Search Results
Results found for "Ethan Dintzner"
- 📰 GPCR Weekly News, May 13 to 19, 2024
for their study on Constitutive internalisation of EP2 differentially regulates G protein signalling Ethan Dintzner, Demet Araç, et al. for their work on The far extracellular CUB domain of the adhesion GPCR
- Why Kinetics Matter More Than Kd in GPCR Drug Discovery
Terry’s Corner: Why Binding Kinetics Matter More Than Affinity In drug discovery today, time wasted is interpret kinetic binding experiments and recognize when a drug’s rate of onset and offset matter more than
- GPCR Drug Discovery at Discovery on Target: Why This Track Is About More Than Receptors
I’m honored to be chairing a session in this track — with none other than Terry Kenakin on the speaker Hearing Terry speak is more than an academic experience — it’s like being handed a new set of tools to
- The Hidden Driver of GPCR Drug Success: Why Target Residence Time Matters More Than You Think
Exploring the kinetic factors that enhance in vivo efficacy beyond traditional potency metrics, as presented by Dr. GPCR. Hey GPCR Fans, This week's breakthroughs are crucial for staying ahead in the rapidly evolving landscape of GPCR research and drug discovery. Dr. Terry Kenakin's insights on target residence time can reshape how you evaluate and advance lead compounds, potentially saving your team from costly late-stage failures. That's exactly what Dr. GPCR delivers every week: practical tools and critical intelligence to elevate your science and sharpen your decisions. Breakthroughs this week: Novo Nordisk cuts Ozempic® cost; Nxera launches obesity pipeline; Superluminal–Lilly cardiometabolic partnership; New GPCR allosteric sites; GPCR signaling potentiation by ATP and sugars. 🔍 This Week in Dr. GPCR Premium: Sneak Peek Get a glimpse of the in-depth intelligence available exclusively to our Premium Members this week: Industry insights: Discover the latest strategic moves in the pharmaceutical sector, from new pipelines targeting obesity to significant collaborations in cardiometabolic disease, and gain insights into novel approaches in neurodegeneration and antibody therapeutics. Upcoming events: Stay informed about key global conferences and symposia focusing on GPCRs, neuropharmacology, drug discovery, and biophysics, ensuring you don't miss crucial networking and learning opportunities. Career opportunities: Explore a selection of high-level job openings in high-throughput screening, research, biologics development, clinical operations, and biostatistics within leading organizations. Must-read publications: Stay updated on cutting-edge research, including the potentiation of GPCR signaling by ATP and sugar monophosphates and the identification of a novel allosteric site on the vasopressin V2 receptor. Terry's Corner - Unlock the Power of Target Residence Time in Your GPCR Drug Discovery Pipeline Gain a critical edge by understanding the in vivo efficacy drivers overlooked by traditional potency metrics. Are your promising in vitro results failing to translate into real-world clinical success? Dr. Terry Kenakin’s latest insights delve into target residence time, revealing why kinetic persistence often trumps binding affinity for in vivo efficacy. Discover how factors like restricted tissue diffusion and receptor density can dramatically alter drug action, potentially unlocking the true potential of your lead compounds. Problem Solved: Eliminate the blind spots in your drug evaluation process, moving beyond simple potency measures to understand the dynamic interactions that govern in vivo effectiveness. Competitive Edge: Identify high-value compounds that might be missed by traditional screening methods, gaining a first-mover advantage in developing more effective therapeutics. Threat Avoided: Prevent costly late-stage failures by incorporating kinetic modeling early in your pipeline, ensuring your candidates have the persistence needed for clinical impact. ➡️ Premium Members get 50%+ discount when they join Terry’s Corner. Access this week’s key insight ➤ Dr GPCR Podcast – Decoding the Deadly Duo: Xylazine, Fentanyl, and Respiratory Depression Understand the synergistic mechanisms driving the escalating opioid crisis and the crucial role of GPCR pharmacology. The opioid crisis is evolving with the dangerous combination of fentanyl and the veterinary sedative xylazine. This week’s featured podcast episode with Catherine Demery explores the distinct yet lethal mechanisms by which these drugs impair respiration. Learn how fentanyl slows inhalation via opioid receptors, while xylazine prolongs exhalation through alpha-2 adrenergic receptors, creating a synergistic effect that drives overdose deaths. Catherine’s research, blending GPCR signaling studies with public health data, offers critical insights into this urgent crisis. Problem Solved: Gain a deeper understanding of the pharmacological underpinnings of opioid overdose, informing the development of more effective intervention strategies. Competitive Edge: Stay informed on emerging public health threats and the scientific research aimed at