Latest Research Posts

JPH203 (Nanvuranlat) LAT1 Inhibition Augments Rapamycin-Insensitive mTOR Protein Synthesis
JPH203 (Nanvuranlat) LAT1 Inhibition Augments Rapamycin-Insensitive mTOR Protein Synthesis
Dorsomorphin Dihydrochloride Dorsomorphin AMPK Inhibition Modulates Neuroinflammatory Cascades
Dorsomorphin Dihydrochloride Dorsomorphin AMPK Inhibition Modulates Neuroinflammatory Cascades
10058-F4 inhibitor suppresses c-MYC/SLC7A5 signaling to block hBMSC osteogenic differentiation
10058-F4 inhibitor suppresses c-MYC/SLC7A5 signaling to block hBMSC osteogenic differentiation
TEPP-46 (ML265) PKM activator selectively promotes PKM2 tetramerization to prevent aortic aneurysm formation
TEPP-46 (ML265) PKM activator selectively promotes PKM2 tetramerization to prevent aortic aneurysm formation
Dimethyloxallyl Glycine (DMOG) Targets PHD to Mitigate Hepatic Ischemia-Reperfusion Injury via HIF-1α Activation
Dimethyloxallyl Glycine (DMOG) Targets PHD to Mitigate Hepatic Ischemia-Reperfusion Injury via HIF-1α Activation
SRI-011381 (C381) SRI-011381 TGF-beta/Smad Agonism Suppresses PEMF Antifibrotic Efficacy
SRI-011381 (C381) SRI-011381 TGF-beta/Smad Agonism Suppresses PEMF Antifibrotic Efficacy
SN-38 from Selleck targets Topoisomerase I to induce double-stranded DNA damage in glioma
SN-38 from Selleck targets Topoisomerase I to induce double-stranded DNA damage in glioma
Ceralasertib (AZD6738) Suppresses ATR Kinase in High-Risk Relapsed Chronic Lymphocytic Leukemia
Ceralasertib (AZD6738) Suppresses ATR Kinase in High-Risk Relapsed Chronic Lymphocytic Leukemia
Cyclosporin A from Selleck Suppresses Calcineurin NFAT Signaling in T-Cells
Cyclosporin A from Selleck Suppresses Calcineurin NFAT Signaling in T-Cells
SC79 Enforced AKT Phosphorylation Mitigates Matrine Induced Glioblastoma Senescence
SC79 Enforced AKT Phosphorylation Mitigates Matrine Induced Glioblastoma Senescence
AZD5363 (Capivasertib) Formulations Display Pharmacokinetic Bioequivalence in Advanced Solid Tumors
AZD5363 (Capivasertib) Formulations Display Pharmacokinetic Bioequivalence in Advanced Solid Tumors
G418 Sulfate (Geneticin) Target Engagement at Escherichia coli DNA Ligase OB-Fold Site 1
G418 Sulfate (Geneticin) Target Engagement at Escherichia coli DNA Ligase OB-Fold Site 1
Actinomycin D (Dactinomycin) Inhibits DNA and RNA Polymerase in Gestational Trophoblastic Neoplasia
Actinomycin D (Dactinomycin) Inhibits DNA and RNA Polymerase in Gestational Trophoblastic Neoplasia
Oligomycin A from Selleck and Oligomycin A (MCH 32) Direct Mitochondrial ATP Synthase Inhibition
Oligomycin A from Selleck and Oligomycin A (MCH 32) Direct Mitochondrial ATP Synthase Inhibition
Q-VD-Oph inhibitor suppresses caspase activation shifting ischemic death toward necroptosis
Q-VD-Oph inhibitor suppresses caspase activation shifting ischemic death toward necroptosis
Mitomycin C Blunts Subconjunctival Fibroblast Proliferation to Preserve Microshunt Bleb Patency
Mitomycin C Blunts Subconjunctival Fibroblast Proliferation to Preserve Microshunt Bleb Patency
Emricasan Caspase inhibitor IDN-6556 dual engagement of ACE2 and caspase-3 in viral pathology
Emricasan Caspase inhibitor IDN-6556 dual engagement of ACE2 and caspase-3 in viral pathology
Navitoclax (ABT-263) Inhibits Bcl-2 and Triggers Beclin-1 Autophagy to Restore Macrophage Function
Navitoclax (ABT-263) Inhibits Bcl-2 and Triggers Beclin-1 Autophagy to Restore Macrophage Function
2-DG (2-Deoxy-D-glucose) 2-DG Carbohydrate Metabol modulator Targets Glycolysis in COVID-19 Clinical Trial
