Year |
Citation |
Score |
2020 |
Purev E, Kondo T, Takemoto D, Niones JT, Ojika M. Identification of ε-Poly-L-lysine as an Antimicrobial Product from an Endophyte and Isolation of Fungal ε-PL Synthetase Gene. Molecules (Basel, Switzerland). 25. PMID 32106587 DOI: 10.3390/Molecules25051032 |
0.304 |
|
2020 |
Nakagawa Y, Sawaki Y, Miyanishi W, Shimomura S, Shibata T, Ojika M. Relationship among structure, cytotoxicity, and Michael acceptor reactivity of quinocidin. Bioorganic & Medicinal Chemistry. 28: 115308. PMID 31956051 DOI: 10.1016/J.Bmc.2020.115308 |
0.339 |
|
2019 |
Ito S, Fujiki Y, Matsui N, Ojika M, Wakamatsu K. Tyrosinase-catalyzed oxidation of resveratrol produces a highly reactive ortho-quinone: implications for melanocyte toxicity. Pigment Cell & Melanoma Research. PMID 31264351 DOI: 10.1111/Pcmr.12808 |
0.302 |
|
2019 |
Soe TW, Han C, Fudou R, Kaida K, Sawaki Y, Tomura T, Ojika M. Clavariopsins C-I, Antifungal Cyclic Depsipeptides from the Aquatic Hyphomycete Clavariopsis aquatica. Journal of Natural Products. PMID 31244144 DOI: 10.1021/Acs.Jnatprod.9B00366 |
0.381 |
|
2018 |
Kasmiati K, Yoshioka Y, Okamoto T, Ojika M. New Crambescidin-Type Alkaloids from the Indonesian Marine Sponge Clathria bulbotoxa. Marine Drugs. 16. PMID 29518039 DOI: 10.3390/Md16030084 |
0.354 |
|
2017 |
Iwai R, Han C, Govindam SVS, Ojika M. Lycosides, Unusual Carotenoid-Derived Terpenoid Glycosides from a Vegetable Juice, Inhibit Asexual Reproduction of the Plant Pathogen Phytophthora. Journal of Agricultural and Food Chemistry. PMID 29224342 DOI: 10.1021/Acs.Jafc.7B04766 |
0.346 |
|
2017 |
Nakagawa Y, Sawaki Y, Kimura T, Tomura T, Igarashi Y, Ojika M. Quinocidin, a Cytotoxic Antibiotic with an Unusual 3,4-Dihydroquinolizinium Ring and Michael Acceptor Reactivity toward Thiols. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29105224 DOI: 10.1002/Chem.201704729 |
0.375 |
|
2017 |
Tomura T, Nagashima S, Yamazaki S, Iizuka T, Fudou R, Ojika M. An Unusual Diterpene-Enhygromic Acid and Deoxyenhygrolides from a Marine Myxobacterium, Enhygromyxa sp. Marine Drugs. 15. PMID 28383484 DOI: 10.3390/Md15040109 |
0.363 |
|
2016 |
Ojima D, Yasui A, Tohyama K, Tokuzumi K, Toriihara E, Ito K, Iwasaki A, Tomura T, Ojika M, Suenaga K. Total Synthesis of Miuraenamides A and D. The Journal of Organic Chemistry. PMID 27662058 DOI: 10.1021/Acs.Joc.6B02061 |
0.346 |
|
2016 |
Sun Y, Feng Z, Tomura T, Suzuki A, Miyano S, Tsuge T, Mori H, Suh JW, Iizuka T, Fudou R, Ojika M. Heterologous Production of the Marine Myxobacterial Antibiotic Haliangicin and Its Unnatural Analogues Generated by Engineering of the Biochemical Pathway. Scientific Reports. 6: 22091. PMID 26915413 DOI: 10.1038/Srep22091 |
0.318 |
|
2016 |
Sun Y, Tomura T, Sato J, Iizuka T, Fudou R, Ojika M. Isolation and Biosynthetic Analysis of Haliamide, a New PKS-NRPS Hybrid Metabolite from the Marine Myxobacterium Haliangium ochraceum. Molecules (Basel, Switzerland). 21. PMID 26751435 DOI: 10.3390/Molecules21010059 |
0.37 |
|
2015 |
Wakamatsu K, Tabuchi K, Ojika M, Zucca FA, Zecca L, Ito S. Norepinephrine and its metabolites are involved in the synthesis of neuromelanin derived from the locus coeruleus. Journal of Neurochemistry. PMID 26156066 DOI: 10.1111/Jnc.13237 |
0.314 |
|
2015 |
Han C, Furukawa H, Tomura T, Fudou R, Kaida K, Choi BK, Imokawa G, Ojika M. Bioactive Maleic Anhydrides and Related Diacids from the Aquatic Hyphomycete Tricladium castaneicola. Journal of Natural Products. 78: 639-44. PMID 25875311 DOI: 10.1021/Np500773S |
