Showing entry for Huntingtin


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT010341
Protein NameHuntingtin
Uniport IdP42858
GeneHTT
Gene Id3064
DomainDUF3652
Pfam PF12372  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
6. Human Diseases 6.4 Neurodegenerative diseases hsa05016 Huntington disease
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0006915 apoptotic process
Biological Process GO:0000132 establishment of mitotic spindle orientation
Biological Process GO:0007030 Golgi organization
Biological Process GO:0099111 microtubule-based transport
Biological Process GO:2001237 negative regulation of extrinsic apoptotic signaling pathway
Biological Process GO:1905337 positive regulation of aggrephagy
Biological Process GO:0043065 positive regulation of apoptotic process
Biological Process GO:1903599 positive regulation of autophagy of mitochondrion
Biological Process GO:0045724 positive regulation of cilium assembly
Biological Process GO:0031587 positive regulation of inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity
Biological Process GO:1904504 positive regulation of lipophagy
Biological Process GO:0031648 protein destabilization
Biological Process GO:1905289 regulation of CAMKK-AMPK signaling cascade
Biological Process GO:2000479 regulation of cAMP-dependent protein kinase activity
Biological Process GO:0043666 regulation of phosphoprotein phosphatase activity
Biological Process GO:0006890 retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum
Biological Process GO:0047496 vesicle transport along microtubule
Biological Process GO:0042297 vocal learning
molecular function GO:0048487 beta-tubulin binding
molecular function GO:0034452 dynactin binding
molecular function GO:0045505 dynein intermediate chain binding
molecular function GO:0031072 heat shock protein binding
molecular function GO:0042802 identical protein binding
molecular function GO:0044325 ion channel binding
molecular function GO:0019900 kinase binding
molecular function GO:0002039 p53 binding
molecular function GO:0005522 profilin binding
cellular component GO:0005776 autophagosome
cellular component GO:0030424 axon
cellular component GO:0005814 centriole
cellular component GO:0005737 cytoplasm
cellular component GO:0030659 cytoplasmic vesicle membrane
cellular component GO:0005829 cytosol
cellular component GO:0030425 dendrite
cellular component GO:0005769 early endosome
cellular component GO:0005783 endoplasmic reticulum
cellular component GO:0005794 Golgi apparatus
cellular component GO:0016234 inclusion body
cellular component GO:0005770 late endosome
cellular component GO:0005654 nucleoplasm
cellular component GO:0005634 nucleus
cellular component GO:0048471 perinuclear region of cytoplasm
cellular component GO:0099524 postsynaptic cytosol
cellular component GO:0032991 protein-containing complex
Reactome
Pathway Id Pathway Name
R-HSA-212436 Generic Transcription Pathway
R-HSA-73857 RNA Polymerase II Transcription
R-HSA-74160 Gene expression (Transcription)
R-HSA-8986944 Transcriptional Regulation by MECP2
R-HSA-9022692 Regulation of MECP2 expression and activity
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0000768 BXGD000007 Congenital Abnormality Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0001973 BXGD000095 Alcoholic Intoxication, Chronic Chemically-Induced Disorders; Mental Disorders
C0002395 BXGD000111 Alzheimer's Disease Nervous System Diseases; Mental Disorders
C0002726 BXGD000125 Amyloidosis Nutritional and Metabolic Diseases
C0002736 BXGD000127 Amyotrophic Lateral Sclerosis Nutritional and Metabolic Diseases; Nervous System Diseases
C0003467 BXGD000194 Anxiety Behavior and Behavior Mechanisms
C0003469 BXGD000195 Anxiety Disorders Mental Disorders
C0004134 BXGD000256 Ataxia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0004352 BXGD000269 Autistic Disorder Mental Disorders
C0004936 BXGD000295 Mental disorders Mental Disorders
C0006111 BXGD000369 Brain Diseases Nervous System Diseases
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0006325 BXGD000393 Bruxism Stomatognathic Diseases
