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Synthesis of photoactivatable analogues of lysophosphatidic acid and covalent labeling of plasma proteins.

ABSTRACT: [reaction: see text] Lysophosphatidic acids bearing a benzophenone group in either the sn-1 or sn-2 chain of an oleoyl-type ester or oleyl-type ether chain and (32)P in the phosphate group were synthesized. The benzophenone moiety was introduced by selective hydroboration of the double bond of enyne 11 at low temperature, followed by a Suzuki reaction with 4-bromobenzophenone. The key intermediates for the preparation of ester-linked lysophosphatidic acid (LPA) 1 and 3 were obtained in one pot by a modified DIBAL-H reduction of orthoformate intermediate 22. These probes were shown to covalently modify a single protein target in rat plasma containing albumin and several protein targets in rat plasma containing a low level of albumin.

SUBMITTER: Li Z

PROVIDER: S-EPMC2533437 | biostudies-literature | 2006 Jan

REPOSITORIES: biostudies-literature

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Synthesis of photoactivatable analogues of lysophosphatidic acid and covalent labeling of plasma proteins.

Li Zaiguo Z Baker Daniel L DL Tigyi Gabor G Bittman Robert R

The Journal of organic chemistry 20060101 2

[reaction: see text] Lysophosphatidic acids bearing a benzophenone group in either the sn-1 or sn-2 chain of an oleoyl-type ester or oleyl-type ether chain and (32)P in the phosphate group were synthesized. The benzophenone moiety was introduced by selective hydroboration of the double bond of enyne 11 at low temperature, followed by a Suzuki reaction with 4-bromobenzophenone. The key intermediates for the preparation of ester-linked lysophosphatidic acid (LPA) 1 and 3 were obtained in one pot b ...[more]

PMID: 16408973

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