2-DG (2-Deoxy-D-glucose) 2-DG Carbohydrate Metabol modulator Targets Glycolysis in COVID-19 Clinical Trial
ABT-199 (Venetoclax) ABT199 Selective BCL2 Inhibition in B-Cell Malignancies
ABT-199 (Venetoclax) ABT199 Selective BCL2 Inhibition in B-Cell Malignancies
MK-2206 Dihydrochloride (MK-2206) suppresses AKT signaling and alters metabolic profiles in solid tumors
MK-2206 Dihydrochloride (MK-2206) suppresses AKT signaling and alters metabolic profiles in solid tumors
Staurosporine (STS) Staurosporine Model Evaluation for Pediatric Cardiac Surgery Mortality Risk
Staurosporine (STS) Staurosporine Model Evaluation for Pediatric Cardiac Surgery Mortality Risk
Forskolin (Colforsin) from Selleck Activates Adenylate Cyclase to Attenuate Vascular Restenosis
Forskolin (Colforsin) from Selleck Activates Adenylate Cyclase to Attenuate Vascular Restenosis
Z-VAD-FMK Caspase inhibitor attenuates smoke-induced airway inflammation and emphysematous tissue destruction
Z-VAD-FMK Caspase inhibitor attenuates smoke-induced airway inflammation and emphysematous tissue destruction
Ezetimibe (SCH-58235) and Ezetimibe from Selleck Target NPC1L1 for Post-ACS Lipid Lowering
Ezetimibe (SCH-58235) and Ezetimibe from Selleck Target NPC1L1 for Post-ACS Lipid Lowering
FB23-2 Target Engagement of FTO Inhibits m6A Demethylation in Hypoxic Hepatocytes
FB23-2 Target Engagement of FTO Inhibits m6A Demethylation in Hypoxic Hepatocytes
Trimetazidine dihydrochloride FAO inhibitor targets 3-KAT to shift metabolism and reduce cancer risk
Trimetazidine dihydrochloride FAO inhibitor targets 3-KAT to shift metabolism and reduce cancer risk
GS-4997 ASK inhibitor suppresses hepatic stellate cell activation and exosomal signaling in fibrosis
GS-4997 ASK inhibitor suppresses hepatic stellate cell activation and exosomal signaling in fibrosis
TH5487 Inhibits OGG1 to Activate PINK1 Parkin Mitophagy in Pulmonary Fibrosis
TH5487 Inhibits OGG1 to Activate PINK1 Parkin Mitophagy in Pulmonary Fibrosis
Olitigaltin (TD139) Olitigaltin from Selleck Galectin-3 Inhibitor in Peritoneal Carcinomatosis
Olitigaltin (TD139) Olitigaltin from Selleck Galectin-3 Inhibitor in Peritoneal Carcinomatosis
Tomivosertib (eFT508) Inhibits MNK1/2 to Suppress eIF4E Phosphorylation and Immune Evasion
Tomivosertib (eFT508) Inhibits MNK1/2 to Suppress eIF4E Phosphorylation and Immune Evasion
Asunaprevir from Selleck targeted HCV NS3 protease inhibition for hepatitis C treatment
Asunaprevir from Selleck targeted HCV NS3 protease inhibition for hepatitis C treatment
WZB117 Inhibition of Class I Glucose Transporters Suppresses Glycolytic Metabolism in Oncology Models
WZB117 Inhibition of Class I Glucose Transporters Suppresses Glycolytic Metabolism in Oncology Models
DSS Crosslinker Mediated Nanosphere Conjugation Reduces CD11b Antibody Binding Affinity
DSS Crosslinker Mediated Nanosphere Conjugation Reduces CD11b Antibody Binding Affinity
Idasanutlin (RG7388) Potentiates p53 Signaling and Apoptosis in Cutaneous Melanoma Models
Idasanutlin (RG7388) Potentiates p53 Signaling and Apoptosis in Cutaneous Melanoma Models
Pentylenetetrazol GABA Receptor Antagonist Mechanisms in Zebrafish Seizure Models
Pentylenetetrazol GABA Receptor Antagonist Mechanisms in Zebrafish Seizure Models
CADD522 from Selleck suppresses RUNX2-mediated ITGBL1 activation to attenuate HBV-induced liver fibrosis
CADD522 from Selleck suppresses RUNX2-mediated ITGBL1 activation to attenuate HBV-induced liver fibrosis
