Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H17N.2C2H3O2.2Cl.Pt.H3N |
Molecular Weight | 552.357 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
N.[Cl-].[Cl-].[Pt+4].CC([O-])=O.CC([O-])=O.NC12CC3CC(CC(C3)C1)C2
InChI
InChIKey=RGCIZXNKLJAKIS-UHFFFAOYSA-J
InChI=1S/C10H17N.2C2H4O2.2ClH.H3N.Pt/c11-10-4-7-1-8(5-10)3-9(2-7)6-10;2*1-2(3)4;;;;/h7-9H,1-6,11H2;2*1H3,(H,3,4);2*1H;1H3;/q;;;;;;+4/p-4
Molecular Formula | H3N |
Molecular Weight | 17.0305 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | Pt |
Molecular Weight | 195.084 |
Charge | 4 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | Cl |
Molecular Weight | 35.453 |
Charge | -1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C2H3O2 |
Molecular Weight | 59.044 |
Charge | -1 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C10H17N |
Molecular Weight | 151.2487 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:29:11 GMT 2023
by
admin
on
Sat Dec 16 11:29:11 GMT 2023
|
Record UNII |
37WM0V5E17
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Record Status |
Validated (UNII)
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Record Version |
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-
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250611-20-2
Created by
admin on Sat Dec 16 11:29:11 GMT 2023 , Edited by admin on Sat Dec 16 11:29:11 GMT 2023
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10007773
Created by
admin on Sat Dec 16 11:29:11 GMT 2023 , Edited by admin on Sat Dec 16 11:29:11 GMT 2023
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37WM0V5E17
Created by
admin on Sat Dec 16 11:29:11 GMT 2023 , Edited by admin on Sat Dec 16 11:29:11 GMT 2023
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300000041380
Created by
admin on Sat Dec 16 11:29:11 GMT 2023 , Edited by admin on Sat Dec 16 11:29:11 GMT 2023
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
The results show that deactivation of adamplatin(IV) by sulfur-containing compounds (such as glutathione or metallothioneins) is likely to play a less significant role in the mechanism of resistance of tumor cells to adamplatin(IV) in contrast to the role of these reactions in the effects of cisplatin. Moreover, the treatment of tumor cells with adamplatin(IV) does not result in DNA modifications that would be markedly different from those produced by cisplatin. In contrast, the effects of other factors, such as enhanced accumulation of the drug in cells, strong inhibition of DNA polymerization by these adducts, lowered DNA repair, and DNA-protein cross-linking are different from the effects of these factors in the mechanism underlying activity of cisplatin.
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