Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H6O4.C5H14N2O2.Pt |
| Molecular Weight | 471.37 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Pt++].NCC(CN)(CO)CO.[O-]C(=O)C1(CCC1)C([O-])=O
InChI
InChIKey=NKUWPVYXJNSCQL-UHFFFAOYSA-L
InChI=1S/C6H8O4.C5H14N2O2.Pt/c7-4(8)6(5(9)10)2-1-3-6;6-1-5(2-7,3-8)4-9;/h1-3H2,(H,7,8)(H,9,10);8-9H,1-4,6-7H2;/q;;+2/p-2
| Molecular Formula | Pt |
| Molecular Weight | 195.084 |
| Charge | 2 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C6H8O4 |
| Molecular Weight | 144.1253 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C5H12N2O2 |
| Molecular Weight | 132.161 |
| Charge | -2 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Zeniplatin is a third-generation organoplatinum compound used in cancer treatment. It is a more water-soluble organoplatinum than cisplatin. On the phase I clinical trial the most prominent non-hematological side-effect of zeniplatin was nausea and vomiting. Other non-hematological side-effects were mild or absent. Zeniplatin did not induce significant neurological or auditory toxicity. Phase II study of zeniplatin on patients with advanced ovarian cancer revealed that zeniplatin may be active in relapsing, platinum-pretreated patients, and has no direct effects on renal function as measured by isotope clearance. Despite these findings, occasional nephrotoxicity may occur in patients with compromised kidney function, even with prophylactic hydration, and thus limit the application of this new analogue. Zeniplatin has a pharmacokinetic profile similar to that of carboplatin. Zeniplatin demonstrated only modest activity in melanoma with significant gastrointestinal and hematologic toxicity.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Zeniplatin in advanced malignant melanoma and renal cancer: phase II studies with unexpected nephrotoxicity. | 1997 |
|
| Zeniplatin in patients with advanced ovarian cancer, a phase II study with a third generation platinum complex. | 1993 |
|
| Can ondansetron hydrochloride (Zofran) enhance the nephrotoxic potential of other drugs? | 1992-11 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7847260
145 mg/m2 over 60-90 minutes every 21 days
Route of Administration:
Intravenous
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:39:49 GMT 2025
by
admin
on
Wed Apr 02 09:39:49 GMT 2025
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| Record UNII |
40ZQ0A17IT
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| Record Status |
Validated (UNII)
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| Record Version |
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NCI_THESAURUS |
C1450
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100000079413
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CC-5
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C1053
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111490-36-9
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DTXSID40891419
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