Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C23H23NO2.CH4O3S |
| Molecular Weight | 441.54 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CS(O)(=O)=O.CC(CO)(CO)NCC1=CC2=C(C=CC3=C2C=CC=C3)C4=CC=CC=C14
InChI
InChIKey=NJWBUDCAWGTQAS-UHFFFAOYSA-N
InChI=1S/C23H23NO2.CH4O3S/c1-23(14-25,15-26)24-13-17-12-22-18-7-3-2-6-16(18)10-11-21(22)20-9-5-4-8-19(17)20;1-5(2,3)4/h2-12,24-26H,13-15H2,1H3;1H3,(H,2,3,4)
| Molecular Formula | C23H23NO2 |
| Molecular Weight | 345.4342 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | CH4O3S |
| Molecular Weight | 96.106 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Crisnatol is a derivative of arylmethylaminopropanediol with significant antineoplastic activity in a variety of murine and human tumor models. Crisnatol functions as a DNA intercalator, with the presence of additional basic amine groups in the sidechain enhancing binding to DNA due to electrostatic interactions. Crisnatol did not show antitumor efficacy in patients with ovarian carcinoma. In another clinical study, 2 of 26 patients with glioma showed complete long-lasting responses to the drug. The dose-limiting side effect was neurotoxicity.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:36:41 GMT 2025
by
admin
on
Mon Mar 31 17:36:41 GMT 2025
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| Record UNII |
R6D31YA2WK
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C582
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Z-10
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C1354
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R6D31YA2WK
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96389-69-4
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CHEMBL61495
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300000055388
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DTXSID70242218
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57061
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PARENT -> SALT/SOLVATE |
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ACTIVE MOIETY |