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Refinado por: assunto: 4-Butyrolactone - Chemistry remover
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Lead Optimization of Butyrolactone I as an Orally Bioavailable Antiallergic Agent Targeting FcγRIIB
Lead Optimization of Butyrolactone I as an Orally Bioavailable Antiallergic Agent Targeting FcγRIIB
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Lead Optimization of Butyrolactone I as an Orally Bioavailable Antiallergic Agent Targeting FcγRIIB

Xie, Chun-Lan ; Xiao, Hong-Xiu ; Song, Pei-Fang ; Liu, Qing-Mei ; Wei, Haoxiang ; Wu, Liang ; Zhu, Guang-Hao ; Liu, Guang-Ming ; Zhang, Yandong ; Wang, Ping ; Yang, Xian-Wen

Journal of medicinal chemistry, 2024-05, Vol.67 (9), p.7504-7515 [Periódico revisado por pares]

United States: American Chemical Society

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2
Metabolites from the Plant Endophytic Fungus Aspergillus sp. CPCC 400735 and Their Anti-HIV Activities
Metabolites from the Plant Endophytic Fungus Aspergillus sp. CPCC 400735 and Their Anti-HIV Activities
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Metabolites from the Plant Endophytic Fungus Aspergillus sp. CPCC 400735 and Their Anti-HIV Activities

Pang, Xu ; Zhao, Jian-Yuan ; Fang, Xiao-Mei ; Zhang, Tao ; Zhang, De-Wu ; Liu, Hong-Yu ; Su, Jing ; Cen, Shan ; Yu, Li-Yan

Journal of natural products (Washington, D.C.), 2017-10, Vol.80 (10), p.2595-2601 [Periódico revisado por pares]

United States: American Chemical Society and American Society of Pharmacognosy

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3
Flavipesides A–C, PKS-NRPS Hybrids as Pancreatic Lipase Inhibitors from a Marine Sponge Symbiotic Fungus Aspergillus flavipes 164013
Flavipesides A–C, PKS-NRPS Hybrids as Pancreatic Lipase Inhibitors from a Marine Sponge Symbiotic Fungus Aspergillus flavipes 164013
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Flavipesides A–C, PKS-NRPS Hybrids as Pancreatic Lipase Inhibitors from a Marine Sponge Symbiotic Fungus Aspergillus flavipes 164013

Jiao, Wei-Hua ; Xu, Qi-Hang ; Ge, Guang-Bo ; Shang, Ru-Yi ; Zhu, Hong-Rui ; Liu, Hong-Yan ; Cui, Jie ; Sun, Fan ; Lin, Hou-Wen

Organic letters, 2020-03, Vol.22 (5), p.1825-1829 [Periódico revisado por pares]

United States: American Chemical Society

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4
Insect‐Associated Bacteria Assemble the Antifungal Butenolide Gladiofungin by Non‐Canonical Polyketide Chain Termination
Insect‐Associated Bacteria Assemble the Antifungal Butenolide Gladiofungin by Non‐Canonical Polyketide Chain Termination
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Insect‐Associated Bacteria Assemble the Antifungal Butenolide Gladiofungin by Non‐Canonical Polyketide Chain Termination

Niehs, Sarah P. ; Kumpfmüller, Jana ; Dose, Benjamin ; Little, Rory F. ; Ishida, Keishi ; Flórez, Laura V. ; Kaltenpoth, Martin ; Hertweck, Christian

Angewandte Chemie (International ed.), 2020-12, Vol.59 (51), p.23122-23126 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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5
Rosmarinic acid is a homoserine lactone mimic produced by plants that activates a bacterial quorum-sensing regulator
Rosmarinic acid is a homoserine lactone mimic produced by plants that activates a bacterial quorum-sensing regulator
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Rosmarinic acid is a homoserine lactone mimic produced by plants that activates a bacterial quorum-sensing regulator

Corral-Lugo, Andrés ; Daddaoua, Abdelali ; Ortega, Alvaro ; Espinosa-Urgel, Manuel ; Krell, Tino