C0006635 BXGD000402 Cadmium poisoning Chemically-Induced Disorders
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007222 BXGD000454 Cardiovascular Diseases Cardiovascular Diseases
C0007758 BXGD000475 Cerebellar Ataxia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0007787 BXGD000487 Transient Ischemic Attack Nervous System Diseases; Cardiovascular Diseases
C0008489 BXGD000546 Chorea Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0009241 BXGD000595 Cognition Disorders Mental Disorders
C0010674 BXGD000683 Cystic Fibrosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Respiratory Tract Diseases
C0011168 BXGD000700 Deglutition Disorders Digestive System Diseases; Otorhinolaryngologic Diseases
C0011265 BXGD000708 Presenile dementia Nervous System Diseases; Mental Disorders
C0011570 BXGD000729 Mental Depression Behavior and Behavior Mechanisms
C0011581 BXGD000733 Depressive disorder Mental Disorders
C0013421 BXGD000837 Dystonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0015674 BXGD001012 Chronic Fatigue Syndrome Infections; Musculoskeletal Diseases; Nervous System Diseases
C0016667 BXGD001072 Fragile X Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0017639 BXGD001133 Gliosis Pathological Conditions, Signs and Symptoms
C0017654 BXGD001136 Glomerular Filtration Rate
C0018799 BXGD001224 Heart Diseases Cardiovascular Diseases
C0019196 BXGD001301 Hepatitis C Digestive System Diseases; Infections
C0019829 BXGD001350 Hodgkin Disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0020179 BXGD001363 Huntington Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
C0020256 BXGD001370 Congenital Hydrocephalus Nervous System Diseases
C0021053 BXGD001476 Immune System Diseases Immune System Diseases
C0021704 BXGD001510 Intelligence Behavior and Behavior Mechanisms
C0022107 BXGD001530 Irritable Mood Behavior and Behavior Mechanisms
C0022336 BXGD001535 Creutzfeldt-Jakob disease Infections; Nervous System Diseases; Mental Disorders
C0022360 BXGD001541 Jaw Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
C0022821 BXGD001590 Kyphosis deformity of spine Musculoskeletal Diseases
C0023418 BXGD001642 leukemia Neoplasms
C0023480 BXGD001664 Leukemia, Myelomonocytic, Chronic Neoplasms; Hemic and Lymphatic Diseases
C0023508 BXGD001675 White Blood Cell Count procedure
C0024408 BXGD001768 Machado-Joseph Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0026650 BXGD001913 Movement Disorders Nervous System Diseases
C0026837 BXGD001937 Muscle Rigidity Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0026838 BXGD001938 Muscle Spasticity Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0026847 BXGD001940 Spinal Muscular Atrophy Nervous System Diseases
C0027066 BXGD001966 Myoclonus Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0027092 BXGD001971 Myopia Eye Diseases
C0027627 BXGD002006 Neoplasm Metastasis Pathological Conditions, Signs and Symptoms; Neoplasms
C0027765 BXGD002033 nervous system disorder Nervous System Diseases
C0027819 BXGD002043 Neuroblastoma Neoplasms
C0028738 BXGD002081 Nystagmus Eye Diseases; Nervous System Diseases
C0028768 BXGD002084 Obsessive-Compulsive Disorder Mental Disorders
C0030193 BXGD002191 Pain Pathological Conditions, Signs and Symptoms
C0030567 BXGD002240 Parkinson Disease Nervous System Diseases
C0032584 BXGD002363 polyps Pathological Conditions, Signs and Symptoms
C0036341 BXGD002600 Schizophrenia Mental Disorders
C0036439 BXGD002615 Scoliosis, unspecified Musculoskeletal Diseases
C0036572 BXGD002625 Seizures Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0036857 BXGD002638 Severe intellectual disability Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0040822 BXGD002885 Tremor Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0041696 BXGD002932 Unipolar Depression Mental Disorders
C0042345 BXGD002977 Varicosity Cardiovascular Diseases
C0085078 BXGD003118 Lysosomal Storage Diseases Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0085631 BXGD003214 Agitation Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0086132 BXGD003264 Depressive Symptoms Behavior and Behavior Mechanisms
