Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H12FN3O4.H2O |
| Molecular Weight | 275.2337 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)\C2=C/F
InChI
InChIKey=XPYQFIISZQCINN-QVXDJYSKSA-N
InChI=1S/C10H12FN3O4.H2O/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);1H2/b5-3+;/t6-,8+,9-;/m1./s1
| Molecular Formula | H2O |
| Molecular Weight | 18.0153 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| 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 |
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
Mon Mar 31 18:03:47 GMT 2025
by
admin
on
Mon Mar 31 18:03:47 GMT 2025
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| Record UNII |
UCC4EQS7WL
|
| Record Status |
Validated (UNII)
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| Record Version |
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Download
| Name | Type | Language | ||
|---|---|---|---|---|
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Official Name | English | ||
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Preferred Name | English | ||
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Code | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C1557
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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FDA ORPHAN DRUG |
164002
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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NCI_THESAURUS |
C2150
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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DTXSID00169020
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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PRIMARY | |||
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C1539
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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PRIMARY | |||
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171176-43-5
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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PRIMARY | |||
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LL-85
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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PRIMARY | |||
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9925544
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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PRIMARY | |||
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TEZACITABINE
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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PRIMARY | |||
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DB06433
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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PRIMARY | |||
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C086432
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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PRIMARY | |||
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UCC4EQS7WL
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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PRIMARY | |||
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CHEMBL2105467
Created by
admin on Mon Mar 31 18:03:47 GMT 2025 , Edited by admin on Mon Mar 31 18:03:47 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ANHYDROUS->SOLVATE | |||
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PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |