class name | count |
---|---|
Spermatophyta | 20 |
rosids | 10 |
asterids | 2 |
eudicotyledons | 2 |
class name | count |
---|---|
Ephedraceae | 20 |
Celastraceae | 4 |
Cistaceae | 2 |
Cyprinidae | 1 |
Convolvulaceae | 1 |
Euphorbiaceae | 1 |
Rubiaceae | 1 |
Salicaceae | 1 |
Proteaceae | 1 |
Urticaceae | 1 |
Apidae | 1 |
Papaveraceae | 1 |
Rutaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Phenylalanine derived alkaloids | 4 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Phenylalanine derived alkaloids | C08300 | C00001405 |
Phenylalanine derived alkaloids | C08301 | C00001406 |
Phenylalanine derived alkaloids | C01575 | C00001409 |
Phenylalanine derived alkaloids | C02765 | C00031097 |
KCF-S ID | # of metabolite |
---|---|
No. 2149 | 5 |
No. 2578 | 4 |
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 |
---|---|---|---|---|---|---|---|
C00001405
![]() |
Pseudoephedrine
/ trans-Ephedrine / (+)-Pseudoephedrine |
CHEMBL357080
CHEMBL211456 CHEMBL1590 CHEMBL1620154 CHEMBL2110656 CHEMBL2110905 |
D054199
|
13 / 12 / 10 | 0 / 50 | No. 2149 |
![]() |
C00032017
![]() |
Benzamide
|
CHEMBL267373
|
19 / 19 / 15 | No. 2149 |
![]() |
||
C00032016
![]() |
Phenylglyoxal
|
CHEMBL233632
|
D010658
|
5 / 1 / 1 | 3 / 0 | No. 2149 |
![]() |
C00001409
![]() |
Methylephedrine
/ N-Methylephedrine / (-)-Methylephedrine |
CHEMBL445001
CHEMBL1589978 |
3 / 0 / 0 | No. 2149 |
![]() |
||
C00031097
![]() |
Acetophenone
|
CHEMBL274467
|
C038699
|
2 / 0 / 0 | 2 / 0 | No. 2149 |
![]() |
C00002685
![]() |
Methylpseudoephedrine
/ (1S,2S)-N-Methylpseudoephedrine |
CHEMBL445001
CHEMBL1589978 |
3 / 0 / 0 | No. 2578 |
![]() |
||
C00001406
![]() |
D-Cathine
|
CHEMBL61006
CHEMBL136560 CHEMBL1412041 CHEMBL1574804 CHEMBL1616525 CHEMBL1788114 CHEMBL2092846 |
13 / 13 / 13 | No. 2578 |
![]() |
||
C00000211
![]() |
Ephedrine
/ L-Ephedrine / 1(R),2(S)-erythro-(-)-Ephedrine |
CHEMBL357080
CHEMBL211456 CHEMBL1590 CHEMBL1620154 CHEMBL2110656 CHEMBL2110905 |
D004809
|
13 / 12 / 10 | 7 / 50 | No. 2578 |
![]() |
C00042277
![]() |
D-Cathinone
|
CHEMBL1124
CHEMBL2104047 |
1 / 0 / 0 | No. 2578 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00001405 C00001409 C00031097 C00042277 | 0 / 1 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00001405 C00001409 C00031097 C00042277 | 1 / 1 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00001405 C00001409 C00031097 | 1 / 0 |
P00352 | Retinal dehydrogenase 1 | Enzyme | C00000211 C00032016 C00032017 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00001409 C00031097 C00042277 | 3 / 3 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00001405 C00032016 C00032017 | 0 / 0 |
P16473 | Thyrotropin receptor | Glycohormone receptor | C00001409 C00031097 C00042277 | 3 / 2 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00001405 C00001409 C00031097 | 0 / 1 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00000211 C00042277 | 0 / 0 |
P40225 | Thrombopoietin | Unclassified protein | C00001409 C00031097 | 1 / 1 |
O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00001409 C00031097 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00032016 C00032017 | 0 / 0 |
P14618 | Pyruvate kinase PKM | Enzyme | C00001409 C00031097 | 0 / 0 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00001409 C00031097 | 0 / 0 |
P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00001409 C00031097 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00000211 C00042277 | 1 / 1 |
P06280 | Alpha-galactosidase A | Enzyme | C00001409 C00031097 | 1 / 1 |
P18054 | Arachidonate 12-lipoxygenase, 12S-type | Enzyme | C00001409 C00031097 | 2 / 0 |
P09874 | Poly [ADP-ribose] polymerase 1 | Enzyme | C00042277 | 0 / 0 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00042277 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00042277 | 0 / 0 |
P49841 | Glycogen synthase kinase-3 beta | Gsk | C00002685 | 0 / 0 |
P35348 | Alpha-1A adrenergic receptor | Adrenergic receptor | C00001405 | 0 / 0 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00000211 | 0 / 0 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00001405 | 0 / 0 |
