oral Hsp90 inhibitor IPI-493
Term · Oncology and biomedicine · MLC-T-ONC-015695
An orally bioavailable formulation of the ansamycin derivative 17-amino-17-demethoxygeldanamycin (17-AG) with potential antineoplastic activity. Oral Hsp90 inhibitor IPI-493 binds to and inhibits Hsp90, which may result the in growth inhibition in sensitive tumor cell populations. Hsp90, a 90 kDa molecular chaperone, may be highly expressed in tumor cells, playing a key role in the conformational maturation, stability and function of other substrate or "client" proteins within the cell; many of these client proteins are involved in signal transduction, cell cycle regulation and apoptosis, and may include kinases, transcription factors and hormone receptors.
| Identifier | MLC-T-ONC-015695 |
|---|---|
| Field | Oncology and biomedicine |
| Synonyms | heat shock protein 90 inhibitor IPI-493 |
| References | National Cancer Institute Thesaurus (CC BY 4.0) |
Record as JSON
{
"id": "MLC-T-ONC-015695",
"term": "oral Hsp90 inhibitor IPI-493",
"field": "Oncology and biomedicine",
"definition": "An orally bioavailable formulation of the ansamycin derivative 17-amino-17-demethoxygeldanamycin (17-AG) with potential antineoplastic activity. Oral Hsp90 inhibitor IPI-493 binds to and inhibits Hsp90, which may result the in growth inhibition in sensitive tumor cell populations. Hsp90, a 90 kDa molecular chaperone, may be highly expressed in tumor cells, playing a key role in the conformational maturation, stability and function of other substrate or \"client\" proteins within the cell; many of these client proteins are involved in signal transduction, cell cycle regulation and apoptosis, and may include kinases, transcription factors and hormone receptors.",
"synonyms": [
"heat shock protein 90 inhibitor IPI-493"
],
"references": [
"National Cancer Institute Thesaurus"
],
"url": "https://mlchart.com/terminology/oncology/oral-hsp90-inhibitor-ipi-493/"
}
Record 12,320 of 17,721 in Oncology and biomedicine terminology (MLC-0111). Request the full dataset.