Organism name | Ostericum koreanum |
---|---|
Genus | Ostericum |
Family | Apiaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Ostericum grosseserratum |
---|---|
Linked NCBI taxonomy ID | 182415 |
Linked level | species |
Family in NCBI taxonomy | Apiaceae |
---|---|
ID | 4037 |
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 |
---|---|---|---|---|---|---|---|---|
C00031084
![]() |
Prim-O-Glucosylcimifugin
|
![]() |
||||||
C00029558
![]() |
5-Caffeoylquinic acid methyl ester
|
CHEMBL416955
CHEMBL596924 CHEMBL1765881 CHEMBL1765882 CHEMBL2048503 CHEMBL2349427 |
6 / 5 / 4 | No. 314 | No. 6 |
![]() |
||
C00029680
![]() |
Ammajin
/ Marmesinin / (-)-Marmesinin |
CHEMBL459825
|
11 / 8 / 6 | No. 399 | No. 25 |
![]() |
||
C00019796
![]() |
Bergaptol-O-beta-D-glucopyranoside
|
C067416
|
No. 491 | No. 25 |
![]() |
|||
C00029480
![]() |
3,4-di-O-Caffeoylquinic acid
/ (-)-4,5-Dicaffeoyl quinic acid |
CHEMBL358821
CHEMBL149674 CHEMBL177126 CHEMBL249448 CHEMBL453276 CHEMBL453537 CHEMBL1972460 |
2 / 0 / 0 | No. 518 | No. 6 |
![]() |
||
C00029481
![]() |
3,5-di-O-caffeate
/ sochlorogenic acid a / 3,5-Dicaffeoylquinic acid |
CHEMBL441250
CHEMBL249447 |
2 / 0 / 0 | No. 518 | No. 6 |
![]() |
||
C00030905
![]() |
Oxypeucedanin hydrate
/ (+)-Oxypeucedanin hydrate |
CHEMBL454060
CHEMBL1438253 |
13 / 5 / 8 | No. 579 | No. 25 |
![]() |
||
C00002668
![]() |
Protocatechuic acid
/ 3,4-Dihydroxybenzoic acid |
CHEMBL37537
|
C009091
|
33 / 19 / 19 | 2 / 0 | No. 817 | No. 81 |
![]() |
C00002421
![]() |
Cimifugin
|
No. 1426 | No. 15 |
![]() |
||||
C00031338
![]() |
sec-O-Glucosylhamaudol
|
CHEMBL2059295
|
No. 5060 |
![]() |
||||
C00030658
![]() |
Ligustiphenol
/ (-)-Ligustiphenol |
No. 6953 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9UNA4 | DNA polymerase iota | Enzyme | C00002668 C00029680 C00030905 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00002668 C00029680 C00030905 | 0 / 0 |
P15121 | Aldose reductase | Enzyme | C00002668 C00029480 C00029481 | 0 / 0 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00002668 C00029680 C00030905 | 0 / 0 |
O60218 | Aldo-keto reductase family 1 member B10 | Enzyme | C00029480 C00029481 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002668 C00030905 | 0 / 0 |
P08254 | Stromelysin-1 | M10A | C00002668 C00029558 | 1 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002668 C00029680 | 1 / 1 |
P14780 | Matrix metalloproteinase-9 | M10A | C00002668 C00029558 | 2 / 2 |
P08253 | 72 kDa type IV collagenase | M10A | C00002668 C00029558 | 1 / 3 |
P06746 | DNA polymerase beta | Enzyme | C00002668 C00030905 | 0 / 0 |
P03956 | Interstitial collagenase | M10A | C00002668 C00029558 | 0 / 1 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00002668 C00030905 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00002668 C00030905 | 1 / 4 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00029680 C00030905 | 2 / 2 |
Q9Y253 | DNA polymerase eta | Enzyme | C00030905 | 1 / 1 |
P16581 | E-selectin | Adhesion | C00002668 | 0 / 0 |
Q9ULX7 | Carbonic anhydrase 14 | Lyase | C00002668 | 0 / 0 |
O43570 | Carbonic anhydrase 12 | Lyase | C00002668 | 1 / 2 |
P23280 | Carbonic anhydrase 6 | Lyase | C00002668 | 0 / 0 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00029680 | 1 / 0 |
P00915 | Carbonic anhydrase 1 | Lyase | C00002668 | 0 / 0 |
P07711 | Cathepsin L1 | C1A | C00002668 | 0 / 0 |
Q9GZT9 | Egl nine homolog 1 | Enzyme | C00002668 | 1 / 1 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00029680 | 0 / 0 |
P02768 | Serum albumin | Secreted protein | C00002668 | 0 / 0 |
P06280 | Alpha-galactosidase A | Enzyme | C00029680 | 1 / 1 |