0.414 |
|
2014 |
Wakamatsu K, Tanaka H, Tabuchi K, Ojika M, Zucca FA, Zecca L, Ito S. Reduction of the nitro group to amine by hydroiodic acid to synthesize o-aminophenol derivatives as putative degradative markers of neuromelanin. Molecules (Basel, Switzerland). 19: 8039-50. PMID 24936706 DOI: 10.3390/Molecules19068039 |
0.301 |
|
2013 |
Oba Y, Yoshida N, Kanie S, Ojika M, Inouye S. Biosynthesis of firefly luciferin in adult lantern: decarboxylation of L-cysteine is a key step for benzothiazole ring formation in firefly luciferin synthesis. Plos One. 8: e84023. PMID 24391868 DOI: 10.1371/Journal.Pone.0084023 |
0.348 |
|
2013 |
Horikawa K, Yagyu T, Yoshioka Y, Fujiwara T, Kanamoto A, Okamoto T, Ojika M. Petrosiols A-E, neurotrophic diyne tetraols isolated from the Okinawan sponge Petrosia strongylata Tetrahedron. 69: 101-106. DOI: 10.1016/J.Tet.2012.10.063 |
0.332 |
|
2012 |
Choi JH, Maeda K, Hirai H, Harada E, Kawade M, Qi J, Ojika M, Kawagishi H. Novel cerebroside, termitomycesphin I, from the mushroom, Termitomyces titanicus. Bioscience, Biotechnology, and Biochemistry. 76: 1407-9. PMID 22785477 DOI: 10.1271/Bbb.120130 |
0.349 |
|
2012 |
Govindam SV, Choi BK, Yoshioka Y, Kanamoto A, Fujiwara T, Okamoto T, Ojika M. Novel cytotoxic polyoxygenated steroids from an Okinawan sponge Dysidea sp. Bioscience, Biotechnology, and Biochemistry. 76: 999-1002. PMID 22738973 DOI: 10.1271/Bbb.120017 |
0.358 |
|
2012 |
Ito S, Nishigaki A, Ishii-Osai Y, Ojika M, Wakamatsu K, Yamashita T, Tamura Y, Ito A, Honda H, Nakayama E, Jimbow K. Mechanism of putative neo-antigen formation from N-propionyl-4-S-cysteaminylphenol, a tyrosinase substrate, in melanoma models. Biochemical Pharmacology. 84: 646-53. PMID 22728921 DOI: 10.1016/J.Bcp.2012.06.015 |
0.302 |
|
2012 |
Qu Y, Sun K, Gao L, Sakagami Y, Kawagishi H, Ojika M, Qi J. Termitomycesphins G and H, additional cerebrosides from the edible Chinese mushroom Termitomyces albuminosus. Bioscience, Biotechnology, and Biochemistry. 76: 791-3. PMID 22484955 DOI: 10.1271/Bbb.110918 |
0.304 |
|
2012 |
Govindam SV, Yoshioka Y, Kanamoto A, Fujiwara T, Okamoto T, Ojika M. Cyclolobatriene, a novel prenylated germacrene diterpene, from the soft coral Lobophytum pauciflorum. Bioorganic & Medicinal Chemistry. 20: 687-92. PMID 22209732 DOI: 10.1016/J.Bmc.2011.12.012 |
0.354 |
|
2012 |
Ojika M, Kigoshi H, Suenaga K, Imamura Y, Yoshikawa K, Ishigaki T, Sakakura A, Mutou T, Yamada K. Aplyronines D-H from the sea hare Aplysia kurodai: Isolation, structures, and cytotoxicity Tetrahedron. 68: 982-987. DOI: 10.1016/J.Tet.2011.11.095 |
0.389 |
|
2011 |
Qu Y, Zhang Y, Pei L, Wang Y, Gao L, Huang Q, Ojika M, Sakagami Y, Qi J. New neuritogenic steroidal saponin from Ophiopogon japonicus (Thunb.) Ker-Gawl. Bioscience, Biotechnology, and Biochemistry. 75: 1201-4. PMID 21670508 DOI: 10.1271/Bbb.110066 |
0.365 |
|
2009 |
Wakita C, Maeshima T, Yamazaki A, Shibata T, Ito S, Akagawa M, Ojika M, Yodoi J, Uchida K. Stereochemical configuration of 4-hydroxy-2-nonenal-cysteine adducts and their stereoselective formation in a redox-regulated protein. The Journal of Biological Chemistry. 284: 28810-22. PMID 19692331 DOI: 10.1074/Jbc.M109.019927 |
0.33 |
|
2009 |
Yamada K, Ojika M, Kigoshi H, Suenaga K. Aplyronine A, a potent antitumour macrolide of marine origin, and the congeners aplyronines B-H: chemistry and biology. Natural Product Reports. 26: 27-43. PMID 19374121 DOI: 10.1039/B800263K |
0.351 |
|
2009 |
