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topscience preclinical compound library  (TargetMol)


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    Structured Review

    TargetMol topscience preclinical compound library
    Topscience Preclinical Compound Library, supplied by TargetMol, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/phenotyping/Preclinical+Compound+Library/ppr0759270-52-17-17
    Average 93 stars, based on 2 article reviews
    topscience preclinical compound library - by Bioz Stars, 2026-11
    93/100 stars

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    Related Articles

    Drug discovery:

    Article Title: Drug Combinations Targeting FAK and MEK Overcomes Tumor Heterogeneity in Glioblastoma.
    Article Snippet: .. Four separate drug libraries were selected, specifically with a drug re-purposing context in mind, and included pre-clinical and/or FDA-approved compounds: the TargetMol anticancer set (L2110, 330 compounds), Kinase Chemogenomic set (KCGS [39], 187 compounds), LOPAC (1280 compounds, Merck), and a custom chemogenomic library set (789 compounds, ‘Comprehensive anti-Cancer small Compound Library, or C3L) [34], with dosing across four concentrations (1000, 300, 100, 30 nM). .. Four separate drug libraries were selected, specifically with a drug re-purposing context in mind, and included pre-clinical and/or FDA-approved compounds: the TargetMol anticancer set (L2110, 330 compounds), Kinase Chemogenomic set (KCGS [39], 187 compounds), LOPAC (1280 compounds, Merck), and a custom chemogenomic library set (789 compounds, ‘Comprehensive anti-Cancer small Compound Library, or C3L) [34], with dosing across four concentrations (1000, 300, 100, 30 nM).

    Article Title: π‐PhenoDrug: A Comprehensive Deep Learning‐Based Pipeline for Phenotypic Drug Screening in High‐Content Analysis
    Article Snippet: .. The melanoma cell line A375 was treated with a library containing 80 bioactive compounds from an FDA-approved kinase inhibitor library (TargetMol Chemicals Inc., L1610), a chemical drug library (TargetMol Chemicals Inc., L2151), and a preclinical compound library (TargetMol Chemicals Inc., L3410) at a concentration of 1.0 μM for all drugs. ..

    Article Title: Identification of a novel small molecule to inhibit gastric cancer cells growth
    Article Snippet: .. CCK-8 assay was rstly applied to assess the growth inhibitory effects of 10 μM compound from the Topscience Preclinical Compound Library (Catalog No.L3410, 450 compounds) against gastric cancer AGS cells. ..

    Concentration Assay:

    Article Title: π‐PhenoDrug: A Comprehensive Deep Learning‐Based Pipeline for Phenotypic Drug Screening in High‐Content Analysis
    Article Snippet: .. The melanoma cell line A375 was treated with a library containing 80 bioactive compounds from an FDA-approved kinase inhibitor library (TargetMol Chemicals Inc., L1610), a chemical drug library (TargetMol Chemicals Inc., L2151), and a preclinical compound library (TargetMol Chemicals Inc., L3410) at a concentration of 1.0 μM for all drugs. ..

    CCK-8 Assay:

    Article Title: Identification of a novel small molecule to inhibit gastric cancer cells growth
    Article Snippet: .. CCK-8 assay was rstly applied to assess the growth inhibitory effects of 10 μM compound from the Topscience Preclinical Compound Library (Catalog No.L3410, 450 compounds) against gastric cancer AGS cells. ..



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    Yeasen Biotechnology phenotypic observations
    The impact of CsBES1-14 silencing on the cold tolerance of tea plant is significant. (a) Examination of the <t>phenotypic</t> traits related to the cold tolerance in various tea plant varieties. Note: normal temperature control; Growth of tea plant treated at 4°C. (b) Expression profiling of CsSK1 , CsTCH4 , and CsCYCD3 , components of the BR signaling pathway. (c) Transcript abundance of CsICE1 , CsCBF1 , and CsCOR47 in cold-stressed tea plant. (d) The analysis of electrical conductivity for the tea leaves of WT, TRV: EV, and TRV: CsBES1-14 was conducted at different temperature ranges. TRV: EV: Empty Vector; TRV: CsBES1-14 : Plants in which the CsBES1-14 was silenced.
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    Image Search Results


