class name | count |
---|---|
Magnoliophyta | 17 |
Liliopsida | 5 |
asterids | 2 |
class name | count |
---|---|
Piperaceae | 12 |
Zingiberaceae | 5 |
Lauraceae | 3 |
Gesneriaceae | 2 |
Annonaceae | 2 |
br08003 Category | # of metabolite |
---|---|
alpha-Pyrones | 5 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
alpha-Pyrones | C09925 | C00002987 |
alpha-Pyrones | C09926 | C00002988 |
alpha-Pyrones | C09947 | C00003000 |
alpha-Pyrones | C09952 | C00003005 |
alpha-Pyrones | C09980 | C00003024 |
alpha-Pyrones | C09925 | C00029550 |
KCF-S ID | # of metabolite |
---|---|
No. 1312 | 7 |
No. 2531 | 4 |
No. 3123 | 3 |
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 |
figure |
---|---|---|---|---|---|---|---|
C00002987
![]() |
p-Hydroxy-5,6-dehydrokawain
/ 4'-Hydroxy-5,6-dehydrokawain |
CHEMBL464111
|
No. 1312 |
![]() |
|||
C00045571
![]() |
Goniothalamin
/ (+)-Goniothalamin |
CHEMBL464443
CHEMBL1170485 CHEMBL1240592 |
C103280
|
22 / 32 / 24 | 16 / 0 | No. 1312 |
![]() |
C00043208
![]() |
Hydroxykavain
|
No. 1312 |
![]() |
||||
C00029551
![]() |
Methysticin
|
CHEMBL579224
CHEMBL1883024 |
C076881
|
10 / 14 / 40 | No. 1312 |
![]() |
|
C00003024
![]() |
10-Methoxyyagonin
|
No. 1312 |
![]() |
||||
C00029373
![]() |
5,6-Dehydromethysticin
|
CHEMBL1946690
|
No. 1312 |
![]() |
|||
C00029550
![]() |
Dihydromethysticin
|
CHEMBL576066
CHEMBL1510786 |
11 / 2 / 3 | No. 1312 |
![]() |
||
C00029378
![]() |
5,6-Dehydro-7,8-dihydromethysticin
|
CHEMBL1376695
|
3 / 0 / 0 | No. 2531 |
![]() |
||
C00003005
![]() |
5,6-Dehydrokawain
|
CHEMBL254218
|
C052297
|
12 / 16 / 44 | No. 2531 |
![]() |
|
C00029583
![]() |
11-Hydroxy-12-methoxydihydrokavain
|
No. 2531 |
![]() |
||||
C00002988
![]() |
Yangonin
|
CHEMBL1098658
|
C110481
|
16 / 25 / 49 | No. 2531 |
![]() |
|
C00037211
![]() |
Kawain
|
CHEMBL578607
CHEMBL1473874 CHEMBL1482039 |
18 / 11 / 7 | No. 3123 |
![]() |
||
C00003000
![]() |
5,6-Dehydrokawain
/ Desmethoxyyangonin |
CHEMBL254218
|
12 / 16 / 44 | No. 3123 |
![]() |
||
C00030497
![]() |
Marindinin
/ 7,8-Dihydrokavain |
CHEMBL569329
CHEMBL1338909 |
C113859
|
5 / 3 / 5 | No. 3123 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P19793 | Retinoic acid receptor RXR-alpha | NR2B1 | C00002987 C00002988 C00003000 C00003005 C00003024 C00029550 C00029583 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00002987 C00002988 C00003000 C00003005 C00003024 C00029550 C00037211 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002987 C00002988 C00003000 C00003005 C00029550 C00029583 | 0 / 1 |
P51449 | Nuclear receptor ROR-gamma | Nuclear hormone receptor subfamily 1 group F member 3 | C00002987 C00002988 C00003000 C00003005 C00003024 C00029550 | 0 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00002987 C00002988 C00003000 C00003005 C00003024 C00029550 | 0 / 0 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00002987 C00003000 C00003005 C00003024 C00029550 | 4 / 1 |
Q96RI1 | Bile acid receptor | NR1H4 | C00002987 C00002988 C00003005 C00003024 C00029550 | 0 / 0 |
Q03181 | Peroxisome proliferator-activated receptor delta | NR1C2 | C00002987 C00002988 C00003000 C00029550 C00029583 | 0 / 0 |
P04637 | Cellular tumor antigen p53 | Transcription Factor | C00002987 C00003005 C00003024 C00029550 | 7 / 37 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00003000 C00003024 C00037211 | 4 / 3 |
O75496 | Geminin | Unclassified protein | C00002988 C00003000 C00037211 | 0 / 0 |
P10275 | Androgen receptor | NR3C4 | C00002987 C00029550 C00029583 | 3 / 4 |
P35869 | Aryl hydrocarbon receptor | Transcription Factor | C00002987 C00003024 C00029550 | 0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00003000 C00037211 C00043208 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00003000 C00037211 C00043208 | 0 / 0 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002987 C00003024 C00029550 | 2 / 2 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00003000 C00037211 | 1 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002988 C00037211 | 0 / 0 |
P10145 | Interleukin-8 | Secreted protein | C00003024 C00029583 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00037211 C00043208 | 0 / 0 |
O60674 | Tyrosine-protein kinase JAK2 | Jakb | C00037211 | 5 / 1 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00037211 | 0 / 0 |
P04150 | Glucocorticoid receptor | NR3C1 | C00003024 | 0 / 1 |
