A. Dombrowski

发表

Resorcylic acid lactones: naturally occurring potent and selective inhibitors of MEK.

O. Hensens, H. Huber, D. Patrick, 1999, The Journal of antibiotics.

Apicidin: a novel antiprotozoal agent that inhibits parasite histone deacetylase.

D M Schmatz, M. Bednarek, D. Schmatz, 1996, Proceedings of the National Academy of Sciences of the United States of America.

The "FERMEX" method for metabolite-enriched fungal extracts.

G. Bills, M. Goetz, A. Dombrowski, 2012, Methods in molecular biology.

Structure, histone deacetylase, and antiprotozoal activities of apicidins B and C, congeners of apicidin with proline and valine substitutions.

D. Schmatz, J. Liesch, D. Zink, 2001, Organic letters.

Integracides: tetracyclic triterpenoid inhibitors of HIV-1 integrase produced by Fusarium sp.

D. Hazuda, J. Hirshfield, P. Felock, 2003, Bioorganic & medicinal chemistry.

Structure and chemistry of apicidins, a class of novel cyclic tetrapeptides without a terminal alpha-keto epoxide as inhibitors of histone deacetylase with potent antiprotozoal activities.

D. Schmatz, R. Mosley, G. Bills, 2002, The Journal of organic chemistry.

Biogeography and relatedness of Nodulisporium strains producing nodulisporic acid

G. Platas, F. Peláez, J. Ondeyka, 2001 .

Production of a family of kinase-inhibiting lactones from fungal fermentations.

Y. Zhang, F. Peláez, G. Bills, 1999, The Journal of antibiotics.

Discovery of structurally diverse natural product antagonists of chemokine receptor CXCR3

Gregory R. Koch, J. Demartino, Z. Guan, 2005, Molecular Diversity.

Recent and future discoveries of pharmacologically active metabolites from tropical fungi.

R. Watling, J. Frankland, A. Ainsworth, 2002 .

Structure, histone deacetylase, and antiprotozoal activities of apicidins B and C, congeners of apicidin with proline and valine substitutions.

D. Schmatz, J. Liesch, D. Zink, 2001, Organic letters.

New fungal metabolite geranylgeranyltransferase inhibitors with antifungal activity

Z. Guan, J. Williamson, T. Kelly, 2005, Natural product research.

Aspercyclide A–C, three novel fungal metabolites from Aspergillus sp. as inhibitors of high-affinity IgE receptor

Sheo B. Singh, D. Zink, A. Dombrowski, 2004 .

Discovery of Novel Antifungal (1,3)-β-d-Glucan Synthase Inhibitors

R. Schwartz, F. Vicente, A. Cabello, 2000, Antimicrobial Agents and Chemotherapy.

Apicidins: Novel cyclic tetrapeptides as coccidiostats and antimalarial agents from Fusarium pallidoroseum

D. Schmatz, Sheo B. Singh, D. Zink, 1996 .

Isolation and Structures of Novel Fungal Metabolites as Chemokine Receptor (CCR2) Antagonists

Z. Guan, A. Cabello, G. Bills, 2005, The Journal of Antibiotics.

Maxikdiol: a novel dihydroxyisoprimane as an agonist of Maxi-K channels

O. McManus, Suresh B. Singh, G. Kaczorowski, 1994 .

Structure of stereochemistry of thysanone: a novel human rhinovirus 3C-protease inhibitor from Thysanophora penicilloides

Jack L. Smith, R. Ball, Sheo B. Singh, 1991 .

Steroidal and Triterpenoidal Fungal Metabolites as Ligands of Liver X Receptors

Ziqiang Guan, Javier Collado, Z. Guan, 2005, The Journal of Antibiotics.

Candelalides A-C: novel diterpenoid pyrones from fermentations of Sesquicillium candelabrum as blockers of the voltage-gated potassium channel Kv1.3.

G. Bills, D. Zink, M. Goetz, 2001, Organic letters.

Isolation and insecticidal activity of mellamide from Aspergillus melleus

Z. Guan, J. Ondeyka, A. Dombrowski, 2003, Journal of Industrial Microbiology and Biotechnology.

Equisetin and a novel opposite stereochemical homolog phomasetin, two fungal metabolites as inhibitors of HIV-1 integrase

D. Hazuda, Sheo B. Singh, D. Zink, 1998 .

Isolation, structure, absolute stereochemistry, and HIV-1 integrase inhibitory activity of integrasone, a novel fungal polyketide.

