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123 items found for "design pharmaceuticals"

  • Design Pharmaceuticals Closes $5 Million Pre-series A Round to Accelerate Commercialization of ...

    April 2022 Design Pharmaceuticals Closes $5 Million Pre-series A Round to Accelerate Commercialization --Design Pharmaceuticals, a company redesigning small molecule drug discovery, today announced the closing Design Pharmaceuticals’ platform is based on ultrahigh-throughput technologies that biomine drug-like

  • Crinetics Pharmaceuticals Announces Pricing Of Underwritten Common Stock Offering

    April 2022 "SAN DIEGO, April 12, 2022 — Crinetics Pharmaceuticals, Inc. (Nasdaq: CRNX), a clinical-stage pharmaceutical company focused on the discovery, development and commercialization

  • Crinetics Pharmaceuticals announced the formation of an independently operated new company...

    December 2021 Crinetics Pharmaceuticals announced the formation of an independently operated new company and Crinetics to Collaborate on Multiple Additional targets SAN DIEGO, October 18, 2021 — Crinetics Pharmaceuticals (Nasdaq: CRNX), a clinical stage pharmaceutical company focused on the discovery, development, and commercialization

  • Crinetics Pharmaceuticals Expands Executive Team With Appointment Of James Hassard As Chief ...

    March 2022 Crinetics Pharmaceuticals Expands Executive Team With Appointment Of James Hassard As Chief Commercial Officer "SAN DIEGO – March 1, 2022 – Crinetics Pharmaceuticals, Inc. (Nasdaq: CRNX), a clinical stage pharmaceutical company focused on the discovery, development, and commercialization

  • Applications of Cryo-EM in small molecule and biologics drug design

    In recent years, pharmaceutical companies have begun to utilize cryo-EM for structure-based drug design In this review, we discuss recent instructive examples of impacts from cryo-EM in therapeutics design

  • Addex's strategic partner The Janssen Pharmaceutical Companies of Johnson & Johnson, Inc. has...

    November 2021 Addex's strategic partner The Janssen Pharmaceutical Companies of Johnson & Johnson, Inc Switzerland, November 15, 2021 – Addex Therapeutics (SIX: ADXN and Nasdaq: ADXN), a clinical-stage pharmaceutical pioneering allosteric modulation-based drug discovery and development, today announced that Janssen Pharmaceuticals , Inc., part of the Janssen Pharmaceutical Companies of Johnson & Johnson, has successfully completed

  • X4 slashes pipeline, lays off staff just three weeks after netting a $55M PIPE

    July 2022 "Not even a PIPE financing could save X4 Pharmaceuticals from enacting layoffs and trimming

  • Crinetics Presents Clinical And Research Results At ENDO 2022

    June 2022 "CRN04894 Selected for Oral Presentation SAN DIEGO, June 8, 2022 — Crinetics Pharmaceuticals

  • TeachOpenCADD - A teaching platform for computer-aided drug design

    bioinformatics are powerful tools to build modular, reproducible, and reusable pipelines for computer-aided drug design

  • Trevena Announce Submission of New Drug Application in China for OLINVYK® by its Partner Jiangsu ...

    Trevena Announces Submission of New Drug Application in China for OLINVYK® by its Partner Jiangsu Nhwa Pharmaceutical The NDA was submitted by Trevena’s partner, Jiangsu Nhwa Pharmaceutical, and follows completion by Nhwa

  • A Chemical Biology Toolbox Targeting the Intracellular Binding Site of CCR9: Fluorescent Ligands ...

