| class name | count | 
|---|---|
| asterids | 5 | 
| rosids | 1 | 
| class name | count | 
|---|---|
| Lamiaceae | 5 | 
| Rutaceae | 1 | 
| KNApSAcK ID | name | ChEMBL link | CTD link | # of proteins in ChEMBL interaction / related OMIM / related KEGG DISEASE | # of genes in CTD interaction / related diseases | figure | 
|---|---|---|---|---|---|---|
| C00003044   | Evodone |   | ||||
| C00003049   | (+)-Menthofuran / (R)-(+)-Menthofuran | CHEMBL1522900 | 10 / 8 / 9 |   | 
| accession | description | class description | KNApSAcK metabolite in interactions | # of diseases (OMIM / KEGG) | 
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00003049 | 1 / 0 | 
| P16473 | Thyrotropin receptor | Glycohormone receptor | C00003049 | 3 / 2 | 
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00003049 | 0 / 1 | 
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00003049 | 0 / 0 | 
| P11509 | Cytochrome P450 2A6 | Cytochrome P450 2A6 | C00003049 | 0 / 0 | 
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00003049 | 0 / 0 | 
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00003049 | 1 / 1 | 
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00003049 | 0 / 1 | 
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00003049 | 0 / 0 | 
| P10275 | Androgen receptor | NR3C4 | C00003049 | 3 / 4 | 
| OMIM | preferred title | UniProt | 
|---|---|---|
| #300068 | Androgen insensitivity syndrome; ais | P10275 | 
| #312300 | Androgen insensitivity, partial; pais | P10275 | 
| #609535 | Drug metabolism, poor, cyp2c19-related | P33261 | 
| #608902 | Drug metabolism, poor, cyp2d6-related | P10635 | 
| #603373 | Hyperthyroidism, familial gestational | P16473 | 
| #609152 | Hyperthyroidism, nonautoimmune | P16473 | 
| #275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 | P16473 | 
| #313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 | P10275 | 
| KEGG | name | UniProt | 
|---|---|---|
| H00036 | Osteosarcoma | P08684
                            (marker) | 
| H00024 | Prostate cancer | P10275
                            (related) | 
| H00062 | Spinal and bulbar muscular atrophy (SBMA) | P10275
                            (related) | 
| H00608 | 46,XY disorders of sex development (Disorders in androgen synthesis or action) | P10275
                            (related) | 
| H00609 | 46,XY disorders of sex development (Other) | P10275
                            (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) |