GSK1349572 Integrase inhibitor (Dolutegravir) mechanisms against HIV-1 strand transfer resistance
GSK1349572 Integrase inhibitor (Dolutegravir) mechanisms against HIV-1 strand transfer resistance
BMS-202 BMS202 PD-1 PD-L1 Checkpoint Inhibitor Hydrogel Loading and Release
BMS-202 BMS202 PD-1 PD-L1 Checkpoint Inhibitor Hydrogel Loading and Release
PF-04418948 antagonist suppresses EP2 and EP4 receptor-mediated airway microvascular leakage
PF-04418948 antagonist suppresses EP2 and EP4 receptor-mediated airway microvascular leakage
Caerulein (Cerulein, FI-6934) from Selleck Induces CCK Receptor-Mediated Pancreatic Microvascular Hyperemia
Caerulein (Cerulein, FI-6934) from Selleck Induces CCK Receptor-Mediated Pancreatic Microvascular Hyperemia
NMS-873 p97 allosteric inhibition attenuates cellular tau seed processing and aggregation
NMS-873 p97 allosteric inhibition attenuates cellular tau seed processing and aggregation
AS1842856 from Selleck Inhibits FoxO1 Transactivation to Suppress Cardiac Fibroblast COX-2 Expression
AS1842856 from Selleck Inhibits FoxO1 Transactivation to Suppress Cardiac Fibroblast COX-2 Expression
BX-795 PDPK1 Inhibition Suppresses Allergic Airway Inflammation via Th-IL-2 Cell Lineage Induction
BX-795 PDPK1 Inhibition Suppresses Allergic Airway Inflammation via Th-IL-2 Cell Lineage Induction
Sulfosuccinimidyl Oleate Sodium from Selleck models Stressor–Strain–Outcome dynamics in digital cyberchondria
Sulfosuccinimidyl Oleate Sodium from Selleck models Stressor–Strain–Outcome dynamics in digital cyberchondria
CA-074 methyl ester (CA-074 Me) inhibits cathepsin B in hypoxic glioma cells
CA-074 methyl ester (CA-074 Me) inhibits cathepsin B in hypoxic glioma cells
CD38 inhibitor 1 CD markers targeting PD-1 PD-L1 immune checkpoint inhibition in multiple myeloma
CD38 inhibitor 1 CD markers targeting PD-1 PD-L1 immune checkpoint inhibition in multiple myeloma
ASP2215 (Gilteritinib) ASP2215 FLT3 inhibitor targeting secondary mutations and microenvironmental resistance in leukemia
ASP2215 (Gilteritinib) ASP2215 FLT3 inhibitor targeting secondary mutations and microenvironmental resistance in leukemia
XMU-MP-1 (XMUMP1) Inhibition of MST1/2 Reverses Hippo-Mediated Protection in Intestinal Sepsis Models
XMU-MP-1 (XMUMP1) Inhibition of MST1/2 Reverses Hippo-Mediated Protection in Intestinal Sepsis Models
Valemetostat (DS-3201) targeting EZH1/2 histone methyltransferases enables disease control in aggressive T-cell lymphoma
Valemetostat (DS-3201) targeting EZH1/2 histone methyltransferases enables disease control in aggressive T-cell lymphoma
UK-5099 (PF-1005023) Mitochondrial pyruva inhibitor Targets Subtype-Specific OXPHOS in Pancreatic Cancer
UK-5099 (PF-1005023) Mitochondrial pyruva inhibitor Targets Subtype-Specific OXPHOS in Pancreatic Cancer
SB-525334 and SB525334 inhibit TGF-beta1 SMAD4 signaling during mild ablation
SB-525334 and SB525334 inhibit TGF-beta1 SMAD4 signaling during mild ablation
LB-100 LB100 PP2A inhibitor Sensitizes Tumors via DNA Repair Suppression
LB-100 LB100 PP2A inhibitor Sensitizes Tumors via DNA Repair Suppression
Ac-CoA Synthase Inhibitor1 (ACSS2 inhibitor) Ac-CoA ACSS2 suppresses raptor/mTORC1 in diabetic nephropathy
Ac-CoA Synthase Inhibitor1 (ACSS2 inhibitor) Ac-CoA ACSS2 suppresses raptor/mTORC1 in diabetic nephropathy
MCC950 from Selleck Inhibits NLRP3 Inflammasome NACHT Domain in Colitis Models
MCC950 from Selleck Inhibits NLRP3 Inflammasome NACHT Domain in Colitis Models
