BIOMAT Database Logo BIOMAT Database Logo

Adriamycin analogs hydroxylated at c-3': synthesis and antitumor activity. 1979

D Horton, and W R Turner

UI MeSH Term Description Entries
D007942 Leukemia, Experimental Leukemia induced experimentally in animals by exposure to leukemogenic agents, such as VIRUSES; RADIATION; or by TRANSPLANTATION of leukemic tissues. Experimental Leukemia,Experimental Leukemias,Leukemia Model, Animal,Leukemias, Experimental,Animal Leukemia Model,Animal Leukemia Models,Leukemia Models, Animal
D003630 Daunorubicin A very toxic anthracycline aminoglycoside antineoplastic isolated from Streptomyces peucetius and others, used in treatment of LEUKEMIA and other NEOPLASMS. Daunomycin,Rubidomycin,Rubomycin,Cerubidine,Dauno-Rubidomycine,Daunoblastin,Daunoblastine,Daunorubicin Hydrochloride,NSC-82151,Dauno Rubidomycine,Hydrochloride, Daunorubicin,NSC 82151,NSC82151
D004317 Doxorubicin Antineoplastic antibiotic obtained from Streptomyces peucetius. It is a hydroxy derivative of DAUNORUBICIN. Adriamycin,Adriablastin,Adriablastine,Adriblastin,Adriblastina,Adriblastine,Adrimedac,DOXO-cell,Doxolem,Doxorubicin Hexal,Doxorubicin Hydrochloride,Doxorubicin NC,Doxorubicina Ferrer Farm,Doxorubicina Funk,Doxorubicina Tedec,Doxorubicine Baxter,Doxotec,Farmiblastina,Myocet,Onkodox,Ribodoxo,Rubex,Urokit Doxo-cell,DOXO cell,Hydrochloride, Doxorubicin,Urokit Doxo cell
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D013329 Structure-Activity Relationship The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups. Relationship, Structure-Activity,Relationships, Structure-Activity,Structure Activity Relationship,Structure-Activity Relationships
D051379 Mice The common name for the genus Mus. Mice, House,Mus,Mus musculus,Mice, Laboratory,Mouse,Mouse, House,Mouse, Laboratory,Mouse, Swiss,Mus domesticus,Mus musculus domesticus,Swiss Mice,House Mice,House Mouse,Laboratory Mice,Laboratory Mouse,Mice, Swiss,Swiss Mouse,domesticus, Mus musculus

Related Publications

D Horton, and W R Turner
Synthesis and antitumor activity of 3'-C-methyl-daunorubicin.
January 1985, Carbohydrate research,
D Horton, and W R Turner
Sparsomycin analogs. VI. Synthesis and antitumor activity of octylsparsomycin analogs.
March 1989, Chemical & pharmaceutical bulletin,
D Horton, and W R Turner
Synthesis and antitumor activity of 2'-bromo- and 2'-chloro-3'-acetoxy-3'-deaminodaunorubicin analogs.
December 1985, Carbohydrate research,
D Horton, and W R Turner
Synthesis and antitumor activity of some curcumin analogs.
April 2005, Archiv der Pharmazie,
D Horton, and W R Turner
Synthesis, antitumor evaluation, and apoptosis-inducing activity of hydroxylated (E)-stilbenes.
February 2005, Journal of medicinal chemistry,
D Horton, and W R Turner
[Antitumor activity of adriamycin].
April 1972, The Japanese journal of antibiotics,
D Horton, and W R Turner
Synthesis and Antitumor Activity of Triazole-Containing Sorafenib Analogs.
October 2017, Molecules (Basel, Switzerland),
D Horton, and W R Turner
Synthesis and antitumor activity of simplified ecteinascidin-saframycin analogs.
March 2006, Bioorganic & medicinal chemistry letters,
D Horton, and W R Turner
Design, synthesis, and antitumor activity evaluation of pretubulysin analogs.
September 2021, Chemical biology & drug design,
D Horton, and W R Turner
Synthesis and Antitumor Activity of New Thiazole Nortopsentin Analogs.
December 2016, Marine drugs,
Copied contents to your clipboard!