Shimozu Y, Shibata T, Ojika M, Uchida K. Identification of advanced reaction products originating from the initial 4-oxo-2-nonenal-cysteine Michael adducts. Chemical Research in Toxicology. 22: 957-64. PMID 19368367 DOI: 10.1021/Tx900059K |
0.33 |
|
2008 |
Ojika M, Inukai Y, Kito Y, Hirata M, Iizuka T, Fudou R. Miuraenamides: antimicrobial cyclic depsipeptides isolated from a rare and slightly halophilic myxobacterium. Chemistry, An Asian Journal. 3: 126-33. PMID 18022981 DOI: 10.1002/Asia.200700233 |
0.381 |
|
2007 |
Mori D, Kimura Y, Kitamura S, Sakagami Y, Yoshioka Y, Shintani T, Okamoto T, Ojika M. Spongolactams, farnesyl transferase inhibitors from a marine sponge: isolation through an LC/MS-guided assay, structures, and semisyntheses. The Journal of Organic Chemistry. 72: 7190-8. PMID 17713950 DOI: 10.1021/Jo071003Y |
0.362 |
|
2007 |
Matsushita S, Yanai Y, Fusyuku A, Fujiwara Y, Ikeda T, Ono M, Han C, Ojika M, Nohara T. Efficient conversion of tomatidine into neuritogenic pregnane derivative. Chemical & Pharmaceutical Bulletin. 55: 1077-8. PMID 17603206 DOI: 10.1248/Cpb.55.1077 |
0.303 |
|
2007 |
Fukatsu T, Onodera K, Ohta Y, Oba Y, Nakamura H, Shintani T, Yoshioka Y, Okamoto T, ten Lohuis M, Miller DJ, Kawachi M, Ojika M. Zooxanthellamide D, a polyhydroxy polyene amide from a marine dinoflagellate, and chemotaxonomic perspective of the Symbiodinium polyols. Journal of Natural Products. 70: 407-11. PMID 17315927 DOI: 10.1021/Np060596P |
0.359 |
|
2007 |
Ojika M, Kigoshi H, Yoshida Y, Ishigaki T, Nisiwaki M, Tsukada I, Arakawa M, Ekimoto H, Yamada K. Aplyronine A, a potent antitumor macrolide of marine origin, and the congeners aplyronines B and C: isolation, structures, and bioactivities Tetrahedron. 63: 3138-3167. DOI: 10.1016/J.Tet.2007.02.011 |
0.37 |
|
2007 |
Han C, Qi J, Ojika M. Linckosides M-Q: Neuritogenic steroid glycosides from the Okinawan starfish Linckia laevigata Journal of Natural Medicines. 61: 138-145. DOI: 10.1007/S11418-006-0107-6 |
0.313 |
|
2006 |
Iizuka T, Fudou R, Jojima Y, Ogawa S, Yamanaka S, Inukai Y, Ojika M. Miuraenamides A and B, novel antimicrobial cyclic depsipeptides from a new slightly halophilic myxobacterium: taxonomy, production, and biological properties. The Journal of Antibiotics. 59: 385-91. PMID 17025014 DOI: 10.1038/Ja.2006.55 |
0.321 |
|
2006 |
Han C, Qi J, Shi X, Sakagami Y, Shibata T, Uchida K, Ojika M. Prostaglandins from a zoanthid: paclitaxel-like neurite-degenerating and microtubule-stabilizating activities. Bioscience, Biotechnology, and Biochemistry. 70: 706-11. PMID 16556989 DOI: 10.1271/Bbb.70.706 |
0.307 |
|
2006 |
Han C, Qi J, Ojika M. Structure-activity relationships of novel neuritogenic steroid glycosides from the Okinawan starfish Linckia laevigata. Bioorganic & Medicinal Chemistry. 14: 4458-65. PMID 16524736 DOI: 10.1016/J.Bmc.2006.02.032 |
0.346 |
|
2006 |
Kundim BA, Qi J, Fudou R, Yamanaka S, Ojika M. Further structure-activity relationships of the myxobacterial antibiotics cystothiazoles Heterocycles. 69: 231-237. DOI: 10.3987/Com-06-S(O)20 |
0.347 |
|
2005 |
Nakamura M, Kakuda T, Qi J, Hirata M, Shintani T, Yoshioka Y, Okamoto T, Oba Y, Nakamura H, Ojika M. Novel relationship between the antifungal activity and cytotoxicity of marine-derived metabolite xestoquinone and its family. Bioscience, Biotechnology, and Biochemistry. 69: 1749-52. PMID 16195594 DOI: 10.1271/Bbb.69.1749 |
0.322 |
|
2005 |
