class name | count |
---|---|
Magnoliophyta | 137 |
eudicotyledons | 97 |
rosids | 4 |
Liliopsida | 3 |
class name | count |
---|---|
Annonaceae | 99 |
Menispermaceae | 61 |
Papaveraceae | 34 |
Lauraceae | 16 |
Magnoliaceae | 8 |
Hernandiaceae | 6 |
Atherospermataceae | 3 |
Pieridae | 3 |
Aristolochiaceae | 3 |
Rutaceae | 2 |
Ranunculaceae | 2 |
Asparagaceae | 2 |
Siparunaceae | 2 |
Rhamnaceae | 1 |
Araceae | 1 |
Euphorbiaceae | 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 |
---|---|---|---|---|---|---|
C00001812
![]() |
Atheroline
|
C001827
|
![]() |
|||
C00001813
![]() |
Atherospermidine
|
C064684
|
![]() |
|||
C00001878
![]() |
Liriodenine
/ Oxoushinsunine / Spermatheridine |
CHEMBL37736
|
C026980
|
5 / 3 / 1 |
![]() |
|
C00024772
![]() |
Oxocompostelline
|
![]() |
||||
C00024773
![]() |
Oxocularine
|
CHEMBL510574
|
![]() |
|||
C00024774
![]() |
Oxosarcocapnidine
|
![]() |
||||
C00024775
![]() |
Oxosarcocapnine
|
![]() |
||||
C00024776
![]() |
Oxosarcophylline
|
![]() |
||||
C00025319
![]() |
Oxoxylopin
/ Oxoxylopine / Lanuginosine |
CHEMBL389400
|
1 / 4 / 2 |
![]() |
||
C00025339
![]() |
Oxocrebanine
/ 8,9-Dimethoxyliriodenine |
![]() |
||||
C00025340
![]() |
Oxostephanine
|
CHEMBL521933
|
![]() |
|||
C00025341
![]() |
Oxostephanosine
|
![]() |
||||
C00025349
![]() |
Thailandine
|
![]() |
||||
C00025354
![]() |
Uthongine
|
![]() |
||||
C00025773
![]() |
Bianfugecine
/ 5,9-Dimethoxy-7H-dibenzo[de,h]quinolin-7-one |
C046292
|
![]() |
|||
C00025774
![]() |
Bianfugedine
|
C046293
|
![]() |
|||
C00025775
![]() |
Bianfugenine
/ Dauriporphine |
C046294
|
![]() |
|||
C00025782
![]() |
Cassameridin
/ Cassameridine |
![]() |
||||
C00025840
![]() |
Dauriporphinoline
|
![]() |
||||
C00025849
![]() |
Dicentrinone
/ Oxodicentrine |
CHEMBL463284
|
1 / 0 / 0 |
![]() |
||
C00025890
![]() |
Liridine
/ Homomoschatoline / O-Methylmoschatoline / O-Methylisomoschatoline |
CHEMBL227533
|
![]() |
|||
C00025898
![]() |
Imenine
|
![]() |
||||
C00025935
![]() |
Lysicamine
/ Oxonuciferine |
CHEMBL510090
|
C069090
|
![]() |
||
C00025940
![]() |
Menisporphine
|
![]() |
||||
C00025992
![]() |
Oxoanolobine
|
![]() |
||||
C00025993
![]() |
Oxobuxifoline
|
![]() |
||||
C00025995
![]() |
Oxonantenine
|
CHEMBL1270949
|
![]() |
|||
C00025996
![]() |
Oxoputerine
|
![]() |
||||
C00026011
![]() |
Peruvianine
|
![]() |
||||
C00026035
![]() |
Splendidine
|
C457226
|
![]() |
|||
C00026052
![]() |
Subsessiline
/ Splendaboline |
![]() |
||||
C00026057
![]() |
Telazoline
|
![]() |
||||
C00027142
![]() |
Duguevalline
|
![]() |
||||
C00027145
![]() |
Isomoschatoline
|
![]() |
||||
C00027298
![]() |
Artabonatine C
|
![]() |
||||
C00027309
![]() |
Cassamedine
|
![]() |
||||
C00027330
![]() |
Glauvine
/ Corunnine |
![]() |
||||
C00027337
![]() |
Daurioxoisoporphine B
|
CHEMBL446816
|
![]() |
|||
C00027338
![]() |
Daurioxoisoporphine C
|
CHEMBL1651051
|
![]() |
|||
C00027339
![]() |
Daurioxoisoporphine D
|
![]() |
||||
C00027364
![]() |
Fissiceine
|
![]() |
||||
C00027404
![]() |
Kuafumine
|
![]() |
||||
C00027456
![]() |
Oxoanolobine
|
![]() |
||||
C00027457
![]() |
Oxoglaucine
/ O-Methylatheroline |
CHEMBL470881
|
C111587
|
25 / 27 / 24 |
![]() |
|
C00027459
![]() |
Oxopurpureine
|
CHEMBL456295
|
20 / 27 / 24 |
![]() |
||
C00027486
![]() |
Teliglazine
|
![]() |
||||
C00027542
![]() |
Hernandonine
|
![]() |
||||
C00027543
![]() |
Hernanymphine
|
![]() |
||||
C00027581
![]() |
Oxobuxifoline
|
![]() |
||||
C00027775
![]() |
7-Oxodehydroasimilobine
|
![]() |
||||
C00027868
![]() |
Annolatine
|
![]() |
||||
C00028596
![]() |
Mollisine
|
![]() |
||||
C00028782
![]() |
Oxocularicine
|
![]() |
||||
C00032676
![]() |
7-Oxohernagine
|
![]() |
||||
C00039441
![]() |
Isofiliformine
|
CHEMBL403551
|
![]() |
|||
C00050097
![]() |
Filiformine
|
![]() |
||||
C00050252
![]() |
Thalicminine
|
CHEMBL450614
|
C069511
|
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
O75496 | Geminin | Unclassified protein | C00027457 C00027459 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00027457 C00027459 | 4 / 3 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00027457 C00027459 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00027457 C00027459 | 0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00027457 C00027459 | 0 / 0 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00027457 C00027459 | 2 / 2 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00027457 C00027459 | 0 / 0 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00027457 C00027459 | 1 / 2 |