    Mechanical force modulates macrophage M2 polarization on PEEK surfaces. (A) The expression levels of mechanical perception (PIEZO1, YAP1) and polarization‐related proteins (iNOS, CD206, STAT6/p‐STAT6, NF‐κB/p‐NF‐κB) in dynamically cultured RAW264.7, determined by Western blot. (B) Gene expression in RAW264.7 were cultured under dynamic and static conditions for 12 h. (C) SEM images of RAW264.7 under static and dynamic culture conditions (scale bar: 10 µm). (D) Confocal fluorescence images of CD206, PIEZO1, iNOS, IL10, YAP1 and ITGB1 in macrophages under dynamic and static conditions (scale bar: 100 µm). The average fluorescence intensity of (E) CD206, IL‐10, (F) PIEZO1, YAP1, and (G) iNOS, ITGB1 were statistically analyzed. Shown are mean values ± SD (n = 3 independent experiments, each with 3 technical replicates), * P < 0.05, ** P < 0.01, and *** P < 0.001, ns, no significant difference. 2‐way ANOVA was used in (B) and (E–G).

    Journal: Advanced Science

    Article Title: Alternating Shear Force of Respiration Regulates Cell Interactions of Fibroblasts and Macrophages to Promote Soft Tissue Integration of Chest Wall Polyetheretherketone Implants

    doi: 10.1002/advs.77118

    Figure Lengend Snippet: Mechanical force modulates macrophage M2 polarization on PEEK surfaces. (A) The expression levels of mechanical perception (PIEZO1, YAP1) and polarization‐related proteins (iNOS, CD206, STAT6/p‐STAT6, NF‐κB/p‐NF‐κB) in dynamically cultured RAW264.7, determined by Western blot. (B) Gene expression in RAW264.7 were cultured under dynamic and static conditions for 12 h. (C) SEM images of RAW264.7 under static and dynamic culture conditions (scale bar: 10 µm). (D) Confocal fluorescence images of CD206, PIEZO1, iNOS, IL10, YAP1 and ITGB1 in macrophages under dynamic and static conditions (scale bar: 100 µm). The average fluorescence intensity of (E) CD206, IL‐10, (F) PIEZO1, YAP1, and (G) iNOS, ITGB1 were statistically analyzed. Shown are mean values ± SD (n = 3 independent experiments, each with 3 technical replicates), * P < 0.05, ** P < 0.01, and *** P < 0.001, ns, no significant difference. 2‐way ANOVA was used in (B) and (E–G).

    Article Snippet: To induce M2 phenotype, M0 macrophages were stimulated with 10 ng/mL IL‐10 (HY‐P70517, MedChemExpress LLC., USA) and 20 ng/mL IL‐4 (HY‐ P70653 , MedChemExpress LLC., USA)

    Techniques: Expressing, Cell Culture, Western Blot, Gene Expression, Fluorescence

    Cobicistat was identified as a novel MEST inhibitor. (A) Eight binding pockets of MEST were identified using the SiteFinder module of MOE software. (B) Virtual docking screening of MEST inhibitor from a library. (C) A preliminary screening of 36 compounds was performed by SPR. (D) Binding affinity of the cobicistat to human MEST assessed by SPR. (E) Molecular structure of cobicistat small molecule. (F) Computational model and the interaction of cobicistat with MEST complex. (G) The interacting amino acids and hydrogen bonds between the complexes.

    Journal: Frontiers in Oncology

    Article Title: Targeting MEST using cobicistat as a therapeutic strategy for gastric cancer through suppressing NF-κB signaling

    doi: 10.3389/fonc.2026.1901635

    Figure Lengend Snippet: Cobicistat was identified as a novel MEST inhibitor. (A) Eight binding pockets of MEST were identified using the SiteFinder module of MOE software. (B) Virtual docking screening of MEST inhibitor from a library. (C) A preliminary screening of 36 compounds was performed by SPR. (D) Binding affinity of the cobicistat to human MEST assessed by SPR. (E) Molecular structure of cobicistat small molecule. (F) Computational model and the interaction of cobicistat with MEST complex. (G) The interacting amino acids and hydrogen bonds between the complexes.