Onodera K, Nakamura H, Oba Y, Ohizumi Y, Ojika M. Zooxanthellamide Cs: vasoconstrictive polyhydroxylated macrolides with the largest lactone ring size from a marine dinoflagellate of Symbiodinium sp. Journal of the American Chemical Society. 127: 10406-11. PMID 16028954 DOI: 10.1021/Ja050810G |
0.37 |
|
2004 |
Okada M, Sato I, Cho SJ, Suzuki Y, Ojika M, Dubnau D, Sakagami Y. Towards structural determination of the ComX pheromone: synthetic studies on peptides containing geranyltryptophan. Bioscience, Biotechnology, and Biochemistry. 68: 2374-87. PMID 15564679 DOI: 10.1271/Bbb.68.2374 |
0.313 |
|
2004 |
Qi J, Ojika M, Sakagami Y. Linckosides C-E, three new neuritogenic steroid glycosides from the Okinawan starfish Linckia laevigata. Bioorganic & Medicinal Chemistry. 12: 4259-65. PMID 15246102 DOI: 10.1016/J.Bmc.2004.04.049 |
0.345 |
|
2004 |
Onodera K, Nakamura H, Oba Y, Ojika M. Zooxanthellamide B, a novel large polyhydroxy metabolite from a marine dinoflagellate of Symbiodinium sp. Bioscience, Biotechnology, and Biochemistry. 68: 955-8. PMID 15118333 DOI: 10.1271/Bbb.68.955 |
0.369 |
|
2004 |
Onodera K, Fukatsu T, Kawai N, Yoshioka Y, Okamoto T, Nakamura H, Ojika M. Zooxanthellactone, a novel gamma-lactone-type oxylipine from dinoflagellates of Symbiodinium sp.: structure, distribution, and biological activity. Bioscience, Biotechnology, and Biochemistry. 68: 848-52. PMID 15118313 DOI: 10.1271/Bbb.68.848 |
0.362 |
|
2004 |
Suzuki Y, Ojika M, Sakagami Y. Biotransformation of cystothiazole A, a myxobacterial antibiotic, into novel derivatives by the mother producer, Cystobacter fuscus. Bioscience, Biotechnology, and Biochemistry. 68: 390-6. PMID 14981303 DOI: 10.1271/Bbb.68.390 |
0.311 |
|
2004 |
Kundim BA, Itou Y, Sakagami Y, Fudou R, Yamanaka S, Ojika M. Novel antifungal polyene amides from the myxobacterium Cystobacter fuscus: Isolation, antifungal activity and absolute structure determination Tetrahedron. 60: 10217-10221. DOI: 10.1016/J.Tet.2004.09.013 |
0.355 |
|
2004 |
Ojika M, Watanabe T, Qi J, Tanino T, Sakagami Y. Syntheses of cystothiazole A and its stereoisomers: Importance of stereochemistry for antifungal activity Tetrahedron. 60: 187-194. DOI: 10.1016/J.Tet.2003.10.078 |
0.32 |
|
2003 |
Kundim BA, Itou Y, Sakagami Y, Fudou R, Iizuka T, Yamanaka S, Ojika M. New haliangicin isomers, potent antifungal metabolites produced by a marine myxobacterium. The Journal of Antibiotics. 56: 630-8. PMID 14513906 DOI: 10.7164/Antibiotics.56.630 |
0.34 |
|
2003 |
Ojika M, Itou Y, Sakagami Y. Structural studies and antifungal activity of unique polyene amides, clathrynamide A and three new derivatives, from a marine sponge, Psammoclemma sp. Bioscience, Biotechnology, and Biochemistry. 67: 1568-73. PMID 12913302 DOI: 10.1271/Bbb.67.1568 |
0.357 |
|
2003 |
Ojika M, Islam MK, Shintani T, Zhang Y, Okamoto T, Sakagami Y. Three new cytotoxic acylspermidines from the soft coral, Sinularia sp. Bioscience, Biotechnology, and Biochemistry. 67: 1410-2. PMID 12843674 DOI: 10.1271/Bbb.67.1410 |
0.331 |
|
2003 |
Suzuki Y, Sakagami Y, Ojika M. Biosynthetic studies on a myxobacterial antibiotic, cystothiazole A: biosynthetic precursors of the carbon skeleton. The Journal of Antibiotics. 56: 372-8. PMID 12817811 DOI: 10.7164/Antibiotics.56.372 |
0.315 |
|
2003 |
Onodera KI, Nakamura H, Oba Y, Ojika M. Zooxanthellamide A, a novel polyhydroxy metabolite from a marine dinoflagellate of Symbiodinium sp. Tetrahedron. 59: 1067-1071. DOI: 10.1016/S0040-4020(02)01630-7 |
0.345 |
|
2001 |
