IMPA1

Inositol monophosphatase 1 · P29218 · IMPA1 on Sugi Atlas →

0 patent compounds predicted against IMPA1, 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 IMPA1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
CMP-MYTHiC Trial and Registry - CardioMyoPathy With MYocarditis THerapy With Colchicine PHASE3RECRUITING
Efficacy of Lithium Against Chemotherapy Induced Neutropenia in Breast Cancer Patients PHASE3COMPLETED
Study Evaluating Toxicity & Efficacy of Lenalidomide(Revlimid®)in Chemotherapy-Naïve AIPC Patients PHASE2COMPLETED
Peptide Vaccine Focusing on Prevention of the Recurrence for Bladder Cancer PHASE2UNKNOWN
IMPase in Treatment-resistant Depression PHASE1UNKNOWN
Effects of Lithium Therapy on Blood-based Therapeutic Targets in Parkinson's Disease. PHASE1COMPLETED
Prognostic Value of Protein IMP3 Expression in Cervical Cancer nanCOMPLETED
United States Hypophosphatasia Molecular Research Center nanCOMPLETED
Genetic Characterization of Parkinson's Disease nanCOMPLETED
Genetic Architecture of Chronic Inflammatory Demyelinating Polyradiculoneuropathy nanUNKNOWN
The Influence of Genetic Variations in ELAPOR1 or ELAPOR2 on Insulin Secretion and Glucose Regulation in Humans nanUNKNOWN
Study of the Pathophysiological Mechanisms Involved in Bleeding Events nanCOMPLETED
Research and Characterization of New Genes Involved in Intellectual Disability nanCOMPLETED
A Real-world, Multi-center, Prospective, Observational Study for PNH in China nanCOMPLETED
Genes-in-Action - Hepcidin Regulation of Iron Supplementation nanCOMPLETED
Role of Genetics in Idiopathic Pulmonary Fibrosis (IPF) nanUNKNOWN
Biomarker in Tissue Samples From Patients With Ewing Sarcoma nanCOMPLETED
Characterization of New Candidate Genes in Cases of Human Inherited Thrombocytopenia (CATCH) nanCOMPLETED
Identification of Acute Intermittent Porphyria Modifying Genes nanRECRUITING
Genetic Variants and Regulation of Specialized Pro-resolving Mediator nanRECRUITING
TSH Receptor Mutations Among a Consanguineous Community nanCOMPLETED
Investigation of Copy Number Variations and Genetic Variants in POI nanRECRUITING
Exome Sequencing for Atypical Femoral Fractures nanCOMPLETED
The Molecular Biology of Paroxysmal Nocturnal Hemoglobinuria (PNH) nanCOMPLETED
Unraveling Genetics of HypoPhosPhatasia (HPP Genetics) nanCOMPLETED
Genetic Studies of Lysosomal Storage Disorders nanENROLLING_BY_INVITATION
Genetic Investigation of Cancer Predisposition nanNOT_YET_RECRUITING
Epigenetics, DNA Methylation Patterns and Periodontal Disease nanCOMPLETED
Targeted Next Generation Sequencing and Intellectual Disability nanCOMPLETED
Family Blood Pressure Program - GenNet Network nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a IMPA1 binder may also engage these)

ProteinNameSimilarity
Q5R4X0 1.000 Q5R4X0 →
P97697 1.000 P97697 →
P20456 1.000 P20456 →
P29219 1.000 P29219 →
O55023 0.997 O55023 →
O77591 0.994 O77591 →
P54927 0.992 P54927 →
Q9M8S8 0.991 Q9M8S8 →
Q8CIN7 0.991 Q8CIN7 →
O49071 0.988 O49071 →
Q91UZ5 0.988 Q91UZ5 →
P54926 0.988 P54926 →
P54928 0.987 P54928 →
Q54U72 0.985 Q54U72 →
Q19420 0.984 Q19420 →
O14732 0.980 O14732 →
Q9JZ07 0.979 Q9JZ07 →
Q05533 0.978 Q05533 →
C4M4T9 0.978 C4M4T9 →
P0ADG4 0.978 P0ADG4 →
Q9KTY5 0.977 Q9KTY5 →
Q9JU03 0.976 Q9JU03 →
Q9XF47 0.976 Q9XF47 →
P0ADG6 0.975 P0ADG6 →
P0ADG5 0.975 P0ADG5 →
P46276 0.975 P46276 →
Q87BG1 0.975 Q87BG1 →
Q9CNV8 0.975 Q9CNV8 →
P44333 0.975 P44333 →
Q8RW99 0.975 Q8RW99 →