class name | count |
---|---|
asterids | 35 |
eudicotyledons | 8 |
Liliopsida | 1 |
rosids | 1 |
class name | count |
---|---|
Lamiaceae | 28 |
Ranunculaceae | 8 |
Apiaceae | 5 |
Boraginaceae | 2 |
Malvaceae | 1 |
Araceae | 1 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
figure |
---|---|---|---|---|---|---|
C00002770
![]() |
Rosmarinic acid
|
CHEMBL66966
CHEMBL324842 CHEMBL1315100 CHEMBL2111558 |
48 / 35 / 38 |
![]() |
||
C00037499
![]() |
Methyl rosmarinate
/ (+)-Methyl rosmarinate |
CHEMBL241405
CHEMBL1765650 |
6 / 5 / 4 |
![]() |
||
C00037774
![]() |
Salvianolic acid D
|
![]() |
||||
C00041433
![]() |
Cimicifugic acid A
/ (+)-Cimicifugic acid A |
CHEMBL517537
|
![]() |
|||
C00041434
![]() |
Cimicifugic acid B
/ (+)-Cimicifugic acid B |
CHEMBL500586
|
![]() |
|||
C00041435
![]() |
Cimicifugic acid D
/ (+)-Cimicifugic acid D |
CHEMBL1095596
|
![]() |
|||
C00041436
![]() |
Cimicifugic acid E
/ (+)-Cimicifugic acid E |
CHEMBL1095920
|
![]() |
|||
C00041437
![]() |
Cimicifugic acid F
/ (+)-Cimicifugic acid F |
CHEMBL1097936
|
![]() |
|||
C00041438
![]() |
Cimicifugic acid G
|
CHEMBL487192
|
1 / 0 / 0 |
![]() |
||
C00041531
![]() |
Fukinolic acid
|
CHEMBL487192
|
C116090
|
1 / 0 / 0 |
![]() |
|
C00047808
![]() |
Clinopodic acid A
/ (+)-Clinopodic acid A |
CHEMBL1079231
|
![]() |
|||
C00047809
![]() |
Clinopodic acid B
/ (+)-Clinopodic acid B |
CHEMBL1080778
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P34969 | 5-hydroxytryptamine receptor 7 | Serotonin receptor | C00041438 C00041531 | 0 / 0 |
P03956 | Interstitial collagenase | M10A | C00002770 C00037499 | 0 / 1 |
P12931 | Proto-oncogene tyrosine-protein kinase Src | Src | C00002770 | 0 / 0 |
P14618 | Pyruvate kinase PKM | Enzyme | C00002770 | 0 / 0 |
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00002770 | 0 / 3 |
Q13093 | Platelet-activating factor acetylhydrolase | Enzyme | C00002770 | 3 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00002770 | 0 / 0 |
P04062 | Glucosylceramidase | Enzyme | C00002770 | 6 / 4 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00002770 | 1 / 1 |
P39900 | Macrophage metalloelastase | M10A | C00037499 | 0 / 0 |
P14780 | Matrix metalloproteinase-9 | M10A | C00037499 | 2 / 2 |
O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00002770 | 0 / 0 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00002770 | 3 / 1 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002770 | 1 / 0 |
P06241 | Tyrosine-protein kinase Fyn | Src | C00002770 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00002770 | 0 / 1 |
P54132 | Bloom syndrome protein | Enzyme | C00002770 | 1 / 2 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00002770 | 1 / 0 |
P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00002770 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00002770 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00002770 | 0 / 0 |
P15121 | Aldose reductase | Enzyme | C00002770 | 0 / 0 |
P40763 | Signal transducer and activator of transcription 3 | Transcription Factor | C00002770 | 1 / 2 |
Q07820 | Induced myeloid leukemia cell differentiation protein Mcl-1 | Other cytosolic protein | C00002770 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00002770 | 1 / 1 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002770 | 0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00002770 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00002770 | 0 / 0 |
P45452 | Collagenase 3 | M10A | C00037499 | 1 / 1 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00002770 | 0 / 0 |
P08253 | 72 kDa type IV collagenase | M10A | C00037499 | 1 / 3 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002770 | 3 / 3 |
P51692 | Signal transducer and activator of transcription 5B | Unclassified protein | C00002770 | 1 / 1 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002770 | 2 / 2 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00002770 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00002770 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002770 | 0 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002770 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00002770 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00002770 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00002770 | 4 / 3 |