addressing them, positioning your work at the forefront of critical biomedical challenges. Threat Avoided: Recognize the growing prevalence and dangers of xylazine-laced opioids, enabling you to contribute to solutions and understand the broader impact on public health. Listen now to understand how two mechanisms intersect—and why pharmacologists are critical in addressing this crisis ➤ Call for Papers – GPCRs: Signal Transduction Volume II With over 21,000 views and 7,785 downloads from Volume I, the Signal Transduction Research Topic is back. Volume II invites experts to deepen our collective understanding of GPCR pathways in health and disease. Manuscript summary deadline: 24 September 2025 . Final submissions: 12 January 2026 . Why contribute: Join a global, like-minded GPCR community. Shape the next generation of cellular biochemistry research. Amplify your work with high-impact visibility. Submit your paper today to secure your work in Volume II ➤ Why Dr. GPCR Premium Membership Gives You an Edge Every week, Premium delivers noise-free intelligence : expert-led courses, classified industry insights, curated events, exclusive job opportunities, and insider commentary. Designed for GPCR scientists and translational teams, Premium keeps you informed on the science, careers, and business moves shaping drug discovery. Unlike fragmented feeds and endless searches, Premium is structured to help you move faster, smarter, and with greater clarity. FAQ: Premium Membership 🔹 What’s included? The complete Weekly News digest, curated jobs, upcoming events, classified GPCR publications, exclusive on-demand expert lectures, and member-only discounts. 🔹 Who is it for? GPCR scientists, translational pharmacologists, biotech discovery teams, and decision-makers who need career-relevant intelligence to stay ahead. 🔹 Why now? The pace of GPCR innovation is accelerating. Those who act on the right signals today will lead tomorrow’s breakthroughs—and avoid delays others won’t see coming. 👉 Don’t Fall Behind—Access the Edge You Need 👉 Already a Premium Member? Access this week’s full Premium Edition here ➤ What our members say 🗣️ “The best pharmacology teacher teaming up with the best GPCR community platform to help train and inspire the next generation of scientists.” — Dr. GPCR University Course Attendee Ready to gain a competitive advantage? 🚀 Upgrade to Premium Membership Today! 🚀 👉 Become a Premium Member Today ➤
- 📅 Dr. GPCR Summit 2022 is less than a month away!
GPCR Summit 2022 is less than a month away!
- Opioid Ligands Addressing Unconventional Binding Sites and More Than One Opioid Receptor Subtype
August 2022 "Opioid receptors (ORs) represent one of the most significant groups of G-protein coupled receptor (GPCR) drug targets and also act as prototypical models for GPCR function. In a constant effort to develop drugs with less side effects, and tools to explore the ORs nature and function, various (poly)pharmacological ligand design approaches have been performed. That is, besides classical ligands, a great number of bivalent ligands (i. e. aiming on two distinct OR subtypes), univalent heteromer-selective ligands and bitopic and allosteric ligands have been synthesized for the ORs. The scope of our review is to present the most important of the aforementioned ligands, highlight their properties and exhibit the current state-of-the-art pallet of promising drug candidates or useful molecular tools for the ORs." Read more at the source #DrGPCR #GPCR #IndustryNews
- Fentanyl and Xylazine: Why Breathing Fails in Overdose
With street-level contamination rising faster than medicine can adapt, Catherine’s work shows why overdose A Crisis That’s Redefining Overdose In 2023, more than 107,000 Americans died from drug overdoses , the The insight is simple but urgent: the drug supply evolves faster than medicine. The Urgency Ahead Every overdose today is more complicated than the last. And the illicit supply is moving faster than clinical medicine can adjust.
- Purpose-Driven Opioid Research: Catherine Demery’s Academic Path
Her story is about more than experiments or data points. Rather than treating opioid pharmacology as a purely theoretical exercise, she collaborates with harm-reduction Academic success is less about prestige than about impact. That urgency, more than titles, positions, or prestige, is what sustains a lasting career in science. Catherine’s story shows that when purpose drives research, science becomes more than a job—it becomes
- From Student to Mentor: What Alessandro Nicoli Learned About Leading in Science
Watch Episode 171 Mentoring in science is more than supervising—it’s about shaping the next generation Mistakes are part of learning—and guiding students through them is more valuable than doing everything
- Building Backwards: Why Top-Down Models Could Revolutionize Pain Research
development... seeing if we can bring preclinical models much closer to the actual human experience than Rather than starting with a molecular hypothesis, Serafini’s team noticed that hamsters infected with
- Unlock the Hidden Lives of Receptors – Are You Ready?