C0087012 BXGD003318 Ataxia, Spinocerebellar Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0151514 BXGD003429 Atrophic condition of skin Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0151611 BXGD003447 Electroencephalogram abnormal Nervous System Diseases
C0151889 BXGD003498 Hyperreflexia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0162429 BXGD003942 Malnutrition Nutritional and Metabolic Diseases
C0178874 BXGD004037 Tumor Progression Pathological Conditions, Signs and Symptoms
C0205682 BXGD004105 Waist-Hip Ratio
C0205710 BXGD004112 Alpers Syndrome (disorder) Immune System Diseases; Nervous System Diseases
C0220597 BXGD004292 Adult Hodgkin Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0231686 BXGD004508 Gait, Unsteady Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0232197 BXGD004536 Fibrillation Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0232466 BXGD004543 Feeding difficulties
C0233401 BXGD004575 Psychiatric symptom
C0233514 BXGD004584 Abnormal behavior Behavior and Behavior Mechanisms
C0233565 BXGD004590 Bradykinesia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0233794 BXGD004618 Memory impairment Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms
C0234132 BXGD004623 Pyramidal sign Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0234985 BXGD004708 Mental deterioration Mental Disorders
C0235031 BXGD004714 Neurologic Symptoms Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0235946 BXGD004789 Cerebral atrophy Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0236642 BXGD004815 Pick Disease of the Brain Nervous System Diseases; Mental Disorders
C0238651 BXGD004951 Ankle clonus
C0240735 BXGD005052 Personality Change Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0242422 BXGD005163 Parkinsonian Disorders Nervous System Diseases
C0266487 BXGD005682 Etat Marbre Nervous System Diseases
C0268407 BXGD005936 Senile cardiac amyloidosis Nutritional and Metabolic Diseases; Cardiovascular Diseases
C0270814 BXGD006109 Spastic syndrome Nervous System Diseases
C0282193 BXGD006798 Iron Overload Nutritional and Metabolic Diseases
C0333463 BXGD006954 Senile Plaques Pathological Conditions, Signs and Symptoms
C0338451 BXGD007176 Frontotemporal dementia Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders
C0338656 BXGD007211 Impaired cognition Mental Disorders
C0344315 BXGD007666 Depressed mood Behavior and Behavior Mechanisms
C0376544 BXGD008001 Hematopoietic Neoplasms Neoplasms; Hemic and Lymphatic Diseases
C0393525 BXGD008081 Progressive cerebellar ataxia Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0393574 BXGD008095 Huntington Disease, Late Onset Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
C0393578 BXGD008098 Pallidoluysian degeneration Nervous System Diseases
C0398568 BXGD008194 Blood group deletion syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0424295 BXGD008524 Hyperactive behavior Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0426980 BXGD008599 Motor symptoms
C0427086 BXGD008605 Involuntary Movements Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0432072 BXGD008718 Dysmorphic features
C0474702 BXGD008957 Sulfate measurement
C0497202 BXGD009055 Abnormal ocular motility
C0497327 BXGD009061 Dementia Nervous System Diseases; Mental Disorders
C0497552 BXGD009067 Congenital neurologic anomalies Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0524528 BXGD009229 Pervasive Development Disorder Mental Disorders
C0524851 BXGD009246 Neurodegenerative Disorders Nervous System Diseases
C0525045 BXGD009255 Mood Disorders Mental Disorders
C0557874 BXGD009444 Global developmental delay
C0575802 BXGD009521 Small hand
C0576226 BXGD009527 Short foot
C0596887 BXGD009648 mathematical ability
C0677050 BXGD009714 Manganese Poisoning Nervous System Diseases; Chemically-Induced Disorders
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0700095 BXGD009875 Central neuroblastoma Neoplasms; Nervous System Diseases
C0740279 BXGD009973 Cerebellar atrophy
C0742028 BXGD010051 Cerebellar vermis atrophy
C0742078 BXGD010055 Mass lesion of brain