Qi J, Ojika M, Sakagami Y. Neuritogenic cerebrosides from an edible Chinese mushroom. Part 2: Structures of two additional termitomycesphins and activity enhancement of an inactive cerebroside by hydroxylation. Bioorganic & Medicinal Chemistry. 9: 2171-7. PMID 11504654 DOI: 10.1016/S0968-0896(01)00125-0 |
0.341 |
|
2001 |
Kaida K, Fudou R, Kameyama T, Tubaki K, Suzuki Y, Ojika M, Sakagami Y. New cyclic depsipeptide antibiotics, clavariopsins A and B, produced by an aquatic hyphomycetes, Clavariopsis aquatica. 1. Taxonomy, fermentation, isolation, and biological properties. The Journal of Antibiotics. 54: 17-21. PMID 11269710 DOI: 10.7164/Antibiotics.54.17 |
0.327 |
|
2001 |
Okamoto Y, Ojika M, Suzuki S, Murakami M, Sakagami Y. Iantherans A and B, unique dimeric polybrominated benzofurans as Na,K-ATPase inhibitors from a marine sponge, Ianthella sp. Bioorganic & Medicinal Chemistry. 9: 179-83. PMID 11197338 DOI: 10.1016/S0968-0896(00)00234-0 |
0.316 |
|
2000 |
Qi J, Ojika M, Sakagami Y. Termitomycesphins A-D, novel neuritogenic cerebrosides from the edible Chinese mushroom Termitomyces albuminosus Tetrahedron. 56: 5835-5841. DOI: 10.1016/S0040-4020(00)00548-2 |
0.349 |
|
2000 |
Okamoto Y, Ojika M, Kato S, Sakagami Y. Ianthesines A-D, four novel dibromotyrosine-derived metabolites from a marine sponge, Ianthella sp. Tetrahedron. 56: 5813-5818. DOI: 10.1016/S0040-4020(00)00544-5 |
0.356 |
|
1999 |
Qi J, Ojika M, Sakagami Y. Differentiation in a rat PC12 cell line induced by ostruthin and (-)-bornyl ferulate, constituents of a Chinese herbal medicine. Bioscience, Biotechnology, and Biochemistry. 63: 1501-2. PMID 10501010 DOI: 10.1271/Bbb.63.1501 |
0.305 |
|
1999 |
Castillo UF, Sakagami Y, Alonso-Amelot M, Ojika M. Pteridanoside, the first protoilludane sesquiterpene glucoside as a toxic component of the neotropical bracken fern Pteridium aquilinum var. caudatum Tetrahedron. 55: 12295-12300. DOI: 10.1016/S0040-4020(99)00728-0 |
0.306 |
|
1998 |
Castillo UF, Ojika M, Alonso-Amelot M, Sakagami Y. Ptaquiloside Z, a new toxic unstable sesquiterpene glucoside from the neotropical bracken fern Pteridium aquilinum var. caudatum. Bioorganic & Medicinal Chemistry. 6: 2229-33. PMID 9881114 DOI: 10.1016/S0968-0896(98)00168-0 |
0.331 |
|
1998 |
Kim SK, Hatori M, Ojika M, Sakagami Y, Marumo S. KM-01, a brassinolide inhibitor, its production, isolation and structure from two fungi Drechslera avenae and Pycnoporus coccineus. Bioorganic & Medicinal Chemistry. 6: 1975-82. PMID 9881090 DOI: 10.1016/S0968-0896(98)00088-1 |
0.372 |
|
1998 |
Ojika M, Suzuki Y, Tsukamoto A, Sakagami Y, Fudou R, Yoshimura T, Yamanaka S. Cystothiazoles A and B, new bithiazole-type antibiotics from the myxobacterium Cystobacter fuscus. The Journal of Antibiotics. 51: 275-81. PMID 9589062 DOI: 10.7164/Antibiotics.51.275 |
0.375 |
|
1998 |
Nemoto T, Ojika M, Takahata Y, Andoh T, Sakagami Y. Structures of topostins, DNA topoisomerase I inhibitors of bacterial origin Tetrahedron. 54: 2683-2690. DOI: 10.1016/S0040-4020(98)83004-4 |
0.379 |
|
1998 |
Suzuki Y, Ojika M, Sakagami Y, Fudou R, Yamanaka S. Cystothiazoles C-F, New Bithiazole-type antibiotics from the myxobacterium cystobacter fuscus Tetrahedron. 54: 11399-11404. DOI: 10.1016/S0040-4020(98)00694-2 |
0.36 |
|
1997 |
Nemoto T, Ojika M, Sakagami Y. Amphimic acids, novel unsaturated C28 fatty acids as DNA topoisomerase I inhibitors from an Australian sponge amphimedon sp Tetrahedron Letters. 38: 5667-5670. DOI: 10.1016/S0040-4039(97)01234-3 |
0.345 |
|
1997 |
Ojika M, Yoshino G, Sakagami Y. Novel ceramide 1-sulfates, potent DNA topoisomerase I inhibitors isolated from the bryozoa Watersipora cucullata Tetrahedron Letters. 38: 4235-4238. DOI: 10.1016/S0040-4039(97)00852-6 |
