Details
| Stereochemistry | MIXED |
| Molecular Formula | C10H20N2 |
| Molecular Weight | 168.2792 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CCC(NC1)C2CCCCN2
InChI
InChIKey=CLBJZAWCBRAMRZ-UHFFFAOYSA-N
InChI=1S/C10H20N2/c1-3-7-11-9(5-1)10-6-2-4-8-12-10/h9-12H,1-8H2
| Molecular Formula | C10H20N2 |
| Molecular Weight | 168.2792 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Origins of the distortions in the base pair step adjacent to platinum anticancer drug-DNA adducts. Fundamental NMR solution studies utilizing right-handed cross-link models having 5'- and 3'-flanking residues. | 2009-09-02 |
|
| Marked dependence on carrier-ligand bulk but not on carrier-ligand chirality of the duplex versus single-strand forms of a DNA oligonucleotide with a series of G-Pt(II)-G intrastrand cross-links modeling cisplatin-DNA adducts. | 2005-11-16 |
|
| Modification of second-sphere communication, leading to an unusually high abundance of the head-to-head conformer of cisplatin cross-link retro models. | 2002-02-11 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 16:22:57 GMT 2025
by
admin
on
Tue Apr 01 16:22:57 GMT 2025
|
| Record UNII |
6B3KS60E1H
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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6B3KS60E1H
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DTXSID501316477
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531-67-9
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208-514-9
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415618
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admin on Tue Apr 01 16:22:57 GMT 2025 , Edited by admin on Tue Apr 01 16:22:57 GMT 2025
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