| class name | count | 
|---|---|
| rosids | 24 | 
| eudicotyledons | 11 | 
| Liliopsida | 9 | 
| class name | count | 
|---|---|
| Hypericaceae | 15 | 
| Polygonaceae | 11 | 
| Xanthorrhoeaceae | 9 | 
| Fabaceae | 4 | 
| Rhamnaceae | 3 | 
| Picramniaceae | 2 | 
| Chaetomiaceae | 1 | 
 
                  
                | br08003 Category | # of metabolite | 
|---|---|
| Anthrone type | 9 | 
| br08003 Category | KEGG ID | KNApSAcK ID | 
|---|---|---|
| Anthrone type | C10305 | C00002797 | 
| Anthrone type | C10307 | C00002799 | 
| Anthrone type | C10314 | C00002806 | 
| Anthrone type | C07606 | C00002829 | 
| Anthrone type | C10404 | C00002863 | 
| Anthrone type | C16801 | C00031651 | 
| Anthrone type | C16800 | C00031652 | 
| Anthrone type | C17778 | C00036708 | 
| Anthrone type | C16799 | C00036884 | 
| 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 | 
|---|---|---|---|---|---|---|---|
| C00002797   | Cassialoin | CHEMBL1721715 | 2 / 0 / 0 | No. 826 |   | ||
| C00044223   | Chrysophanic acid 9-anthrone | CHEMBL122196 | C010430 | No. 826 |   | ||
| C00044143   | Pseudohypericin | CHEMBL1614664 | C056602 | 1 / 0 | No. 826 |   | |
| C00044047   | Hypericin | CHEMBL286494 | C004965 | 23 / 24 / 24 | 7 / 2 | No. 826 |   | 
| C00036708   | Mayoside C / (-)-Mayoside C | No. 826 |   | ||||
| C00034664   | Picramnioside F / (-)-Picramnioside F | No. 826 |   | ||||
| C00034663   | 10-Hydroxycascaroside C / (-)-10-Hydroxycascaroside C | No. 826 |   | ||||
| C00034662   | Cascaroside A | No. 826 |   | ||||
| C00034661   | Cascaroside B / (-)-Cascaroside B | No. 826 |   | ||||
| C00031656   | Deacetyllittoraloin / (-)-Deacetyllittoraloin | No. 826 |   | ||||
| C00034660   | Cascaroside D | No. 826 |   | ||||
| C00044224   | Sennoside A | CHEMBL54481 CHEMBL448894 CHEMBL445268 CHEMBL1314924 CHEMBL1356785 CHEMBL1362935 CHEMBL1644069 | 58 / 59 / 53 | No. 1163 |   | ||
| C00002799   | 10-Hydroxyaloin B | No. 1163 |   | ||||
| C00031652   | Aloin / Aloin A / Barbaloin | CHEMBL123026 CHEMBL497001 CHEMBL1569106 | C045601 | 2 / 2 / 2 | No. 1163 |   | |
| C00031651   | Aloin B | CHEMBL123026 CHEMBL497001 CHEMBL1569106 | 2 / 2 / 2 | No. 1163 |   | ||
| C00031490   | Rumejaposide C / (-)-Rumejaposide C | No. 1163 |   | ||||
| C00037637   | Protopseudohypericin | C108324 | No. 1163 |   | |||
| C00037488   | Protohypericin | CHEMBL1078768 | C108325 | No. 1163 |   | ||
| C00036884   | Littoraloside / (-)-Littoraloside | No. 1163 |   | ||||
| C00002855   | Rumejaposide A / (+)-Rumejaposide A | No. 2632 |   | ||||
| C00034650   | Littoraloin / (-)-Littoraloin | No. 2632 |   | ||||
| C00002829   | Rumejaposide E / (-)-Rumejaposide E | No. 2632 |   | ||||
| C00034651   | Cascaroside C | No. 2632 |   | ||||
| C00002806   | Rumejaposide D / (-)-Rumejaposide D | No. 3961 |   | ||||
| C00002863   | Rumejaposide B / (-)-Rumejaposide B | No. 7714 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| Q99700 | Ataxin-2 | Unclassified protein | C00002797 C00002863 C00036708 | 1 / 1 | 
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00002829 C00002863 C00031656 | 0 / 0 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00002829 C00002863 | 4 / 3 | 
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002829 C00002863 | 1 / 2 | 
| O00255 | Menin | Unclassified protein | C00002829 C00002863 | 2 / 5 | 
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00002829 C00002863 | 1 / 1 | 
| Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00002829 C00002863 | 1 / 4 | 
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00002829 C00002863 | 0 / 0 | 
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00002829 C00002863 | 0 / 0 | 
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00002829 C00002863 | 3 / 1 | 
| Q13951 | Core-binding factor subunit beta | Unclassified protein | C00002829 C00002863 | 0 / 1 | 
| P54132 | Bloom syndrome protein | Enzyme | C00002829 C00002863 | 1 / 2 | 
| P11473 | Vitamin D3 receptor | NR1I1 | C00002829 C00002863 | 2 / 3 | 
| O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00002829 C00002863 | 0 / 0 | 
