SFXN3

Sideroflexin-3 · Q9BWM7 · SFXN3 on Sugi Atlas →

0 patent compounds predicted against SFXN3, 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 SFXN3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
A Trial to Assess the Safety and Efficacy of KRN23 in Epidermal Nevus Syndrome (ENS) PHASE4COMPLETED
Bovine Lactoferrin to Prevent and Cure Iron Deficiency and Iron Deficiency Anemia in Complicated Pregnancies PHASE4COMPLETED
A Study of KRN23 in Pediatric Patients With X-linked Hypophosphatemic Rickets/Osteomalacia PHASE3COMPLETED
Safety and Tolerability of Lacosamide in Patients With Gain-of-function Nav1.7 Mutations Related Small Fiber Neuropathy PHASE3COMPLETED
Effect of Pioglitazone Administered to Patients With Friedreich's Ataxia: Proof of Concept PHASE3COMPLETED
Efficacy and Safety Assessment of Oral LBH589 in Adult Patients With Advanced Soft TIssue Sarcoma After Pre-treatment Failure PHASE2COMPLETED
A Study to Assess the Safety and Efficacy of 3 Doses of ALX1-11 (50, 75, and 100µg) in the Treatment of Postmenopausal Osteoporosis PHASE2COMPLETED
Open Trail of γIFN for Friedreich Ataxia PHASE2COMPLETED
A Phase II Clinical Trial Evaluating the Combination of Olaparib and Temozolomide for the Treatment of Advanced Uterine Leiomyosarcoma PHASE2ACTIVE_NOT_RECRUITING
Effects of Vitamin D Replacement on Hormones Regulating Iron Metabolism in Individuals With Chronic Kidney Disease EARLY_PHASE1COMPLETED
Hydroxychloroquin (HCQ) in chILD of Genetic Defect nanCOMPLETED
Biocollection in MyeloDysplastic Syndrome (P-MDS) nanRECRUITING
Genetic Causes and Clinical Features of Childhood Interstitial Lung Diseases in China nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Personalized Medicine Program on Myelodysplastic Syndromes: Characterization of the Patient's Genome for Clinical Decision Making and Systematic Collection of Real World Data to Improve Quality of Health Care nanCOMPLETED
Role of USP35 in the Detection of Ferroptosis in Juvenile Autoimmune Hepatitis nanNOT_YET_RECRUITING
Natural History Study of FDXR Mutation-related Mitochondriopathy nanCOMPLETED
Genetic Regulation of Surfactant Deficiency nanCOMPLETED
Hemochromatosis and Iron Overload Screening Study (HEIRS) nanCOMPLETED
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
GDF 15 in Sickle Cell Disease and Hereditary Spherocytosis nanUNKNOWN
Investigations Into ISCU Myopathy or Iron Sulfur Scaffold U Protein Myopathy nanCOMPLETED
Pumilio1 (PUM1) Expression, Sickle Cell Anemia, β-thalassemia Intermedia nanNOT_YET_RECRUITING
Role of Inflammasome in Platelet Activation in Sickle Cell Disease Patient nanCOMPLETED
Incidence of Iron Deficiency in Polycythemia Vera (PV) and Association With Disease Features nanUNKNOWN
Analysis of Post-Translational Modifications of a Critical Protein Implicated in Amyotrophic Lateral Sclerosis nanCOMPLETED
Use of miRNAs in Growth Hormone Deficiency (GHD) nanUNKNOWN
Better Delineation of DDX3X Related Phenotype and Epigenetic Signature. nanUNKNOWN
Study of the Genetic Factors Involved in Autism and Related Disorders nanRECRUITING
Pilot Study of Non-Invasive Assessment of Hepatic And Myocardial Iron Through T2* Magnet Resonance Imaging (MRI) In Patients With Iron Overload nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a SFXN3 binder may also engage these)

ProteinNameSimilarity
Q5RD16 1.000 Q5RD16 →
A6QP55 1.000 A6QP55 →
Q9JHY2 1.000 Q9JHY2 →
Q91V61 1.000 Q91V61 →
Q9VN13 1.000 Q9VN13 →
B2LU20 1.000 B2LU20 →
Q925N2 1.000 Q925N2 →
SFXN1 Sideroflexin-1 1.000 landscape →
Q12029 1.000 Q12029 →
Q63965 1.000 Q63965 →
Q99JR1 1.000 Q99JR1 →
Q5FC79 1.000 Q5FC79 →
Q5E9M8 1.000 Q5E9M8 →
Q5EA43 1.000 Q5EA43 →
Q96NB2 1.000 Q96NB2 →
A5A761 1.000 A5A761 →
O13793 1.000 O13793 →
Q3T0M2 1.000 Q3T0M2 →
Q9VVW3 0.999 Q9VVW3 →
A8E7G5 0.998 A8E7G5 →
Q09201 0.997 Q09201 →
Q54NQ9 0.996 Q54NQ9 →
Q6P4A7 0.995 Q6P4A7 →
Q925N1 0.991 Q925N1 →
P53311 0.984 P53311 →
P38857 0.983 P38857 →
Q9VW12 0.983 Q9VW12 →
B4LE89 0.982 B4LE89 →
Q8IQ56 0.982 Q8IQ56 →
B4KZ16 0.982 B4KZ16 →