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Publikationer som ChEBI hänvisar till för elliptinium acetate. Visa hela publikationsregistret

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Publikationer i urvalet

6 träffar

Bibliografisk träff 1994-07-01

Anticancer specificity of some ellipticinium salts against human brain tumors in vitro.

Acton EM, Narayanan VL, Risbood PA, Shoemaker RH, Vistica DT, Boyd MR.

J Med Chem · research support, u.s. gov't, p.h.s.; journal article · DOI 10.1021/jm00040a010

Bibliografisk träff 1994-07-01

Synthesis and evaluation of 9-hydroxy-5-methyl-(and 5,6-dimethyl)-6H-pyrido[4,3-b]carbazole-1-N- [(dialkylamino)alkyl]carboxamides, a new promising series of antitumor olivacine derivatives.

Jasztold-Howorko R, Landras C, Pierré A, Atassi G, Guilbaud N, Kraus-Berthier L, Léonce S, Rolland Y, Prost JF, Bisagni E.

J Med Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/jm00041a024

Bibliografisk träff 1994-06-01

Design, synthesis, and study of 9-substituted ellipticine and 2-methylellipticinium analogues as potential CNS-selective antitumor agents.

Anderson WK, Gopalsamy A, Reddy PS.

J Med Chem · comparative study; research support, u.s. gov't, p.h.s.; research support, u.s. gov't, non-p.h.s.; journal article · DOI 10.1021/jm00039a007

Bibliografisk träff 1988-07-01

Synthesis and antitumor activity of quaternary ellipticine glycosides, a series of novel and highly active antitumor agents.

Honda T, Kato M, Inoue M, Shimamoto T, Shima K, Nakanishi T, Yoshida T, Noguchi T.

J Med Chem · comparative study; journal article · DOI 10.1021/jm00402a007

Bibliografisk träff 1986-09-01

Synthesis of 11H-pyridocarbazoles and derivatives. Comparison of their DNA binding and antitumor activity with those of 6H- and 7H-pyridocarbazoles.

Lescot E, Muzard G, Markovits J, Belleney J, Roques BP, Le Pecq JB.

J Med Chem · comparative study; research support, non-u.s. gov't; journal article · DOI 10.1021/jm00159a028

Bibliografisk träff 1986-08-01

Ribose as the preferential target for the oxidized form of elliptinium acetate in ribonucleos(t)ides. Biological activities of the resulting adducts.

Pratviel G, Bernadou J, Ha T, Meunier G, Cros S, Meunier B, Gillet B, Guittet E.

J Med Chem · research support, non-u.s. gov't; journal article · DOI 10.1021/jm00158a005