VAMP8

Vesicle-associated membrane protein 8 · Q9BV40 · VAMP8 on Sugi Atlas →

0 patent compounds predicted against VAMP8, 0 high-confidence (nearest known ligand ≥ 0.5)

Top predicted compounds (top 20 by supporting neighbours, then confidence)

CompoundConfidenceSupporting neighbours

Clinical trials — most relevant to VAMP8 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Prehospital Early Administration of Ketamine for Status Epilepticus in Epileptic Kids (PEAK-SEEK) PHASE2/PHASE3RECRUITING
Melpida: Recombinant Adeno-associated Virus (serotype 9) Encoding a Codon Optimized Human AP4M1 Transgene (hAP4M1opt) PHASE1/PHASE2RECRUITING
Safety and Efficacy of AAV9/AP4B1 (BFB-101) For Patients With AP4B1-related Hereditary Spastic Paraplegia Type 47 (SPG47) PHASE1/PHASE2NOT_YET_RECRUITING
The Synapse Project PHASE2COMPLETED
Nilotinib in Huntington's Disease PHASE1UNKNOWN
Phenylbutyrate for Monogenetic Developmental and Epileptic Encephalopathy EARLY_PHASE1ACTIVE_NOT_RECRUITING
Stem Cell Models of Best Disease and Other Retinal Degenerative Diseases. nanCOMPLETED
Identification of New Biomarkers of Insulin Resistance nanACTIVE_NOT_RECRUITING
Nuclear Myosin VI - a Therapeutic Target in Breast Cancer nanUNKNOWN
Long COVID-19 on the Human Brain nanCOMPLETED
Transcriptomic Profile of Patients Treated With Different Modalities of Spinal Cord Stimulation nanUNKNOWN
Biomarker Research in Inherited Movement Disorders nanRECRUITING
Gene-STEPS: Shortening Time of Evaluation in Paediatric Epilepsy Services nanUNKNOWN
Combined Aerobic Exercise and Cognitive Training in Seniors at Increased Risk for Alzheimer's Disease nanNOT_YET_RECRUITING
Genetics of Recurrent Early Onset Major Depression nanCOMPLETED
Study of Chediak-Higashi Syndrome nanRECRUITING
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Study of the Genetic Factors Involved in Autism and Related Disorders nanRECRUITING
Cell Free Circulating Nucleic Acids as New Tumor Diagnostics From Human Plasma Samples. nanUNKNOWN
Genetic Variation in CLTCL1 and Whole-body Glucose Control nanCOMPLETED
The Influence of Genetic Variations in ELAPOR1 or ELAPOR2 on Insulin Secretion and Glucose Regulation in Humans nanUNKNOWN
Investigating Phenotypic, Epigenetic, and NeuroGenetic Traits in Rare and Ultra-rare Neurodevelopmental Disorders (Project PENGUIN) nanRECRUITING
The Effect of Probiotics on Systemic Inflammation and Metabolic Endotoxemia in Patients Undergoing Bariatric Surgery nanUNKNOWN
Insulin Detemir in Obesity Management nanACTIVE_NOT_RECRUITING
Toward Molecular Profiling of Parkinson's Disease in Easily Accessible Biological Matrices nanACTIVE_NOT_RECRUITING
Genes, Proteins, and Metabolites in Drug-resistant Epilepsy (DRE) Patients nanNOT_YET_RECRUITING
Neurophysiologic Biomarkers in Rett Syndrome nanRECRUITING
miR-142-3p as Potential Biomarker of Synaptopathy in MS nanUNKNOWN
STXBP1 and SYNGAP1 Related Disorders Natural History Study nanRECRUITING
Inherited Reproductive Disorders nanRECRUITING

Related proteins — ESM-2 sequence neighbours (a VAMP8 binder may also engage these)

ProteinNameSimilarity
Q5REQ5 1.000 Q5REQ5 →
Q3T0Y8 1.000 Q3T0Y8 →
O70404 1.000 O70404 →
Q9WUF4 0.999 Q9WUF4 →
P33328 0.969 P33328 →
Q9Z2J5 0.968 Q9Z2J5 →
Q9Z2P8 0.968 Q9Z2P8 →
P31109 0.967 P31109 →
Q92356 0.964 Q92356 →
O75379 0.960 O75379 →
Q32L97 0.956 Q32L97 →
O70480 0.955 O70480 →
Q2KHY2 0.954 Q2KHY2 →
Q15836 0.935 Q15836 →
O95183 0.934 O95183 →
P63025 0.934 P63025 →
P63024 0.934 P63024 →
Q2KJD2 0.932 Q2KJD2 →
Q9JHW5 0.931 Q9JHW5 →
O02495 0.930 O02495 →
O15400 0.930 O15400 →
Q60WU2 0.930 Q60WU2 →
Q5R602 0.929 Q5R602 →
Q4R8T0 0.929 Q4R8T0 →
G3V7P1 0.925 G3V7P1 →
O70439 0.925 O70439 →
P58200 0.925 P58200 →
Q5ZL74 0.924 Q5ZL74 →
Q9UEU0 0.924 Q9UEU0 →
O70257 0.924 O70257 →