Methods of inhibiting transmission of a costimulatory signal of lymphocytes
View Patent ↗Activated haptens useful for generating immunogens to the HIV protease inhibitor atazanavir, immunogens useful for producing antibodies to atazanavir, and antibodies and labeled conjugates useful in immunoassays for determination of atazanavir. The haptens feature an activated functionality at the central, non-terminal hydroxyl group.
1. A compound having the structure
wherein Y is O, S, or NH, m is 0 or 1, L is a linker comprising from 0 to 40 carbon atoms arranged in a straight chain or a branched chain, saturated or unsaturated, and further comprising up to two ring structures and 0–20 heteroatoms, with the proviso that not more than two heteroatoms are linked in sequence, Z is a moiety selected from the group consisting of —CONH—, —NHCO—, —NHCONH—, —NHCSNH—, —OCONH—, —NHOCO—, —S—, —NH(C═NH)—, —N═N—, —NH—, and
P is selected, from the group consisting of polypeptides, polysaccharides and synthetic polymers, and n is a number from 1 to 50 per 50 kilodaltons molecular weight of P.
2. The compound of claim 1 wherein Y is O, m is 1, and P is selected from the group consisting of polypeptides and polysaccharides.
3. The compound O c -[4′-(succinimido-oxycarbonyl)-benzoyl-aminocaproyl]-atazanavir conjugate with BSA.
4. The compound O c -(succinimido-oxycarbonyl-butyryl-aminocaproyl)-atazanavir conjugate with KLH.
5. The compound O c -(succinimido-oxycarbonyl-butyryl-aminocaproyl)-atazanavir.
6. The compound O c -[4′-(succinimido-oxycarbonyl)-benzoyl-aminocaproyl]-atazanavir.
7. A compound having the structure
wherein Y is O, S, or NH, m is 0 or 1, L is a linker comprising from 0 to 40 carbon atoms arranged in a straight chain or a branched chain saturated or unsaturated, and further comprising up to two ring structures and 0–20 heteroatoms, with the proviso that not more than two heteroatoms are linked in sequence, Z is a moiety selected from the group consisting of —CONH—, —NHCO—, —NHCONH—, —NHCSNH—, —OCONH—, —NHOCO—, —S—, —NH(C═NH)—, —N═N—, —NH—, and
Q is selected from the group consisting of non-isotopic labels, and n is a number from 1 to 50 per 50 kilodaltons molecular Q.
8. The compound of claim 7 wherein Y is O, m is 1, and Q is selected from the group consisting of non-isotopic labels.
9. An antibody generated in response to a compound having the structure
wherein Y is O, S, or NH, m is 0 or 1, L is a linker comprising from 0 to 40 carbon atoms arranged in a straight chain or a branch chain, saturated or unsaturated, and further comprising up to two ring structures and 0–20 heteroatoms, with the proviso that not more than two heteroatoms are linked in sequence, Z is a moiety selected from the group consisting of —CONH—, —NHCO—, —NHCONH—, —NHCSNH—, —OCONH—, —NHOCO—, —S—, —NH(C═NH)—, —N═N—, and
P is selected from the group consisting of polypeptides, a polysaccharides, and synthetic polymers, and n is a number from 1 to 50 per 50 kilodaltons molecular weight of P.
10. A monoclonal antibody specific for atazanavir having less than 1% cross-reactivity with an HIV protease inhibitor selected from the group consisting of saquinavir, nelfinavir, indinavir, amprenavir, ritonavir, and lopinavir.
11. A monoclonal antibody specific for atazanavir having less than 1% cross-reactivity with 4-pyridin-2-yl-benzoic acid.
12. Murine hybridoma ATZ 4.1 having ATCC No. PTA-6257.