Necrosulfonamide targets GSDMD-N to inhibit dendritic cell pyroptosis in allergic rhinitis
Necrosulfonamide targets GSDMD-N to inhibit dendritic cell pyroptosis in allergic rhinitis
IACS-010759 (IACS-10759) and IACS-10759 from Selleck Target Complex I in Resistant Melanoma
IACS-010759 (IACS-10759) and IACS-10759 from Selleck Target Complex I in Resistant Melanoma
Denifanstat (TVB-2640) targets FASN to disrupt de novo palmitate synthesis in endocrine-resistant breast cancer
Denifanstat (TVB-2640) targets FASN to disrupt de novo palmitate synthesis in endocrine-resistant breast cancer
Atglistatin Lipase inhibitor PNPLA2 Suppression Selectively Uncouples Macrophage Differentiation From Tumor Phagocytosis
Atglistatin Lipase inhibitor PNPLA2 Suppression Selectively Uncouples Macrophage Differentiation From Tumor Phagocytosis
BMS-927711 (Rimegepant) BMS-927711 CGRP receptor blockade attenuates migraine frequency
BMS-927711 (Rimegepant) BMS-927711 CGRP receptor blockade attenuates migraine frequency
Finerenone (BAY 94-8862) Nonsteroidal Mineralocorticoid Receptor Antagonism in Renal Disease
Finerenone (BAY 94-8862) Nonsteroidal Mineralocorticoid Receptor Antagonism in Renal Disease
LY2109761 Inhibition of TβRI/II Suppresses TGFβ1/Smad-Mediated Stem Cell Transdifferentiation
LY2109761 Inhibition of TβRI/II Suppresses TGFβ1/Smad-Mediated Stem Cell Transdifferentiation
SB505124 Targeting of TGF-β Receptor Reverses High-Risk Programmed Cell Death Phenotypes in KIRC
SB505124 Targeting of TGF-β Receptor Reverses High-Risk Programmed Cell Death Phenotypes in KIRC
PDD00017273 targets PARG to sensitize colorectal cancer cells to standard chemotherapy regimens.
PDD00017273 targets PARG to sensitize colorectal cancer cells to standard chemotherapy regimens.
EN6 Lipopeptide Biosurfactant Enhances Electrokinetic Remediation of Soil Chromium Contamination
EN6 Lipopeptide Biosurfactant Enhances Electrokinetic Remediation of Soil Chromium Contamination
Importazole from Selleck Inhibits KPNB1 Nucleocytoplasmic Transport and Prostate Cancer Growth
Importazole from Selleck Inhibits KPNB1 Nucleocytoplasmic Transport and Prostate Cancer Growth
Thiamet G Selective Glycosidase Inhibition Profile Against Beta-N-Acetylglucosaminidase Enzymes
Thiamet G Selective Glycosidase Inhibition Profile Against Beta-N-Acetylglucosaminidase Enzymes
Epacadostat (INCB024360) IDO1 Inhibition in First-Line Metastatic Renal Cell Carcinoma Phase 3 Trial
Epacadostat (INCB024360) IDO1 Inhibition in First-Line Metastatic Renal Cell Carcinoma Phase 3 Trial
Talabostat inhibitor Talabostat (Val-boroPro, PT-100) Mesylate targets DPP4 DPP8 DPP9 FAP
Talabostat inhibitor Talabostat (Val-boroPro, PT-100) Mesylate targets DPP4 DPP8 DPP9 FAP
NMDA (N-Methyl-D-aspartic acid) NMethylDaspartic NMDAR Excitotoxicity in Alzheimer Disease
NMDA (N-Methyl-D-aspartic acid) NMethylDaspartic NMDAR Excitotoxicity in Alzheimer Disease
Relacorilant from Selleck (CORT125134) selectively antagonizes glucocorticoid receptors in hypercortisolism disorders
Relacorilant from Selleck (CORT125134) selectively antagonizes glucocorticoid receptors in hypercortisolism disorders
Ko143 BCRP inhibitor Blocks ABCG2 Efflux at Blood-Placenta Barrier
Ko143 BCRP inhibitor Blocks ABCG2 Efflux at Blood-Placenta Barrier
Gsk484 Hydrochloride (Gsk484) Inhibits PADI4 to Reverse Lenvatinib Resistance in Hepatocellular Carcinoma
Gsk484 Hydrochloride (Gsk484) Inhibits PADI4 to Reverse Lenvatinib Resistance in Hepatocellular Carcinoma