C0750901 BXGD010242 Alzheimer Disease, Early Onset Nervous System Diseases; Mental Disorders
C0751072 BXGD010312 Frontotemporal Lobar Degeneration Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders
C0751207 BXGD010348 Akinetic-Rigid Variant of Huntington Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
C0751208 BXGD010349 Juvenile Huntington Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
C0751706 BXGD010559 Primary Progressive Nonfluent Aphasia Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Nervous System Diseases; Mental Disorders
C0751781 BXGD010590 Dentatorubral-Pallidoluysian Atrophy Nervous System Diseases
C0751837 BXGD010604 Gait Ataxia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751870 BXGD010622 Heredodegenerative Disorders, Nervous System Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0752120 BXGD010668 Spinocerebellar Ataxia Type 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0752125 BXGD010673 Spinocerebellar Ataxia Type 7 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0854193 BXGD011005 Cognitive deterioration
C0854723 BXGD011026 Retinal Dystrophies Eye Diseases
C0856863 BXGD011122 Broad-based gait
C0856975 BXGD011127 Autistic behavior Behavior and Behavior Mechanisms
C0878544 BXGD011368 Cardiomyopathies Cardiovascular Diseases
C0948163 BXGD011511 Leukoaraiosis Pathological Conditions, Signs and Symptoms
C0949664 BXGD011583 Tauopathies Nervous System Diseases
C1262477 BXGD011882 Weight decreased Pathological Conditions, Signs and Symptoms
C1269683 BXGD012001 Major Depressive Disorder Mental Disorders
C1269955 BXGD012005 Tumor Cell Invasion
C1285162 BXGD012167 Degenerative disorder Pathological Conditions, Signs and Symptoms
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1334804 BXGD012740 Motor Manifestations Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1458155 BXGD013136 Mammary Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C1531647 BXGD013301 Cerebral ventriculomegaly Nervous System Diseases
C1535926 BXGD013322 Neurodevelopmental Disorders Mental Disorders
C1611743 BXGD013456 Familial (FPAH)
C1836830 BXGD014165 Developmental regression Mental Disorders
C1839259 BXGD014363 Bulbo-Spinal Atrophy, X-Linked Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C1846707 BXGD014836 SPINOCEREBELLAR ATAXIA 17 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C1847987 BXGD014900 HUNTINGTON DISEASE-LIKE 2 Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
C1848673 BXGD014963 Hypoplastic feet
C1850496 BXGD015147 Neuronal loss in central nervous system
C1853743 BXGD015358 Muscular hypotonia of the trunk Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1854882 BXGD015439 Absent speech Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1855008 BXGD015449 Mitochondrial Complex II Deficiency Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C1859098 BXGD015850 Chorea, Benign Familial Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1963060 BXGD016679 Agitation, CTCAE 3.0
C2220255 BXGD016956 Motor disturbances
C2700617 BXGD017474 Irritation - emotion Behavior and Behavior Mechanisms
C2718001 BXGD017521 Protein Misfolding Disorders Nutritional and Metabolic Diseases
C2718017 BXGD017522 TDP-43 Proteinopathies Nutritional and Metabolic Diseases; Nervous System Diseases
C2750913 BXGD017685 Neuronal loss in basal ganglia
C2752147 BXGD017769 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C2936349 BXGD018109 Plaque, Amyloid Pathological Conditions, Signs and Symptoms
C2939419 BXGD018178 Secondary Neoplasm Pathological Conditions, Signs and Symptoms; Neoplasms
C3273225 BXGD018648 Hereditary Neurodegenerative Disorder Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C3278923 BXGD018748 Dilated ventricles (finding)
C3711380 BXGD019386 Huntington Disease-Like Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C3714756 BXGD019429 Intellectual Disability Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C4021776 BXGD020772 Abnormality of the voice
C4022592 BXGD020932 Oral motor hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C4022855 BXGD021013 Abnormal involuntary eye movements
