15 articles for FC Huang
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
23
Quaternary substituted PDE IV inhibitors II: the synthesis and in vitro evaluation of a novel series of gamma-lactams.

Rh£Ne-Poulenc Rorer Central Research
13
Quaternary substituted PDE4 inhibitors I: the synthesis and in vitro evaluation of a novel series of oxindoles.

Rh£Ne-Poulenc Rorer Central Research
25
The synthesis and biological evaluation of a novel series of indole PDE4 inhibitors I.

Rh£Ne-Poulenc Rorer Central Research
3
Structure-based design, synthesis and evaluation of novel anthra[1,2-d]imidazole-6,11-dione derivatives as telomerase inhibitors and potential for cancer polypharmacology.

National Defense Medical Center
2
Synthesis, human telomerase inhibition and anti-proliferative studies of a series of 2,7-bis-substituted amido-anthraquinone derivatives.

National Defense Medical Center
1
Novel cytokine release inhibitors. Part I: Triterpenes.

RhóNe-Poulenc Rorer Central Research
3
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.

RhôNe-Poulenc Rorer
3
A novel series of [2-[methyl(2-phenethyl)amino]-2-oxoethyl] benzene-containing leukotriene B4 antagonists: initial structure-activity relationships.

Rhone-Poulenc Rorer Central Research
17
Novel cyclic compounds as potent phosphodiesterase 4 inhibitors.

Sw 8 Rh£Ne-Poulenc Rorer Central Research
29
Differential effects of a series of hydroxamic acid derivatives on 5-lipoxygenase and cyclooxygenase from neutrophils and 12-lipoxygenase from platelets and their in vivo effects on inflammation and anaphylaxis.

Rorer Central Research
37
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.

Rorer Central Research
35
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.

Rorer Central Research
27
Development of a novel series of (2-quinolinylmethoxy)phenyl-containing compounds as high-affinity leukotriene receptor antagonists. 1. Initial structure-activity relationships.

Rorer Central Research
17
Development of a novel series of (2-quinolinylmethoxy)phenyl-containing compounds as high-affinity leukotriene D4 receptor antagonists. 4. Addition of chromone moiety enhances leukotriene D4 receptor binding affinity.

Rhone-Poulenc Rorer Central Research
4
4-[2-[Methyl(2-phenethyl)amino]-2-oxoethyl]-8-(phenylmethoxy)-2- naphthalenecarboxylic acid: a high affinity, competitive, orally active leukotriene B4 receptor antagonist.

Rhone-Poulenc Rorer Central Research