Happolabiileja kytkentämolekyylejä

This invention relates to the field of immune therapy of cancer, more specifically to immunoconjugates of a cytotoxic moiety with a targeting moiety, more specifically to immunoconjugates of antibodies or fragments or functional derivatives of antibodies coupled to a cytotoxic substance such as drug...

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Main Authors BOS,EBO SYBREN, BOON,PETRUS JOHANNES, KASPERSEN,FRANCISCUS MICHAEL
Format Patent
LanguageFinnish
Swedish
Published 14.08.1998
Edition6
Subjects
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Abstract This invention relates to the field of immune therapy of cancer, more specifically to immunoconjugates of a cytotoxic moiety with a targeting moiety, more specifically to immunoconjugates of antibodies or fragments or functional derivatives of antibodies coupled to a cytotoxic substance such as drugs, toxins or radioisotopes. It especially relates to the release of substances bound to a targeting moiety through the use of acid-cleavable linker molecules derived from compounds of formula I. wherein: R1 = H, lower alkyl, -N-lower alkyl, -O-lower alkyl, -S-lower alkyl, -N-lower aralkyl, -O-lower aralkyl, -S-lower aralkyl, -N-lower alkylene, -O-lower alkylene, -S-lower alkylene, -N-lower aryl, -O-lower aryl, -S-lower aryl, R2 = H, lower alkyl, lower aralkyl, lower aryl R3 is or another chemical structure which is able to decolize the lone pair electrons of the Nitrogen and R4 is a pendant reactive group, capable of linking R3 to a carrier molecule, a proteinaceous substance, an antibody (fragment), a polymer or a nucleic acid.
AbstractList This invention relates to the field of immune therapy of cancer, more specifically to immunoconjugates of a cytotoxic moiety with a targeting moiety, more specifically to immunoconjugates of antibodies or fragments or functional derivatives of antibodies coupled to a cytotoxic substance such as drugs, toxins or radioisotopes. It especially relates to the release of substances bound to a targeting moiety through the use of acid-cleavable linker molecules derived from compounds of formula I. wherein: R1 = H, lower alkyl, -N-lower alkyl, -O-lower alkyl, -S-lower alkyl, -N-lower aralkyl, -O-lower aralkyl, -S-lower aralkyl, -N-lower alkylene, -O-lower alkylene, -S-lower alkylene, -N-lower aryl, -O-lower aryl, -S-lower aryl, R2 = H, lower alkyl, lower aralkyl, lower aryl R3 is or another chemical structure which is able to decolize the lone pair electrons of the Nitrogen and R4 is a pendant reactive group, capable of linking R3 to a carrier molecule, a proteinaceous substance, an antibody (fragment), a polymer or a nucleic acid.
Author KASPERSEN,FRANCISCUS MICHAEL
BOON,PETRUS JOHANNES
BOS,EBO SYBREN
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Snippet This invention relates to the field of immune therapy of cancer, more specifically to immunoconjugates of a cytotoxic moiety with a targeting moiety, more...
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SubjectTerms CHEMISTRY
DERIVATIVES THEREOF
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
NUCLEIC ACIDS
NUCLEOSIDES
NUCLEOTIDES
ORGANIC CHEMISTRY
PEPTIDES
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
SUGARS
Title Happolabiileja kytkentämolekyylejä
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