Titlebook: International Symposium on Adriamycin; Milan, 9th-10th Sept Stephen K. Carter,A. Di Marco,G. Mathé Conference proceedings 1972 Springer-Ver

cauda-equina

菊花

Antitumor Effects of Adriamycin on Yoshida Rat Sarcoma and L 1210 Mouse Leukemia — Cross-resistance stitution of a hydroxyl group for a hydrogen atom in the acetyl radical of the aglycone moiety of daunomycin [2]. Adriamycin was reported to possess a higher therapeutic index than daunomycin in serval experimental tumor systems [3, 4]. This paper deals with cross-resistance studies using various re

Inflamed

Cross-resistance between Adriamycin, Daunomycin and Vincristine in Ehrlich Ascites Tumor been done using experimental tumors as model systems. In the present investigation, the development of resistance to several drugs, including daunomycin and adriamycin, was studied in Ehrlich ascites tumor . in mice.

物質(zhì)

賞心悅目

trigger

Structure and Physicochemical Properties of Adriamycin (Doxorubicin)he tetracyclic quinoid aglycone adriamycinone (14-hydroxydaunomycinone) linked to the amino- sugar daunosamine. The chemical name for adriamycin is therefore the following: (7S : 9S)-9-hydroxyacetyl-4-methoxy-7,8,9,10-tetrahydro-6,7,9, ll-tetrahydroxy-7-0- (2′3′6′-trideoxy-3′-amino-α-L-lyxohexopyranosyl)-5,12-naphthacenedione.

FLORA

詞匯

Meditative

DNR215

Short Summary of the Informal Meeting Preceeding the Adriamycin SymposiumDespite the large number of growth-inhibiting compounds isolated and proved to be active against neoplastic cells in . cultures or in animal tumors, the final goal of a highly efficient and safe therapy of human tumor is not yet achieved.