Tanaka A - Search Results

1

Synthesis and biological activity of novel macrocyclic antifungals: acylated conjugates of the ornithine moiety of the lipopeptidolactone FR901469.

Barrett D, Tanaka A, Harada K, Ohki H, Watabe E, Maki K, Ikeda F. Barrett D, et al. Among authors: tanaka a. Bioorg Med Chem Lett. 2001 Feb 26;11(4):479-82. doi: 10.1016/s0960-894x(00)00705-8. Bioorg Med Chem Lett. 2001. PMID: 11229752

2

Synthesis and biological activity of novel macrocyclic antifungals. modification of the tyrosine moiety of the lipopeptidolactone FR901469.

Barrett D, Tanaka A, Harada K, Watabe E, Maki K, Ikeda F. Barrett D, et al. Among authors: tanaka a. Bioorg Med Chem Lett. 2001 Jul 23;11(14):1843-9. doi: 10.1016/s0960-894x(01)00317-1. Bioorg Med Chem Lett. 2001. PMID: 11459644

3

Novel amidine conjugates of the ornithine moiety of the macrocyclic antifungal lipopeptidolactone FR901469.

Barrett D, Tanaka A, Watabe E, Maki K, Ikeda F. Barrett D, et al. Among authors: tanaka a. J Antibiot (Tokyo). 2001 Oct;54(10):844-7. doi: 10.7164/antibiotics.54.844. J Antibiot (Tokyo). 2001. PMID: 11776442 Free article. No abstract available.

4

Site-specific structural transformation of the novel antifungal cyclic depsipeptide FR901469: synthesis and biological activity of FR203903.

Tanaka A, Barrett D, Fujie A, Shigematsu N, Hashimoto M, Hashimoto S, Ikeda F. Tanaka A, et al. J Antibiot (Tokyo). 2001 Feb;54(2):193-7. doi: 10.7164/antibiotics.54.193. J Antibiot (Tokyo). 2001. PMID: 11302496 Free article. No abstract available.

5

Synthesis and antibacterial activity of novel 4-pyrrolidinylthio carbapenems Part IV. 2-Alkyl substituents containing cationic heteroaromatics linked via a C-C bond.

Zam HA, Barrett D, Tanaka A, Sasaki H, Matsuda K, Sakurai M, Terasawa T, Shirai F, Chiba T, Matsumoto Y, Tawara S. Zam HA, et al. Among authors: tanaka a. Bioorg Med Chem. 2001 Apr;9(4):961-82. doi: 10.1016/s0968-0896(00)00314-x. Bioorg Med Chem. 2001. PMID: 11354680

6

Molecular design, synthesis, and hypoglycemic activity of a series of thiazolidine-2,4-diones.

Oguchi M, Wada K, Honma H, Tanaka A, Kaneko T, Sakakibara S, Ohsumi J, Serizawa N, Fujiwara T, Horikoshi H, Fujita T. Oguchi M, et al. Among authors: tanaka a. J Med Chem. 2000 Aug 10;43(16):3052-66. doi: 10.1021/jm990522t. J Med Chem. 2000. PMID: 10956213

7

Synthesis, X-ray crystal structure, and biological activity of FR186054, a novel, potent, orally active inhibitor of acyl-CoA:cholesterol O-acyltransferase (ACAT) bearing a pyrazole ring.

Tanaka A, Terasawa T, Hagihara H, Kinoshita T, Sakuma Y, Ishibe N, Sawada M, Takasugi H, Tanaka H. Tanaka A, et al. Among authors: tanaka h. Bioorg Med Chem Lett. 1998 Jan 6;8(1):81-6. doi: 10.1016/s0960-894x(97)10191-3. Bioorg Med Chem Lett. 1998. PMID: 9871633

8

Inhibitors of acyl-CoA:cholesterol O-acyltransferase. 2. Identification and structure-activity relationships of a novel series of N-alkyl-N-(heteroaryl-substituted benzyl)-N'-arylureas.

Tanaka A, Terasawa T, Hagihara H, Sakuma Y, Ishibe N, Sawada M, Takasugi H, Tanaka H. Tanaka A, et al. Among authors: tanaka h. J Med Chem. 1998 Jun 18;41(13):2390-410. doi: 10.1021/jm9800853. J Med Chem. 1998. PMID: 9632372

9

Inhibitors of acyl-CoA:cholesterol O-acyltransferase (ACAT). Part 1: identification and structure-activity relationships of a novel series of substituted N-alkyl-N-biphenylylmethyl-N'-arylureas.

Tanaka A, Terasawa T, Hagihara H, Sakuma Y, Ishibe N, Sawada M, Takasugi H, Tanaka H. Tanaka A, et al. Among authors: tanaka h. Bioorg Med Chem. 1998 Jan;6(1):15-30. doi: 10.1016/s0968-0896(97)10009-8. Bioorg Med Chem. 1998. PMID: 9502102

10

QSAR study of the peptidic fibrinogen inhibitors FK633, FR158999 and related derivatives, using a novel and useful hydrophobic descriptor (logPmw).

Tanaka A, Murata M, Fujiwara H. Tanaka A, et al. Bioorg Med Chem Lett. 1998 Sep 22;8(18):2483-8. doi: 10.1016/s0960-894x(98)00405-3. Bioorg Med Chem Lett. 1998. PMID: 9873566

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