Abstract:
Thienothiazine derivs. (I; A formed B or C with two carbons, R1 = lower alkyl, R2 = aromatic heterocyclic residues, Ph, R3, R4 = H, lower alkyl) useful as antiphlogistic, anodyne, and antirheumatic, were prepd. by treating I(NHR2 = OR, R - lower alkyl) with amine (III), decyclizing IV, lower alkylizing I(R' = H), reacting I(OH = O, COHNR2 = H2) with isocyanate (O = C = N-R2) in the presence of strong base, or hydrolizing enamines (I; OH = NR5R6, R5, R6 = lower alkyl).
Abstract:
Benzene-ring substituted (2-methylhydrazino)-methyl-benzene compounds and intermediates therefore are described. The former compounds are useful as cytostatic agents and, particularly, inhibit the growth of transplantable tumors in both mice and rats. Thus, they are active, for example, against Walker tumors, Ehrlich carcinoma and Ehrlich ascites carcinoma.
Abstract:
BENZENE-RING SUBSTITUTED (2-METHYLHYDRAZINO)-METHYLBENZENE COMPOUNDS AND INTERMEDIATES THEREFOR ARE DESCRIBED. THE FORMER COMPOUNDS ARE USEFUL AS CYTOSTATIC AGENTS AND, PARTICUARLY, INHIBIT THE GROWTH OF TRANSPLANTABLE TUMORS IN BOTH MICE AND RATS. THUS, THEY ARE ACTIVE, FOR EXAMPLE, AGAINST WALKER TUMORS, EHRLICH CARCINOMA AND EHRLICH ASCITES CARCINOMA.
Abstract:
BEBZENE-RING SUBSTITUTED (2-METHYLHYDRAZINO)-METHYLBENZENE COMPOUNDS AND INTERMEIATES THEREOF ARE DESCRIBED. THE FORMED COMPOUNDS ARE USEFUL AS CYTOSTATIC AGENTS AND, PARTICULARLY, INIBIT THE ROOWTH OF TRANSPLANTALE TUMORS IN BOTH MICE AND RATS. THUS, THENY ARE ACTIVE FOR EXAMPLE, AGAINST WALKER TUMORS, ERLICH CARCINMA AND ERILICH ASCITES CARINOMA.
Abstract:
BENZENE-RING SUBSTITUTED (2-METHYLHYDRAZINO)-METHYLBENZENE COMPOUNDS AND INTERMEDIATES THEREFOR ARE DESCRIBED. THE FORMER COMPOUNDS ARE USEFUL AS CYTOSTATIC AGENTS AND, PARTICULARLY, IN HIBIT THE GROWTH OF TRANSPLANTABLE TOUMORS IN BOTH MICE AND RATS. THUS, THEY ARE ACTIVE, FOR EXAMPLE,AGAINST WALKER TUMORS, EHRILICH CARCINOMA AND EHRILICH ASCITES CARCINOMA.