Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C18H23N7O10 |
| Molecular Weight | 497.4161 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=NC=C(N1CCOC(=O)CN(CC(O)=O)CC(=O)OCCN2C(C)=NC=C2[N+]([O-])=O)[N+]([O-])=O
InChI
InChIKey=AWSWJRUMDBPELJ-UHFFFAOYSA-N
InChI=1S/C18H23N7O10/c1-12-19-7-14(24(30)31)22(12)3-5-34-17(28)10-21(9-16(26)27)11-18(29)35-6-4-23-13(2)20-8-15(23)25(32)33/h7-8H,3-6,9-11H2,1-2H3,(H,26,27)
| Molecular Formula | C18H23N7O10 |
| Molecular Weight | 497.4161 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Sodium glycididazole (CMNA), a nitroimidazole compound that has a radiation-enhancing effect. This drug was studied in the treatment of patients with various tumors, such as non-small-cell lung cancer, esophageal carcinoma. CMNA combined with chemoradiotherapy participated in phase II clinical trials in patients with locally recurrent squamous cell esophageal carcinoma. It was shown, that CMNA improved curative effects without increasing adverse reactions, and significantly increase survival rates of the patients. The precise mechanism of action CMNA is not clear but is known that it acts through downregulation of ATM signaling pathway.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 09:21:55 GMT 2023
by
admin
on
Sat Dec 16 09:21:55 GMT 2023
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| Record UNII |
B2PT4D6Q3B
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| Record Status |
Validated (UNII)
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| Record Version |
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9914615
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DTXSID20432743
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298688-51-4
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B2PT4D6Q3B
Created by
admin on Sat Dec 16 09:21:55 GMT 2023 , Edited by admin on Sat Dec 16 09:21:55 GMT 2023
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