大学院薬学研究院

北島 満里子

キタジマ マリコ  (Mariko Kitajima)

基本情報

所属
千葉大学 大学院薬学研究院 准教授
学位
博士(薬学)(千葉大学)

J-GLOBAL ID
200901059580656008
researchmap会員ID
1000191975

外部リンク

受賞

 3

論文

 271
  • Go Yoshimura, Jukiya Sakamoto, Mariko Kitajima, Hayato Ishikawa
    e202401153 2024年4月7日  査読有り
  • Sho Imaoka, Yuta Nakashima, Mariko Kitajima, Hayato Ishikawa
    Chemical & Pharmaceutical Bulletin 72(1) 68-74 2024年  査読有り
    The first enantioselective total synthesis of kopsiyunnanine B, which has a unique folded and complex pentacyclic structure containing six contiguous chiral centers, has been achieved along our originally proposed biosynthetic pathway. The key reaction of this synthesis includes a bioinspired cascade that builds three ring structures and three chiral centers in one step and features the stereoselective reduction of a β-acrylate and oxidation to an oxindole.
  • Yoshihiro Ataka, Mariko Kitajima, Hayato Ishikawa
    Organic Letters 25(42) 7601-7605 2023年10月27日  査読有り
    The enantioselective total syntheses of (-)-silicine and (-)-20-episilicine, which contain a chiral piperidine with three contiguous chiral centers (D-ring) and a strained seven-membered ring (C-ring) attached to an indole, were achieved. The key steps of these syntheses included a chiral secondary amine-catalyzed formal aza-[3 + 3] cycloaddition reaction and Lewis acid-mediated irreversible ring-closing reaction. In addition, the stereochemistry at C20 was controlled at a later stage in the syntheses.
  • Yuma Ito, Huiyan Lu, Mariko Kitajima, Hayato Ishikawa, Yoshihiro Nakata, Yasumasa Iwatani, Tyuji Hoshino
    Journal of Natural Products 86(11) 2487-2495 2023年10月  査読有り
  • Yuta Nakashima, Taichi Inoshita, Mariko Kitajima, Hayato Ishikawa
    Organic Letters 25(7) 1151-1155 2023年2月24日  査読有り
    The first asymmetric total synthesis of the Lycopodium alkaloid senepodine F, which contains a decahydroquinoline ring (AB-ring) and a quinolizidine ring (CD-ring) connected by a methylene tether, has been achieved. The key steps of this synthesis include an organocatalytic asymmetric Diels-Alder reaction, a diastereoselective intramolecular aza-Michael reaction, and an intramolecular SN2 cyclization to construct multisubstituted nitrogen-containing heterocycles. In addition, our total synthesis led to the stereochemical reassignment on the decahydroquinoline ring of senepodine F.

MISC

 5
  • TH Kang, Y Murakami, K Matsumoto, H Takayama, M Kitajima, N Aimi, H Watanabe
    JOURNAL OF PHARMACOLOGICAL SCIENCES 91 232P-232P 2003年  
  • 北島 満里子, 丹羽 美苗, 柳沢 知恵子, 高山 廣光, 斉藤 和季, 山崎 真巳, 須藤 浩, 相見 則郎
    日本薬学会年会要旨集 122年会(2) 130-130 2002年3月  
  • O. Ohmori, H. Takayama, M. Kitajima, N. Aimi
    Towards Natural Medicine Research in the 21st Century (Proceedings of the International Symposium on Natural Medicines) 1157 573-582 1998年  
  • 北島 満里子, Stockigt Joachim, 中村 美緒, 益本 誠二, 大沢 美香, 上野 正弘, 高山 廣光, 山崎 真巳, 斉藤 和季, 相見 則郎
    天然有機化合物討論会講演要旨集 38 283-288 1996年  
    Camptothecin (1) is well known for the remarkable inhibitory activities against tumor cells and topoisomerase I. Synthetic and biological studies about camptothecin and related compounds have been extensively carried out. In the course of chemical studies of camptothecins, we have already found that Ophiorrhiza pumila Champ. (Rubiaceae) produces not only camptothecin (1) but also a variety of related alkaloids (2-5). We herein report the synthetic studies of these alkaloids based on a biogenetic hypothesis as well as the chemical investigation of the secondary metabolites in cell cultures of this plant. I. Synthetic Studies of Camptothecin Related Compounds Vincoside lactam (8) was converted to 3(R)-deoxypumiloside tetraacetate (13) through a reductive deoxygenation at C-7 position in 3(R)-pumiloside tetraacetate (10). Synthetic 13 was identified with the tetraacetate of natural deoxypumiloside. From this result, H-3 stereochemistry of natural deoxypumiloside, which has been previously reported as α-form, was revised to be β orientation. Strictosamide (7) could also be converted to 3(S)-deoxypumiloside tetraacetate (14). By exhaustive investigation of the chemical constituents in O. pumila, it was found that O. pumila produces both of 3(R)-deoxypumiloside (16) and 3(S)-deoxypumiloside (17). II. Chemical Investigation of the Metabolites in Cell Cultures of Ophiorrhiza pumila From callus cultures induced from leaf segments of O. pumila, eight anthraquinones including two new ones and cholesterol were isolated. No trace of camptothecin related alkaloids was detected. New anthraquinones were identified as 1-hydroxy-2-hydroxymethyl-3-methoxyanthraquinone (22) and 2-butoxymethyl-1,3-dihydroxyanthraquinone (25) by spectroscopic analyses. Regenerated plant, which was formed from callus cultures through differentiation, produced camptothecin (1), pumiloside (4), 3(R)-deoxypumiloside (16), strictosamide (7) and loganin. New camptothecin alkaloid (26) was also isolated from acetylated n-BuOH fraction and identified as 9-O-β-D-glucosylcamptothecin pentaacetate (26). Hairy roots of O. pumila were obtained by the inoculation of Agrobacterium rhizogenes to regenerated plants. From hairy roots, pumiloside (4), 3(R)- and 3(S)-deoxypumiloside (16, 17), strictsamide (7), and two anthraquinones (24, 27) were isolated.

書籍等出版物

 8

講演・口頭発表等

 211

所属学協会

 2

共同研究・競争的資金等の研究課題

 25