    A conserved intracellular allosteric binding site (IABS) has recently been identified at several G protein-coupled receptors (GPCRs). Starting from vercirnon, an intracellular C-C chemokine receptor type 9 (CCR9) antagonist and previous phase III clinical candidate for the treatment of Crohn's disease, we developed a chemical biology toolbox targeting the IABS of CCR9. We first synthesized a fluorescent ligand enabling equilibrium and kinetic binding studies via NanoBRET as well as fluorescence microscopy. Applying this molecular tool in a membrane-based setup and in living cells, we discovered a 4-aminopyrimidine analogue as a new intracellular CCR9 antagonist with improved affinity. To chemically induce CCR9 degradation, we then developed the first PROTAC targeting the IABS of GPCRs. In a proof-of-principle study, we succeeded in showing that our CCR9-PROTAC is able to reduce CCR9 levels, thereby offering an unprecedented approach to modulate GPCR activity. Read full article

  • GPCR Agonist-to-Antagonist Conversion: Enabling the Design of Nucleoside Functional Switches for...

    October 2022 GPCR Agonist-to-Antagonist Conversion: Enabling the Design of Nucleoside Functional Switches This approach can expand the repertoire of adenosine receptor antagonists that can be designed based

  • AlphaFold2 versus experimental structures: evaluation on G protein-coupled receptors

    differences impeded the use of predicted structure models in the functional study and structure-based drug design

  • Design and validation of recombinant protein standards for quantitative Western blot analysis of...

    October 2022 Design and validation of recombinant protein standards for quantitative Western blot analysis

  • Targeted Activation of G-Protein Coupled Receptor-Mediated Ca 2+ Signaling Drives Enhanced Cartilage

    One such platform is the chemogenetic DREADD (designer receptor exclusively activated by designer drugs

  • Ono Enters into Collaboration Agreement with Domain Therapeutics and Université de Montréal for ...

    with Domain Therapeutics and Université de Montréal for GPCR-Targeted Drug Discovery "Apr.19.2022 Ono Pharmaceutical

  • PH-Binding Motif in PAR4 Oncogene: From Molecular Mechanism to Drug Design

    October 2022 "While the role of G-protein-coupled receptors (GPCR) in cancer is acknowledged, their underlying signaling pathways are understudied. Protease-activated receptors (PAR), a subgroup of GPCRs, form a family of four members (PAR1-4) centrally involved in epithelial malignancies. PAR4 emerges as a potent oncogene, capable of inducing tumor generation. Here, we demonstrate identification of a pleckstrin-homology (PH)-binding motif within PAR4, critical for colon cancer growth. In addition to PH-Akt/PKB association, other PH-containing signal proteins such as Gab1 and Sos1 also associate with PAR4. Point mutations are in the C-tail of PAR4 PH-binding domain; F347 L and D349A, but not E346A, abrogate these associations. Pc(4-4), a lead backbone cyclic peptide, was selected out of a mini-library, directed toward PAR2&4 PH-binding motifs. It effectively attenuates PAR2&4-Akt/PKB associations; PAR4 instigated Matrigel invasion and migration in vitro and tumor development in vivo. EGFR/erbB is among the most prominent cancer targets. AYPGKF peptide ligand activation of PAR4 induces EGF receptor (EGFR) Tyr-phosphorylation, effectively inhibited by Pc(4-4). The presence of PAR2 and PAR4 in biopsies of aggressive breast and colon cancer tissue specimens is demonstrated. We propose that Pc(4-4) may serve as a powerful drug not only toward PAR-expressing tumors but also for treating EGFR/erbB-expressing tumors in cases of resistance to traditional therapies. Overall, our studies are expected to allocate new targets for cancer therapy. Pc(4-4) may become a promising candidate for future therapeutic cancer treatment." Read more at the source #DrGPCR #GPCR #IndustryNews

  • Cancer Research UK and Sosei Heptares sign agreement to advance cancer immunotherapy candidate ...

    , an international biopharmaceutical company and world-leader in GPCR1-focused structure-based drug design

  • 📰 GPCR Weekly News, February 27 to March 5, 2023

    Industry News Design Pharmaceuticals has a new website Confo Therapeutics Announces Global Licensing Computational drug design PhD student at the Department of Drug Design and Pharmacology. Computational drug design postdoc at the Department of Drug Design and Pharmacology. Software / database development PhD student at Department of Drug Design and Pharmacology. Software / database development postdoc at the Department of Drug Design and Pharmacology.