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00002829 C00002863 | 0 / 0 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002829 C00002863 | 0 / 1 | 
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002829 C00002863 | 2 / 2 | 
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00002829 C00002863 | 0 / 0 | 
| Q9H244 | P2Y purinoceptor 12 | Purine receptor | C00002797 C00036708 | 1 / 1 | 
| O75496 | Geminin | Unclassified protein | C00002863 C00031656 | 0 / 0 | 
| Q2TB90 | Putative hexokinase HKDC1 | Enzyme | C00002863 | 0 / 0 | 
| P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00002863 | 4 / 2 | 
| P35462 | D(3) dopamine receptor | Dopamine receptor | C00002829 | 1 / 0 | 
| Q9Y253 | DNA polymerase eta | Enzyme | C00002863 | 1 / 1 | 
| Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00002863 | 0 / 0 | 
| P11308 | Transcriptional regulator ERG | Unclassified protein | C00002863 | 1 / 2 | 
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002863 | 0 / 0 | 
| P11021 | 78 kDa glucose-regulated protein | Unclassified protein | C00002829 | 0 / 0 | 
| O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00002863 | 0 / 0 | 
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00002863 | 2 / 0 | 
| P06280 | Alpha-galactosidase A | Enzyme | C00002863 | 1 / 1 | 
| P18054 | Arachidonate 12-lipoxygenase, 12S-type | Enzyme | C00002829 | 2 / 0 | 
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00002863 | 0 / 0 | 
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002863 | 3 / 3 | 
| P39748 | Flap endonuclease 1 | Enzyme | C00002863 | 0 / 0 | 
| O15118 | Niemann-Pick C1 protein | Unclassified protein | C00002863 | 1 / 1 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00002863 | 0 / 0 | 
| P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00002863 | 0 / 0 | 
| P55210 | Caspase-7 | C14 | C00002863 | 0 / 0 | 
| P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00002863 | 2 / 2 | 
| O75164 | Lysine-specific demethylase 4A | Enzyme | C00002863 | 0 / 0 | 
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00002829 | 0 / 0 | 
| P34998 | Corticotropin-releasing factor receptor 1 | Corticotropin releasing factor receptor | C00002829 | 0 / 0 | 
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00002863 | 0 / 0 | 
| P02545 | Prelamin-A/C | Unclassified protein | C00002863 | 11 / 10 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002863 | 0 / 0 | 
| O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00002863 | 0 / 0 | 
| O00167 | Eyes absent homolog 2 | Enzyme | C00002863 | 0 / 0 | 
| P51151 | Ras-related protein Rab-9A | Unclassified protein | C00002863 | 0 / 0 | 
| Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00002863 | 0 / 0 | 
| P29466 | Caspase-1 | C14 | C00002863 | 0 / 0 | 
| P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00002863 | 0 / 3 | 
| P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00002863 | 2 / 0 | 
| Q16637 | Survival motor neuron protein | Unclassified protein | C00002829 | 4 / 1 | 
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00002863 | 0 / 0 | 
| Q92731 | Estrogen receptor beta | NR3A2 | C00002863 | 0 / 1 | 
| P03372 | Estrogen receptor | NR3A1 | C00002863 | 1 / 1 | 
| P19429 | Troponin I, cardiac muscle | Unclassified protein | C00002863 | 4 / 4 | 
| P45379 | Troponin T, cardiac muscle | Unclassified protein | C00002863 | 3 / 5 | 
| P63316 | Troponin C, slow skeletal and cardiac muscles | Other cytosolic protein | C00002863 | 2 / 2 | 
| P63165 | Small ubiquitin-related modifier 1 | Unclassified protein | C00002863 | 1 / 1 | 
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00002863 | 0 / 0 | 
| Q9H0H5 | Rac GTPase-activating protein 1 | Unclassified protein | C00002863 | 0 / 0 | 
| Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00002863 | 2 / 1 | 
| Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00002863 | 1 / 1 | 
| gene | gene name | gene description | KNApSAcK metabolite in interactions | 
|---|---|---|---|
| 1543 | CYP1A1, AHH, AHRR, CP11, CYP1, P1-450, P450-C, P450DX | cytochrome P450, family 1, subfamily A, polypeptide 1 (EC:1.14.14.1) | C00002829
