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The Complestatins as HIV-1 Integrase Inhibitors. Efficient Isolation, Structure Elucidation, and Inhibitory Activities of Isocomplestatin, Chloropeptin I, New Complestatins, A and B, and Acid-Hydrolysis Products of Chloropeptin I

Journal of natural products (Washington, D.C.), 2001-07, Vol.64 (7), p.874-882

2001

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Selective inhibition of farnesyl-protein transferase blocks ras processing in vivo

The Journal of biological chemistry, 1993-04, Vol.268 (11), p.7617-7620

1993

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Resorcylic Acid Lactones: Naturally Occurring Potent and Selective Inhibitors of MEK

The Journal of Antibiotics, 1999/12/25, Vol.52(12), pp.1086-1094

1999

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Inhibitors of farnesylation of Ras from a microbial natural products screening program

Journal of industrial microbiology & biotechnology, 2000-12, Vol.25 (6), p.315-327

2000

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Clavaric acid: a triterpenoid inhibitor of farnesyl-protein transferase from Clavariadelphus truncatus

Journal of natural products (Washington, D.C.), 1998-12, Vol.61 (12), p.1568-1570

1998

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Efficient syntheses, human and yeast farnesyl-protein transferase inhibitory activities of chaetomellic acids and analogues

Bioorganic & medicinal chemistry, 2000-03, Vol.8 (3), p.571-580

2000

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Kampanols: novel ras farnesyl-protein transferase inhibitors from Stachybotrys kampalensis

Bioorganic & medicinal chemistry letters, 1998-08, Vol.8 (16), p.2071-2076

1998

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Clavaric Acid and Steroidal Analogues as Ras- and FPP-Directed Inhibitors of Human Farnesyl-Protein Transferase

Journal of medicinal chemistry, 1998-11, Vol.41 (23), p.4492-4501

1998

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Prenatal ethanol exposure impairs lesion-induced plasticity in a dopaminergic synapse after maturity

Neuroscience, 1989, Vol.29 (3), p.715-723

1989

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L-696, 474, A NOVEL CYTOCHALASIN AS AN INHIBITOR OF HIV-1 PROTEASE: II. ISOLATION AND STRUCTURE

The Journal of Antibiotics, 1992/05/25, Vol.45(5), pp.679-685

1992

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Contractions of the isolated uterus stimulated by epidermal growth factor

The FASEB journal, 1987-09, Vol.1 (3), p.224-228

1987

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Isolation and structure of chaetomellic acids A and B from Chaetomella acutiseta: farnesyl pyrophosphate mimic inhibitors of ras farnesyl-protein transferase

Tetrahedron, 1993-07, Vol.49 (27), p.5917-5926

1993

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Microbial Transformation of L-696, 474, a Novel Cytochalasin as an Inhibitor of HIV-1 Protease

Journal of natural products (Washington, D.C.), 1993-05, Vol.56 (5), p.755-761

1993

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Deafferentation elicits increased dopamine-sensitive adenylate cyclase and receptor binding in the olfactory tubercle

The Journal of neuroscience, 1986-08, Vol.6 (8), p.2208-2214

1986

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Estrogen regulation of epidermal growth factor receptor messenger ribonucleic-acid

Molecular endocrinology (Baltimore, Md.), 1988-03, Vol.2 (3), p.230-235

1988

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Quinoxapeptins: Novel Chromodepsipeptide Inhibitors of HIV-1 and HIV-2 Reverse Transcriptase: I. The Producing Organism and Biological Activity

The Journal of Antibiotics, 1996/03/25, Vol.49(3), pp.253-259

1996

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Barceloneic Acid A, a New Farnesyl-Protein Transferase Inhibitor from a Phoma Species

Journal of natural products (Washington, D.C.), 1995-07, Vol.58 (7), p.986-991

1995

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HIV-1 protease inhibitory activity of L-694,746, a novel metabolite of L-689,502

Biochemical and biophysical research communications, 1991-12, Vol.181 (3), p.1456-1461

1991

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Fusidienol: A novel inhibitor of Ras farnesyl-protein transferase from Fusidium griseum

Tetrahedron letters, 1994-07, Vol.35 (27), p.4693-4696

1994

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Oreganic Acid, a Potent Inhibitor of Ras Farnesyl-Protein Transferase

