SIN3A

Paired amphipathic helix protein Sin3a · Q96ST3 · SIN3A on Sugi Atlas →

0 patent compounds predicted against SIN3A, 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 SIN3A by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Efficacy and Safety Assessment of Oral LBH589 in Adult Patients With Advanced Soft TIssue Sarcoma After Pre-treatment Failure PHASE2COMPLETED
A Study of Bezafibrate in Mitochondrial Myopathy PHASE2COMPLETED
Temsirolimus and Sorafenib in Advanced Hepatocellular Carcinoma PHASE1COMPLETED
Study on the Interplay Between Twist1 and Other EMT Regulators Through microRNA-29 Family. nanUNKNOWN
Autophagy in Systemic Lupus Erythematosus nanUNKNOWN
Immune Cell Response to Stimuli nanRECRUITING
MiRNA223 and HMGB1 as Apredictos for Drug Resistant Epilepsy nanUNKNOWN
Association of SNPs in Long Intergenic Noncoding RNA 00511 (LINC00511) With Breast Cancer Among the Egyptian Population nanCOMPLETED
Role of SF3B1 Mutation in Assessment of Acute and Chronic Lymphatic Leukemia nanNOT_YET_RECRUITING
Role of the Nuclear Pore Component RANBP2 in Inflammatory Responses to Viral Infections nanCOMPLETED
SMYD3-Driven Metabolic Rewiring in Colorectal Liver Metastases nanNOT_YET_RECRUITING
Mapping Disease Pathways for Biliary Atresia nanRECRUITING
Thermogenic Silencer Regulatory Factors in Humans nanACTIVE_NOT_RECRUITING
High Altitude Medical Research Expedition Himlung 2013 - a Study of Human Adaption to Hypoxia nanCOMPLETED
Investigation of the Genetic Causes of Kallmann Syndrome and Reproductive Disorders nanCOMPLETED
Defining an Obesity QTL on Chromosome 3q nanCOMPLETED
Genetic Variants Associated With Adolescent Suicide Attempts nanCOMPLETED
Diagnosis of RSTS: Identification of the Acetylation Profiles as Epigenetic Markers for Assessing Causality of CREBBP and EP300 Variants. nanUNKNOWN
Defining the Brain Phenotype of Children With Williams Syndrome nanRECRUITING
Genetic Analysis of Heart Channelopathies in Brazilian Patients and Their Relatives nanUNKNOWN
Prevalence of a Non-Expressing 11B Mutation in Aka Peoples of the Central African Republic nanCOMPLETED
Changes in Skin Innervation of Neurologically Asymptomatic Type 2 Diabetic Patients: the Correlation With the Diabetic Parameters and Neurotrophins. nanUNKNOWN
Gene Analysis of Parkinson's Disease nanCOMPLETED
Pathogenesis of Primary Ciliary Dyskinesia (PCD) Lung Disease nanRECRUITING
Study of the Genetic Factors Involved in Autism and Related Disorders nanRECRUITING
Identification of a New Gene Involved in Hereditary Lipodystrophy nanCOMPLETED
Family Blood Pressure Program - HyperGEN nanCOMPLETED
The Phenotyping and Genotyping of Taiwanese Patients With Obstructive Sleep Apnea nanUNKNOWN
Transcripts with Retained H/ACA Box SnoRNA Sequences As Biomarkers for Estrogen Dependence in Lum-B Breast Carcinomas nanACTIVE_NOT_RECRUITING
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a SIN3A binder may also engage these)

ProteinNameSimilarity
Q60520 1.000 Q60520 →
Q62141 0.994 Q62141 →
SMARCC2 SWI/SNF complex subunit SMARCC2 0.992 landscape →
Q96G25 0.988 Q96G25 →
P70210 0.987 P70210 →
Q9D7W5 0.987 Q9D7W5 →
Q6PDG5 0.986 Q6PDG5 →
A5D794 0.986 A5D794 →
F4HPA7 0.986 F4HPA7 →
O54772 0.985 O54772 →
Q6P9Z1 0.985 Q6P9Z1 →
Q80TJ1 0.985 Q80TJ1 →
Q90701 0.984 Q90701 →
KAT2A Histone acetyltransferase KAT2A 0.984 landscape →
O75182 0.984 O75182 →
TEAD4 Transcriptional enhancer factor TEF-3 0.984 landscape →
Q69ZZ6 0.984 Q69ZZ6 →
CNOT1 CCR4-NOT transcription complex subunit 1 0.984 landscape →
O94915 0.984 O94915 →
Q3UQU0 0.984 Q3UQU0 →
O43439 0.984 O43439 →
SMARCC1 SWI/SNF complex subunit SMARCC1 0.984 landscape →
Q9H3P2 0.983 Q9H3P2 →
Q62296 0.983 Q62296 →
P97496 0.983 P97496 →
Q9EP53 0.983 Q9EP53 →
Q5R8Q4 0.983 Q5R8Q4 →
Q6GLR7 0.983 Q6GLR7 →
Q8BMP6 0.983 Q8BMP6 →
Q02225 0.983 Q02225 →