P45452 | Collagenase 3 | M10A | C00029558 | 1 / 1 |
P56817 | Beta-secretase 1 | A1A | C00030905 | 0 / 0 |
Q16790 | Carbonic anhydrase 9 | Lyase | C00002668 | 0 / 1 |
P00918 | Carbonic anhydrase 2 | Lyase | C00002668 | 1 / 2 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00029680 | 2 / 2 |
P03372 | Estrogen receptor | NR3A1 | C00002668 | 1 / 1 |
P22303 | Acetylcholinesterase | Hydrolase | C00029680 | 1 / 0 |
P14151 | L-selectin | Adhesion | C00002668 | 0 / 0 |
P16109 | P-selectin | Adhesion | C00002668 | 1 / 0 |
P39900 | Macrophage metalloelastase | M10A | C00029558 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00030905 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00002668 | 4 / 3 |
P22894 | Neutrophil collagenase | M10A | C00002668 | 0 / 0 |
P22748 | Carbonic anhydrase 4 | Lyase | C00002668 | 1 / 1 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00030905 | 0 / 0 |
P43166 | Carbonic anhydrase 7 | Lyase | C00002668 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00029680 | 0 / 0 |
Q13093 | Platelet-activating factor acetylhydrolase | Enzyme | C00002668 | 3 / 0 |
P09917 | Arachidonate 5-lipoxygenase | Oxidoreductase | C00002668 | 0 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00002668 | 0 / 0 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00030905 | 1 / 1 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
1312 | COMT | catechol-O-methyltransferase (EC:2.1.1.6) |
C00002668
|
2023 | ENO1, ENO1L1, MPB1, NNE, PPH | enolase 1, (alpha) (EC:4.2.1.11) |
C00002668
|
OMIM | preferred title | UniProt |
---|---|---|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#600807 | Asthma, susceptibility to |
Q13093
|
#614466 | Coronary heart disease, susceptibility to, 6; chds6 |
P08254
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#609820 | Erythrocytosis, familial, 3; ecyt3 |
Q9GZT9
|
#615363 | Estrogen resistance; estrr |
P03372
|
#301500 | Fabry disease |
P06280
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#232300 | Glycogen storage disease ii |
P10253
|
#143860 | Hyperchlorhidrosis, isolated |
O43570
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#147050 | Ige responsiveness, atopic; iger |
Q13093
|
#603932 | Intervertebral disc disease; idd |
P14780
|
#613073 | Metaphyseal anadysplasia 2; mandp2 |
P14780
|
#259600 | Multicentric osteolysis, nodulosis, and arthropathy; mona |
P08253
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#614278 | Platelet-activating factor acetylhydrolase deficiency; pafad |
Q13093
|
#600852 | Retinitis pigmentosa 17; rp17 |
P22748
|
#602111 | Spondyloepimetaphyseal dysplasia, missouri type |
P45452
|
#601367 | Stroke, ischemic |
P16109
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
#112100 | Yt blood group antigen |
P22303
|
KEGG | name | UniProt |
---|---|---|
H01302 | Hyperchlorhidrosis isolated (HCHLH) |
O43570
(related)
|
H00021 | Renal cell carcinoma |
O43570
(marker)
Q16790 (marker) |
H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
H00436 | Osteopetrosis |
P00918
(related)
|
H00026 | Endometrial Cancer |
P03372
(marker)
|
H00028 | Choriocarcinoma |
P03956
(related)
P08253 (related) |
H00125 | Fabry disease |
P06280
(related)
|
H00025 | Penile cancer |
P08253
(related)
P14780 (related) |
H00472 | Torg-Winchester syndrome |
P08253
(related)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00479 | Metaphyseal dysplasias |
P14780
(related)
P45452 (related) |
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H00527 | Retinitis pigmentosa (RP) |
P22748
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00236 | Congenital polycythemia |
Q9GZT9
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|