With the right lens, you’ll see why efficacy is more than signal strength: it's a fingerprint of conformational
- Accelerating GPCR Drug Discovery: What 40 Years of Pharmacology Reveal
Earlier than many teams do. Modern real-time assays can deliver these insights earlier, faster, and cheaper than most teams assume It’s less bureaucratic than most outsiders think. Why kinetic profiling matters more than most teams realize.
- The Quiet Power of RGS Proteins: Rethinking Pain Pathways through GPCR Biology
despite these targets falling short clinically: “The downstream cascade is probably a little bit weaker than hitting a GPCR... and honestly, like with the trials, they were not really that sufficiently better than
- Fluorescence Polarization in GPCR Research
Research FP assays work on the principle that a fluorescent ligand bound to protein rotates slower than This makes them very useful for GPCR drug discovery, since receptors are a lot bigger than their small They are more accessible than radioligand assays, since they do not require complex equipment for analysis
- Ever Wondered How Drugs Are Discovered?
unique ability to combine storytelling, real-world experience, and scientific clarity makes this more than
- Optimizing HTRF Assays with Fluorescent Ligands: Time-Resolved Fluorescence in GPCR Research
The donors used in this technique have longer half-lives than other fluorophores (between 300μs–1 ms Terbium, a second-generation donor, is brighter than Europium (10-20 times), which increases sensitivity The donor lanthanum fluorophores are more stable than regular fluorophores and quite resistant to photobleaching
- Dr. GPCR Updates
article GPCR Publication Highlights βCGRP breaks the mold: Distinct signaling patterns reveal it’s more than
- Antibodies That Don’t Block, They Activate: A New Angle on Autoimmunity and GPCRs
.” — Tom Sakmar This makes them more than biomarkers — they’re potential drivers of disease .
- Gαs and Gαq/11 protein coupling bias of two AVPR2 mutants (R68W and V162A) that cause nephrogenic di
Recent studies showed that some AVPR2 mutations could cause biased Gαq/11 protein coupling rather than R68W showed bias to coupling with Gαq/11 protein rather than V162A and wild-type receptor.
- Enzyme Inhibition Pharmacology: The Hidden Gatekeepers of GPCR Drug Discovery
By visualizing enzymes as dynamic molecular partners rather than static filters, drug discovery scientists Cytochrome P450: Friend, Foe, and FDA Focus No enzyme class is more important—or more unpredictable—than Yet many discovery teams still relegate them to the “ADME” checklist, rather than the strategic design
- Learn about Dr. GPCR Ecosystem!
GPCR is much more than a podcast? Come check out the brand new Dr.
- Roles of Focal Adhesion Kinase PTK2 and Integrin αIIbβ3 Signaling in Collagen- and GPVI-Dependent...
The suppressive rather than activating effects of pGRP were confined to blood flow at a high shear rate Blockage of PTK2 or interference of CIB1 no more than slightly affected thrombus formation at a low shear
- Carola Weiss joins InterAx Biotech AG as VP Business Development
Carola Weiss is a Senior Executive with more than 20 years of international experience in the biopharmaceutical
- How a Failed Med School Dream Sparked a GPCR Biotech Revolution
More than a technical overview, this is a story of curiosity, persistence, and using science to meet Rather than being discouraged by challenges, he views them as forcing functions for creativity and growth
- Illuminating the draggable GPCR-ome
This time with none other than Dr. Bryan Roth There are 10 open tickets available. Get yours now!
- X4 slashes pipeline, lays off staff just three weeks after netting a $55M PIPE
The move comes less than three weeks after X4 pulled together a $55 million PIPE and amended a loan facility
- Dr. Marta Filizola - Dr. GPCR Podcast
GPCR Podcast, we have none other than Dr. Marta Filizola!
- Dr. Juan José Fung - Dr. GPCR Podcast
Our guest is none other than Dr. Juan Jose Fung, Principal Scientist, at GPCR Therapeutics.
- Unconventional GPCR-PKA Communication in the Hedgehog Pathway
Our first guest speaker is none other than Dr. Ben Myers!
- Structural basis of GPCR coupling to distinct signal transducers: implications for biased signaling
determine partner preference; or (iii) the dynamics of GPCR binding to different types of partners rather than
























