CLIC1

Chloride intracellular channel protein 1 · O00299 · CLIC1 on Sugi Atlas →

1,422 patent compounds predicted against CLIC1, 1,291 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL4699731 SCHEMBL4699731 1.00 2/20
SCHEMBL4697866 SCHEMBL4697866 0.89 2/20
SCHEMBL4697696 SCHEMBL4697696 0.86 2/20
SCHEMBL4699947 SCHEMBL4699947 0.83 2/20
SCHEMBL4699140 SCHEMBL4699140 0.80 2/20
SCHEMBL4922941 SCHEMBL4922941 0.80 2/20
SCHEMBL4916509 SCHEMBL4916509 0.78 2/20
SCHEMBL4700123 SCHEMBL4700123 0.77 2/20
SCHEMBL4698636 SCHEMBL4698636 0.76 2/20
SCHEMBL4914334 SCHEMBL4914334 0.76 2/20
SCHEMBL4917606 SCHEMBL4917606 0.76 2/20
SCHEMBL4908396 SCHEMBL4908396 0.74 2/20
SCHEMBL4699183 SCHEMBL4699183 0.74 2/20
SCHEMBL4914310 SCHEMBL4914310 0.73 2/20
SCHEMBL4915098 SCHEMBL4915098 0.73 2/20
SCHEMBL4696222 SCHEMBL4696222 0.72 2/20
SCHEMBL4701699 SCHEMBL4701699 0.70 2/20
SCHEMBL4698169 SCHEMBL4698169 0.70 2/20
SCHEMBL4696537 SCHEMBL4696537 0.68 2/20
SCHEMBL4920392 SCHEMBL4920392 0.66 2/20

Clinical trials — most relevant to CLIC1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Efficacy and Safety of Tigerase® vs. Pulmozyme® in Patients With Cystic Fibrosis PHASE3COMPLETED
Safety, Tolerability, and Efficacy of PLX-200 in Patients With CLN3 PHASE3NOT_YET_RECRUITING
Intravitreal ERT to Prevent Retinal Disease Progression in Children With CLN2 PHASE1/PHASE2ACTIVE_NOT_RECRUITING
Safety and Tolerability of Inhaled Nitric Oxide in Patients With Cystic Fibrosis PHASE1/PHASE2COMPLETED
Aerosolized Hypertonic Xylitol Versus Hypertonic Saline in Cystic Fibrosis (CF) Subjects PHASE1/PHASE2COMPLETED
Inhaled Xylitol Versus Saline in Stable Subjects With Cystic Fibrosis PHASE1/PHASE2COMPLETED
Ivacaftor for Acquired CFTR Dysfunction in Chronic Rhinosinusitis EARLY_PHASE1RECRUITING
Mechanism and Effects of Manipulating Chloride Homeostasis in Stable Heart Failure EARLY_PHASE1COMPLETED
Examining Developmental Outcomes of Children Diagnosed With CLN2 Disease nanENROLLING_BY_INVITATION
A Natural History Study of RYR1-Related Disorders nanRECRUITING
Natural History of Neuronal Ceroid Lipofuscinosis, Batten's CLN6 Diseae nanACTIVE_NOT_RECRUITING
Microbiome Acquisition and Progression of Inflammation and Airway Disease in Infants and Children With Cystic Fibrosis nanCOMPLETED
Investigations of Juvenile Neuronal Ceroid Lipofuscinosis nanRECRUITING
Comparison Between Ultra-low-dose Computed Tomography and Lung MRI in Cystic Fibrosis nanCOMPLETED
Genetics of Reproductive Disorders (Including Kallmann Syndrome) and Cleft Lip and/or Palate nanRECRUITING
The Effect of Adding Lubiprostone to Standard Large-Volume PEG-ELS on The Quality of Inpatient Colonoscopy Preparation nanWITHDRAWN
Development of an Artificial Intelligence Algorithm to Detect Pathological Repolarization Disorders on the ECG and the Risk of Ventricular Arrhythmias nanRECRUITING
Wolfram Syndrome and WFS1-related Disorders International Registry and Clinical Study nanRECRUITING
Genetic Analysis of Craniosynostosis, Philadelphia Type nanCOMPLETED
Genome Sequencing in the Intensive Care Unit Population nanENROLLING_BY_INVITATION
A Single Center Prospective Study in an Estimated 570 Patients Who Underwent Genetic Screening at UZ Brussel in the Context of a Primary Cardiac Arrhythmia. Patients Showing a Variant Class 3,4 or 5 in SCN4A or CLCN1 Will Undergo a Clinical and Electrophysiological Review After IC. nanNOT_YET_RECRUITING
Energy Balance and Weight Gain With Ivacaftor Treatment nanCOMPLETED
Na+ Channel mRNA Regulation in Heart Failure nanCOMPLETED
Bone Microarchitecture at the Radius: a Pilot Comparison Between Children With Cystic Fibrosis and Healthy Controls nanCOMPLETED
Clinical and Genetic Analysis of Enlarged Vestibular Aqueducts nanCOMPLETED
Genomic Sequencing for Evaluation of Fetal Structural Anomalies nanENROLLING_BY_INVITATION
Neurogenetics Patient Registry nanRECRUITING
Gastrostomy-Biliary Diversion: Innovative Management for Bile Canalicular Transport Disorders nanUNKNOWN
Clinical and Genetic Analysis in Congenital Hypothyroidism Due to Thyroid Dysgenesis. nanCOMPLETED
Genetic Analysis of Parkinson's Disease nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a CLIC1 binder may also engage these)

ProteinNameSimilarity
Q9Z1Q5 1.000 Q9Z1Q5 →
Q6MG61 1.000 Q6MG61 →
Q5E9B7 1.000 Q5E9B7 →
Q95MF9 1.000 Q95MF9 →
Q9EPT8 0.997 Q9EPT8 →
Q9Z0W7 0.996 Q9Z0W7 →
Q5M883 0.996 Q5M883 →
Q5R957 0.994 Q5R957 →
CLIC4 Chloride intracellular channel protein 4 0.994 landscape →
Q9FG59 0.993 Q9FG59 →
Q9XSA7 0.993 Q9XSA7 →
Q9QYB1 0.993 Q9QYB1 →
Q8BXK9 0.992 Q8BXK9 →
O15247 0.991 O15247 →
Q6NLB0 0.990 Q6NLB0 →
P25317 0.989 P25317 →
Q9D7P7 0.988 Q9D7P7 →
O45405 0.988 O45405 →
Q65XA0 0.987 Q65XA0 →
Q4WB03 0.987 Q4WB03 →
A0A1U8QXK4 0.987 A0A1U8QXK4 →
O95833 0.987 O95833 →
Q9FUT0 0.986 Q9FUT0 →
P34277 0.986 P34277 →
Q10N44 0.985 Q10N44 →
Q9C8M3 0.985 Q9C8M3 →
P49248 0.985 P49248 →
Q9LZ06 0.984 Q9LZ06 →
Q29238 0.984 Q29238 →
GSTA1 Glutathione S-transferase A1 0.984 landscape →