                          C00002855 | 
| 1576 | CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 | cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) | C00002829 | 
| 5243 | ABCB1, ABC20, CD243, CLCS, GP170, MDR1, P-GP, PGY1 | ATP-binding cassette, sub-family B (MDR/TAP), member 1 (EC:3.6.3.44) | C00002829 | 
| 213 | ALB, PRO0883, PRO0903, PRO1341 | albumin | C00002829 | 
| 2938 | GSTA1, GST2, GSTA1-1, GTH1 | glutathione S-transferase alpha 1 (EC:2.5.1.18) | C00002829 | 
| 2950 | GSTP1, DFN7, FAEES3, GST3, GSTP, PI | glutathione S-transferase pi 1 (EC:2.5.1.18) | C00002829 | 
| 7153 | TOP2A, TOP2, TP2A | topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) | C00002829 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency | Q99714 | 
| #612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 | Q13148 | 
| #609821 | Bleeding disorder, platelet-type, 8; bdplt8 | Q9H244 | 
| #210900 | Bloom syndrome; blm | P54132 | 
| #114480 | Breast cancer | P38398 | 
| #604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 | P38398 | 
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a | P02545 | 
| #601494 | Cardiomyopathy, dilated, 1d; cmd1d | P45379 | 
| #613286 | Cardiomyopathy, dilated, 1ff; cmd1ff | P19429 | 
| #611879 | Cardiomyopathy, dilated, 1z; cmd1z | P63316 | 
| #611880 | Cardiomyopathy, dilated, 2a; cmd2a | P19429 | 
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism | P02545 | 
| #613243 | Cardiomyopathy, familial hypertrophic, 13; cmh13 | P63316 | 
| #115195 | Cardiomyopathy, familial hypertrophic, 2; cmh2 | P45379 | 
| #613690 | Cardiomyopathy, familial hypertrophic, 7; cmh7 | P19429 | 
| #115210 | Cardiomyopathy, familial restrictive, 1; rcm1 | P19429 | 
| #612422 | Cardiomyopathy, familial restrictive, 3; rcm3 | P45379 | 
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 | P02545 | 
| #114500 | Colorectal cancer; crc | P18054 P84022 Q14191 | 
| #119900 | Digital clubbing, isolated congenital | P15428 | 
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 | P02545 | 
| #133239 | Esophageal cancer | P18054 | 
| #615363 | Estrogen resistance; estrr | P03372 | 
| #612219 | Ewing sarcoma; es | P11308 | 
| #301500 | Fabry disease | P06280 | 
| #600274 | Frontotemporal dementia; ftd | P10636 | 
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay | Q03164 | 
| #610140 | Heart-hand syndrome, slovenian type | P02545 | 
| #176670 | Hutchinson-gilford progeria syndrome; hgps | P02545 | 
| #145000 | Hyperparathyroidism 1; hrpt1 | O00255 | 
| #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 | 
| #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 | 
| #607948 | Mycobacterium tuberculosis, susceptibility to | P11473 | 
| #257200 | Niemann-pick disease, type a | P17405 | 
| #607616 | Niemann-pick disease, type b | P17405 | 
| #257220 | Niemann-pick disease, type c1; npc1 | O15118 | 
| #613705 | Orofacial cleft 10; ofc10 | P63165 | 
| #167000 | Ovarian cancer | P38398 | 
| #614320 | Pancreatic cancer, susceptibility to, 4; pnca4 | P38398 | 
| #260540 | Parkinson-dementia syndrome | P10636 | 
| #172700 | Pick disease of brain | P10636 | 
| #601399 | Platelet disorder, familial, with associated myeloid malignancy | Q01196 | 
| #275210 | Restrictive dermopathy, lethal | P02545 | 
| #604906 | Schizophrenia 9; sczd9 | P49798 | 
| #181500 | Schizophrenia; sczd | P49798 | 
| #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 | 
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | P10636 | 
| #188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth | P10828 | 
| #274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth | P10828 | 
| #145650 | Thyroid hormone resistance, selective pituitary; prth | P10828 | 
| #190300 | Tremor, hereditary essential, 1; etm1 | P35462 | 
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a | P11473 | 
| #277700 | Werner syndrome; wrn | Q14191 | 
| #278750 | Xeroderma pigmentosum, variant type; xpv | Q9Y253 | 
| KEGG | name | UniProt | 
|---|---|---|
