Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H32N4 |
| Molecular Weight | 256.4307 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCNCCCNC\C=C/CNCCCNCC
InChI
InChIKey=XFWLTFZLLXVKDY-WAYWQWQTSA-N
InChI=1S/C14H32N4/c1-3-15-11-7-13-17-9-5-6-10-18-14-8-12-16-4-2/h5-6,15-18H,3-4,7-14H2,1-2H3/b6-5-
| Molecular Formula | C14H32N4 |
| Molecular Weight | 256.4307 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
CGC-11047 is a polyamine analog designed to halt cell growth and induce apoptosis of cancer cells. In preclinical models CGC-11047 significantly inhibited tumor development in both lung and prostate cancer models when administered as a single agent. In the lung cancer model, CGC-11047 potentiated the antitumor effect of cisplatin. Although potent activity was observed with CGC-11047 and bevacizumab when administered as single agents in the prostate cancer model, the combination arm significantly enhanced antitumor activity compared with either agent alone. In all experiments, CGC-11047 was well tolerated with no adverse effects on bodyweight gain.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:25:58 GMT 2025
by
admin
on
Mon Mar 31 23:25:58 GMT 2025
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| Record UNII |
2C4Y86R2AX
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| Record Status |
Validated (UNII)
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| Record Version |
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2C4Y86R2AX
Created by
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100000175494
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308145-19-9
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admin on Mon Mar 31 23:25:58 GMT 2025 , Edited by admin on Mon Mar 31 23:25:58 GMT 2025
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1227404-21-8
Created by
admin on Mon Mar 31 23:25:58 GMT 2025 , Edited by admin on Mon Mar 31 23:25:58 GMT 2025
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6475492
Created by
admin on Mon Mar 31 23:25:58 GMT 2025 , Edited by admin on Mon Mar 31 23:25:58 GMT 2025
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |