| Organism name | Teucrium ramosissimum | 
|---|---|
| Genus | Teucrium | 
| Family | Labiatae | 
| Kingdom | Plantae | 
| Linked NCBI taxonomy name | Teucrium | 
|---|---|
| Linked NCBI taxonomy ID | 21896 | 
| Linked level | genus | 
| Family in NCBI taxonomy | Lamiaceae | 
|---|---|
| ID | 4136 | 
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae | 
|---|---|
| ID | 33090 | 
| Plant class | asterids | 
|---|---|
| ID | 71274 | 
| 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 | 
|---|---|---|---|---|---|---|---|---|
| C00001016   | 7-O-Methylacacetin / Acacetin 7-methyl ether / Genkwanin 4'-methyl ether / Apigenin 7,4'-dimethyl ether / 5-Hydroxy-4',7-dimethoxyflavone / 5-Hydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one | CHEMBL350958 | C044998 | 1 / 0 / 0 | No. 3 | No. 15 |   | |
| C00001043   | Genkwanin | CHEMBL210635 | C014568 | 5 / 4 / 5 | 3 / 0 | No. 3 | No. 15 |   | 
| C00003837   | Cirsimaritin | CHEMBL348436 | C007072 | 13 / 18 / 14 | No. 3 | No. 15 |   | |
| C00003840   | Salvigenin | CHEMBL376644 | C014049 | No. 35 | No. 15 |   | ||
| C00048255   | 1beta,4beta,6beta-Trihydroxyeudesmane | No. 351 |   | |||||
| C00033538   | 1beta,4beta,7alpha-Trihydroxyeudesmane / (-)-1beta,4beta,7alpha-Trihydroxyeudesmane | No. 351 |   | |||||
| C00033918   | Homalomenol C / (-)-Homalomenol C | No. 1209 |   | |||||
| C00048288   | 4alpha-Hydroxy-homalomenol C | No. 1209 |   | |||||
| C00020240   | Oplopanone / (-)-Oplopanone | No. 1395 |   | |||||
| C00048558   | Teucmosin | No. 5825 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| P33765 | Adenosine receptor A3 | Adenosine receptor | C00001016 C00003837 | 0 / 0 | 
| P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00003837 | 7 / 3 | 
| Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00003837 | 0 / 0 | 
| P06746 | DNA polymerase beta | Enzyme | C00003837 | 0 / 0 | 
| P04062 | Glucosylceramidase | Enzyme | C00003837 | 6 / 4 | 
| P04798 | Cytochrome P450 1A1 | Cytochrome P450 1A1 | C00001043 | 0 / 0 | 
| P23219 | Prostaglandin G/H synthase 1 | Oxidoreductase | C00003837 | 0 / 0 | 
| Q9Y3R4 | Sialidase-2 | Enzyme | C00001043 | 0 / 0 | 
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00003837 | 0 / 0 | 
| P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00003837 | 0 / 3 | 
| Q9Y253 | DNA polymerase eta | Enzyme | C00003837 | 1 / 1 | 
| Q16678 | Cytochrome P450 1B1 | Cytochrome P450 1B1 | C00001043 | 4 / 4 | 
| P04745 | Alpha-amylase 1 | Enzyme | C00001043 | 0 / 0 | 
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00003837 | 0 / 0 | 
| Q9UNA4 | DNA polymerase iota | Enzyme | C00003837 | 0 / 0 | 
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00003837 | 4 / 3 | 
| P06239 | Tyrosine-protein kinase Lck | Src | C00001043 | 0 / 1 | 
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00003837 | 0 / 0 | 
| 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) | C00001043 | 
| 1544 | CYP1A2, CP12, P3-450, P450(PA) | cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) | C00001043 | 
| 1545 | CYP1B1, CP1B, CYPIB1, GLC3A, P4501B1 | cytochrome P450, family 1, subfamily B, polypeptide 1 (EC:1.14.14.1) | C00001043 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #219080 | Acth-independent macronodular adrenal hyperplasia; aimah | P63092 | 
| #600274 | Frontotemporal dementia; ftd | P10636 | 
| #608013 | Gaucher disease, perinatal lethal | P04062 | 
| #230800 | Gaucher disease, type i | P04062 | 
| #230900 | Gaucher disease, type ii | P04062 | 
| #231000 | Gaucher disease, type iii | P04062 | 
| #231005 | Gaucher disease, type iiic | P04062 | 
| #137750 | Glaucoma 1, open angle, a; glc1a | Q16678 | 
| #231300 | Glaucoma 3, primary congenital, a; glc3a | Q16678 | 
| #137760 | Glaucoma, primary open angle; poag | Q16678 | 
| #174800 | Mccune-albright syndrome; mas | P63092 | 
| #166350 | Osseous heteroplasia, progressive; poh | P63092 | 
| #168600 | Parkinson disease, late-onset; pd | P04062 | 
| #260540 | Parkinson-dementia syndrome | P10636 | 
| #604229 | Peters anomaly | Q16678 | 
| #172700 | Pick disease of brain | P10636 | 
| #102200 | Pituitary adenoma, growth hormone-secreting | P63092 | 
| #103580 | Pseudohypoparathyroidism, type ia; php1a | P63092 | 
| #603233 | Pseudohypoparathyroidism, type ib; php1b | P63092 | 
| #612462 | Pseudohypoparathyroidism, type ic; php1c | P63092 | 
| #601104 | Supranuclear palsy, progressive, 1; psnp1 | P10636 | 
| #278750 | Xeroderma pigmentosum, variant type; xpv | Q9Y253 | 
| KEGG | name | UniProt | 
|---|---|---|
| H00066 | Lewy body dementia (LBD) | P04062
                            (related) | 
| H00126 | Gaucher disease | P04062
                            (related) | 
| H00426 | Defects in the degradation of ganglioside | P04062
                            (related) | 
| H00810 | Progressive myoclonic epilepsy (PME) | P04062
                            (related) | 
| H00093 | Combined immunodeficiencies (CIDs) | P06239
                            (related) | 
| H00058 | Amyotrophic lateral sclerosis (ALS) | P10636
                            (related) | 
| H00077 | Progressive supranuclear palsy (PSP) | P10636
                            (related) | 
| H00078 | Frontotemporal lobar degeneration (FTLD) | P10636
                            (related) | 
| H00017 | Esophageal cancer | P35354
                            (related) | 
| H00025 | Penile cancer | P35354
                            (related) | 
| H00046 | Cholangiocarcinoma | P35354
                            (related) | 
| H00244 | Pseudohypoparathyroidism | P63092
                            (related) | 
| H00441 | Progressive osseous heteroplasia (POH) | P63092
                            (related) | 
| H00501 | Fibrous dysplasia, polyostotic | P63092
                            (related) | 
| H00612 | Primary open angle glaucoma | Q16678
                            (related) | 
| H01075 | Peters anomaly | Q16678
                            (related) | 
| H01159 | Anterior segment dysgenesis (ASD) | Q16678
                            (related) | 
| H01203 | Primary congenital glaucoma (PCG) | Q16678
                            (related) | 
| H00403 | Disorders of nucleotide excision repair | Q9Y253
                            (related) |