Species

KNApSAcK Entry

Organism name Vitex cannabifolia Sieb.et.Zucc.
Genus Vitex
Family Labiatae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Vitex
Linked NCBI taxonomy ID 54476
Linked level genus

Family

Family in NCBI taxonomy Lamiaceae
ID 4136

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (10)

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
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
C00000320 External link 512 Geniposide
CHEMBL462894
CHEMBL1417490
CHEMBL1718933
C007835
3 / 2 / 3 3 / 0 No. 100 No. 36
C00032499 External link 512 Vitecannaside B
No. 174 No. 22
C00032498 External link 512 Vitecannaside A
No. 174 No. 22
C00030122 External link 512 Detetrahydroconidendrin
CHEMBL486411
No. 561
C00032502 External link 512 Vitrofolal F
CHEMBL486413
No. 561
C00032501 External link 512 Vitrofolal E
CHEMBL486412
No. 561
C00003068 External link 512 Agnuside
/ Buddlejoside A
CHEMBL391454
CHEMBL483223
1 / 0 / 0 No. 1380 No. 36
C00029374 External link 512 10-O-vanillate
/ (-)-Pedunculariside
/ 10-o-Vanilloyl aucubin
No. 1380 No. 36

Human Protein / Gene in interactions

30 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00001055 C00001078 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001055 C00001078 1 / 2
O00255 Menin Unclassified protein C00001055 C00001078 2 / 5
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
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00001055 C00001078 1 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00001055 C00001078 0 / 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
Q9Y253 DNA polymerase eta Enzyme C00001055 C00001078 1 / 1
Q9Y468 Lethal(3)malignant brain tumor-like protein 1 Unclassified protein C00001055 C00001078 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000320 C00001055 0 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00001055 C00001078 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00001055 C00001078 0 / 0
O75496 Geminin Unclassified protein C00000320 0 / 0
P39748 Flap endonuclease 1 Enzyme C00001055 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00001078 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00000320 2 / 3
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00001078 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00001078 3 / 1
P09917 Arachidonate 5-lipoxygenase Oxidoreductase C00003068 0 / 0
Q99700 Ataxin-2 Unclassified protein C00001078 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

3 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
581 BAX, BCL2L4 BCL2-associated X protein C00000320
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00000320
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00000320

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (20)

OMIM preferred title UniProt
#114500 Colorectal cancer; crc Q14191
#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
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#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
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (21)

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)
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)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (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)
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