P06239 | Tyrosine-protein kinase Lck | Src | C00002770 | 0 / 1 |
P08254 | Stromelysin-1 | M10A | C00037499 | 1 / 0 |
Q12794 | Hyaluronidase-1 | Enzyme | C00002770 | 1 / 2 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00002770 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002770 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00002770 | 0 / 0 |
P42224 | Signal transducer and activator of transcription 1-alpha/beta | Unclassified protein | C00002770 | 3 / 3 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00002770 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00002770 | 1 / 1 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00002770 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00002770 | 1 / 4 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00002770 | 0 / 0 |
Q9H0H5 | Rac GTPase-activating protein 1 | Unclassified protein | C00002770 | 0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#600807 | Asthma, susceptibility to |
Q13093
|
#209950 | Atypical mycobacteriosis, familial |
P42224
|
#210900 | Bloom syndrome; blm |
P54132
|
#614162 | Candidiasis, familial, 7; candf7 |
P42224
|
#614466 | Coronary heart disease, susceptibility to, 6; chds6 |
P08254
|
#119900 | Digital clubbing, isolated congenital |
P15428
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#608013 | Gaucher disease, perinatal lethal |
P04062
|
#230800 | Gaucher disease, type i |
P04062
|
#230900 | Gaucher disease, type ii |
P04062
|
#231000 | Gaucher disease, type iii |
P04062
|
#231005 | Gaucher disease, type iiic |
P04062
|
#232300 | Glycogen storage disease ii |
P10253
|
#245590 | Growth hormone insensitivity with immunodeficiency |
P51692
|
#147060 | Hyper-ige recurrent infection syndrome, autosomal dominant |
P40763
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#147050 | Ige responsiveness, atopic; iger |
Q13093
|
#603932 | Intervertebral disc disease; idd |
P14780
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#613073 | Metaphyseal anadysplasia 2; mandp2 |
P14780
|
#601492 | Mucopolysaccharidosis, type ix; mps9 |
Q12794
|
#259600 | Multicentric osteolysis, nodulosis, and arthropathy; mona |
P08253
|
#613796 | Mycobacterial and viral infections, susceptibility to, autosomal recessive |
P42224
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#168600 | Parkinson disease, late-onset; pd |
P04062
|
#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
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#602111 | Spondyloepimetaphyseal dysplasia, missouri type |
P45452
|
#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
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00028 | Choriocarcinoma |
P03956
(related)
P08253 (related) |
H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
H00126 | Gaucher disease |
P04062
(related)
|
H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
H00093 | Combined immunodeficiencies (CIDs) |
P06239
(related)
|
H00025 | Penile cancer |
P08253
(related)
P14780 (related) P35354 (related) |
H00472 | Torg-Winchester syndrome |
P08253
(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)
|
H00479 | Metaphyseal dysplasias |
P14780
(related)
P45452 (related) |
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00017 | Esophageal cancer |
P35354
(related)
|
H00046 | Cholangiocarcinoma |
P35354
(related)
|
H00016 | Oral cancer |
P40763
(related)
|
H00107 | Other well-defined immunodeficiency syndromes |
P40763
(related)
|
H00089 | IFN-gamma/IL-12 axis |
P42224
(related)
|
H00363 | Candidiasis |
P42224
(related)
|
H01109 | Chronic mucocutaneous candidiasis (CMC) |
P42224
(related)
|
H00931 | Growth hormone insensitivity with immunodeficiency |
P51692
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(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)
|
H00133 | Mucopolysaccharidosis type IX (MPS9) |
Q12794
(related)
|
H00421 | Mucopolysaccharidosis (MPS) |
Q12794
(related)
|
H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|