Huang F - Search Results

1

Design, synthesis and QSAR study of novel isatin analogues inspired Michael acceptor as potential anticancer compounds.

Wang J, Yun D, Yao J, Fu W, Huang F, Chen L, Wei T, Yu C, Xu H, Zhou X, Huang Y, Wu J, Qiu P, Li W. Wang J, et al. Among authors: huang f, huang y. Eur J Med Chem. 2018 Jan 20;144:493-503. doi: 10.1016/j.ejmech.2017.12.043. Epub 2017 Dec 18. Eur J Med Chem. 2018. PMID: 29288946

2

Novel cyclic compounds as potent phosphodiesterase 4 inhibitors.

He W, Huang FC, Hanney B, Souness J, Miller B, Liang G, Mason J, Djuric S. He W, et al. Among authors: huang fc. J Med Chem. 1998 Oct 22;41(22):4216-23. doi: 10.1021/jm970575f. J Med Chem. 1998. PMID: 9784096

3

Synthesis of 2-(2,3-dihydro-2-oxo-1,3,4-oxadiazol-5-yl) benzo heterocycles. A novel series of orally active antiallergic agents.

Musser JH, Brown RE, Loev B, Bailey K, Jones H, Kahen R, Huang FC, Khandwala A, Leibowitz M, Sonnino-Goldman P, et al. Musser JH, et al. Among authors: huang fc. J Med Chem. 1984 Feb;27(2):121-5. doi: 10.1021/jm00368a004. J Med Chem. 1984. PMID: 6198518

4

The development of a novel series of (quinolin-2-ylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 3. Structural variation of the acidic side chain to give antagonists of enhanced potency.

Galemmo RA Jr, Johnson WH Jr, Learn KS, Lee TD, Huang FC, Campbell HF, Youssefyeh R, O'Rourke SV, Schuessler G, Sweeney DM, et al. Galemmo RA Jr, et al. Among authors: huang fc. J Med Chem. 1990 Oct;33(10):2828-41. doi: 10.1021/jm00172a024. J Med Chem. 1990. PMID: 2170649

5

Structure-activity relationships study of two series of leukotriene B4 antagonists: novel indolyl and naphthyl compounds substituted with a 2-[methyl(2-phenethyl)amino]-2-oxoethyl side chain.

Chan WK, Huang FC, Morrissette MM, Warus JD, Moriarty KJ, Galemmo RA, Dankulich WD, Poli G, Sutherland CA. Chan WK, et al. Among authors: huang fc. J Med Chem. 1996 Sep 13;39(19):3756-68. doi: 10.1021/jm950699x. J Med Chem. 1996. PMID: 8809164

6

Quaternary substituted PDE IV inhibitors II: the synthesis and in vitro evaluation of a novel series of gamma-lactams.

Hulme C, Moriarty K, Huang FC, Mason J, McGarry D, Labaudiniere R, Souness J, Djuric S. Hulme C, et al. Among authors: huang fc. Bioorg Med Chem Lett. 1998 Feb 17;8(4):399-404. doi: 10.1016/s0960-894x(98)00036-5. Bioorg Med Chem Lett. 1998. PMID: 9871693

7

A novel series of [2-[methyl(2-phenethyl)amino]-2-oxoethyl] benzene-containing leukotriene B4 antagonists: initial structure-activity relationships.

Huang FC, Chan WK, Moriarty KJ, Poli G, Morrissette MM, Galemmo RA, Warus JD, Dankulich WP, Sutherland CA. Huang FC, et al. J Med Chem. 1996 Sep 13;39(19):3748-55. doi: 10.1021/jm9506985. J Med Chem. 1996. PMID: 8809163

8

Quaternary substituted PDE4 inhibitors I: the synthesis and in vitro evaluation of a novel series of oxindoles.

Hulme C, Poli GB, Huang FC, Souness JE, Djuric SW. Hulme C, et al. Among authors: huang fc. Bioorg Med Chem Lett. 1998 Jan 20;8(2):175-8. doi: 10.1016/s0960-894x(97)10206-2. Bioorg Med Chem Lett. 1998. PMID: 9871649

9

1,2,4-Triazolo[4,3-a]quinoxaline-1,4-diones as antiallergic agents.

Loev B, Musser JH, Brown RE, Jones H, Kahen R, Huang FC, Khandwala A, Sonnino-Goldman P, Leibowitz MJ. Loev B, et al. Among authors: huang fc. J Med Chem. 1985 Mar;28(3):363-6. doi: 10.1021/jm00381a016. J Med Chem. 1985. PMID: 2579236

10

Development of a novel series of (2-quinolinylmethoxy)phenyl-containing compounds as high-affinity leukotriene D4 receptor antagonists. 2. Effects of an additional phenyl ring on receptor affinity.

Huang FC, Galemmo RA Jr, Johnson WH Jr, Poli GB, Morrissette MM, Mencel JJ, Warus JD, Campbell HF, Nuss GW, Carnathan GW, et al. Huang FC, et al. J Med Chem. 1990 Apr;33(4):1194-200. doi: 10.1021/jm00166a017. J Med Chem. 1990. PMID: 2157010

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