| Organism name | Rhamnus cathartica | 
|---|---|
| Genus | Rhamnus | 
| Family | Rhamnaceae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Rhamnus cathartica | 
|---|---|
| Linked NCBI taxonomy ID | 3610 | 
| Linked level | species | 
| Family in NCBI taxonomy | Rhamnaceae | 
|---|---|
| ID | 3608 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | rosids | 
|---|---|
| ID | 71275 | 
| Species | Activity | 
|---|---|
| Rhamnus cathartica L. | Antitumor | 
| Rhamnus cathartica L. | Collyrium | 
| Rhamnus cathartica L. | Depurative | 
| Rhamnus cathartica L. | Diuretic | 
| Rhamnus cathartica L. | Emetic | 
| Rhamnus cathartica L. | Laxative | 
| Rhamnus cathartica L. | Peristaltic | 
| 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 | phytochemical cluster | figure | 
|---|---|---|---|---|---|---|---|---|
| C00004634   | Rhamnetin / 7-Methoxyquercetin / 3,5,3',4'-Tetrahydroxy-7-methoxyflavone / 2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-4H-1- benzopyran-4-one | CHEMBL312163 | C063423 | 20 / 27 / 27 | No. 3 | No. 15 |   | |
| C00004642   | Rhamnazin / 7,3'-Di-O-methylquercetin / 3,4',5-Trihydroxy-3',7-dimethoxyflavone / 3,5-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-4H-1-benzopyran-4-one | CHEMBL457148 | No. 3 | No. 15 |   | |||
| C00004567   | Rhamnocitrin / 7-Methylkaempferol / 3,4',5-Trihydroxy-7-methoxyflavone / 3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-1-benzopyran-4-one | CHEMBL442289 | No. 3 | No. 15 |   | |||
| C00005518   | Rhamnetin 3-rhamninoside / Rhamnetin 3-O-rhamninoside | CHEMBL500372 | No. 5 | No. 15 |   | |||
| C00002825   | Frangulin B | CHEMBL496999 | C007781 | 2 / 1 / 1 | No. 568 | No. 62 |   | |
| C00002824   | Frangulin A | CHEMBL1172006 | 1 / 1 / 1 | No. 568 | No. 62 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| Q9H244 | P2Y purinoceptor 12 | Purine receptor | C00002824 C00002825 | 1 / 1 | 
| P45983 | Mitogen-activated protein kinase 8 | Jnk | C00004634 | 0 / 0 | 
| P02545 | Prelamin-A/C | Unclassified protein | C00004634 | 11 / 10 | 
| P10828 | Thyroid hormone receptor beta | NR1A2 | C00004634 | 3 / 1 | 
| P04792 | Heat shock protein beta-1 | Unclassified protein | C00004634 | 2 / 1 | 
| P11388 | DNA topoisomerase 2-alpha | Isomerase | C00002825 | 0 / 0 | 
| O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00004634 | 0 / 0 | 
| P15121 | Aldose reductase | Enzyme | C00004634 | 0 / 0 | 
| P45984 | Mitogen-activated protein kinase 9 | Jnk | C00004634 | 0 / 0 | 
| P04745 | Alpha-amylase 1 | Enzyme | C00004634 | 0 / 0 | 
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00004634 | 0 / 0 | 
| P27361 | Mitogen-activated protein kinase 3 | Erk | C00004634 | 0 / 0 | 
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00004634 | 3 / 3 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00004634 | 0 / 1 | 
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00004634 | 0 / 0 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00004634 | 4 / 3 | 
| Q9UBT6 | DNA polymerase kappa | Enzyme | C00004634 | 0 / 0 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00004634 | 0 / 0 | 
| P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00004634 | 0 / 0 | 
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00004634 | 1 / 1 | 
| O00255 | Menin | Unclassified protein | C00004634 | 2 / 5 | 
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00004634 | 1 / 2 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency | Q99714 | 
| #609821 | Bleeding disorder, platelet-type, 8; bdplt8 | Q9H244 | 
| #115200 | Cardiomyopathy, dilated, 1a; cmd1a | P02545 | 
| #212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism | P02545 | 
| #605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 | P02545 | 
| #606595 | Charcot-marie-tooth disease, axonal, type 2f; cmt2f | P04792 | 
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 | P02545 | 
| #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 | 
| #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 | 
| #131100 | Multiple endocrine neoplasia, type i; men1 | O00255 | 
| #613205 | Muscular dystrophy, congenital, lmna-related | P02545 | 
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b | P02545 | 
| #608634 | Neuronopathy, distal hereditary motor, type iib; hmn2b | P04792 | 
| #260540 | Parkinson-dementia syndrome | P10636 | 
| #172700 | Pick disease of brain | P10636 | 
| #275210 | Restrictive dermopathy, lethal | P02545 | 
| #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 | 
| 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) | 
| 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) | 
| H00856 | Distal hereditary motor neuropathies (dHMN) | P04792
                            (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) | 
| H00249 | Thyroid hormone resistance syndrome | P10828
                            (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) | 
| 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) | 
| H00063 | Spinocerebellar ataxia (SCA) | Q9NUW8
                            (related) |