Science signaling, 2016-01, Vol.9 (409), p.ra1-ra1 [Periódico revisado por pares]

United States

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6
Ligustilide covalently binds to Cys703 in the pre-S1 helix of TRPA1, blocking the opening of channel and relieving pain in rats with acute soft tissue injury
Ligustilide covalently binds to Cys703 in the pre-S1 helix of TRPA1, blocking the opening of channel and relieving pain in rats with acute soft tissue injury
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Ligustilide covalently binds to Cys703 in the pre-S1 helix of TRPA1, blocking the opening of channel and relieving pain in rats with acute soft tissue injury

Zhang, Kaixue ; Liu, Wenjuan ; Shen, Fukui ; Luan, Guoqing ; Han, Yanqi ; Xu, Jun ; Fu, Cheng ; Wu, Weidong ; Hou, Yuanyuan ; Jiang, Min ; Zhang, Tiejun ; Bai, Gang

Journal of ethnopharmacology, 2024-08, Vol.330, p.118217-118217, Article 118217 [Periódico revisado por pares]

Ireland: Elsevier B.V

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7
Parthenolide inhibits ubiquitin-specific peptidase 7 (USP7), Wnt signaling, and colorectal cancer cell growth
Parthenolide inhibits ubiquitin-specific peptidase 7 (USP7), Wnt signaling, and colorectal cancer cell growth
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Parthenolide inhibits ubiquitin-specific peptidase 7 (USP7), Wnt signaling, and colorectal cancer cell growth

Li, Xue ; Kong, Lingmei ; Yang, Qihong ; Duan, Aizhu ; Ju, Xiaoman ; Cai, Bicheng ; Chen, Lin ; An, Tao ; Li, Yan

The Journal of biological chemistry, 2020-03, Vol.295 (11), p.3576-3589 [Periódico revisado por pares]

United States: Elsevier Inc

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8
Chojalactones A–C, Cytotoxic Butanolides Isolated from Streptomyces sp. Cultivated with Mycolic Acid Containing Bacterium
Chojalactones A–C, Cytotoxic Butanolides Isolated from Streptomyces sp. Cultivated with Mycolic Acid Containing Bacterium
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Chojalactones A–C, Cytotoxic Butanolides Isolated from Streptomyces sp. Cultivated with Mycolic Acid Containing Bacterium

Hoshino, Shotaro ; Wakimoto, Toshiyuki ; Onaka, Hiroyasu ; Abe, Ikuro

Organic letters, 2015-03, Vol.17 (6), p.1501-1504 [Periódico revisado por pares]

United States: American Chemical Society

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9
A Review of the Pharmacological Activities and Recent Synthetic Advances of γ-Butyrolactones
A Review of the Pharmacological Activities and Recent Synthetic Advances of γ-Butyrolactones
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A Review of the Pharmacological Activities and Recent Synthetic Advances of γ-Butyrolactones

Hur, Joonseong ; Jang, Jaebong ; Sim, Jaehoon

International journal of molecular sciences, 2021-03, Vol.22 (5), p.2769 [Periódico revisado por pares]

Switzerland: MDPI

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10
Butenolides from a marine-derived fungus Aspergillus terreus with antitumor activities against pancreatic ductal adenocarcinoma cells
Butenolides from a marine-derived fungus Aspergillus terreus with antitumor activities against pancreatic ductal adenocarcinoma cells
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Butenolides from a marine-derived fungus Aspergillus terreus with antitumor activities against pancreatic ductal adenocarcinoma cells

Qi, Changxing ; Gao, Weixi ; Guan, Danyingzi ; Wang, Jianping ; Liu, Mengting ; Chen, Chunmei ; Zhu, Hucheng ; Zhou, Yuan ; Lai, Yongji ; Hu, Zhengxi ; Zhou, Qun ; Zhang, Yonghui

Bioorganic & medicinal chemistry, 2018-12, Vol.26 (22), p.5903-5910 [Periódico revisado por pares]

England: Elsevier Ltd

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