| Project/Area Number |
06558090
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 試験 |
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| Research Field |
Bioorganic chemistry
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| Research Institution | Gifu University |
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Principal Investigator |
SUZUKI Masaaki Gifu University, Faculty of engineering, Department of Biomolecular Science, Professor, 工学部, 教授 (90093046)
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| Co-Investigator(Kenkyū-buntansha) |
KUROZUMI Seiji TEIJIN LIMITED,Planning Department Medical & Pharmaceutical Group, Director & Ge, 医薬事業本部, 部長(研究職)
NEGISHI Manabu Kyoto University, Faculty of Pharmaceutical Sciences, Department of Physiologica, 薬学部, 教授 (60201696)
NOYORI Ryoji Nagoya University, Department of Chemistry and Molecular Chirality Research Unit, 理学部, 教授 (50022554)
成宮 周 京都大学, 医学部, 教授 (70144350)
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| Project Period (FY) |
1994 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥18,600,000 (Direct Cost: ¥18,600,000)
Fiscal Year 1996: ¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1995: ¥4,700,000 (Direct Cost: ¥4,700,000)
Fiscal Year 1994: ¥12,000,000 (Direct Cost: ¥12,000,000)
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| Keywords | Prostacyclin / Isocarbacyclin / Receptor / 15R-TIC / 受容体探索子 / APNIC / 受容体タンパク質 / クローニング |
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| Research Abstract |
Isocarbacyclin, a stable carbocyclic analog of prostacyclin, has efficiently been synthesized by combination of rationally designed organic reactions starting a universal intermediate readily obtained by our three-component coupling process. An efficient photoaffinity probe, APNIC,for the PGI_2 receptor (IP_1) has been elaborated by modification of isocarbacyclin. APNIC has proven to exhibit a strong and high specific affinity with the PGI_2 receptor protein (IC_<50>=3nM) in mastocytoma P-815 cells and act as a PGI_2 receptor agonist. The photoaffinity labeling experiment allowed for the first time the idenification of the PGI_2 receptor proteins of approximately 43 kDa (mastocytoma cells), 45 kDa (porcine platelets), and 52 kDa (human platelets) as glycoproteins. We discovered a novel prostacyclin (PGI_2) receptor (IP_2) expressed in the central nervous system (CNS) and succeeded in creating a stable ligand, (15R) -16-m-tolyl-17,18,19,20-tetranorisocarba- cyclin (15R-TIC), with high b
… More
inding affinity and selectivity for this receptor. 15R-TIC exhibited high binding affinity (IC_<50>=30nM) for a novel PGI_2 receptor (IP_2) in the thalamus but showed very weak binding (IC_<50>=1.2muM) for the PGI_2 receptor (IP_1) in the NTS (nucleus tractus solitarius). We examined the reaction of methyl iodide and tributylphenylstannane (excess), giving toluene, with the focus on the realization of rapid coupling applicable to short-lived ^<11>C radionuclide (t_<1/2>=20min). Although methylation by usual Stille reaction conditions failed. We accomplished this methylation in >90% yield using 40 equiv of tributylphenylstannane within 5 min at 60 ﾟC in the presence of bis(tri-o-tolylphosphine) palladium (0), Cu (I) salt, and K_2CO_3 in DMF.This new protocol provided a firm chemical basis for the synthesis of ^<11>CH_3-incorporated PET tracers and, actually, it was successfully applied to the synthesis of [^<11>C] 15R-TIC which realized clear imaging of the IP_2 receptor in the living monkey brain. Less
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