CHD1

Chromodomain-helicase-DNA-binding protein 1 · O14646 · CHD1 on Sugi Atlas →

1,033 patent compounds predicted against CHD1, 863 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
SCHEMBL14844528 SCHEMBL14844528 1.00 3/20
SCHEMBL25205454 SCHEMBL25205454 1.00 3/20
SCHEMBL25228095 SCHEMBL25228095 0.87 3/20
SCHEMBL25239433 SCHEMBL25239433 0.87 3/20
SCHEMBL23682942 SCHEMBL23682942 0.83 3/20
SCHEMBL23682930 SCHEMBL23682930 0.81 3/20
SCHEMBL23682932 SCHEMBL23682932 0.81 3/20
SCHEMBL18179252 SCHEMBL18179252 0.80 3/20
SCHEMBL20525068 SCHEMBL20525068 0.80 3/20
SCHEMBL19598912 SCHEMBL19598912 0.80 3/20
SCHEMBL25198767 SCHEMBL25198767 0.79 3/20
SCHEMBL25203229 SCHEMBL25203229 0.78 3/20
SCHEMBL25239635 SCHEMBL25239635 0.78 3/20
SCHEMBL23718000 SCHEMBL23718000 0.74 3/20
SCHEMBL22265265 SCHEMBL22265265 0.74 3/20
SCHEMBL16568970 SCHEMBL16568970 0.73 3/20
SCHEMBL20303897 SCHEMBL20303897 0.72 3/20
SCHEMBL20351018 SCHEMBL20351018 0.72 3/20
Formic Acid Formic Acid (SCHEMBL20336820) 0.67 3/20
SCHEMBL20720595 SCHEMBL20720595 0.67 3/20

Clinical trials — most relevant to CHD1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Cornelia De Lange Syndrome: Assessing Positive Effects of Lithium Treatment PHASE2/PHASE3RECRUITING
Compared the Efficacy and Safety of CDOP Combined With Chidamide and CDOP in de Novo Peripheral T Cell Lymphoma Patients PHASE3UNKNOWN
PhII 5-Azacytidine Plus Valproic Acid and Eventually Atra in Intermediate II and High Risk MDS PHASE2COMPLETED
Trial of the Histone-Deacetylase Inhibitor ITF2357 Followed by Mechlorethamine in Relapsed/Refractory Hodgkin's Lymphoma PHASE1/PHASE2COMPLETED
An Open-Label, Proof of Consent Study of Vorinostat for the Treatment of Mdoerate-to-Severe Crohn s Disease and Maintenance Therapy With Ustekinumab PHASE1/PHASE2RECRUITING
Panobinostat and Epirubicin in Treating Patients With Metastatic Malignant Solid Tumors PHASE1COMPLETED
Evaluation of the Safety and the Tolerability of a Combination of Two HIV Inducers in Patients With Undetectable Viral Load PHASE1COMPLETED
Study of Cytolytic Viral Activation Therapy (CVAT) for Recurrent/Metastatic Nasopharyngeal Carcinoma PHASE1UNKNOWN
Studying The Role of Key Epigenetic Mediators in Breast Cancer Patients nanRECRUITING
Global Profiling of Gene and Protein Expression Associated With Coronary Heart Disease Reversal nanCOMPLETED
Genetics of Congenital Heart Disease nanRECRUITING
Accelerated Aging in Newborns and Adults With Congenital Heart Disease nanUNKNOWN
Genes Associated With Development of Pulmonary Arterial Hypertension in Patients With Congenital Shunt Lesions nanRECRUITING
UTHealth Turner Syndrome Research Registry nanRECRUITING
X-chromosome Inactivation, Epigenetics and the Transcriptome nanCOMPLETED
Research for Genetic Factors Involved in Congenital Dislocation of Hip: Genome-wide Association Study in Grand West France nanCOMPLETED
Clinical and Molecular Study of CHARGE Syndrom nanCOMPLETED
CMOP Regimen and Chidamide in the Treatment of Newly Diagnosed Peripheral T-cell Lymphoma nanUNKNOWN
dbGaP Protocol: The Pediatric Cardiac Genetics Consortium (PCGC) nanCOMPLETED
Studying Genes in Samples From Younger Patients With Relapsed Acute Lymphoblastic Leukemia nanCOMPLETED
Antenatal Investigation of Fetuses With Complex Congenital Heart Defects Using multiOMICS nanRECRUITING
Molecular Genetic Epidemiology of Three Cardiac Defects -SCOR in Pediatric Cardiovascular Disease nanCOMPLETED
The Sequencing for Detection in Congenital Heart Disease (SD-CHD) Study nanRECRUITING
DNA Methylation and Autoimmune Thyroid Diseases nanCOMPLETED
Chromosomal Abnormalities in Patients With Congenital Heart Disease at Assiut University Children's Hospital nanNOT_YET_RECRUITING
Genetic Markers of Coronary Heart Disease in Type 2 Diabetes nanCOMPLETED
Effect of Adenovirus E1A Oncogene on DNA Replication Dynamics nanUNKNOWN
Proteomic-Based Profiling of Lymphomas: Chromatin Proteomics; Composition and Modification of Histone and Non-Histone Chromosomal Proteins nanCOMPLETED
Diagnosis of RSTS: Identification of the Acetylation Profiles as Epigenetic Markers for Assessing Causality of CREBBP and EP300 Variants. nanUNKNOWN
Genetic of SportS Induced Endofibrotic Remodeling nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a CHD1 binder may also engage these)

ProteinNameSimilarity
B6ZLK2 1.000 B6ZLK2 →
P40201 1.000 P40201 →
E9PZM4 1.000 E9PZM4 →
O14647 1.000 O14647 →
D3ZA12 1.000 D3ZA12 →
A3KFM7 1.000 A3KFM7 →
Q8TD26 0.999 Q8TD26 →
Q7G8Y3 0.996 Q7G8Y3 →
Q04692 0.996 Q04692 →
B0R061 0.996 B0R061 →
Q8RWY3 0.995 Q8RWY3 →
B5VE38 0.995 B5VE38 →
F4JY24 0.995 F4JY24 →
Q7KU24 0.995 Q7KU24 →
Q7ZU90 0.994 Q7ZU90 →
O14139 0.994 O14139 →
Q9S775 0.994 Q9S775 →
Q9Y4B4 0.993 Q9Y4B4 →
E1B7X9 0.993 E1B7X9 →
D3Z9Z9 0.993 D3Z9Z9 →
P32657 0.993 P32657 →
C7GQI8 0.993 C7GQI8 →
O16102 0.993 O16102 →
A5E3K3 0.993 A5E3K3 →
P34739 0.992 P34739 →
Q9H4L7 0.992 Q9H4L7 →
A6ZL17 0.992 A6ZL17 →
Q9US25 0.992 Q9US25 →
O74393 0.992 O74393 →
Q9H1H9 0.992 Q9H1H9 →