NDUFV2

NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial · P19404 · NDUFV2 on Sugi Atlas →

2,237 patent compounds predicted against NDUFV2, 1,369 high-confidence (nearest known ligand ≥ 0.5)

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

CompoundConfidenceSupporting neighbours
Auraptene Auraptene (SCHEMBL2535029) 1.00 5/20
Auraptene Auraptene (SCHEMBL2535034) 1.00 5/20
SCHEMBL8491443 SCHEMBL8491443 0.56 4/20
SCHEMBL8489900 SCHEMBL8489900 0.52 4/20
SCHEMBL8489907 SCHEMBL8489907 0.52 4/20
SCHEMBL8492838 SCHEMBL8492838 0.52 4/20
SCHEMBL8492845 SCHEMBL8492845 0.52 4/20
SCHEMBL8489902 SCHEMBL8489902 0.51 4/20
SCHEMBL8489908 SCHEMBL8489908 0.51 4/20
SCHEMBL8491154 SCHEMBL8491154 0.51 4/20
SCHEMBL8491160 SCHEMBL8491160 0.51 4/20
SCHEMBL8491619 SCHEMBL8491619 0.50 4/20
SCHEMBL8491624 SCHEMBL8491624 0.50 4/20
SCHEMBL8491634 SCHEMBL8491634 0.50 4/20
SCHEMBL8494171 SCHEMBL8494171 0.50 4/20
SCHEMBL8494175 SCHEMBL8494175 0.50 4/20
SCHEMBL8494177 SCHEMBL8494177 0.50 4/20
7-Prenyloxycoumarin 7-Prenyloxycoumarin (SCHEMBL4898255) 0.79 3/20
SCHEMBL712741 SCHEMBL712741 0.57 3/20
Geiparvarin Geiparvarin (SCHEMBL2532495) 0.56 3/20

Clinical trials — most relevant to NDUFV2 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Phase III Trial of Coenzyme Q10 in Mitochondrial Disease PHASE3COMPLETED
A Study of the Efficacy and Safety of MT1621 in Thymidine Kinase 2 (TK2) Deficiency (Treatment naïve) PHASE3WITHDRAWN
Coenzyme Q10 as a Symptomatic Treatment in Parkinson's Disease PHASE3COMPLETED
Mitochondrial Dysfunction in the Pathophysiology and Treatment of Bipolar Disorder PHASE2WITHDRAWN
Trial of Nicotinamide Riboside and Co-enzyme Q10 in Chronic Kidney Disease PHASE2COMPLETED
Efficacy of KL1333 in Adult Patients With Primary Mitochondrial Disease PHASE2RECRUITING
A Study to Evaluate Vitamin B3 Derivative to Treat Mitochondrial Myopathy PHASE2ACTIVE_NOT_RECRUITING
A Study of Bezafibrate in Mitochondrial Myopathy PHASE2COMPLETED
Nicotinamide Riboside on Mitochondrial Function in Li-Fraumeni Syndrome PHASE1/PHASE2COMPLETED
Does Clinical Treatment of Mitochondrial Dysfunction Impact Autism Spectrum Disorder (ASD)? PHASE1UNKNOWN
Genomic Profiling of Mitochondrial Disease - Imaging Analysis for Precise Mitochondrial Medicine nanCOMPLETED
Evaluation of Impact of Disease and Visual Disability on Quality of Life and Loss of Independence of Patients Living in France With Leber's Hereditary Optic Neuropathy (LHON) Through Qualitative and Quantitative Data Collection nanCOMPLETED
North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC) nanRECRUITING
Tissue Sample Study for Mitochondrial Disorders nanENROLLING_BY_INVITATION
MITOMICS : a Multi-OMICS Approach for the Diagnosis of Mitochondrial Diseases nanRECRUITING
The Natural History of Mitochondrial Diseases nanRECRUITING
Identification of Large-Scale Mutations of POLG Gene by QMPSF in Patients With Mitochondrial DNA Instability. nanUNKNOWN
Nicotinamide Riboside and Mitochondrial Biogenesis nanCOMPLETED
GDF-15 as a Biomarker for Mitochondrial Disease nanCOMPLETED
Natural History in Primary Mitochondrial Myopathies nanRECRUITING
Identification of New Candidate Genes in Patients With Mitochondrial Disease by High Resolution Chromosome Analysis on DNA Chip nanCOMPLETED
Effect of Subtle Energy Transmission and Tao Calligraphy Mindfulness Practice on Mitochondrial DNA in Peripheral Blood Leukocytes nanNOT_YET_RECRUITING
Survey on Supplement Use in Mitochondrial Disease nanCOMPLETED
The Genetics of Diabetes in Southern California Chinese Americans nanWITHDRAWN
Safety and Efficacy Study of rAAV2-ND4 Treatment of Leber Hereditary Optic Neuropathy (LHON) nanCOMPLETED
Ccf mtDNA as a Neurodegenerative Biomarker nanUNKNOWN
Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants nanRECRUITING
Cardiac Mitochondrial Function in Explanted Human Hearts nanUNKNOWN
A Study Into the Underlying Biochemical Pathways Involved in Parkinson's Disease, Such as Mitochondrial (Cellular Powerhouse) Dysfunction nanCOMPLETED
Mitoquines in COPD nanUNKNOWN

Related proteins — ESM-2 sequence neighbours (a NDUFV2 binder may also engage these)

ProteinNameSimilarity
Q0MQI9 1.000 Q0MQI9 →
P04394 1.000 P04394 →
Q0MQI7 1.000 Q0MQI7 →
Q0MQI8 1.000 Q0MQI8 →
Q9D6J6 0.999 Q9D6J6 →
P19234 0.997 P19234 →
Q20719 0.996 Q20719 →
P40915 0.995 P40915 →
Q54F10 0.982 Q54F10 →
O22769 0.979 O22769 →
P29914 0.971 P29914 →
Q11190 0.968 Q11190 →
P22944 0.964 P22944 →
Q4K8L6 0.964 Q4K8L6 →
SPTLC3 Serine palmitoyltransferase 3 0.964 landscape →
O23813 0.964 O23813 →
P46643 0.963 P46643 →
Q8IQF1 0.963 Q8IQF1 →
A9UZ24 0.962 A9UZ24 →
P45575 0.962 P45575 →
P94694 0.962 P94694 →
Q02252 0.962 Q02252 →
Q43644 0.962 Q43644 →
GOT2 Aspartate aminotransferase, mitochondrial 0.962 landscape →
Q9V7Y2 0.962 Q9V7Y2 →
A7SDA8 0.962 A7SDA8 →
Q5REB0 0.961 Q5REB0 →
Q54XM6 0.961 Q54XM6 →
Q4UM09 0.961 Q4UM09 →
O04630 0.961 O04630 →