SCN3A

Sodium channel protein type 3 subunit alpha · Q9NY46 · SCN3A on Sugi Atlas →

90,417 patent compounds predicted against SCN3A, 57,026 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
Ambucaine Ambucaine (SCHEMBL82280) 0.91 8/20
SCHEMBL135105 SCHEMBL135105 0.56 8/20
SCHEMBL135106 SCHEMBL135106 0.56 8/20
Metabutoxycaine Metabutoxycaine (SCHEMBL25778) 0.58 7/20
Propoxycaine Propoxycaine (SCHEMBL83073) 1.00 6/20
Propoxycaine Propoxycaine (SCHEMBL24720) 0.98 6/20
Biphenamine Biphenamine (SCHEMBL25980) 0.81 6/20
Chloroprocaine Chloroprocaine (SCHEMBL6676) 0.67 6/20
Benoxinate Benoxinate (SCHEMBL25087) 1.00 5/20
Betoxycaine Betoxycaine (SCHEMBL25758) 0.77 5/20
Procaine Procaine (SCHEMBL3524) 0.68 5/20
Chloroprocaine Chloroprocaine (SCHEMBL24096) 0.66 5/20
Phthalylsulfacetamide Phthalylsulfacetamide (SCHEMBL49529) 0.59 5/20
Pramipexole Pramipexole (SCHEMBL35376) 0.56 5/20
Dexpramipexole Dexpramipexole (SCHEMBL74780) 0.56 5/20
Pramipexole Pramipexole (SCHEMBL42113) 0.55 5/20
SCHEMBL517 SCHEMBL517 0.40 5/20
Proparacaine Proparacaine (SCHEMBL23334) 1.00 4/20
SCHEMBL25906 SCHEMBL25906 1.00 4/20
SCHEMBL25907 SCHEMBL25907 1.00 4/20

Clinical trials — most relevant to SCN3A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Carbamazapine for Inherited Erythromelalgia Patients With NaV1.7 Mutations PHASE4COMPLETED
A Double-blind Study Evaluating the Efficacy, Safety, and Tolerability of Zorevunersen in Patients With Dravet Syndrome PHASE3RECRUITING
Safety and Tolerability of Lacosamide in Patients With Gain-of-function Nav1.7 Mutations Related Small Fiber Neuropathy PHASE3COMPLETED
Suzetrigine in Total Hip Arthroplasty PHASE3RECRUITING
An Open-Label Study to Investigate the Safety of Single and Multiple Ascending Doses in Children and Adolescents With Dravet Syndrome PHASE1/PHASE2COMPLETED
Verapamil as Therapy for Children and Young Adults With Dravet Syndrome PHASE2COMPLETED
Safety and Tolerability Study of ST-503 for Refractory Pain Due to Peripheral Neuropathy (Small Fiber Predominant, SFN) PHASE1/PHASE2RECRUITING
Mutation-specific Therapy for the Long QT Syndrome PHASE2COMPLETED
An Open-Label Extension Study of STK-001 for Patients With Dravet Syndrome PHASE2ACTIVE_NOT_RECRUITING
Sodium Channel Splicing in Obstructive Sleep Apnea (SOCS-OSA) nanCOMPLETED
Sodium Channel Splicing in Heart Failure Trial nanCOMPLETED
Sodium Channel Splicing in Heart Failure Trial (SOCS-HEFT) Prospective Study nanUNKNOWN
Prospective Study to Determine the Prevalence of Signs of Central Sensitization in Adults With ASD Without Intellectual Developmental Disorders nanRECRUITING
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Evaluation of the Effects of KCNQ1 Mutation on Insulin Tolerance and Obsessive Compulsive Features in Long QT Romano-Ward Syndrome Patients. nanUNKNOWN
Factors Affecting Salt Intake in Young Adults nanUNKNOWN
A Prospective, Remote Observational Study in Pediatric Participants With Early-Onset SCN2A-Developmental and Epileptic Encephalopathy nanCOMPLETED
Treatment of Gait Disorders in Children With Dravet Syndrome nanCOMPLETED
SCN1A Horizons A Natural History Study of SCN1A-related Epilepsies in the United Kingdom nanRECRUITING
Longitudinal Study of Phenotypic and Developmental Severity in Patients With Dravet Syndrome With SCN1A Gene Mutation nanRECRUITING
Painful Channelopathies Study nanUNKNOWN
Role of SNP and DIGOXIN Response in Atrial Fibrillation Patients nanCOMPLETED
fMRI-study in Patients With Small Fiber Neuropathy nanUNKNOWN
Genetic Determinants of Sudden Cardiac Death nanCOMPLETED
Probing the Role of Sodium Channels in Painful Neuropathies nanUNKNOWN
Gene-STEPS: Shortening Time of Evaluation in Paediatric Epilepsy Services nanUNKNOWN
A Single Center Prospective Study in an Estimated 570 Patients Who Underwent Genetic Screening at UZ Brussel in the Context of a Primary Cardiac Arrhythmia. Patients Showing a Variant Class 3,4 or 5 in SCN4A or CLCN1 Will Undergo a Clinical and Electrophysiological Review After IC. nanNOT_YET_RECRUITING
Multicenter Study of Patients With SHANK3 Mutations: Identification of Genes Modificators in Phelan-McDermid Syndrome (EUQ13) nanNOT_YET_RECRUITING
Exploring the Genetics of Neuropathic Pain nanRECRUITING
The Influence of Genetic Predisposition on Outcome After Catheter Ablation of Atrial Fibrillation. nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a SCN3A binder may also engage these)

ProteinNameSimilarity
SCN2A Sodium channel protein type 2 subunit alpha 1.000 landscape →
P04775 1.000 P04775 →
P08104 1.000 P08104 →
B1AWN6 1.000 B1AWN6 →
A2ASI5 1.000 A2ASI5 →
O88420 1.000 O88420 →
Q62205 1.000 Q62205 →
Q28644 1.000 Q28644 →
SCN1A Sodium channel protein type 1 subunit alpha 1.000 landscape →
Q9WTU3 1.000 Q9WTU3 →
Q2XVR7 1.000 Q2XVR7 →
Q62968 1.000 Q62968 →
SCN9A Sodium channel protein type 9 subunit alpha 1.000 landscape →
P15390 1.000 P15390 →
Q2XVR3 1.000 Q2XVR3 →
A2APX8 1.000 A2APX8 →
SCN8A Sodium channel protein type 8 subunit alpha 1.000 landscape →
P04774 1.000 P04774 →
Q6QIY3 1.000 Q6QIY3 →
P15389 0.999 P15389 →
Q9JJV9 0.999 Q9JJV9 →
O08562 0.998 O08562 →
P02719 0.998 P02719 →
Q20JQ7 0.998 Q20JQ7 →
Q9ER60 0.998 Q9ER60 →
Q2XVR6 0.998 Q2XVR6 →
P35500 0.997 P35500 →
Q28371 0.997 Q28371 →
SCN10A Sodium channel protein type 10 subunit alpha 0.996 landscape →
SCN5A Sodium channel protein type 5 subunit alpha 0.996 landscape →