P37231 | Peroxisome proliferator-activated receptor gamma | NR1C3 | C00003024 | 5 / 3 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00037211 | 1 / 2 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00037211 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00003000 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00003024 | 3 / 3 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00037211 | 2 / 0 |
P42858 | Huntingtin | Unclassified protein | C00037211 | 1 / 1 |
Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00003000 | 0 / 0 |
P03372 | Estrogen receptor | NR3A1 | C00002988 | 1 / 1 |
P55210 | Caspase-7 | C14 | C00003024 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00003000 | 1 / 1 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00003000 | 0 / 1 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00003005 | 3 / 2 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00037211 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00037211 | 11 / 10 |
P29466 | Caspase-1 | C14 | C00003024 | 0 / 0 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00037211 | 2 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00037211 | 1 / 1 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00003005 | 0 / 0 |
O14980 | Exportin-1 | Unclassified protein | C00037211 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00003000 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00002988 | 1 / 1 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00037211 | 1 / 0 |
O00255 | Menin | Unclassified protein | C00037211 | 2 / 5 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00037211 | 2 / 1 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00003000 | 1 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
306 | ANXA3, ANX3 | annexin A3 (EC:3.1.4.43) |
C00037211
|
581 | BAX, BCL2L4 | BCL2-associated X protein |
C00037211
|
596 | BCL2, Bcl-2, PPP1R50 | B-cell CLL/lymphoma 2 |
C00037211
|
835 | CASP2, CASP-2, ICH1, NEDD-2, NEDD2, PPP1R57 | caspase 2, apoptosis-related cysteine peptidase (EC:3.4.22.55) |
C00037211
|
836 | CASP3, CPP32, CPP32B, SCA-1 | caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) |
C00037211
|
841 | CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 | caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) |
C00037211
|
842 | CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 | caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) |
C00037211
|
54205 | CYCS, CYC, HCS, THC4 | cytochrome c, somatic |
C00037211
|
4193 | MDM2, ACTFS, HDMX, hdm2 | MDM2 oncogene, E3 ubiquitin protein ligase |
C00037211
|
4842 | NOS1, IHPS1, N-NOS, NC-NOS, NOS, bNOS, nNOS | nitric oxide synthase 1 (neuronal) (EC:1.14.13.39) |
C00037211
|
4846 | NOS3, ECNOS, eNOS | nitric oxide synthase 3 (endothelial cell) (EC:1.14.13.39) |
C00037211
|
142 | PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 | poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) |
C00037211
|
5366 | PMAIP1, APR, NOXA | phorbol-12-myristate-13-acetate-induced protein 1 |
C00037211
|
5970 | RELA, NFKB3, p65 | v-rel avian reticuloendotheliosis viral oncogene homolog A |
C00037211
|
7132 | TNFRSF1A, CD120a, FPF, MS5, TBP1, TNF-R, TNF-R-I, TNF-R55, TNFAR, TNFR1, TNFR1-d2, TNFR55, TNFR60, p55, p55-R, p60 | tumor necrosis factor receptor superfamily, member 1A |
C00037211
|
7157 | TP53, BCC7, LFS1, P53, TRP53 | tumor protein p53 |
C00037211
|
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#202300 | Adrenocortical carcinoma, hereditary; adcc |
P04637
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#300068 | Androgen insensitivity syndrome; ais |
P10275
|
#312300 | Androgen insensitivity, partial; pais |
P10275
|
#614740 | Basal cell carcinoma, susceptibility to, 7; bcc7 |
P04637
|
%606641 | Body mass index; bmi |
P37231
|
#600880 | Budd-chiari syndrome; bdchs |
O60674
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#609338 | Carotid intimal medial thickness 1 |
P37231
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#114500 | Colorectal cancer; crc |
P84022
Q14191 |
#119900 | Digital clubbing, isolated congenital |
P15428
|
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#133239 | Esophageal cancer |
P04637
|
#615363 | Estrogen resistance; estrr |
P03372
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
P37231 |
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#143100 | Huntington disease; hd |
