Species

KNApSAcK Entry

Organism name Polygonum orientale
Genus Polygonum
Family Polygonaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Persicaria orientalis
Linked NCBI taxonomy ID 467334
Linked level species

Family

Family in NCBI taxonomy Polygonaceae
ID 3615

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class eudicotyledons
ID 71240

Metabolite list (9)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00005071 External link 512 3,5,8,3'-Tetramethoxy-6,7:4',5'-bis(methylenedioxy)flavone
No. 8 No. 15
C00005070 External link 512 3'-Hydroxy-3,5,8,4',5'-pentamethoxy-6,7-methylenedioxyflavone
No. 8 No. 15
C00005069 External link 512 5,3'-Dihydroxy-3,8,4',5'-tetramethoxy-6,7-methylenedioxyflavone
No. 8 No. 15
C00004867 External link 512 Digicitrin
CHEMBL470677
No. 8 No. 15
C00004871 External link 512 Exoticin
No. 8 No. 15
C00004869 External link 512 3'-Hydroxy-3,5,6,7,8,4',5'-heptamethoxyflavone
No. 8 No. 15
C00001078 External link 512 Lutexin
/ Orientin
/ Luteolin 8-C-beta-D-glucopyranoside
/ 8-beta-D-Glucopyranosyl-3',4',5,7-tetrahydroxyflavone
CHEMBL520866
CHEMBL1468796
C065886
20 / 15 / 14 No. 22 No. 15
C00001055 External link 512 Isoorientin
/ Homoorientin
/ Lespecapitioside
/ Luteolin 6-C-beta-D-glucopyranoside
/ 2-(3,4-Dihydroxyphenyl)-6-beta-D-glucopyranosyl-5,7-dihydroxy-4H-1-benzopyran-4-one
CHEMBL239559
CHEMBL1302308
C057912
23 / 14 / 17 0 / 1 No. 22 No. 15
C00000609 External link 512 (-)-Arctigenin
CHEMBL369142
CHEMBL435734
CHEMBL1966556
C071942
13 / 7 / 6 No. 223 No. 21

Human Protein / Gene in interactions

38 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UNA4 DNA polymerase iota Enzyme C00000609 C00001055 C00001078 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001055 C00001078 0 / 0
O00255 Menin Unclassified protein C00001055 C00001078 2 / 5
Q99700 Ataxin-2 Unclassified protein C00000609 C00001078 1 / 1
P06746 DNA polymerase beta Enzyme C00001055 C00001078 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00001055 C00001078 1 / 1
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00001055 C00001078 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001055 C00001078 1 / 1
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001055 C00001078 1 / 2
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00001055 C00001078 1 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00001055 C00001078 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00001055 C00001078 4 / 3
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00001055 C00001078 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00001055 C00001078 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00001055 C00001078 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00001055 C00001078 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00001055 C00001078 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00000609 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000609 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000609 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00001055 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000609 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000609 0 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00000609 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00000609 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000609 2 / 0
P39748 Flap endonuclease 1 Enzyme C00001055 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001078 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000609 0 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001078 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00001078 3 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000609 1 / 0
Q02750 Dual specificity mitogen-activated protein kinase kinase 1 Ste7 C00000609 1 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00001055 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00001055 1 / 4
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001055 0 / 0
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00001055 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00001055 2 / 1

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (23)

OMIM preferred title UniProt
#615279 Cardiofaciocutaneous syndrome 3; cfc3 Q02750
#114500 Colorectal cancer; crc P84022
Q14191
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#600274 Frontotemporal dementia; ftd P10636
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#257220 Niemann-pick disease, type c1; npc1 O15118
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (23)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00523 Noonan syndrome and related disorders Q02750 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00296 Defects in RecQ helicases Q14191 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D008104 Liver Cirrhosis, Alcoholic C00001055