SLC22A3

Solute carrier family 22 member 3 · O75751 · SLC22A3 on Sugi Atlas →

30,929 patent compounds predicted against SLC22A3, 25,711 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL166140 SCHEMBL166140 1.00 7/20
Phenylguanidine Phenylguanidine (SCHEMBL467577) 1.00 6/20
SCHEMBL164098 SCHEMBL164098 0.56 6/20
SCHEMBL247052 SCHEMBL247052 0.52 6/20
Iodide Iodide (SCHEMBL82245) 0.42 3/20
Famotidine Famotidine (SCHEMBL973) 1.00 2/20
Imipramine Imipramine (SCHEMBL34282) 1.00 2/20
Desipramine Desipramine (SCHEMBL34384) 1.00 2/20
Famotidine Famotidine (SCHEMBL39237) 1.00 2/20
Famotidine Famotidine (SCHEMBL458654) 1.00 2/20
Imipramine Imipramine (SCHEMBL41765) 0.97 2/20
Imipramine Imipramine (SCHEMBL41766) 0.97 2/20
Desipramine Desipramine (SCHEMBL41992) 0.97 2/20
Desipramine Desipramine (SCHEMBL41993) 0.94 2/20
11Beta-Hydroxyprogesterone 11Beta-Hydroxyprogesterone (SCHEMBL572275) 0.79 2/20
Desoxycorticosterone Desoxycorticosterone (SCHEMBL4065) 0.78 2/20
Desoxycorticosterone Desoxycorticosterone (SCHEMBL4066) 0.78 2/20
Quinaldine Blue Quinaldine Blue (SCHEMBL58012) 0.77 2/20
Quinaldine Blue Quinaldine Blue (SCHEMBL466982) 0.74 2/20
Famotidine Famotidine (SCHEMBL188452) 0.67 2/20

Clinical trials — most relevant to SLC22A3 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Genetic Basis for Variation in the Renal Elimination of Metformin PHASE4COMPLETED
Applying Proton Pump Inhibitor to Prevent and Treat Acute Fluctuating Hearing Loss in Patients With SLC26A4 Mutation PHASE2/PHASE3UNKNOWN
Treatment of Ectopic Calcification in Fahr's Disease or Syndrome PHASE2RECRUITING
Effect of, OAT3, on the Renal Secretion of Cefotaxime PHASE1COMPLETED
Pharmacokinetic Drug-Drug Interaction Study to Identify Biomarkers of Kidney Transporters EARLY_PHASE1COMPLETED
Gadoxetate Sodium Enhanced MRI as a Biomarker for Aggressive Prostate Cancer EARLY_PHASE1UNKNOWN
Natural History Study of SLC25A46 Mutation-related Mitochondriopathy nanCOMPLETED
Cancer and Hearing Loss Related in Children nanCOMPLETED
SLC13A5 Deficiency Natural History Study - Remote Only nanENROLLING_BY_INVITATION
Influence of OCTN2 Variants on Carnitine Status and Plasma Triglycerides nanCOMPLETED
Impact of Polymorphisms of OAT1, OAT3, and OCT2 on Transportation of Potential Nephrotoxic Drugs nanCOMPLETED
Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts nanCOMPLETED
Oxalate and Citrate in Humans - Response to Citrate nanRECRUITING
Study of ABCB1,SLC22A16 Drug Transporter Genes and Doxorubicin and Cyclophosphamide Toxicity in Brest Cancer Patient nanUNKNOWN
Bile Acid Effects in Fetal Arrhythmia Study nanUNKNOWN
Understanding Methotrexate Induced Gastrointestinal Intolerance in Juvenile Idiopathic Arthritis and Childhood Leukemia nanCOMPLETED
Effect of SLC01B1 (rs2306283) Polymorphism on the Efficacy and Safety Profile of Atorvastatin in Pakistani Population nanCOMPLETED
Autonomic Function in Patients With COPD nanCOMPLETED
Gastrostomy-Biliary Diversion: Innovative Management for Bile Canalicular Transport Disorders nanUNKNOWN
Genetics of Hyperuricemia Therapy in Hmong nanCOMPLETED
Cardiovascular Effects of Empagliflozine nanUNKNOWN
Coproporphyrine Isomers and Methotrexate Elimination nanCOMPLETED
Gyrate Atrophy Ocular and Systemic Study nanACTIVE_NOT_RECRUITING
Renal and Hepatic Clearance Following High-Dose Methotrexate in Childhood ALL nanCOMPLETED
Impact of Genetics on Metformin Pharmacokinetics nanCOMPLETED
Secondary Sclerosing Cholangitis in Critically Ill Patients nanACTIVE_NOT_RECRUITING
SLC13A5 Deficiency Natural History Study - United States Only nanENROLLING_BY_INVITATION
Role of the ATP7A Transporter in Ovarian Cancer nanCOMPLETED
Demographic, Metabolic, and Genomic Description of Neonates With Severe Hyperbilirubinemia nanCOMPLETED
Effect of Pharmacogenetics on Imatinib Plasma Level and Response nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a SLC22A3 binder may also engage these)

ProteinNameSimilarity
O88446 0.999 O88446 →
O02713 0.994 O02713 →
Q9WTW5 0.993 Q9WTW5 →
Q8MJI6 0.993 Q8MJI6 →
Q9R0W2 0.993 Q9R0W2 →
Q5R5H7 0.991 Q5R5H7 →
O76082 0.990 O76082 →
SLC22A2 Solute carrier family 22 member 2 0.989 landscape →
SLC22A1 Solute carrier family 22 member 1 0.989 landscape →
O08966 0.989 O08966 →
Q863T6 0.988 Q863T6 →
Q91WU2 0.988 Q91WU2 →
O77504 0.987 O77504 →
A9CB25 0.987 A9CB25 →
Q9R141 0.987 Q9R141 →
SLC22A4 Solute carrier family 22 member 4 0.987 landscape →
O70577 0.986 O70577 →
A7MBE0 0.985 A7MBE0 →
Q9Z306 0.985 Q9Z306 →
B2GV36 0.985 B2GV36 →
Q9Z0E8 0.985 Q9Z0E8 →
Q63089 0.984 Q63089 →
Q9WTN6 0.982 Q9WTN6 →
O70594 0.982 O70594 →
Q9Y226 0.981 Q9Y226 →
Q961J5 0.981 Q961J5 →
Q9R1U7 0.979 Q9R1U7 →
O57379 0.979 O57379 →
Q17QN9 0.977 Q17QN9 →
SLC22A16 Solute carrier family 22 member 16 0.977 landscape →