P02545 | Prelamin-A/C | Unclassified protein | C00027457 C00027459 | 11 / 10 |
P42858 | Huntingtin | Unclassified protein | C00027457 C00027459 | 1 / 1 |
P39748 | Flap endonuclease 1 | Enzyme | C00027457 C00027459 | 0 / 0 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00027457 C00027459 | 1 / 0 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00027457 | 1 / 0 |
P43681 | Neuronal acetylcholine receptor subunit alpha-4 | CHRN alpha | C00001878 | 1 / 1 |
P32297 | Neuronal acetylcholine receptor subunit alpha-3 | CHRN alpha | C00001878 | 1 / 0 |
P11387 | DNA topoisomerase 1 | Isomerase | C00025849 | 0 / 0 |
Q14761 | Protein tyrosine phosphatase receptor type C-associated protein | Enzyme | C00001878 | 0 / 0 |
P30926 | Neuronal acetylcholine receptor subunit beta-4 | CHRN beta | C00001878 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00027457 | 0 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00027457 | 2 / 0 |
P17787 | Neuronal acetylcholine receptor subunit beta-2 | CHRN beta | C00001878 | 1 / 1 |
Q9Y253 | DNA polymerase eta | Enzyme | C00027457 | 1 / 1 |
Q92793 | CREB-binding protein | Enzyme | C00027457 | 1 / 1 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00027457 | 0 / 0 |
P00734 | Prothrombin | S1A | C00025319 | 4 / 2 |
Q13315 | Serine-protein kinase ATM | Atypical serine/threonine protein kinase PIKK subfamily | C00027459 | 1 / 4 |
P29466 | Caspase-1 | C14 | C00027457 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00027457 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00027457 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00027457 | 0 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00027459 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00027459 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00027459 | 1 / 1 |
Q16637 | Survival motor neuron protein | Unclassified protein | C00027459 | 4 / 1 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00027457 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00027457 | 0 / 0 |
Q2TB90 | Putative hexokinase HKDC1 | Enzyme | C00027459 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00027459 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00027457 | 1 / 1 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00027459 | 1 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#208900 | Ataxia-telangiectasia; at |
Q13315
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#114500 | Colorectal cancer; crc |
P84022
|
#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
|
#600513 | Epilepsy, nocturnal frontal lobe, 1; enfl1 |
P43681
|
#605375 | Epilepsy, nocturnal frontal lobe, 3; enfl3 |
P17787
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#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
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#614390 | Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 |
P00734
|
#613679 | Prothrombin deficiency, congenital |
P00734
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#180849 | Rubinstein-taybi syndrome 1; rsts1 |
Q92793
|
#612052 | Smoking as a quantitative trait locus 3; sqtl3 |
P32297
|
#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
|
#601367 | Stroke, ischemic |
P00734
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#188050 | Thrombophilia due to thrombin defect; thph1 |
P00734
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00223 | Inherited thrombophilia |
P00734
(related)
|
H01254 | Congenital prothrombin deficiency |
P00734
(related)
|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
|
H00420 | Familial partial lipodystrophy (FPL) |
P02545
(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)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(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)
|
H00807 | Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) |
P17787
(related)
P43681 (related) |
H01171 | Poor drug metabolism (PM) |
P33261
(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)
|
H00005 | Chronic lymphocytic leukemia (CLL) |
Q13315
(related)
|
H00064 | Ataxia telangiectasia (AT) |
Q13315
(related)
|
H00094 | DNA repair defects |
Q13315
(related)
|
H00848 | Ataxia with ocular apraxia (AOA) |
Q13315
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00504 | Rubinstein-Taybi syndrome |
Q92793
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|