Z. Li

发表

Polyamines with N-(3-phenylpropyl) substituents are effective competitive inhibitors of trypanothione reductase and trypanocidal agents.

Matthew T. Hancock, B. Ganem, D. Rattendi, 2001, Bioorganic & medicinal chemistry letters.

Development and activities of a new melphalan prodrug designed for tumor-selective activation.

N. Siemers, D. Kerr, P. Senter, 1998, Bioconjugate chemistry.

Polyamine derivatives as inhibitors of trypanothione reductase and assessment of their trypanocidal activities.

D. Rattendi, C. Bacchi, T. Durham, 1997, Bioorganic & medicinal chemistry.

Preparation of (R)- and (S)-N-protected 3-hydroxypyrrolidines by hydroxylation with Sphingomonas sp. HXN-200, a highly active, regio- and stereoselective, and easy to handle biocatalyst.

B. Witholt, J. B. van Beilen, W. Duetz, 2001, The Journal of organic chemistry.

Antitumor 8-chlorobenzocycloheptapyridines: a new class of selective, nonpeptidic, nonsulfhydryl inhibitors of ras farnesylation.

W. R. Bishop, M. Snow, P. Kirschmeier, 1997, Bioorganic & medicinal chemistry.

Design and synthesis of a novel class of histone deacetylase inhibitors.

S. Leit, S. Fréchette, G. Bouchain, 2001, Bioorganic & medicinal chemistry letters.

1 alpha,25-dihydroxyvitamin D3 analogs featuring aromatic and heteroaromatic rings: design, synthesis, and preliminary biological testing.

T. Kensler, S. Guggino, M. White, 1995, Journal of medicinal chemistry.

Synthesis of 3-indolyl-2,5-dihydroxybenzoquinones.

M. Pirrung, K. Park, Z. Li, 2001, Organic letters.

Zn(OAc)2 catalyzed microwave irradiated synthesis of substituted thieno[2,3-d]pyrimidin-4(3H)-one

C. Yan, Z. Li, L. Wu, 2011 .

Design and synthesis of Pfmrk inhibitors as potential antimalarial agents.

N. Waters, C. Woodard, Z. Li, 2001, Bioorganic & medicinal chemistry letters.

Biotinylated isocoumarins, new inhibitors and reagents for detection, localization, and isolation of serine proteases.

J. Powers, C. Kam, D. Hudig, 1993, Bioconjugate chemistry.

Structural, dynamic, and theoretical studies of [AunPt2(PPh3)4(mu-S)2-n(mu 3-S)nL][PF6]n [n = 1, L = PPh3; n = 2, L = Ph2PCH2PPh2, (C5H4PPh2)2Fe].

T. Hor, Z. Loh, Z. Li, 2000, Inorganic chemistry.

Preparation of (S)-N-substituted 4-hydroxy-pyrrolidin-2-ones by regio- and stereoselective hydroxylation with Sphingomonas sp. HXN-200.

B. Witholt, Zhi Li, Z. Li, 2000, Organic letters.

Inhibitors of farnesyl protein transferase. 4-Amido, 4-carbamoyl, and 4-carboxamido derivatives of 1-(8-chloro-6,11-dihydro-5H-benzo[5,6]- cyclohepta[1,2-b]pyridin-11-yl)piperazine and 1-(3-bromo-8-chloro-6,11- dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)piperazine.

Walter A. Korfmacher, W. R. Bishop, J. Chen, 1998, Journal of medicinal chemistry.

Structure-activity relationship of 3-substituted N-(pyridinylacetyl)-4- (8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene )- piperidine inhibitors of farnesyl-protein transferase: design and synthesis of in vivo active antitumor compounds.

W. R. Bishop, J. Catino, M. Malkowski, 1997, Journal of medicinal chemistry.

Syntheses and absolute stereochemistry of chiral 9,10-dihydro-9,10-ethanoanthracenes and their tricarbonylchromium complexes

A. Werner, Z. Li, K. Schlögl, 1993 .

Intercalation of the (1R,2S,3R,4S)-N6-[1-(1,2,3,4-tetrahydro-2,3,4-trihydroxybenz[a]anthracenyl)]-2'-deoxyadenosyl adduct in the N-ras codon 61 sequence: DNA sequence effects.

C. Harris, T. Harris, M. Stone, 2001, Biochemistry.

Intercalation of the (1S,2R,3S,4R)-N6-[1-(1,2,3,4-tetrahydro-2,3, 4-trihydroxybenz[a]anthracenyl)]-2'-deoxyadenosyl adduct in an oligodeoxynucleotide containing the human N-ras codon 61 sequence.

C. Harris, T. Harris, M. Stone, 1999, Biochemistry.

Role of a polycyclic aromatic hydrocarbon bay region ring in modulating DNA adduct structure: the non-bay region (8S,9R,10S, 11R)-N(6)-[11-(8,9,10,11-tetrahydro-8,9, 10-trihydroxybenz[a]anthracenyl)]-2'-deoxyadenosyl adduct in codon 61 of the human N-ras protooncogene.

C. Harris, T. Harris, M. Stone, 1999, Biochemistry.

Intercalation of the (-)-(1R,2S,3R, 4S)-N6-[1-benz[a]anthracenyl]-2'-deoxyadenosyl adduct in an oligodeoxynucleotide containing the human N-ras codon 61 sequence.

C. Harris, T. Harris, M. Stone, 1999, Biochemistry.

6-(1-Hydroxyalkyl))penam sulfone derivatives as inhibitors of class A and class C beta-lactamases II.

P. Petersen, G. Francisco, E. Lenoy, 1999, Bioorganic & medicinal chemistry letters.

PTP1B inhibition and antihyperglycemic activity in the ob/ob mouse model of novel 11-arylbenzo[b]naphtho[2,3-d]furans and 11-arylbenzo[b]naphtho[2,3-d]thiophenes.

C. Moxham, Z. Zhang, J. Sredy, 1999, Journal of medicinal chemistry.