| H00033 | Adrenal carcinoma | O00255
                            (related) | 
| H00034 | Carcinoid | O00255
                            (related) | 
| H00045 | Malignant islet cell carcinoma | O00255
                            (related) | 
| H00246 | Primary hyperparathyroidism | O00255
                            (related) | 
| H01102 | Pituitary adenomas | O00255
                            (related) | 
| H00136 | Niemann-Pick disease type C (NPC) | O15118
                            (related) | 
| H00264 | Charcot-Marie-Tooth disease (CMT) | P02545
                            (related) | 
| H00294 | Dilated cardiomyopathy (DCM) | P02545
                            (related) P19429 (related) P45379 (related) P63316 (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) P45379 (related) | 
| H00026 | Endometrial Cancer | P03372
                            (marker) Q92731 (marker) | 
| H00125 | Fabry disease | P06280
                            (related) | 
| H00036 | Osteosarcoma | P08684
                            (marker) | 
| H00058 | Amyotrophic lateral sclerosis (ALS) | P10636
                            (related) Q13148 (related) | 
| H00077 | Progressive supranuclear palsy (PSP) | P10636
                            (related) | 
| H00078 | Frontotemporal lobar degeneration (FTLD) | P10636
                            (related) | 
| H00249 | Thyroid hormone resistance syndrome | P10828
                            (related) | 
| H00024 | Prostate cancer | P11308
                            (related) | 
| H00035 | Ewing's sarcoma | P11308
                            (related) | 
| H00342 | Tuberculosis | P11473
                            (related) | 
| H00784 | Localized autosomal recessive hypotrichosis | P11473
                            (related) | 
| H01143 | Vitamin D-dependent rickets | P11473
                            (related) | 
| H00457 | Primary hypertrophic osteoarthropathy (PHO) | P15428
                            (related) | 
| H01246 | Isolated congenital nail clubbing (ICNC) | P15428
                            (related) | 
| H00137 | Niemann-Pick disease (NPD) typeA and B | P17405
                            (related) | 
| H00424 | Defects in the degradation of sphingomyelin | P17405
                            (related) | 
| H00292 | Hypertrophic cardiomyopathy (HCM) | P19429
                            (related) P45379 (related) P63316 (related) | 
| H01219 | Restrictive cardiomyopathy (RCM) | P19429
                            (related) P45379 (related) | 
| H00295 | Viral myocarditis | P19429
                            (marker) P45379 (marker) | 
| H00017 | Esophageal cancer | P35354
                            (related) | 
| H00025 | Penile cancer | P35354
                            (related) | 
| H00046 | Cholangiocarcinoma | P35354
                            (related) | 
| H00027 | Ovarian cancer | P38398
                            (related) | 
| H00031 | Breast cancer | P38398
                            (related) | 
| H00094 | DNA repair defects | P54132
                            (related) | 
| H00296 | Defects in RecQ helicases | P54132
                            (related) Q14191 (related) | 
| H00516 | Isolated orofacial clefts | P63165
                            (related) | 
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) | Q01196
                            (related) Q01196 (marker) Q03164 (related) Q03164 (marker) | 
| H00003 | Acute myeloid leukemia (AML) | Q01196
                            (related) Q01196 (marker) Q13951 (marker) | 
| H00004 | Chronic myeloid leukemia (CML) | Q01196
                            (related) | 
| H00978 | Thrombocytopenia (THC) | Q01196
                            (related) | 
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) | Q03164
                            (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) | 
| H01235 | Bleeding disorder platelet-type | Q9H244
                            (related) | 
| H00403 | Disorders of nucleotide excision repair | Q9Y253
                            (related) |