Organism name | Vitex cannabifolia Sieb.et.Zucc. |
---|---|
Genus | Vitex |
Family | Labiatae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Vitex |
---|---|
Linked NCBI taxonomy ID | 54476 |
Linked level | genus |
Family in NCBI taxonomy | Lamiaceae |
---|---|
ID | 4136 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | asterids |
---|---|
ID | 71274 |
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
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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
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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
![]() |
Geniposide
|
CHEMBL462894
CHEMBL1417490 CHEMBL1718933 |
C007835
|
3 / 2 / 3 | 3 / 0 | No. 100 | No. 36 |
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C00032499
![]() |
Vitecannaside B
|
No. 174 | No. 22 |
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||||
C00032498
![]() |
Vitecannaside A
|
No. 174 | No. 22 |
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||||
C00030122
![]() |
Detetrahydroconidendrin
|
CHEMBL486411
|
No. 561 |
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||||
C00032502
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Vitrofolal F
|
CHEMBL486413
|
No. 561 |
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||||
C00032501
![]() |
Vitrofolal E
|
CHEMBL486412
|
No. 561 |
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||||
C00003068
![]() |
Agnuside
/ Buddlejoside A |
CHEMBL391454
CHEMBL483223 |
1 / 0 / 0 | No. 1380 | No. 36 |
![]() |
||
C00029374
![]() |
10-O-vanillate
/ (-)-Pedunculariside / 10-o-Vanilloyl aucubin |
No. 1380 | No. 36 |
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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 |
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
|
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 | 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)
|