SCN7A

Sodium channel protein type 7 subunit alpha · Q01118 · SCN7A on Sugi Atlas →

17,809 patent compounds predicted against SCN7A, 12,300 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL160752 SCHEMBL160752 0.35 5/20
Noxiptiline Noxiptiline (SCHEMBL49824) 0.49 2/20
Mexiletine Mexiletine (SCHEMBL16081) 1.00 1/20
(R)-Mexiletine (R)-Mexiletine (SCHEMBL16082) 1.00 1/20
Diltiazem Diltiazem (SCHEMBL17776) 1.00 1/20
Ajmaline Ajmaline (SCHEMBL18950) 1.00 1/20
Ajmaline Ajmaline (SCHEMBL34501) 1.00 1/20
Tetracaine Tetracaine (SCHEMBL34714) 1.00 1/20
Mibefradil Mibefradil (SCHEMBL39551) 1.00 1/20
Sertindole Sertindole (SCHEMBL112092) 1.00 1/20
Cifenline Cifenline (SCHEMBL122806) 1.00 1/20
Tedisamil Tedisamil (SCHEMBL157918) 1.00 1/20
Mibefradil Mibefradil (SCHEMBL120810) 0.99 1/20
Diltiazem Diltiazem (SCHEMBL15457) 0.98 1/20
Tetracaine Tetracaine (SCHEMBL24370) 0.97 1/20
Mexiletine Mexiletine (SCHEMBL42226) 0.96 1/20
Diltiazem Diltiazem (SCHEMBL120772) 0.83 1/20
Cifenline Cifenline (SCHEMBL121044) 0.79 1/20
SCHEMBL281173 SCHEMBL281173 0.79 1/20
Clentiazem Clentiazem (SCHEMBL33909) 0.77 1/20

Clinical trials — most relevant to SCN7A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Carbamazapine for Inherited Erythromelalgia Patients With NaV1.7 Mutations PHASE4COMPLETED
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
Safety and Tolerability Study of ST-503 for Refractory Pain Due to Peripheral Neuropathy (Small Fiber Predominant, SFN) PHASE1/PHASE2RECRUITING
Verapamil as Therapy for Children and Young Adults With Dravet Syndrome PHASE2COMPLETED
Pathophysiology Based Therapy of Early Onset Epileptic Encephalopathies PHASE2WITHDRAWN
A First-in-human Study of S230815 in Pediatric Participants With KCNT1-related Developmental and Epileptic Encephalopathy PHASE1/PHASE2RECRUITING
An Open-Label Extension Study of STK-001 for Patients With Dravet Syndrome PHASE2ACTIVE_NOT_RECRUITING
Mechanism of Human Cold Pain Perception - Involvement of TRPA1, TRPM8, Nav1.7 and Nav1.8 EARLY_PHASE1COMPLETED
Sodium Channel Splicing in Heart Failure Trial nanCOMPLETED
Sodium Channel Splicing in Heart Failure Trial (SOCS-HEFT) Prospective Study nanUNKNOWN
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
Evaluation of the Effects of KCNQ1 Mutation on Insulin Tolerance and Obsessive Compulsive Features in Long QT Romano-Ward Syndrome Patients. nanUNKNOWN
Longitudinal Study of Phenotypic and Developmental Severity in Patients With Dravet Syndrome With SCN1A Gene Mutation nanRECRUITING
Sodium Channel Splicing in Obstructive Sleep Apnea (SOCS-OSA) nanCOMPLETED
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
GABA Biomarkers in Dravet Syndrome nanRECRUITING
Probing the Role of Sodium Channels in Painful Neuropathies nanUNKNOWN
Role of SNP and DIGOXIN Response in Atrial Fibrillation Patients nanCOMPLETED
Gene-STEPS: Shortening Time of Evaluation in Paediatric Epilepsy Services nanUNKNOWN
EXploring novEl Molecular Determinants of DRAvet Syndrome Phenotype Heterogeneity nanUNKNOWN
A Prospective, Remote Observational Study in Pediatric Participants With Early-Onset SCN2A-Developmental and Epileptic Encephalopathy nanCOMPLETED
The Influence of Genetic Predisposition on Outcome After Catheter Ablation of Atrial Fibrillation. nanUNKNOWN
Factors Affecting Salt Intake in Young Adults nanUNKNOWN
fMRI-study in Patients With Small Fiber Neuropathy nanUNKNOWN
Painful Channelopathies Study nanUNKNOWN
Copy Number Variation in CHRNA7 Gene in Migraine and Gene Expression nanCOMPLETED
Exploring the Genetics of Neuropathic Pain nanRECRUITING
A Study to Gather Information About Overall Occurrence and New Cases of Dravet and Lennox-Gastaut Syndromes in Children, Teenagers and Adults in Spain nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a SCN7A binder may also engage these)

ProteinNameSimilarity
B1AYL1 1.000 B1AYL1 →
F1LQQ7 1.000 F1LQQ7 →
P02719 0.994 P02719 →
P27732 0.992 P27732 →
Q6AXP6 0.992 Q6AXP6 →
Q9R053 0.992 Q9R053 →
SCN11A Sodium channel protein type 11 subunit alpha 0.991 landscape →
Q8BVN3 0.991 Q8BVN3 →
P15390 0.991 P15390 →
Q62968 0.991 Q62968 →
Q28644 0.991 Q28644 →
Q28371 0.991 Q28371 →
Q80W99 0.991 Q80W99 →
O08562 0.990 O08562 →
Q62205 0.990 Q62205 →
P22002 0.990 P22002 →
SCN2A Sodium channel protein type 2 subunit alpha 0.990 landscape →
CACNA1C Voltage-dependent L-type calcium channel subunit alpha-1C 0.990 landscape →
SCN10A Sodium channel protein type 10 subunit alpha 0.989 landscape →
O88457 0.989 O88457 →
O73700 0.989 O73700 →
Q6QIY3 0.989 Q6QIY3 →
Q25452 0.989 Q25452 →
CACNA1D Voltage-dependent L-type calcium channel subunit alpha-1D 0.988 landscape →
P56698 0.988 P56698 →
SCN3A Sodium channel protein type 3 subunit alpha 0.988 landscape →
Q02789 0.988 Q02789 →
Q2XVR6 0.988 Q2XVR6 →
CACNA1G Voltage-dependent T-type calcium channel subunit alpha-1G 0.988 landscape →
O14234 0.988 O14234 →