0.332 |
|
1997 |
Nemoto T, Yoshino G, Ojika M, Sakagami Y. Amphimic acids and related long-chain fatty acids as DNA topoisomerase I inhibitors from an Australian sponge, Amphimedon sp.: Isolation, structure, synthesis, and biological evaluation Tetrahedron. 53: 16699-16710. DOI: 10.1016/S0040-4020(97)10099-0 |
0.35 |
|
1996 |
Mutou T, Kondo T, Ojika M, Yamada K. Isolation and Stereostructures of Dolastatin G and Nordolastatin G, Cytotoxic 35-Membered Cyclodepsipeptides from the Japanese Sea Hare Dolabella auricularia. The Journal of Organic Chemistry. 61: 6340-6345. PMID 11667475 DOI: 10.1021/Jo9608228 |
0.324 |
|
1996 |
Kigoshi H, Suenaga K, Mutou T, Ishigaki T, Atsumi T, Ishiwata H, Sakakura A, Ogawa T, Ojika M, Yamada K. Aplyronine A, a potent antitumor substance of marine origin, aplyronines B and C, and artificial analogues: Total synthesis and structure-cytotoxicity relationships Journal of Organic Chemistry. 61: 5326-5351. DOI: 10.1021/Jo9606113 |
0.314 |
|
1996 |
Sone H, Shibata T, Fujita T, Ojika M, Yamada K. Dolastatin H and isodolastatin H, potent cytotoxic peptides from the sea hare Dolabella auricularia: Isolation, stereostructures, and synthesis Journal of the American Chemical Society. 118: 1874-1880. DOI: 10.1021/Ja9519086 |
0.378 |
|
1995 |
Sone H, Kondo T, Kiryu M, Ishiwata H, Ojika M, Yamada K. Dolabellin, a cytotoxic bisthiazole metabolite from the sea hare Dolabella auricularia: Structural determination and synthesis The Journal of Organic Chemistry. 60: 4774-4781. DOI: 10.1021/Jo00120A021 |
0.341 |
|
1995 |
Ojika M, Nagoya T, Yamada K. Dolabelides A and B, cytotoxic 22-membered macrolides isolated from the sea hare Dolabella auricularia Tetrahedron Letters. 36: 7491-7494. DOI: 10.1016/0040-4039(95)01605-8 |
0.372 |
|
1995 |
Nakamura M, Shibata T, Nakane K, Nemoto T, Ojika M, Yamada K. Stereochemistry and total synthesis of dolastatin E Tetrahedron Letters. 36: 5059-5062. DOI: 10.1016/0040-4039(95)00923-Z |
0.301 |
|
1995 |
Ojika M, Nemoto T, Nakamura M, Yamada K. Dolastatin E, a new cyclic hexapeptide isolated from the sea hare Dolabella auricularia Tetrahedron Letters. 36: 5057-5058. DOI: 10.1016/0040-4039(95)00922-Y |
0.341 |
|
1994 |
Ishiwata H, Nemoto T, Ojika M, Yamada K. Isolation and stereostructure of doliculide, a cytotoxic cyclodepsipeptide from the Japanese sea hare Dolabella auricularia Journal of Organic Chemistry. 59: 4710-4711. DOI: 10.1021/Jo00096A002 |
0.315 |
|
1994 |
Kigoshi H, Ojika M, Ishigaki T, Suenaga K, Mutou T, Sakakura A, Ogawa T, Yamada K. Total synthesis of aplyronine A, a potent antitumor substance of marine origin Journal of the American Chemical Society. 116: 7443-7444. DOI: 10.1021/Ja00095A072 |
0.304 |
|
1994 |
Ojika M, Kigoshi H, Ishigaki T, Tsukada I, Tsuboi T, Ogawa T, Yamada K. Absolute stereochemistry of aplyronine A, a potent antitumor substance of marine origin Journal of the American Chemical Society. 116: 7441-7442. DOI: 10.1021/Ja00095A071 |
0.304 |
|
1993 |
Yamada K, Ojika M, Ishigaki T, Yoshida Y, Ekimoto H, Arakawa M. Aplyronine A, a potent antitumor substance, and the congeners aplyronines B and C isolated from the sea hare Aplysia kurodai Journal of the American Chemical Society. 115: 11020-11021. DOI: 10.1021/Ja00076A082 |
0.308 |
|
1993 |
Ojika M, Nemoto T, Yamada K. Doliculols A and B, the non-halogenated C15 acetogenins with cyclic ether from the sea hare Dolabella auricularia Tetrahedron Letters. 34: 3461-3462. DOI: 10.1016/S0040-4039(00)79183-0 |
