Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H3F3N2O2 |
| Molecular Weight | 180.0847 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FC(F)(F)C1=CNC(=O)NC1=O
InChI
InChIKey=LMNPKIOZMGYQIU-UHFFFAOYSA-N
InChI=1S/C5H3F3N2O2/c6-5(7,8)2-1-9-4(12)10-3(2)11/h1H,(H2,9,10,11,12)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii. | 1994 Aug 17 |
|
| Synthesis and herbicidal activity of novel heterocyclic protoporphyrinogen oxidase inhibitors. | 2004 Dec |
|
| The novel pyrimidine and purine derivatives of l-ascorbic acid: synthesis, one- and two-dimensional 1H and 13C NMR study, cytostatic and antiviral evaluation. | 2005 Jan 3 |
|
| Simple and rapid enzymatic method for the synthesis of single-strand oligonucleotides containing trifluorothymidine. | 2010 Nov |
|
| The unsaturated acyclic nucleoside analogues bearing a sterically constrained (Z)-4'-benzamido-2'-butenyl moiety: Synthesis, X-ray crystal structure study, cytostatic and antiviral activity evaluations. | 2010 Sep 1 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
200-197-5
Created by
admin on Sat Dec 16 04:59:32 UTC 2023 , Edited by admin on Sat Dec 16 04:59:32 UTC 2023
|
PRIMARY | |||
|
5899
Created by
admin on Sat Dec 16 04:59:32 UTC 2023 , Edited by admin on Sat Dec 16 04:59:32 UTC 2023
|
PRIMARY | |||
|
54-20-6
Created by
admin on Sat Dec 16 04:59:32 UTC 2023 , Edited by admin on Sat Dec 16 04:59:32 UTC 2023
|
PRIMARY | |||
|
73757
Created by
admin on Sat Dec 16 04:59:32 UTC 2023 , Edited by admin on Sat Dec 16 04:59:32 UTC 2023
|
PRIMARY | |||
|
DTXSID40202304
Created by
admin on Sat Dec 16 04:59:32 UTC 2023 , Edited by admin on Sat Dec 16 04:59:32 UTC 2023
|
PRIMARY | |||
|
4U846R5P34
Created by
admin on Sat Dec 16 04:59:32 UTC 2023 , Edited by admin on Sat Dec 16 04:59:32 UTC 2023
|
PRIMARY |
PARENT (METABOLITE INACTIVE)
SUBSTANCE RECORD
