Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H12FN3O4 |
| Molecular Weight | 257.2184 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO)[C@@H](O)\C2=C/F
InChI
InChIKey=GFFXZLZWLOBBLO-ASKVSEFXSA-N
InChI=1S/C10H12FN3O4/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)/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 |
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 19:12:46 GMT 2025
by
admin
on
Mon Mar 31 19:12:46 GMT 2025
|
| Record UNII |
7607Y95N9S
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C1557
Created by
admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
|
||
|
NCI_THESAURUS |
C2150
Created by
admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
8003
Created by
admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
|
PRIMARY | |||
|
7607Y95N9S
Created by
admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
|
PRIMARY | |||
|
DTXSID10156446
Created by
admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
|
PRIMARY | |||
|
300000036939
Created by
admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
|
PRIMARY | |||
|
130306-02-4
Created by
admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
|
PRIMARY | |||
|
C95916
Created by
admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
|
PRIMARY | |||
|
6435808
Created by
admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
|
PRIMARY | |||
|
171233-40-2
Created by
admin on Mon Mar 31 19:12:46 GMT 2025 , Edited by admin on Mon Mar 31 19:12:46 GMT 2025
|
NON-SPECIFIC STEREOCHEMISTRY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
SOLVATE->ANHYDROUS | |||
|
|
SALT/SOLVATE -> PARENT | |||
|
|
SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |