U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Structure of ADAMPLATIN-IV

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

HIDE SMILES / InChI

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 Sat Dec 16 11:29:11 GMT 2023
Edited
by admin
on Sat Dec 16 11:29:11 GMT 2023
Record UNII
37WM0V5E17
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ADAMPLATIN-IV
Common Name English
LA 12 (PLATINUM COMPLEX)
Code English
PLD-147
Code English
LA 12
Code English
PLATINUM, BIS(ACETATO-.KAPPA.O)AMMINEDICHLORO(TRICYCLO(3.3.1.13,7)DECAN-1-AMINE)-, (OC-6-43)-
Systematic Name English
LA-12
Code English
Code System Code Type Description
CAS
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
PRIMARY
PUBCHEM
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
PRIMARY
FDA UNII
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
PRIMARY
SMS_ID
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
PRIMARY
Related Record Type Details
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.