    Article Snippet: Here, we identified a candidate MEST-inhibitory compound, cobicistat, by screening the TargetMol and Selleck small-molecule compound libraries based on its catalytic site, ASN163.

    Techniques: Binding Assay, Software, Docking Assay, Screening

    The impact of CsBES1-14 silencing on the cold tolerance of tea plant is significant. (a) Examination of the phenotypic traits related to the cold tolerance in various tea plant varieties. Note: normal temperature control; Growth of tea plant treated at 4°C. (b) Expression profiling of CsSK1 , CsTCH4 , and CsCYCD3 , components of the BR signaling pathway. (c) Transcript abundance of CsICE1 , CsCBF1 , and CsCOR47 in cold-stressed tea plant. (d) The analysis of electrical conductivity for the tea leaves of WT, TRV: EV, and TRV: CsBES1-14 was conducted at different temperature ranges. TRV: EV: Empty Vector; TRV: CsBES1-14 : Plants in which the CsBES1-14 was silenced.

    Journal: Horticulture Research

    Article Title: The CsBES1-14-CsCOR413 module mediated by brassinolide positively regulates cold resistance in tea plant

    doi: 10.1093/hr/uhag098

    Figure Lengend Snippet: The impact of CsBES1-14 silencing on the cold tolerance of tea plant is significant. (a) Examination of the phenotypic traits related to the cold tolerance in various tea plant varieties. Note: normal temperature control; Growth of tea plant treated at 4°C. (b) Expression profiling of CsSK1 , CsTCH4 , and CsCYCD3 , components of the BR signaling pathway. (c) Transcript abundance of CsICE1 , CsCBF1 , and CsCOR47 in cold-stressed tea plant. (d) The analysis of electrical conductivity for the tea leaves of WT, TRV: EV, and TRV: CsBES1-14 was conducted at different temperature ranges. TRV: EV: Empty Vector; TRV: CsBES1-14 : Plants in which the CsBES1-14 was silenced.

    Article Snippet: After 2–3 days of incubation at 30°C, phenotypic observations (growth and color) were made for experimental and control sets (Yeasen, Shanghai, China; Cat. 10923ES05).

    Techniques: Control, Expressing, Plasmid Preparation

    Expression pattern of CsCOR413 and analysis of cold resistance in tea plant following its silencing. (a) Transcriptional levels of CsCOR413 following cold treatment of tea plant after BL application. (b) Transcriptional levels of CsCOR413 following cold treatment of tea plant after BRZ application. (c) Analysis of CsCOR413 expression in silenced plants. (d) Analysis of leaf relative conductivity of different plants under cold stress. (e) Phenotypic analysis of plants silenced by CsCOR413 under low-temperature stress.

    Journal: Horticulture Research

    Article Title: The CsBES1-14-CsCOR413 module mediated by brassinolide positively regulates cold resistance in tea plant

    doi: 10.1093/hr/uhag098

    Figure Lengend Snippet: Expression pattern of CsCOR413 and analysis of cold resistance in tea plant following its silencing. (a) Transcriptional levels of CsCOR413 following cold treatment of tea plant after BL application. (b) Transcriptional levels of CsCOR413 following cold treatment of tea plant after BRZ application. (c) Analysis of CsCOR413 expression in silenced plants. (d) Analysis of leaf relative conductivity of different plants under cold stress. (e) Phenotypic analysis of plants silenced by CsCOR413 under low-temperature stress.

    Article Snippet: After 2–3 days of incubation at 30°C, phenotypic observations (growth and color) were made for experimental and control sets (Yeasen, Shanghai, China; Cat. 10923ES05).

    Techniques: Expressing