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Activity of Estrogen Receptor β Agonists in Therapy-Resistant Estrogen Receptor-Positive Breast Cancer

Frontiers in oncology, 2022-04, Vol.12, p.857590-857590

2022

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Target specificity, in vivo pharmacokinetics, and efficacy of the putative STAT3 inhibitor LY5 in osteosarcoma, Ewing's sarcoma, and rhabdomyosarcoma

PloS one, 2017-07, Vol.12 (7), p.e0181885

2017

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Acid-Promoted Prins Cyclizations of Enol Ethers To Form Tetrahydropyrans

Organic letters, 2003-05, Vol.5 (9), p.1499-1502

2003

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The elucidation of species-specific receptor pharmacology: a case study using subtype selective para - and meta -carborane estrogen receptor agonists

The Journal of pharmacology and experimental therapeutics, 2024-06, p.JPET-AR-2023-001874

2024

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Fused tricyclic mGluR1 antagonists for the treatment of neuropathic pain

Bioorganic & medicinal chemistry letters, 2012-02, Vol.22 (4), p.1575-1578

2012

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Substituent Effects on the Regiochemical and Stereochemical Course of the Nussbaumer-Frater Variation of the Prins Cyclization

Heterocycles, 2006-12, Vol.70 (1), p.119

2006

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The Practical Synthesis of a Novel and Highly Potent Analogue of Bryostatin

Journal of the American Chemical Society, 2002-11, Vol.124 (46), p.13648-13649

2002

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A Highly Stereoselective Synthesis of 2-Deoxy-β-glycosides Using 2-Deoxy-2-iodo-glucopyranosyl Acetate Donors

Journal of the American Chemical Society, 1999-04, Vol.121 (14), p.3541-3542

1999

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Iminoheterocycles as γ-secretase modulators

Bioorganic & medicinal chemistry letters, 2010-09, Vol.20 (18), p.5380-5384

2010

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Synthesis and SAR development of novel mGluR1 antagonists for the treatment of chronic pain

Bioorganic & medicinal chemistry letters, 2012-12, Vol.22 (23), p.7223-7226

2012

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Synthesis of Furans by SN2' Cyclization of .gamma.-Alkynyl Allylic Alcohol Derivatives

Journal of organic chemistry, 1994-10, Vol.59 (20), p.6110-6113

1994

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A Highly Stereoselective Synthesis of the Landomycin A Hexasaccharide Unit

Journal of the American Chemical Society, 2000-06, Vol.122 (25), p.6124-6125

2000

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The Potent Dihydroorotate Dehydrogenase Inhibitor, Hosu-53, Exhibits Compelling Monotherapy Efficacy in Multiple Myeloma and Augments CD47 Targeted Therapy

Blood, 2023-11, Vol.142 (Supplement 1), p.4692-4692

2023

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2-Deoxy-2-iodo- and 2-Deoxy-2-bromo-α-glucopyranosyl Trichloroacetimidates: Highly Reactive and Stereoselective Donors for the Synthesis of 2-Deoxy-β-glycosides

Organic letters, 1999-09, Vol.1 (6), p.891-893

1999

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Studies on the Synthesis of Landomycin A: Synthesis and Glycosidation Reactions of l-Rhodinosyl Acetate Derivatives

Journal of organic chemistry, 2001-09, Vol.66 (19), p.6389-6393

2001

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Iodoacetoxylation of Glycals Using Cerium(IV) Ammonium Nitrate, Sodium Iodide, and Acetic Acid: Stereoselective Synthesis of 2-Deoxy-2-iodo-α-mannopyranosyl Acetates

Organic letters, 1999-09, Vol.1 (6), p.895-897

1999

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Abstract 1060: Introducing a novel DHODH inhibitor with superior in vivo activity as monotherapy or in novel combination regimen with immunotherapy for hematological malignancies

Cancer research (Chicago, Ill.), 2022-06, Vol.82 (12_Supplement), p.1060-1060

2022

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Synthesis of Furans by SN2' Cyclization of .gamma.-Alkynyl Allylic Alcohol Derivatives. [Erratum to document cited in CA122:31231]

Journal of organic chemistry, 1995-04, Vol.60 (8), p.2644-2644

1995

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Iminoheterocycles as g-secretase modulators

Bioorganic & medicinal chemistry letters, 2010-09, Vol.20 (18), p.5380-5384

2010

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Stereoselective synthesis of 2-deoxy-β-glycosides from glycal precursors. 1. Stereochemistry of the reactions of d-glucal derivatives with phenylsulfenyl chloride and phenylselenenyl chloride

Tetrahedron, 1997-06, Vol.53 (26), p.8825-8836

1997

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Acid-Promoted Prins Cyclizations of Enol Ethers to Form Tetrahydropyrans

