Abstract: The present invention provides a lysine ester triisocyanate represented by general formula (I): (wherein R represents lower alkylene), characterized in that the change in a hue value (APHA) of the lysine ester triisocyanate is 20 or less when it is stored for two weeks at 40° C. in a nitrogen atmosphere under blocking light; and a process for producing the same.

Abstract: The present invention provides the following [1] to [3], etc.

Abstract: This invention pertains to the polyurethane composition with hydrophilicity and hydrolysis resistance. The purpose of this invention is achieved by:1) A polyurethane molecule containing at least one acidic hydrophilic group in the molecule which is neutralized with piperidine derivatives and piperazinone derivatives, or2) A mixture containing polyurethane and compounds(s) having at least one acidic hydrophilic group which is neutralized with piperidine derivatives and piperazinone derivatives.The invention polyurethane compositions which have excellent hydrolysis resistance and rupture strength are useful for adhesives, paints, and bonding agents for magnetic recording media.

Abstract: Mitomycin derivatives having potent antitumour activity have the formula: ##STR1## wherein R represents lower alkyl, cycloalkyl or unsubstituted or substituted aralkyl;X represents hydrogen or carbamoyl;Y and Z each independently represents hydrogen or methyl;and represents an .alpha. or .beta. bond.

Abstract: Mitomycin derivatives having potent antitumor activity having the formula: ##STR1## wherein A is ON--or R.sub.4 N.dbd.N--[wherein R.sub.4 is selected from ##STR2## and optionally substituted heterocyclic groups (wherein R.sub.5 and R.sub.8 are each independently selected from hydrogen, lower alkyl and lower cycloalkyl; R.sub.6 is selected from hydrogen, halogen, hydroxy, lower alkoxy, amino and nitro; R.sub.7 is selected from lower alkyl and lower cycloalkyl; and X is selected from oxygen, sulphur and imino)];R.sub.1 and R.sub.2 are each independently selected from hydrogen, lower alkyl, lower cycloalkyl, optionally substituted aralkyl, optionally substituted alkanoyl, optionally substituted arylcarbonyl, optionally substituted alkanesulfonyl, arylsulfonyl and aralkylsulfonyl;R.sub.3 is hydrogen or carbamoyl;Y is hydrogen or methyl;Z is selected from hydrogen, methyl and acetyl;and is an .alpha. or .beta. bond.