SCN2A

Sodium channel protein type 2 subunit alpha · Q99250 · SCN2A on Sugi Atlas →

106,058 patent compounds predicted against SCN2A, 69,144 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
Metabutoxycaine Metabutoxycaine (SCHEMBL25778) 0.58 7/20
Propoxycaine Propoxycaine (SCHEMBL83073) 1.00 6/20
Propoxycaine Propoxycaine (SCHEMBL24720) 0.98 6/20
SCHEMBL85047 SCHEMBL85047 0.81 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
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
Parethoxycaine Parethoxycaine (SCHEMBL25944) 1.00 4/20
Proparacaine Proparacaine (SCHEMBL23333) 0.98 4/20
Proparacaine Proparacaine (SCHEMBL93880) 0.98 4/20
SCHEMBL25553 SCHEMBL25553 0.81 4/20
Hydroquinine Hydroquinine (SCHEMBL109600) 0.81 4/20

Clinical trials — most relevant to SCN2A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Carbamazapine for Inherited Erythromelalgia Patients With NaV1.7 Mutations PHASE4COMPLETED
A Clinical Trial of Elsunersen in Pediatric SCN2A-DEE to Assess Efficacy and Safety PHASE3RECRUITING
A Double-blind Study Evaluating the Efficacy, Safety, and Tolerability of Zorevunersen in Patients With Dravet Syndrome PHASE3RECRUITING
A Clinical Trial of PRAX-562 in Subjects With Developmental and Epileptic Encephalopathies (DEE) PHASE2/PHASE3ACTIVE_NOT_RECRUITING
Safety and Tolerability of Lacosamide in Patients With Gain-of-function Nav1.7 Mutations Related Small Fiber Neuropathy PHASE3COMPLETED
An Open-Label Study to Investigate the Safety of Single and Multiple Ascending Doses in Children and Adolescents With Dravet Syndrome PHASE1/PHASE2COMPLETED
Mutation-specific Therapy for the Long QT Syndrome PHASE2COMPLETED
4-Aminopyridine in Episodic Ataxia Type 2 PHASE2WITHDRAWN
Personalized Antisense Oligonucleotide Therapy for Rare Pediatric Genetic Disease: SCN2A PHASE1/PHASE2ACTIVE_NOT_RECRUITING
Pathophysiology Based Therapy of Early Onset Epileptic Encephalopathies PHASE2WITHDRAWN
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
A Clinical Trial of PRAX-222 in Pediatric Participants With Early Onset SCN2A Developmental and Epileptic Encephalopathy PHASE1/PHASE2RECRUITING
Sodium Channel Splicing in Heart Failure Trial nanCOMPLETED
A Prospective, Remote Observational Study in Pediatric Participants With Early-Onset SCN2A-Developmental and Epileptic Encephalopathy nanCOMPLETED
Sodium Channel Splicing in Heart Failure Trial (SOCS-HEFT) Prospective Study nanUNKNOWN
Evaluation of the Effects of KCNQ1 Mutation on Insulin Tolerance and Obsessive Compulsive Features in Long QT Romano-Ward Syndrome Patients. nanUNKNOWN
SCN2A Polymorphisms Are Associated With Response to Valproic Acid in Paediatric Population(Pakistan) nanCOMPLETED
Sodium Channel Splicing in Obstructive Sleep Apnea (SOCS-OSA) nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Genotype, Phenotype, and Disease Progression of Developmental Epileptic Encephalopathy With Onset Before 2 Years of Age nanRECRUITING
Treatment of Gait Disorders in Children With Dravet Syndrome nanCOMPLETED
Longitudinal Study of Phenotypic and Developmental Severity in Patients With Dravet Syndrome With SCN1A Gene Mutation nanRECRUITING
Role of SNP and DIGOXIN Response in Atrial Fibrillation Patients nanCOMPLETED
SCN1A Horizons A Natural History Study of SCN1A-related Epilepsies in the United Kingdom nanRECRUITING
ST-segment Elevation as an AF Endophenotype nanCOMPLETED
Piezo2-related Arthrogryposis & physiopathOLOgy 3 nanNOT_YET_RECRUITING
Post-stroke Epilepsy: Primary Prophylaxis Study nanUNKNOWN
fMRI-study in Patients With Small Fiber Neuropathy nanUNKNOWN
Factors Affecting Salt Intake in Young Adults nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a SCN2A binder may also engage these)

ProteinNameSimilarity
P04775 1.000 P04775 →
SCN3A Sodium channel protein type 3 subunit alpha 1.000 landscape →
B1AWN6 1.000 B1AWN6 →
Q28644 1.000 Q28644 →
P08104 1.000 P08104 →
Q62205 1.000 Q62205 →
A2ASI5 1.000 A2ASI5 →
O88420 1.000 O88420 →
SCN1A Sodium channel protein type 1 subunit alpha 1.000 landscape →
A2APX8 1.000 A2APX8 →
Q9WTU3 1.000 Q9WTU3 →
P15390 1.000 P15390 →
SCN9A Sodium channel protein type 9 subunit alpha 1.000 landscape →
Q62968 1.000 Q62968 →
O08562 1.000 O08562 →
SCN8A Sodium channel protein type 8 subunit alpha 1.000 landscape →
P15389 1.000 P15389 →
Q6QIY3 0.999 Q6QIY3 →
P04774 0.999 P04774 →
Q9JJV9 0.999 Q9JJV9 →
Q2XVR7 0.999 Q2XVR7 →
P02719 0.998 P02719 →
Q2XVR6 0.998 Q2XVR6 →
Q2XVR3 0.998 Q2XVR3 →
SCN5A Sodium channel protein type 5 subunit alpha 0.997 landscape →
Q20JQ7 0.997 Q20JQ7 →
Q9ER60 0.997 Q9ER60 →
P35500 0.997 P35500 →
SCN10A Sodium channel protein type 10 subunit alpha 0.996 landscape →
Q28371 0.996 Q28371 →