Page last updated: 2024-08-05 11:15:57
organic phosphonate
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ChEBI ID: 37592
Members (13)
| Member | Definition | Role |
|---|---|---|
| adefovir dipivoxil | An organic phosphonate that is the dipivoxil ester of adefovir. A prodrug for adefovir, an HIV-1 reverse transcriptase inhibitor, adefovir pivoxil is used to treat chronic hepatitis B viral infection. | adefovir pivoxil |
| armin | ethyl 4-nitrophenyl ethylphosphonate | |
| bay 93820 | isocarbophos | |
| diisopropyl methylphosphonate | An organic phosphonate that is the diisopropyl ester of methylphosphonic acid. | diisopropyl methylphosphonate |
| fosthiazate | fosthiazate | |
| fotemustine | A member of the class of N-nitrosoureas that is ethyl diethylphosphonate in the hydrogen at position 1 of the ethyl group attached to the phosphorus has been replaced by a [(2-chloroethyl)(nitroso)carbamoyl]amino group. | diethyl (1-{[(2-chloroethyl)(nitroso)carbamoyl]amino}ethyl)phosphonate |
| hydroxy-2-naphthalenyl-methyl phosphonic acid trisacetoxymethylester | An organic phosphonate that is the trisacetoxymethylester derivative of naphthalene substituted hydroxymethylphosphonic acid. It has been found to inhibit insulin receptor tyrosine kinase activity and insulin stimulated glucose oxidation. | hydroxy-2-naphthalenyl-methyl phosphonic acid trisacetoxymethylester |
| isofenphos | isofenphos | |
| leptophos | An organic phosphonate that is phenylphosphonothioic O,O-acid in which the hydroxy groups are substituted by methoxy and 4-bromo-2,5-dichlorophenoxy groups. | O-(4-bromo-2,5-dichlorophenyl) O-methyl phenylphosphonothioate |
| phenylphosphonothioic acid, 2-ethyl 2-(4-nitrophenyl) ester | EPN | |
| phosphonoacetohydroxamate | The hydroxamate of phosphonoacetic acid. | phosphonoacetohydroxamic acid |
| sr 12813 | An organic phosphonate that is the tetraethyl ester of [2-(3,5-di-tert-butyl-4-hydroxyphenyl)ethene-1,1-diyl]bis(phosphonic acid). | SR12813 |
| trichlorfon | A phosphonic ester that is dimethyl phosphonate in which the hydrogen atom attched to the phosphorous is substituted by a 2,2,2-trichloro-1-hydroxyethyl group. | trichlorfon |
Research
Studies (2,192)
| Timeframe | Studies, Drugs in This Class (%) | All Drugs % |
|---|---|---|
| pre-1990 | 756 (34.49) | 18.7374 |
| 1990's | 354 (16.15) | 18.2507 |
| 2000's | 540 (24.64) | 29.6817 |
| 2010's | 458 (20.89) | 24.3611 |
| 2020's | 84 (3.83) | 2.80 |
Study Types
| Publication Type | Studies, Drugs in This Class (%) | All Drugs (%) |
|---|---|---|
| Trials | 309 (12.39%) | 5.53% |
| Reviews | 207 (8.30%) | 6.00% |
| Case Studies | 128 (5.13%) | 4.05% |
| Observational | 2 (0.08%) | 0.25% |
| Other | 1,848 (74.10%) | 84.16% |