D. Hazuda, Z. Guan, G. Bills, 2004, Journal of natural products.

Structure and conformation of ophiobolin K and 6- epiophiobolin K from Aspergillus ustus as a nematocidal agent.

Suresh B. Singh, Jack L. Smith, J. Schaeffer, 1991 .

Isolation and Insecticidal/Anthelmintic Activity of Xanthonol, a Novel Bis-xanthone, from a Non-sporulating Fungal species

Z. Guan, Sheo B. Singh, J. Ondeyka, 2006, The Journal of Antibiotics.

Isolation and structure of nodulisporic acid A1 and A2, novel insecticides from a Nodulisporium sp.

O. Hensens, D. Zink, J. Ondeyka, 1999 .

Integramides A and B, two novel non-ribosomal linear peptides containing nine C(alpha)-methyl amino acids produced by fungal fermentations that are inhibitors of HIV-1 integrase.

D. Hazuda, Z. Guan, K. Silverman, 2002, Organic letters.

A Carotane Sesquiterpene as a Potent Modulator of the Maxi-K Channel from Arthrinium phaesospermum

G. Kaczorowski, G. Bills, R. Ball, 1995 .

Preussomerin D from the Endophyte Hormonema Dematioides

G. Salituro, N. Tsou, A. Dombrowski, 1993 .

L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease. I. The producing organism and its fermentation.

R. Monaghan, G. Bills, R. Giacobbe, 1992, The Journal of antibiotics.

Nodulisporic Acid A, a Novel and Potent Insecticide from a Nodulisporium Sp. Isolation, Structure Determination, and Chemical Transformations

O. Hensens, G. Helms, R. Ball, 1997 .

L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease. II. Isolation and structure.

O. Hensens, G. Bills, D. Zink, 1992, The Journal of antibiotics.

Isolation, structure, and HIV-1-integrase inhibitory activity of structurally diverse fungal metabolites

D. Hazuda, Z. Guan, G. Platas, 2003, Journal of Industrial Microbiology and Biotechnology.

Identification of Diverse Microbial Metabolites as Potent Inhibitors of HIV‐1 Tat Transactivation

J. Tomassini, O. Genilloud, F. Peláez, 2005, Chemistry & biodiversity.

Dietary tocopherols inhibit cell proliferation, regulate expression of ERα, PPARγ, and Nrf2, and decrease serum inflammatory markers during the development of mammary hyperplasia

A. Kong, N. Suh, J. So, 2013, Molecular carcinogenesis.

Isolation and structure of antagonists of chemokine receptor (CCR5).

Ziqiang Guan, Z. Guan, D. Stevenson, 2004, Journal of natural products.

SPORANDOL: A NOVEL ANTIPARASITIC BINAPHTHALENE FROM CHRYSOSPORIUM MERIDARIUM

O. Hensens, J. Williamson, R. Ball, 1997 .

Dihydrocarbazole alkaloids from Aspergillus tubingensis.

H. Sings, G. Harris, A. Dombrowski, 2001, Journal of natural products.

Isolation, structure, and HIV-1 integrase inhibitory activity of Cytosporic acid, a fungal metabolite produced by a Cytospora sp.

D. Hazuda, Z. Guan, P. Felock, 2003, Journal of natural products.

Isolation, structure and HIV-1 integrase inhibitory activity of exophillic acid, a novel fungal metabolite from Exophiala pisciphila.

D. Hazuda, P. Felock, Sheo B. Singh, 2003, The Journal of antibiotics.

Isolation, Structure and HIV‐1 Integrase Inhibitory Activity of Exophillic Acid, a Novel Fungal Metabolite from Exophiala pisciphila.

D. Hazuda, P. Felock, Sheo B. Singh, 2004 .

L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease. III. Biological activity.

P. Darke, K. Silverman, G. Bills, 1992, The Journal of antibiotics.

Novel sesquiterpenoids from the fermentation of Xylaria persicaria are selective ligands for the NPY Y5 receptor.

Scott K. Smith, N. Morin, D. Macneil, 2002, The Journal of organic chemistry.

Diterpenoid pyrones, novel blockers of the voltage-gated potassium channel Kv1.3 from fungal fermentations

Sheo B. Singh, D. Zink, M. Goetz, 2001 .