C4086165 BXGD022126 Childhood Neuroblastoma Neoplasms
C4479476 BXGD022936 MENTAL RETARDATION, AUTOSOMAL RECESSIVE 60
C4479491 BXGD022937 LOPES-MACIEL-RODAN SYNDROME
C4551583 BXGD023361 Cerebral cortical atrophy
C4551584 BXGD023362 Brain atrophy Nervous System Diseases
C4552810 BXGD023525 Irritability, CTCAE
C4552855 BXGD023528 Agitation, CTCAE 5.0
C4553743 BXGD023548 Spasticity, CTCAE
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0000164 Oxoglaucine 351.35
BXGC0000194 Sanguinarine 332.33
BXGC0000430 Gossypol 518.55
BXGC0000504 Vanillic acid 168.15
BXGC0000573 Dantron 240.21
BXGC0001544 Harmaline 214.26
BXGC0001767 (E)-Resveratrol 228.25
BXGC0001988 4-Acetyl-2-prenylphenol 204.26
BXGC0002616 Copper 63.55
BXGC0003249 5-Hexyl-2-methylpyridine 270.37
BXGC0003696 Quercetin 3-O-methyl-ether 316.26
BXGC0004576 2-tert-Butyl-1,4-benzenediol 166.22
BXGC0005043 1-Hydroxy-10-methylacridone 225.24
BXGC0005458 Oxopurpureine 381.38
BXGC0005982 Curcumin 368.38
BXGC0006306 Myricetin 318.24
BXGC0006422 Mercenene 214.05
BXGC0007028 beta-Thujaplicin 164.2
BXGC0012377 Nagilactone B 364.15
BXGC0013414 Trehalose 342.12
BXGC0015314 1-(2,6-Dihydroxyphenyl)Dodecan-1-One 292.2
BXGC0015879 Chlorhexidine 504.2
BXGC0016333 artesunic acid 384.18
BXGC0016470 Camptothecin 348.11
BXGC0016891 Nortriptyline 263.17
BXGC0017232 Dipyrithione 252
BXGC0018004 \N 186.08
BXGC0019091 D-Tryptophan 204.09
BXGC0019348 Angustibalin 304.13
BXGC0019377 Cumingianoside A 738.46
BXGC0020737 Protoapigenone 286.05
BXGC0020873 Aromaticin 246.13
BXGC0021716 (R)-Verapamil 454.28
BXGC0023633 Kamebanin 334.21
BXGC0024428 3-(1H-Benzimidazol-2-Yl)-7-(Diethylamino)Chromen-2-One 333.15
BXGC0025200 2-Anilinonaphthalene-1,4-Dione 249.08
BXGC0025603 [(9R,10R)-10-Acetyloxy-8,8-Dimethyl-2-Oxo-9,10-Dihydropyrano[2,3-F]Chromen-9-Yl] (Z)-2-Methylbut-2-Enoate 386.14
BXGC0025757 Calcimycin 523.27
BXGC0026480 Osajin 404.16
BXGC0027259 Tryptanthrin 248.06
BXGC0027583 dihydroartemisinin 284.16
BXGC0028067 Enniatin B 639.41
BXGC0029291 Diphyllin 380.09
BXGC0031326 Paxilline 435.24
BXGC0033577 Interiotherin C 556.23
BXGC0034768 Vincristine 824.4
BXGC0035575 6-(2-Methylbut-3-En-2-Yl)Furo[3,2-G]Chromen-7-One 254.09
BXGC0036860 Helenalin 262.12
BXGC0037718 Ethacrynic Acid 302.01
BXGC0038183 Artemisin 282.15
BXGC0038400 [(9R,10R)-8,8-Dimethyl-9-[(Z)-2-Methylbut-2-Enoyl]Oxy-2-Oxo-9,10-Dihydropyrano[2,3-F]Chromen-10-Yl] (Z)-2-Methylbut-2-Enoate 426.17
BXGC0038486 (2S)-3-[(2S,3S)-5,7-Dihydroxy-2-(4-Methoxyphenyl)-4-Oxo-2,3-Dihydrochromen-3-Yl]-5,7-Dihydroxy-2-(4-Methoxyphenyl)-2,3-Dihydrochromen-4-One 570.15
BXGC0038546 [(3Ar,4S,6Z,9E,11S,11Ar)-11-Hydroxy-6,10-Dimethyl-3-Methylidene-2,8-Dioxo-4,5,11,11A-Tetrahydro-3Ah-Cyclodeca[B]Furan-4-Yl] 2-Methylprop-2-Enoate 346.14
BXGC0038807 curine 594.27
BXGC0039281 Methyl (1S,4As,5As,6R,10As)-1-Methyl-2'-Oxospiro[1,4A,5,5A,7,8,10,10A-Octahydropyrano[3,4-F]Indolizine-6,3'-1H-Indole]-4-Carboxylate 368.17
BXGC0039520 [(3Ar,4S,6Z,9E,11S,11Ar)-11-Hydroxy-6,10-Dimethyl-3-Methylidene-2,8-Dioxo-4,5,11,11A-Tetrahydro-3Ah-Cyclodeca[B]Furan-4-Yl] (E)-2-Methylbut-2-Enoate 360.16
BXGC0039684 Berberine Chloride 336.12
BXGC0040949 Hydroxyprogesterone Caproate 428.29
BXGC0041560 Thiram 239.99
BXGC0042035 raubasine 352.18
BXGC0042046 Actinodaphnine 311.12
BXGC0042091 Dequalinium 456.33
BXGC0042252 Homoharringtonine 545.26
BXGC0042414 2-[(E)-2-Phenylethenyl]-2,3-Dihydropyran-6-One 200.08
BXGC0042510 Fluoxetine 309.13
BXGC0044245 2,4-Dibromo-6-(2,4-Dibromophenoxy)Phenol 497.71
BXGC0046281 Cucurbitacin B 558.32
BXGC0046510 Tpck 351.07
BXGC0047086 4-[(2R)-2-[(1R,3R,5S)-3,5-Dimethyl-2-Oxocyclohexyl]-2-Hydroxyethyl]Piperidine-2,6-Dione 281.16
BXGC0049049 Haplamine 257.11
BXGC0049758 Corosolic Acid 472.36
BXGC0050471 Fluorouracil 130.02
BXGC0052595 (5R,9R,10R,13S,14S,17S)-4,4,10,13,14-Pentamethyl-17-[(2S,4R,5S)-4,5,6-Trihydroxy-6-Methylheptan-2-Yl]-1,2,5,6,9,11,12,15,16,17-Decahydrocyclopenta[A]Phenanthren-3-One 474.37
BXGC0053334 2,3-Diphenylcycloprop-2-En-1-One 206.07
BXGC0053641 Nagilactone A 348.16
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein