| 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
|