WebHere we have identified novel Top1 inhibitors as potential anticancer agents by using a combination of structure- and ligand-based molecular modelling methods. Pharmacophore models have been developed based on the molecular characteristics of derivatives of the alkaloid camptothecin (CPT), which represent potent antitumour agents and the main ... WebApr 10, 2024 · The crystal structure of M. oryzae single-stranded DNA binding protein (PDB ID: 4AGH at 1.79 Å resolution), and ... ARG71 formed electrostatic interactions. (B) Camptothecin formed a hydrogen bond with A:TYR73, A:ASN69, and A:SER60 and hydrophobic interactions with residues A:PHE67.2D interaction analysis is shown on the …
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WebMar 1, 1989 · From the structure-activity relations, the regions of interaction between the camptothecin ring system and the receptor site were inferred. Striking correlations were observed between activity against topoisomerase I and reported activity against murine leukemias, indicating that an action on topoisomerase I is responsible for the antitumor ... qtc in harlingen
Passive and active targeting strategies for the delivery of the ...
WebCamptotecina. La camptotecina (CPT) és un inhibidor de la topoisomerasa tipus I. Va ser descobert el 1966 per M. E. Wall i M. C. Wani en un cribratge sistemàtic de productes naturals per a antineoplàstics. Va ser aïllat de l' escorça i la tija de Camptotheca acuminata, un arbre originari de la Xina utilitzat com a tractament contra el ... WebDec 8, 2003 · Total Structure Weight: 81.14 kDa Atom Count: 5,386 Modelled Residue Count: 538 Deposited Residue Count: 609 Unique protein chains: 1 Unique nucleic acid … WebDownload scientific diagram Camptothecin structure and equilibrium between the active lactone form and the inactive carboxylate form. from publication: Camptothecin … qtc hospital monitor