complex to collide with the replication fork, leading to a DNA double … WebSDS (+)-Camptothecin, 98%, Thermo Scientific Chemicals 100 mg, Glass bottle Quantity: 100 mg 1 g Packaging: Glass bottle Description This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand.

Camptothecin mw

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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. 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 …

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. … WebApr 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 …

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. 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 …

WebDec 5, 2024 · The highly toxic payloads, for instance, maytansine, camptothecin derivatives, auristatin, or doxorubicin are recommended to choose in the conjugates. 9 Finally, ... and the purified DM1-B6 was analyzed with HPLC and ESI-MS for purity and molecular weight. The collected fractions with the target molecule were combined, …

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 ... list of popular star wars charactersWebCamptothecin, Camptotheca acuminata - CAS 2114454. BRD-A30437061-001-01-9. BRD-A30437061-001-04-3. Q27163449. 4-Ethyl-4-hydroxy-1H,12H-6,12a-diaza-2-oxa-13H-dibenzo [b,h]fluorene-3,13 (4H) … list of popular software applicationsWebCamptothetin (CPT) is a quinoline alkaloid originally isolated from the Chinese tree, Camptotheca acuminata Decne. CPT was found to have anticancerous and antiviral properties. Derivatives of... imgtown 4310WebJan 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 … list of pork meatsWebCamptothecin is a cytotoxic plant alkaloid with antitumor properties; prototypic DNA topoisomerase I inhibitor. Induces single strand DNA breaks and protein-DNA crosslinks. … imgtown 4008imgtown 6000WebCamptothecin 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 ... imgtown 3101