ARSA

Arylsulfatase A · P15289 · ARSA on Sugi Atlas →

262 patent compounds predicted against ARSA, 84 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL17384095 SCHEMBL17384095 0.64 1/20
SCHEMBL64776 SCHEMBL64776 0.58 1/20
SCHEMBL33372528 SCHEMBL33372528 0.58 1/20
SCHEMBL893374 SCHEMBL893374 0.57 1/20
SCHEMBL30702421 SCHEMBL30702421 0.57 1/20
SCHEMBL3081576 SCHEMBL3081576 0.56 1/20
SCHEMBL17384169 SCHEMBL17384169 0.53 1/20
SCHEMBL17384172 SCHEMBL17384172 0.53 1/20
SCHEMBL7915211 SCHEMBL7915211 0.50 1/20
SCHEMBL21190538 SCHEMBL21190538 0.50 1/20
SCHEMBL22260258 SCHEMBL22260258 0.50 1/20
SCHEMBL7577681 SCHEMBL7577681 0.49 1/20
SCHEMBL3584746 SCHEMBL3584746 0.49 1/20
SCHEMBL5470220 SCHEMBL5470220 0.49 1/20
SCHEMBL30154375 SCHEMBL30154375 0.49 1/20
SCHEMBL7912329 SCHEMBL7912329 0.48 1/20
SCHEMBL22609991 SCHEMBL22609991 0.48 1/20
SCHEMBL11480829 SCHEMBL11480829 0.47 1/20
SCHEMBL2957612 SCHEMBL2957612 0.47 1/20
SCHEMBL3192410 SCHEMBL3192410 0.47 1/20

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

TrialPhaseStatus
A Study of Elaprase in Children and Adults With Hunter Syndrome (Mucopolysaccharidosis II) in India PHASE4COMPLETED
Safety and Clinical Outcomes in Hunter Syndrome Patients 5 Years of Age and Younger Receiving Idursulfase Therapy PHASE4COMPLETED
OTL-200 in Patients With Late Juvenile Metachromatic Leukodystrophy (MLD) PHASE3ACTIVE_NOT_RECRUITING
Iduronate-2-sulfatase Enzyme Replacement Therapy in Mucopolysaccharidosis II (MPS II) PHASE2/PHASE3COMPLETED
Study of Intrathecal Idursulfase-IT Administered in Conjunction With Elaprase® in Pediatric Patients With Hunter Syndrome and Early Cognitive Impairment PHASE2/PHASE3COMPLETED
An Extension Study to Assess the Long-term Safety and Efficacy of Hunterase (Idursulfase Beta) PHASE3COMPLETED
Efficacy METAZYM for the Treatment Metachromatic Leukodystrophy Treated With Hematopoietic Stem Cell Transplantation PHASE2COMPLETED
Intracerebral Gene Therapy for Children With Early Onset Forms of Metachromatic Leukodystrophy PHASE1/PHASE2COMPLETED
A Study in MPS VI to Assess Safety and Efficacy of Odiparcil PHASE2COMPLETED
Multicenter Study of HGT-1110 Administered Intrathecally in Children With Metachromatic Leukodystrophy (MLD) PHASE1/PHASE2COMPLETED
Gene Therapy in Patients With Mucopolysaccharidosis Disease PHASE1/PHASE2COMPLETED
A Study of Intrathecal SHP611 in Children With Metachromatic Leukodystrophy PHASE2ACTIVE_NOT_RECRUITING
Long-term Metazym Treatment of Patients With Late Infantile Metachromatic Leukodystrophy (MLD) PHASE1/PHASE2COMPLETED
A Safety and Efficacy Study of Cryopreserved OTL-200 for Treatment of Metachromatic Leukodystrophy (MLD) PHASE2COMPLETED
Autologous Hematopoietic Stem Cell Gene Therapy for Metachromatic Leukodystrophy and Adrenoleukodystrophy PHASE1/PHASE2UNKNOWN
Gene Therapy for Metachromatic Leukodystrophy (MLD) PHASE1/PHASE2COMPLETED
An Efficacy and Safety Study of HGT-1110 in Participants With Metachromatic Leukodystrophy PHASE1/PHASE2COMPLETED
Safety and Dose Ranging Study of Insulin Receptor MoAb-IDS Fusion Protein in Patients With Hunter Syndrome PHASE1COMPLETED
A Study of the Tolerance, Safety, and Pharmacokinetics of GNR-055 in Healthy Volunteers PHASE1COMPLETED
Mucopolysaccharidosis (MPS) VI Clinical Surveillance Program (CSP) nanCOMPLETED
Imaging Study of the White Matter Lesions in Children With Metachromatic Leucodystrophy nanCOMPLETED
Lentiviral Hematopoietic Stem Cell Gene Therapy for MLD nanRECRUITING
Biomarker for Maroteaux-Lamy Disease (BioMaroteaux) nanWITHDRAWN
Direct Lentiviral Injection Gene Therapy for MLD nanRECRUITING
BMN 110 US Expanded Access Program nanAPPROVED_FOR_MARKETING
Chest Wall Deformities in Children - Epidemiological Data nanCOMPLETED
A Natural History Study of Biomarkers and Clinical Outcomes in Mucopolysaccharidosis Type IIIA (MPS IIIA; Sanfilippo Syndrome) nanCOMPLETED
Post-trial Access Program of Idursulfase-IT Along With Elaprase in Children With Hunter Syndrome nanAVAILABLE
A Study of Patients With Sanfilippo Syndrome Type A (MPS IIIA) nanCOMPLETED
Returning Genetic Results on Arsenic Susceptibility nanCOMPLETED

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

ProteinNameSimilarity
Q08DD1 1.000 Q08DD1 →
P50428 1.000 P50428 →
P15589 0.986 P15589 →
P51689 0.982 P51689 →
Q3TYD4 0.981 Q3TYD4 →
Q32KJ9 0.974 Q32KJ9 →
P50429 0.972 P50429 →
Q5FYA8 0.971 Q5FYA8 →
P15848 0.971 P15848 →
P51690 0.971 P51690 →
Q96EG1 0.970 Q96EG1 →
P50427 0.970 P50427 →
Q60HH5 0.970 Q60HH5 →
P14000 0.968 P14000 →
P50430 0.968 P50430 →
P54793 0.967 P54793 →
P21836 0.967 P21836 →
P33727 0.967 P33727 →
P23795 0.966 P23795 →
P37136 0.966 P37136 →
O97524 0.965 O97524 →
P51688 0.965 P51688 →
O18835 0.965 O18835 →
GAA Lysosomal alpha-glucosidase 0.964 landscape →
O62763 0.964 O62763 →
P51840 0.963 P51840 →
ACHE Acetylcholinesterase 0.963 landscape →
Q29499 0.963 Q29499 →
Q32KH8 0.963 Q32KH8 →
P51839 0.963 P51839 →