| 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)
|