ChemInform, 2003-09, Vol.34 (36), p.no-no

2003

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ChemInform Abstract: A Highly Stereoselective Synthesis of 2-Deoxy-β-glycosides Using 2-Deoxy-2-iodo-glucopyranosyl Acetate Donors

ChemInform, 1999-08, Vol.30 (34), p.no-no

1999

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ChemInform Abstract: Iodoacetoxylation of Glycals Using Cerium(IV) Ammonium Nitrate, Sodium Iodide, and Acetic Acid: Stereoselective Synthesis of 2-Deoxy-2-iodo-α-mannopyranosyl Acetates

ChemInform, 1999-11, Vol.30 (48), p.no-no

1999

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ChemInform Abstract: 2-Deoxy-2-iodo- and 2-Deoxy-2-bromo-α-glucopyranosyl Trichloroacetimidates: Highly Reactive and Stereoselective Donors for the Synthesis of 2-Deoxy-β-glycosides

ChemInform, 1999-11, Vol.30 (47), p.no-no

1999

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Activity of Estrogen Receptor β Agonists in Therapy-Resistant Estrogen Receptor-Positive Breast Cancer

Target specificity, in vivo pharmacokinetics, and efficacy of the putative STAT3 inhibitor LY5 in osteosarcoma, Ewing's sarcoma, and rhabdomyosarcoma

Acid-Promoted Prins Cyclizations of Enol Ethers To Form Tetrahydropyrans

The elucidation of species-specific receptor pharmacology: a case study using subtype selective para - and meta -carborane estrogen receptor agonists

Pyrimidine depletion enhances targeted and immune therapy combinations in acute myeloid leukemia

Fused tricyclic mGluR1 antagonists for the treatment of neuropathic pain

Substituent Effects on the Regiochemical and Stereochemical Course of the Nussbaumer-Frater Variation of the Prins Cyclization

The Practical Synthesis of a Novel and Highly Potent Analogue of Bryostatin

A Highly Stereoselective Synthesis of 2-Deoxy-β-glycosides Using 2-Deoxy-2-iodo-glucopyranosyl Acetate Donors

Iminoheterocycles as γ-secretase modulators

Synthesis and SAR development of novel mGluR1 antagonists for the treatment of chronic pain

Synthesis of Furans by SN2' Cyclization of .gamma.-Alkynyl Allylic Alcohol Derivatives

A Highly Stereoselective Synthesis of the Landomycin A Hexasaccharide Unit

The Potent Dihydroorotate Dehydrogenase Inhibitor, Hosu-53, Exhibits Compelling Monotherapy Efficacy in Multiple Myeloma and Augments CD47 Targeted Therapy

2-Deoxy-2-iodo- and 2-Deoxy-2-bromo-α-glucopyranosyl Trichloroacetimidates: Highly Reactive and Stereoselective Donors for the Synthesis of 2-Deoxy-β-glycosides

Studies on the Synthesis of Landomycin A: Synthesis and Glycosidation Reactions of l-Rhodinosyl Acetate Derivatives

Iodoacetoxylation of Glycals Using Cerium(IV) Ammonium Nitrate, Sodium Iodide, and Acetic Acid: Stereoselective Synthesis of 2-Deoxy-2-iodo-α-mannopyranosyl Acetates

Abstract 1060: Introducing a novel DHODH inhibitor with superior in vivo activity as monotherapy or in novel combination regimen with immunotherapy for hematological malignancies

Synthesis of Furans by SN2' Cyclization of .gamma.-Alkynyl Allylic Alcohol Derivatives. [Erratum to document cited in CA122:31231]

Iminoheterocycles as g-secretase modulators

Stereoselective synthesis of 2-deoxy-β-glycosides from glycal precursors. 1. Stereochemistry of the reactions of d-glucal derivatives with phenylsulfenyl chloride and phenylselenenyl chloride

Acid-Promoted Prins Cyclizations of Enol Ethers to Form Tetrahydropyrans

ChemInform Abstract: A Highly Stereoselective Synthesis of 2-Deoxy-β-glycosides Using 2-Deoxy-2-iodo-glucopyranosyl Acetate Donors

ChemInform Abstract: Iodoacetoxylation of Glycals Using Cerium(IV) Ammonium Nitrate, Sodium Iodide, and Acetic Acid: Stereoselective Synthesis of 2-Deoxy-2-iodo-α-mannopyranosyl Acetates

ChemInform Abstract: 2-Deoxy-2-iodo- and 2-Deoxy-2-bromo-α-glucopyranosyl Trichloroacetimidates: Highly Reactive and Stereoselective Donors for the Synthesis of 2-Deoxy-β-glycosides

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