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Neoplasma ; 24(4): 401-4, 1977.
Article in English | MEDLINE | ID: mdl-904741

ABSTRACT

It is shown that L-cystine-bis-(N,N-beta-chloroethyl)-hydrazide-hydro-bromide possesses strong (50-100%) inhibitory effect in vivo against myeloma P-8, carcinosarcoma Walker, lymphosarcoma Pliss, sarcoma Yoshida, sarcoma Jensen and sarcoma 180 in doses 5-12 mg/kg/day. No suppression of the growth of Ehrlich ascites tumor was observed. The acute toxicity (LD50) of this substance on mice and rats is 71 mg/kg and 47 mg/kg respectively.


Subject(s)
Neoplasms, Experimental/drug therapy , Nitrogen Mustard Compounds/therapeutic use , Alkylation , Animals , Carcinoma, Ehrlich Tumor/drug therapy , Cats , Cystine/analogs & derivatives , Cystine/therapeutic use , Lethal Dose 50 , Mice , Mice, Inbred BALB C , Multiple Myeloma/drug therapy , Neoplasm Transplantation , Rats , Sarcoma, Experimental/drug therapy , Transplantation, Homologous
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