Any compound that inhibits one or more steps in the pathway leading to the synthesis of brassinosteroids.
ChEBI ID: 73189
| Member | Definition | Class |
|---|---|---|
| methampicillin | A member of the class of triazoles that is butan-2-ol which is substituted at positions 2, 3, and 4 by phenyl, 1H-1,2,4-triazol-1-yl and p-chlorophenyl groups, respectively. An inhibitor of brassinosteroid biosynthesis. | brassinazole |
| Timeframe | Studies, Drugs with This Role(%) | All Drugs % |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (1.45) | 18.2507 |
| 2000's | 20 (28.99) | 29.6817 |
| 2010's | 26 (37.68) | 24.3611 |
| 2020's | 22 (31.88) | 2.80 |
| Publication Type | Studies, Drugs with this Role (%) | All Drugs (%) |
|---|---|---|
| Trials | 0 (0.00%) | 5.53% |
| Reviews | 2 (2.90%) | 6.00% |
| Case Studies | 0 (0.00%) | 4.05% |
| Observational | 0 (0.00%) | 0.25% |
| Other | 67 (97.10%) | 84.16% |
| Protein | Taxonomy | Measurement | Average (mM) | Bioassay(s) | Drugs |
|---|---|---|---|---|---|
| cytochrome P450 2C9, partial | Homo sapiens (human) | Potency | 0.9522 | 1 | 1 |
| cytochrome P450 2D6 | Homo sapiens (human) | Potency | 21.3174 | 1 | 1 |
| cytochrome P450 family 3 subfamily A polypeptide 4 | Homo sapiens (human) | Potency | 0.4253 | 1 | 1 |
| G | Vesicular stomatitis virus | Potency | 0.9522 | 1 | 1 |
| HLA class I histocompatibility antigen, B alpha chain | Homo sapiens (human) | Potency | 0.9522 | 1 | 1 |
| Inositol hexakisphosphate kinase 1 | Homo sapiens (human) | Potency | 0.9522 | 1 | 2 |
| Interferon beta | Homo sapiens (human) | Potency | 0.9522 | 1 | 1 |