Vinyl substituted radiohalogen and methods of use conjugates

Details Vinyl substituted radiohalogen and methods of use conjugates Vinyl substituted radiohalogen and methods of use conjugates

1988-04-05

1989-10-24

Maples, John S.

Drug, bio-affecting and body treating compositions

Radionuclide or intended radionuclide containing; adjuvant...

424 9, 424 8591, 530402, 530403, 530387, 514 2, 514 21, A61K 4902, A61K 3702, A61K 3944

Patent

active

048760811

ABSTRACT:
Vinyl radiohalogenated small molecules shown in formulas I and II: ##STR1## wherein *X is a radiohalogen, C.dbd.C is a double bonded set of sp.sup.2 hybridized carbon atoms, and substituents R.sub.1, R.sub.2, and Y are as defined below. R.sub.1 and R.sub.2 are substituents independently selected from among hydrogen; alkyl or substituted alkyl, provided that any sp.sup.2 or sp carbon atom substituted on the alkyl is separated from C.dbd.C by at least one fully substituted sp.sup.3 carbon atom; aryl or substituted aryl, provided that the aryl is bonded directly to C.dbd.C; heteroalkyl, provided, first, that no heteroatom of the heteroalkyl bonds directly to C.dbd.C and, second, that any sp.sup.2 or sp hybridized carbon bonded to a heteroatom of the heteroalkyl is not bonded directly to or otherwise conjugated with C.dbd.C and, third, that where a single sp.sup.3 carbon intervenes between C.dbd.C and an sp.sup.2 or sp carbon bonded to a heteroatom, that intervening sp.sup.3 carbon must be fully substituted; heteroaryl, provided that a heteroatom of the heteroaryl is not bonded directly with C.dbd.C; mixed alkylaryl, provided, first, that no heteroatom is bonded to C.dbd.C and, second, that either an aryl moiety of the mixed alkylaryl is directly bonded to C.dbd.C or that any aryl moiety is separated from C.dbd.C by at least one sp.sup.3 carbon atom and, where only one sp.sup.3 hybridized carbon atom intervenes between C.dbd.C and an aryl moiety, that intervening sp.sup.3 carbon must be fully substituted. Y is a substituent containing any of the groups described above for R.sub.1 and R.sub.2, except that Y cannot be hydrogen, and bearing a functional group suitable for binding to protein under conditions that preserve the biological activity of the protein. The compounds of formulas I and II can be coupled to proteins such as monoclonal antibodies to provide reagents for diagnostic and therapeutic applications. Also metalated precursors of compounds I and II, as well as radiopharmaceutical reagent kits containing any of the subject small molecules.

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