P42858
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#601626 | Leukemia, acute myeloid; aml |
O60674
|
#151623 | Li-fraumeni syndrome 1; lfs1 |
P04637
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#604367 | Lipodystrophy, familial partial, type 3; fpld3 |
P37231
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#211980 | Lung cancer |
P04637
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
#300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#254450 | Myelofibrosis |
O60674
|
#601665 | Obesity |
P37231
|
#260500 | Papilloma of choroid plexus; cpp |
P04637
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#263300 | Polycythemia vera; pv |
O60674
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
#253300 | Spinal muscular atrophy, type i; sma1 |
Q16637
|
#253550 | Spinal muscular atrophy, type ii; sma2 |
Q16637
|
#253400 | Spinal muscular atrophy, type iii; sma3 |
Q16637
|
#271150 | Spinal muscular atrophy, type iv; sma4 |
Q16637
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#275355 | Squamous cell carcinoma, head and neck; hnscc |
P04637
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#614521 | Thrombocythemia 3; thcyt3 |
O60674
|
#277700 | Werner syndrome; wrn |
Q14191
|
KEGG | name | UniProt |
---|---|---|
H00033 | Adrenal carcinoma |
O00255
(related)
P04637 (related) |
H00034 | Carcinoid |
O00255
(related)
|
H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
H00246 | Primary hyperparathyroidism |
O00255
(related)
|
H01102 | Pituitary adenomas |
O00255
(related)
|
H00012 | Polycythemia vera |
O60674
(related)
O60674 (marker) |
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
P37231 (related) |
H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
H00663 | Restrictive dermopathy |
P02545
(related)
|
H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
|
H00026 | Endometrial Cancer |
P03372
(marker)
P04637 (related) |
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P04150
(related)
|
H00004 | Chronic myeloid leukemia (CML) |
P04637
(related)
|
H00005 | Chronic lymphocytic leukemia (CLL) |
P04637
(related)
|
H00006 | Hairy-cell leukemia |
P04637
(related)
|
H00008 | Burkitt lymphoma |
P04637
(related)
|
H00009 | Adult T-cell leukemia |
P04637
(related)
|
H00010 | Multiple myeloma |
P04637
(related)
|
H00013 | Small cell lung cancer |
P04637
(related)
|
H00014 | Non-small cell lung cancer |
P04637
(related)
|
H00015 | Malignant pleural mesothelioma |
P04637
(related)
|
H00016 | Oral cancer |
P04637
(related)
P04637 (marker) |
H00017 | Esophageal cancer |
P04637
(related)
P04637 (marker) |
H00018 | Gastric cancer |
P04637
(related)
|
H00019 | Pancreatic cancer |
P04637
(related)
P04637 (marker) |
H00020 | Colorectal cancer |
P04637
(related)
P04637 (marker) |
H00022 | Bladder cancer |
P04637
(related)
|
H00025 | Penile cancer |
P04637
(related)
P04637 (marker) |
H00027 | Ovarian cancer |
P04637
(related)
|
H00028 | Choriocarcinoma |
P04637
(related)
|
H00029 | Vulvar cancer |
P04637
(related)
|
H00031 | Breast cancer |
P04637
(related)
|
H00032 | Thyroid cancer |
P04637
(related)
P37231 (related) |
H00036 | Osteosarcoma |
P04637
(related)
P08684 (marker) |
H00038 | Malignant melanoma |
P04637
(related)
|
H00039 | Basal cell carcinoma |
P04637
(related)
|
H00040 | Squamous cell carcinoma |
P04637
(related)
|
H00041 | Kaposi's sarcoma |
P04637
(related)
|
H00042 | Glioma |
P04637
(related)
P04637 (marker) |
H00044 | Cancer of the anal canal |
P04637
(related)
|
H00046 | Cholangiocarcinoma |
P04637
(related)
|
H00047 | Gallbladder cancer |
P04637
(related)
|
H00048 | Hepatocellular carcinoma |
P04637
(related)
|
H00055 | Laryngeal cancer |
P04637
(related)
P04637 (marker) |
H00881 | Li-Fraumeni syndrome |
P04637
(related)
|
H01007 | Choroid plexus papilloma |
P04637
(related)
|
H00021 | Renal cell carcinoma |
P04637
(marker)
|
H00024 | Prostate cancer |
P10275
(related)
|
H00062 | Spinal and bulbar muscular atrophy (SBMA) |
P10275
(related)
|
H00608 | 46,XY disorders of sex development (Disorders in androgen synthesis or action) |
P10275
(related)
|
H00609 | 46,XY disorders of sex development (Other) |
P10275
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00409 | Type II diabetes mellitus |
P37231
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (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)
|