Cho H - Search Results

1

Structure-activity relationships of potent and selective factor Xa inhibitors: benzimidazole derivatives with the side chain oriented to the prime site of factor Xa.

Ueno H, Katoh S, Yokota K, Hoshi J, Hayashi M, Uchida I, Aisaka K, Hase Y, Cho H. Ueno H, et al. Among authors: cho h. Bioorg Med Chem Lett. 2004 Aug 16;14(16):4281-6. doi: 10.1016/j.bmcl.2004.05.092. Bioorg Med Chem Lett. 2004. PMID: 15261287

2

Synthesis and structure-activity relationships of 5,6,7,8-tetrahydro-4H-thieno[3,2-b]azepine derivatives: novel arginine vasopressin antagonists.

Cho H, Murakami K, Nakanishi H, Fujisawa A, Isoshima H, Niwa M, Hayakawa K, Hase Y, Uchida I, Watanabe H, Wakitani K, Aisaka K. Cho H, et al. J Med Chem. 2004 Jan 1;47(1):101-9. doi: 10.1021/jm030287l. J Med Chem. 2004. PMID: 14695824

A variety of novel heterocyclic compounds having thienoazepine, pyrroloazepine, furoazepine, and thienodiazepine skeletons were synthesized, most of which exhibited potent antagonism of [(3)H]-AVP specific binding in assays using rat liver (V1), rat kidney (V2), human plat …

A variety of novel heterocyclic compounds having thienoazepine, pyrroloazepine, furoazepine, and thienodiazepine skeletons were synthesized, …

3

Discovery of novel tetrahydroisoquinoline derivatives as potent and selective factor Xa inhibitors.

Ueno H, Yokota K, Hoshi J, Yasue K, Hayashi M, Uchida I, Aisaka K, Hase Y, Katoh S, Cho H. Ueno H, et al. Among authors: cho h. Bioorg Med Chem Lett. 2005 Jan 3;15(1):185-9. doi: 10.1016/j.bmcl.2004.10.033. Bioorg Med Chem Lett. 2005. PMID: 15582437

4

Synthesis and structure-activity relationships of novel selective factor Xa inhibitors with a tetrahydroisoquinoline ring.

Ueno H, Yokota K, Hoshi J, Yasue K, Hayashi M, Hase Y, Uchida I, Aisaka K, Katoh S, Cho H. Ueno H, et al. Among authors: cho h. J Med Chem. 2005 May 19;48(10):3586-604. doi: 10.1021/jm058160e. J Med Chem. 2005. PMID: 15887966

5

Synthesis and selective coronary vasodilatory activity of 3,4-dihydro-2,2-bis(methoxymethyl)-2H-1-benzopyran-3-ol derivatives: novel potassium channel openers.

Cho H, Katoh S, Sayama S, Murakami K, Nakanishi H, Kajimoto Y, Ueno H, Kawasaki H, Aisaka K, Uchida I. Cho H, et al. J Med Chem. 1996 Sep 13;39(19):3797-805. doi: 10.1021/jm960270l. J Med Chem. 1996. PMID: 8809167

6

Novel caffeic acid derivatives: extremely potent inhibitors of 12-lipoxygenase.

Cho H, Ueda M, Tamaoka M, Hamaguchi M, Aisaka K, Kiso Y, Inoue T, Ogino R, Tatsuoka T, Ishihara T, et al. Cho H, et al. J Med Chem. 1991 Apr;34(4):1503-5. doi: 10.1021/jm00108a039. J Med Chem. 1991. PMID: 2016727 No abstract available.

7

Dihydropyrimidines: novel calcium antagonists with potent and long-lasting vasodilative and antihypertensive activity.

Cho H, Ueda M, Shima K, Mizuno A, Hayashimatsu M, Ohnaka Y, Takeuchi Y, Hamaguchi M, Aisaka K, Hidaka T, et al. Cho H, et al. J Med Chem. 1989 Oct;32(10):2399-406. doi: 10.1021/jm00130a029. J Med Chem. 1989. PMID: 2552119

8

Synthesis of novel 2-chloro-1,4-dihydropyridines by chlorination of 2-hydroxy-1,4-dihydropyridines with phosphorus oxychloride.

Cho H, Ueda M, Mizuno A, Ishihara T, Aisaka K, Noguchi T. Cho H, et al. Chem Pharm Bull (Tokyo). 1989 Aug;37(8):2117-21. doi: 10.1248/cpb.37.2117. Chem Pharm Bull (Tokyo). 1989. PMID: 2598311

9

Novel benzthiodiazepinones as antiherpetic agents: SAR improvement of therapeutic index by alterations of the seven-membered ring.

Hamilton HW, Nishiguchi G, Hagen SE, Domagala JD, Weber PC, Gracheck S, Boulware SL, Nordby EC, Cho H, Nakamura T, Ikeda S, Watanabe W. Hamilton HW, et al. Among authors: cho h. Bioorg Med Chem Lett. 2002 Oct 21;12(20):2981-3. doi: 10.1016/s0960-894x(02)00578-4. Bioorg Med Chem Lett. 2002. PMID: 12270188

10

Formation of Wrinkled Nanostructures via Surface-Bulk Curing Disparity in Ethyl Cyanoacrylate: Toward Superhydrophobic Surface Applications.

Lee C, Choi HJ, Jeong K, Lee K, Cho H. Lee C, et al. Among authors: cho h. Nanomaterials (Basel). 2024 Dec 25;15(1):12. doi: 10.3390/nano15010012. Nanomaterials (Basel). 2024. PMID: 39791772

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