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 | , , |
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Format | Patent |
Language | Finnish Swedish |
Published |
14.08.1998
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Edition | 6 |
Subjects | |
Online Access | Get full text |
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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. |
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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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DocumentTitleAlternate | Syralabila kopplingsmolekyler |
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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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