0.328 |
|
1993 |
Ojika M, Yoshida T, Yamada K. Aplysepine, a novel 1,4-benzodiazepine alkaloid from the sea hare Aplysia kurodai Tetrahedron Letters. 34: 5307-5308. DOI: 10.1016/S0040-4039(00)73981-5 |
0.35 |
|
1993 |
Ojika M, Kigoshi H, Ishigaki T, Nisiwaki M, Tsukada I, Mizuta K, Yamada K. Studies on the stereochemistry of aplyronine A: Determination of the stereochemistry of the C21C34 fragment Tetrahedron Letters. 34: 8505-8508. DOI: 10.1016/S0040-4039(00)61370-9 |
0.328 |
|
1993 |
Ojika M, Kigoshi H, Ishigaki T, Yamada K. Further studies on aplyronine A, an antitumor substance isolated from the sea hare Aplysia kurodai Tetrahedron Letters. 34: 8501-8504. DOI: 10.1016/S0040-4039(00)61369-2 |
0.374 |
|
1993 |
Sone H, Nemoto T, Ishiwata H, Ojika M, Yamada K. Isolation, structure, and synthesis of dolastatin D, a cytotoxic cyclic depsipeptide from the sea gare Dolabella auricularia Tetrahedron Letters. 34: 8449-8452. DOI: 10.1016/S0040-4039(00)61356-4 |
0.334 |
|
1993 |
Sone H, Nemoto T, Ojika M, Yamada K. Isolation, structure, and synthesis of dolastatin C, a new depsipeptide from the sea hare Dolabella auricularia Tetrahedron Letters. 34: 8445-8448. DOI: 10.1016/S0040-4039(00)61355-2 |
0.389 |
|
1992 |
Ojika M, Kigoshi H, Yoshikawa K, Nakayama Y, Yamada K. A New Bromo Diterpene,epi-Aplysin-20, andent-Isoconcinndiol from the Marine MolluscAplysia kurodai Bulletin of the Chemical Society of Japan. 65: 2300-2302. DOI: 10.1246/Bcsj.65.2300 |
0.349 |
|
1990 |
Meyers HV, Ojika M, Wiesler WT, Nakanishi K. Oligosaccharide microanalysis by c.d. spectroscopy. Reference curves for D-mannose derivatives. Carbohydrate Research. 197: 15-32. PMID 2346947 DOI: 10.1016/0008-6215(90)84126-F |
0.62 |
|
1990 |
Nishiwaki S, Fujiki H, Suganuma M, Furuya-Suguri H, Matsushima R, Iida Y, Ojika M, Yamada K, Uemura D, Yasumoto T. Structure-activity relationship within a series of okadaic acid derivatives. Carcinogenesis. 11: 1837-41. PMID 2170047 DOI: 10.1093/Carcin/11.10.1837 |
0.31 |
|
1990 |
Ojika M, Yoshida Y, Nakayama Y, Yamada K. Aplydilactone, a novel fatty acid metabolite from the marine mollusc aplysia kurodai Tetrahedron Letters. 31: 4907-4910. DOI: 10.1016/S0040-4039(00)97765-7 |
0.357 |
|
1990 |
Wiesler WT, Berova N, Ojika M, Meyers HV, Chang M, Zhou P, Lo L, Niwa M, Takeda R, Nakanishi K. A CD-Spectroscopic Alternative to Methylation Analysis of Oligosaccharides: Reference Spectra for Identification of Chromophoric Glycopyranoside Derivatives Helvetica Chimica Acta. 73: 509-551. DOI: 10.1002/Hlca.19900730302 |
0.44 |
|
1990 |
WIESLER WT, BEROVA N, OJIKA M, MEYERS HV, CHANG M, ZHOU P, LO L, NIWA M, TAKEDA R, NAKANISHI K. ChemInform Abstract: A CD-Spectroscopic Alternative to Methylation Analysis of Oligosaccharides: Reference Spectra for Identification of Chromophoric Glycopyranoside Derivatives. Cheminform. 21. DOI: 10.1002/chin.199030286 |
0.515 |
|
1989 |
Oltz EM, Pollack S, Delohery T, Smith MJ, Ojika M, Lee S, Kustin K, Nakanishi K. Distribution of tunichrome and vanadium in sea squirt blood cells sorted by flow cytometry. Experientia. 45: 186-90. PMID 2920805 DOI: 10.1007/Bf01954871 |
0.595 |
|
1989 |
Chang M, Nakanishi K, Meyers HV, Park MH, Takeda R, Ojika M, Hill J, Vázquez JT, Wiesler WT. Microscale structure determination of oligosaccharides by the exciton chirality method Pure and Applied Chemistry. 61: 1193-1200. DOI: 10.1351/Pac198961071193 |
0.678 |
|
1989 |