Setmelanotide (RM-493) and Setmelanotide from Selleck Target MC4R in Rare Genetic Obesity
Setmelanotide (RM-493) and Setmelanotide from Selleck Target MC4R in Rare Genetic Obesity
Vorapaxar (MK-5348) Reversibly Inhibits Protease-Activated Receptor-1 Signaling in Atherothrombosis
Vorapaxar (MK-5348) Reversibly Inhibits Protease-Activated Receptor-1 Signaling in Atherothrombosis
SF1670 Regulates PTEN AKT Signaling to Modulate Non-Small Cell Lung Cancer Invasion
SF1670 Regulates PTEN AKT Signaling to Modulate Non-Small Cell Lung Cancer Invasion
Crenigacestat (LY3039478) Suppresses GINS1-Driven Notch/PI3K/AKT/mTORC1 Signaling in LUAD
Crenigacestat (LY3039478) Suppresses GINS1-Driven Notch/PI3K/AKT/mTORC1 Signaling in LUAD
Compstatin from Selleck inhibits C3 cleavage to block C3b dependent platelet aggregation
Compstatin from Selleck inhibits C3 cleavage to block C3b dependent platelet aggregation
MK571 MK-571 (L-660711) Mediates ABCC5 Efflux Transporter Inhibition in Hepatocellular Carcinoma
MK571 MK-571 (L-660711) Mediates ABCC5 Efflux Transporter Inhibition in Hepatocellular Carcinoma
Monastrol Inhibition of Kinesin Eg5 Induces Monopolar Spindle Arrest in Cancer Cells
Monastrol Inhibition of Kinesin Eg5 Induces Monopolar Spindle Arrest in Cancer Cells
Tat-beclin 1 Beclin activator Restores Autophagic Flux in Klebsiella pneumoniae Sepsis
Tat-beclin 1 Beclin activator Restores Autophagic Flux in Klebsiella pneumoniae Sepsis
PKR-IN-C16 PKRINC16 PKR inhibitor targets SPT1 in de novo ceramide synthesis
PKR-IN-C16 PKRINC16 PKR inhibitor targets SPT1 in de novo ceramide synthesis
Firsocostat inhibitor Firsocostat (GS-0976, ND-630) Targets ACC1 in Renal Fibrosis
Firsocostat inhibitor Firsocostat (GS-0976, ND-630) Targets ACC1 in Renal Fibrosis
Auranofin (SKF-39162) Auranofin Bacterial inhibitor Targets Thioredoxin Reductase in Toxoplasma
Auranofin (SKF-39162) Auranofin Bacterial inhibitor Targets Thioredoxin Reductase in Toxoplasma
Tiplaxtinin (PAI-039) from Selleck Targets PAI-1 to Attenuate Microvascular Thrombosis Post-TBI
Tiplaxtinin (PAI-039) from Selleck Targets PAI-1 to Attenuate Microvascular Thrombosis Post-TBI
Dooku1 Selective Antagonism of Yoda1-Induced Piezo1 Mechanosensitive Ion Channel Activation
Dooku1 Selective Antagonism of Yoda1-Induced Piezo1 Mechanosensitive Ion Channel Activation
NNMTi Targeted Inhibition Depletes 1-MNA and Restores Epigenetic Methylation in Solid Tumors
NNMTi Targeted Inhibition Depletes 1-MNA and Restores Epigenetic Methylation in Solid Tumors
BMS-303141 inhibitor targets ATP citrate lyase to suppress hepatic alanine transamination and gluconeogenesis
BMS-303141 inhibitor targets ATP citrate lyase to suppress hepatic alanine transamination and gluconeogenesis
BMS-309403 Inhibition of FABP4 Mitigates Ischemia-Reperfusion Injury in Steatotic Livers
BMS-309403 Inhibition of FABP4 Mitigates Ischemia-Reperfusion Injury in Steatotic Livers
WRW4 antagonist suppression of FPR2 blocks peripheral inflammatory pain resolution
WRW4 antagonist suppression of FPR2 blocks peripheral inflammatory pain resolution
ABR-215757 from Selleck Blockade of S100A9 Restores Cardiac Mitochondrial Homeostasis
ABR-215757 from Selleck Blockade of S100A9 Restores Cardiac Mitochondrial Homeostasis
MitoPQ from Selleck Targets Mitochondrial Complex I to Generate Selective Superoxide
MitoPQ from Selleck Targets Mitochondrial Complex I to Generate Selective Superoxide
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