P08913 | Alpha-2A adrenergic receptor | Adrenergic receptor | C00001405 | 0 / 0 |
Q01453 | Peripheral myelin protein 22 | Unclassified protein | C00042277 | 5 / 2 |
P51449 | Nuclear receptor ROR-gamma | Nuclear hormone receptor subfamily 1 group F member 3 | C00000211 | 0 / 0 |
O75496 | Geminin | Unclassified protein | C00042277 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00001405 | 0 / 0 |
Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00001405 | 0 / 0 |
Q13464 | Rho-associated protein kinase 1 | Rock | C00002685 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00042277 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00042277 | 4 / 3 |
Q99549 | M-phase phosphoprotein 8 | Unclassified protein | C00042277 | 0 / 0 |
P54132 | Bloom syndrome protein | Enzyme | C00042277 | 1 / 2 |
Q86W56 | Poly(ADP-ribose) glycohydrolase | Enzyme | C00042277 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00042277 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00001405 | 11 / 10 |
P06746 | DNA polymerase beta | Enzyme | C00042277 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00042277 | 1 / 1 |
P35368 | Alpha-1B adrenergic receptor | Adrenergic receptor | C00001405 | 0 / 0 |
P25100 | Alpha-1D adrenergic receptor | Adrenergic receptor | C00001405 | 0 / 0 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00001406 | 0 / 0 |
gene | gene name | gene description | KNApSAcK metabolite in interactions |
---|---|---|---|
217 | ALDH2, ALDH-E2, ALDHI, ALDM | aldehyde dehydrogenase 2 family (mitochondrial) (EC:1.2.1.3) |
C00002685
|
250 | ALPP, ALP, PALP, PLAP, PLAP-1 | alkaline phosphatase, placental (EC:3.1.3.1) |
C00002685
|
335 | APOA1 | apolipoprotein A-I |
C00001409
|
336 | APOA2, Apo-AII, ApoA-II, apoAII | apolipoprotein A-II |
C00001409
|
338 | APOB, FLDB, LDLCQ4 | apolipoprotein B |
C00001409
|
341 | APOC1 | apolipoprotein C-I |
C00001409
|
344 | APOC2, APO-CII, APOC-II | apolipoprotein C-II |
C00001409
|
345 | APOC3, APOCIII, HALP2 | apolipoprotein C-III |
C00001409
|
2353 | FOS, AP-1, C-FOS, p55 | FBJ murine osteosarcoma viral oncogene homolog |
C00001409
|
10327 | AKR1A1, ALDR1, ALR, ARM, DD3 | aldo-keto reductase family 1, member A1 (aldehyde reductase) (EC:1.1.1.2) |
C00000211
|
231 | AKR1B1, ADR, ALDR1, ALR2, AR | aldo-keto reductase family 1, member B1 (aldose reductase) (EC:1.1.1.21) |
C00000211
|
2530 | FUT8 | fucosyltransferase 8 (alpha (1,6) fucosyltransferase) (EC:2.4.1.68) |
C00000211
|
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#210900 | Bloom syndrome; blm |
P54132
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#118300 | Charcot-marie-tooth disease and deafness |
Q01453
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#118220 | Charcot-marie-tooth disease, demyelinating, type 1a; cmt1a |
Q01453
|
#114500 | Colorectal cancer; crc |
P18054
|
#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 |
P18054
|
#301500 | Fabry disease |
P06280
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#139393 | Guillain-barre syndrome, familial; gbs |
Q01453
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#603373 | Hyperthyroidism, familial gestational |
P16473
|
#609152 | Hyperthyroidism, nonautoimmune |
P16473
|
#145900 | Hypertrophic neuropathy of dejerine-sottas |
Q01453
|
#275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#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
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#162500 | Neuropathy, hereditary, with liability to pressure palsies; hnpp |
Q01453
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#187950 | Thrombocythemia 1; thcyt1 |
P40225
|
KEGG | name | UniProt |
---|---|---|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
Q01453 (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)
|
H00125 | Fabry disease |
P06280
(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)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
|
H01269 | Congenital hyperthyroidism |
P16473