Ojika M, Meyers HV, Chang M, Nakanishi K. Microscale glycosidic cleavage of oligosaccharide bromobenzoates for circular dichroism analysis Journal of the American Chemical Society. 111: 8944-8946. DOI: 10.1021/Ja00206A042 |
0.598 |
|
1989 |
Ojika M, Meyers HV, Chang M, Nakanishi K. Microscale glycosidic cleavage of oligosaccharide bromobenzoates for circular dichroism analysis Journal of the American Chemical Society. 111: 8944-8946. |
0.521 |
|
1987 |
Ojika M, Wakamatsu K, Niwa H, Yamada K. Structures of new p-hydroxystyrene glycosides, ptelatoside-a and ptelatoside-b isolated from bracken fern, pteridium aquilinumvar. latiusculum, and synthesis of ptelatoside-a Tetrahedron. 43: 5275-5280. DOI: 10.1016/S0040-4020(01)87703-6 |
0.352 |
|
1987 |
Ojika M, Wakamatsu K, Niwa H, Yamada K. Ptaquiloside, a potent carcinogen isolated from bracken fern pteridium aquilinum var. latiusculum: structure elucidation based on chemical and spectral evidence, and reactions with amino acids, nucleosides, and nucleotides Tetrahedron. 43: 5261-5274. DOI: 10.1016/S0040-4020(01)87702-4 |
0.373 |
|
1986 |
Kigoshi H, Ojika M, Shizuri Y, Niwa H, Yamada K. Isolation of (10R,11R)-(+)-squalene-10,11-epoxide from the red alga laurencia okamurai and its enantioselective synthesis Tetrahedron. 42: 3789-3792. DOI: 10.1016/S0040-4020(01)87533-5 |
0.306 |
|
1986 |
Yamada K, Tan H, Tatematsu H, Ojika M. Dictyoprolene and neodictyoprolene, two new odoriferous compounds from the brown alga Dictyopteris prolifera: structures and synthesis Tetrahedron. 42: 3775-3780. DOI: 10.1016/S0040-4020(01)87531-1 |
0.382 |
|
1984 |
Ojika M, Wakamatsu K, Niwa H, Yamada K, Hirono I. ISOLATION AND STRUCTURES OF TWO NEWp-HYDROXYSTYRENE GLYCOSIDES, PTELATOSIDE-A AND PTELATOSIDE-B FROM BRACKEN,PTERIDIUM AQUILINUMVAR.LATIUSCULUM, AND SYNTHESIS OF PTELATOSIDE-A Chemistry Letters. 13: 397-400. DOI: 10.1246/Cl.1984.397 |
0.329 |
|
1983 |
Niwa H, Ojika M, Wakamatsu K, Yamada K, Hirono I, Matsushita K. Ptaquiloside, a novel norsesquiterpene glucoside from bracken, Pteridium aquilinum var. latiusculum Tetrahedron Letters. 24: 4117-4120. DOI: 10.1016/S0040-4039(00)88276-3 |
0.365 |
|
1983 |
Niwa H, Ojika M, Wakamatsu K, Yamada K, Ohba S, Saito Y, Hirono I, Matsushita K. Stereochemistry of ptaquiloside, a novel norsesquiterpene glucoside from bracken, Pteridium aquilinum var. latiusculum Tetrahedron Letters. 24: 5371-5372. DOI: 10.1016/S0040-4039(00)87871-5 |
0.301 |
|
1982 |
Ojika M, Shizuri Y, Niwa H, Yamada K, Iwadare S. Structure and synthesis of reductiline, a novel metabolite from a variant of streptomyces orientalis Tetrahedron Letters. 23: 4977-4980. DOI: 10.1016/S0040-4039(00)85765-2 |
0.336 |
|
1982 |
Shizuri Y, Matsukawa S, Ojika M, Yamada K. Two new farnesylacetone derivatives from the brown alga Sargassum micracanthum Phytochemistry. 21: 1808-1809. DOI: 10.1016/S0031-9422(82)85074-7 |
0.366 |
|
1982 |
Ojika M, Shizuri Y, Yamada K. A halogenated chamigrane epoxide and six related halogen-containing sesquiterpenes from the red alga Laurencia okamurai Phytochemistry. 21: 2410-2411. DOI: 10.1016/0031-9422(82)85220-5 |
0.352 |
|
1981 |
Shizuri Y, Ojika M, Yamada K. Structure of an antitumor antibiotic, reductiomycin Tetrahedron Letters. 22: 4291-4294. DOI: 10.1016/S0040-4039(01)82937-3 |
0.329 |
|
1980 |
Yamada K, Ojika M, Tan H. ISOLATION AND STRUCTURE OF NEODICTYOPROLENE, A NEW C11-COMPOUND OF BIOGENETIC SIGNIFICANCE FROM A BROWN ALGADICTYOPTERIS PROLIFERA Chemistry Letters. 9: 1633-1634. DOI: 10.1246/Cl.1980.1633 |
0.345 |
|
Show low-probability matches. |