  • 📰 GPCR Weekly News, March 13 to 19, 2023

    GPCR Binders, Drugs, and more Design of Drug Efficacy Guided by Free Energy Simulations of the β2-Adrenoceptor GPCRs in Cardiology, Endocrinology, and Taste Structure-based design of novel melanin-concentrating hormone Therapy An extraordinary opportunity to generate proprietary chemo-informatics for GPCR drug discovery - Design Pharmaceuticals Call for GPCR Papers GPCRs: Signal Transduction.

  • SYnAbs is now officially accredited as a Research Tax Credit by the French Ministry of Higher...

    monoclonalantibodies #drugdiscovery #biotechnology #research #ionchannels #biologics #biotech #pharma #pharmaindustry #pharmaceuticals

  • 📰 GPCR Weekly News, October 9 to 15, 2023

    Submit a logo design by Nov 1st on the Logo Contest page. No registration is needed to submit your logo design. Subscribe to Dr. , Drugs, and more Development of Photoswitchable Tethered Ligands that Target the µ-Opioid Receptor Design Jobs NEW Head of Human Resource Business Partners Senior Scientist, In vitro pharmacology - Crinetics Pharmaceuticals Senior Director, In vitro pharmacology - Crinetics Pharmaceuticals In vivo Antibody Discovery Research

  • 📰 GPCR Weekly News, October 2 to 8, 2023

    Submit a logo design by Nov 1st on the Logo Contest page. No registration is needed to submit your logo design. Subscribe now to Dr. - 4, 2024 | Chemotactic Cytokines GPCR Jobs NEW Senior Scientist, In vitro pharmacology - Crinetics Pharmaceuticals NEW Senior Director, In vitro pharmacology - Crinetics Pharmaceuticals In vivo Antibody Discovery Research

  • 📰 GPCR Weekly News, July 31 to August 6, 2023

    pro-inflammatory G-protein coupled receptor GPR84 GPCR Binders, Drugs, and more Computational Peptide Design Therapeutics To Release Half-Year 2023 Financial Results And Host Conference Call On August 10, 2023 X4 Pharmaceuticals adverse cardiovascular events by 20% in adults with overweight or obesity in the SELECT trial Crinetics Pharmaceuticals Reports Second Quarter 2023 Financial Results And Provides Corporate Update X4 Pharmaceuticals Announces

  • 📰 GPCR Weekly News, October 23 to 29, 2023

    Chemotactic Cytokines GPCR Jobs NEW Staff Scientist (AC-TAP) in Database Development at Department of Drug Design Apprentice Head of Human Resource Business Partners Senior Scientist, In vitro pharmacology - Crinetics Pharmaceuticals Senior Director, In vitro pharmacology - Crinetics Pharmaceuticals In vivo Antibody Discovery Research

  • 📰 GPCR Weekly News, October 16 to 22, 2023

    Submit your logo design by Nov 1st on the Logo Contest page. to Buy Hypertension Treatment from KBP Biosciences Exscientia to Present New Preclinical Data for AI-designed GPCR Jobs Head of Human Resource Business Partners Senior Scientist, In vitro pharmacology - Crinetics Pharmaceuticals Senior Director, In vitro pharmacology - Crinetics Pharmaceuticals In vivo Antibody Discovery Research

  • Jan Steyaert Named 2022 Jacob and Louise Gabbay Award Winner

    research in biomedical sciences with the mechanistic understanding of one of the biggest classes of pharmaceutical

  • 📰 GPCR Weekly News, January 1 to 7, 2024

    expansion as the leading GPCR immuno-oncology company Sosei Group Announces Appointment of Experienced Pharmaceutical Executive Toshihiro Maeda as Chief Operating Officer Rhythm Pharmaceuticals and LG Chem Life Sciences Showcase™ 2024 Establishing our first international translational research project - Institute for Protein Design

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