Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H12FN3O4.ClH |
| Molecular Weight | 293.679 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)\C2=C/F
InChI
InChIKey=GMEZRYKSEMDDQQ-QVXDJYSKSA-N
InChI=1S/C10H12FN3O4.ClH/c11-3-5-8(16)6(4-15)18-9(5)14-2-1-7(12)13-10(14)17;/h1-3,6,8-9,15-16H,4H2,(H2,12,13,17);1H/b5-3+;/t6-,8+,9-;/m1./s1
| Molecular Formula | C10H12FN3O4 |
| Molecular Weight | 257.2184 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 1 |
| Optical Activity | UNSPECIFIED |
| Molecular Formula | ClH |
| Molecular Weight | 36.461 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Tezacitabine is a cytidine derivative patented by Merrell Dow Pharmaceuticals, Inc. as an antineoplastic and antiviral agent. Tezacitabine acts as irreversible ribonucleotide reductase inhibitor and DNA chain terminator. Tezacitabine shows as potent activity in a broad spectrum of tumor cell lines and in vivo tumor models, including human colon, prostate, and breast tumor xenografts, In clinical trials combination of Tezacitabine and 5-Fluorouracil exerts favor influences in patients with advanced solid tumors particularly in patients with esophageal and other gastrointestinal carcinomas.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15772958
150-350 mg/m^2 on Day 1 of a 14-day cycle
Route of Administration:
Intravenous
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 18:40:45 GMT 2025
by
admin
on
Tue Apr 01 18:40:45 GMT 2025
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| Record UNII |
Y19296N8M6
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| Record Status |
Validated (UNII)
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| Record Version |
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121596369
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153586-81-3
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