Biochemical and biophysical research communications, 1997-03, Vol.232 (2), p.478-481

1997

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Isolation and structure determination of pycnidione, A novel bistropolone stromelysin inhibitor from a Phoma sp

Tetrahedron, 1993-03, Vol.49 (11), p.2139-2144

1993

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L-696, 474, A NOVEL CYTOCHALASIN AS AN INHIBITOR OF HIV-1 PROTEASE: III. BIOLOGICAL ACTIVITY

The Journal of Antibiotics, 1992/05/25, Vol.45(5), pp.686-691

1992

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Structure, Stereochemistry, and Biological Activity of Integramycin, a Novel Hexacyclic Natural Product Produced by Actinoplanes sp. that Inhibits HIV-1 Integrase

Organic letters, 2002-04, Vol.4 (7), p.1123-1126

2002

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Chaetomella acutiseta produces chaetomellic acids A and B which are reversible inhibitors of farnesyl-protein transferase

Applied microbiology and biotechnology, 1993-11, Vol.40 (2-3), p.370-374

1993

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Durhamycin A, a Potent Inhibitor of HIV Tat Transactivation

Journal of natural products (Washington, D.C.), 2002-08, Vol.65 (8), p.1091-1095

2002

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The Complestatins as HIV-1 Integrase Inhibitors. Efficient Isolation, Structure Elucidation, and Inhibitory Activities of Isocomplestatin, Chloropeptin I, New Complestatins, A and B, and Acid-Hydrolysis Products of Chloropeptin I

Selective inhibition of farnesyl-protein transferase blocks ras processing in vivo

Resorcylic Acid Lactones: Naturally Occurring Potent and Selective Inhibitors of MEK

Inhibitors of farnesylation of Ras from a microbial natural products screening program

Clavaric acid: a triterpenoid inhibitor of farnesyl-protein transferase from Clavariadelphus truncatus

Efficient syntheses, human and yeast farnesyl-protein transferase inhibitory activities of chaetomellic acids and analogues

Kampanols: novel ras farnesyl-protein transferase inhibitors from Stachybotrys kampalensis

Clavaric Acid and Steroidal Analogues as Ras- and FPP-Directed Inhibitors of Human Farnesyl-Protein Transferase

Prenatal ethanol exposure impairs lesion-induced plasticity in a dopaminergic synapse after maturity

L-696, 474, A NOVEL CYTOCHALASIN AS AN INHIBITOR OF HIV-1 PROTEASE: II. ISOLATION AND STRUCTURE

Contractions of the isolated uterus stimulated by epidermal growth factor

Isolation and structure of chaetomellic acids A and B from Chaetomella acutiseta: farnesyl pyrophosphate mimic inhibitors of ras farnesyl-protein transferase

Microbial Transformation of L-696, 474, a Novel Cytochalasin as an Inhibitor of HIV-1 Protease

Deafferentation elicits increased dopamine-sensitive adenylate cyclase and receptor binding in the olfactory tubercle

Estrogen regulation of epidermal growth factor receptor messenger ribonucleic-acid

Quinoxapeptins: Novel Chromodepsipeptide Inhibitors of HIV-1 and HIV-2 Reverse Transcriptase: I. The Producing Organism and Biological Activity

Barceloneic Acid A, a New Farnesyl-Protein Transferase Inhibitor from a Phoma Species

HIV-1 protease inhibitory activity of L-694,746, a novel metabolite of L-689,502

Fusidienol: A novel inhibitor of Ras farnesyl-protein transferase from Fusidium griseum

Oreganic Acid, a Potent Inhibitor of Ras Farnesyl-Protein Transferase

Isolation and structure determination of pycnidione, A novel bistropolone stromelysin inhibitor from a Phoma sp

L-696, 474, A NOVEL CYTOCHALASIN AS AN INHIBITOR OF HIV-1 PROTEASE: III. BIOLOGICAL ACTIVITY

Structure, Stereochemistry, and Biological Activity of Integramycin, a Novel Hexacyclic Natural Product Produced by Actinoplanes sp. that Inhibits HIV-1 Integrase

Chaetomella acutiseta produces chaetomellic acids A and B which are reversible inhibitors of farnesyl-protein transferase

Durhamycin A, a Potent Inhibitor of HIV Tat Transactivation

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