(related)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00227 | Congenital amegakaryocytic thrombocytopenia (CAMT) |
P40225
(marker)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
|
H01296 | Hereditary neuropathy with liability to pressure palsies (HNPP) |
Q01453
(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)
|
MESH or OMIM | name |
KNApSAcK
metabolite |
---|---|---|
D058186 | Acute Kidney Injury |
C00001409
C00031097 |
D017180 | Tachycardia, Ventricular |
C00001409
C00031097 |
D012640 | Seizures |
C00001409
C00031097 |
D011605 | Psychoses, Substance-Induced |
C00001409
C00031097 |
D009203 | Myocardial Infarction |
C00001409
C00031097 |
D020343 | Hypertensive Encephalopathy |
C00001409
C00031097 |
D009202 | Cardiomyopathies |
C00001409
C00031097 |
D006973 | Hypertension |
C00001409
C00031097 |
D002543 | Cerebral Hemorrhage |
C00001409
C00031097 |
D006967 | Hypersensitivity |
C00001409
C00031097 |
D006261 | Headache |
C00001409
C00031097 |
D003329 | Coronary Vasospasm |
C00001409
C00031097 |
D053609 | Lethargy |
C00031097
|
D004830 | Epilepsy, Tonic-Clonic |
C00001409
|
D005315 | Fetal Diseases |
C00001409
|
D005334 | Fever |
C00001409
|
D006212 | Hallucinations |
C00001409
|
D003327 | Coronary Disease |
C00001409
|
D006323 | Heart Arrest |
C00001409
|
D006470 | Hemorrhage |
C00001409
|
D006948 | Hyperkinesis |
C00001409
|
D003128 | COMA |
C00001409
|
D002311 | Cardiomyopathy, Dilated |
C00001409
|
D002303 | Cardiac Output, Low |
C00001409
|
D007022 | Hypotension |
C00001409
|
D007024 | Hypotension, Orthostatic |
C00001409
|
D007333 | Insulin Resistance |
C00001409
|
D007431 | Intraoperative Complications |
C00001409
|
D007669 | Kidney Calculi |
C00001409
|
D017114 | Liver Failure, Acute |
C00001409
|
D008269 | Macular Edema |
C00001409
|
D015878 | Mydriasis |
C00001409
|
D001919 | Bradycardia |
C00001409
|
D009336 | Necrosis |
C00001409
|
D019636 | Neurodegenerative Diseases |
C00001409
|
D009765 | Obesity |
C00001409
|
D007744 | Obstetric Labor Complications |
C00001409
|
D010146 | Pain |
C00001409
|
D001763 | Blepharoptosis |
C00001409
|
D011654 | Pulmonary Edema |
C00001409
|
D012131 | Respiratory Insufficiency |
C00001409
|
D012206 | Rhabdomyolysis |
C00001409
|
D012607 | Scotoma |
C00001409
|
D054537 | Atrioventricular Block |
C00001409
|
D054138 | Sinus Arrest, Cardiac |
C00001409
|
D013610 | Tachycardia |
C00001409
|
D013616 | Tachycardia, Sinus |
C00001409
|
D001249 | Asthma |
C00001409
|
D014549 | Urinary Incontinence |
C00001409
|
D014786 | Vision Disorders |
C00001409
|
D054058 | Acute Coronary Syndrome |
C00031097
|
D000787 | Angina Pectoris |
C00031097
|
D000799 | Angioedema |
C00031097
|
D001146 | Arrhythmia, Sinus |
C00031097
|
D001259 | Ataxia |
C00031097
|
D001714 | Bipolar Disorder |
C00031097
|
D001929 | Brain Edema |
C00031097
|
D017091 | Colitis, Ischemic |
C00031097
|
D003139 | Common Cold |
C00031097
|
D003873 | Dermatitis, Exfoliative |
C00031097
|
D006970 | Disorders of Excessive Somnolence |
C00031097
|
D004244 | Dizziness |
C00031097
|
D004342 | Drug Hypersensitivity |
C00031097
|
D062787 | Drug Overdose |
C00031097
|
D006333 | Heart Failure |
C00031097
|
D007251 | Influenza, Human |
C00031097
|
D056486 | Drug-Induced Liver Injury |
C00001409
|
D009207 | Myoclonus |
C00031097
|
D009668 | Nose Diseases |
C00031097
|
D010554 | Personality Disorders |
C00031097
|
D010612 | Pharyngitis |
C00031097
|
D011644 | Puerperal Disorders |
C00031097
|
D012220 | Rhinitis |
C00031097
|
D012221 | Rhinitis, Allergic, Perennial |
C00031097
|
D006255 | Rhinitis, Allergic, Seasonal |
C00031097
|
D012852 | Sinusitis |
C00031097
|
D020521 | Stroke |
C00031097
|
D013575 | Syncope |
C00031097
|
D013614 | Tachycardia, Paroxysmal |
C00031097
|
D013617 | Tachycardia, Supraventricular |
C00031097
|
D014202 | Tremor |
C00031097
|
D014545 | Urinary Calculi |
C00031097
|
D016055 | Urinary Retention |
C00031097
|
D052878 | Urolithiasis |
C00031097
|
D014581 | Urticaria |
C00031097
|
D018879 | Ventricular Premature Complexes |
C00031097
|
D014839 | Vomiting |
C00031097
|
D014987 | Xerostomia |
C00031097
|