Cart
sales@molnova.com
Thymectacin
CAS No. 232925-18-7
Thymectacin( —— )
Catalog No. M34040 CAS No. 232925-18-7
Thymectacin (NB 1011) is a selective thymidine synthase (TS) inhibitor with anticancer activity for the study of colon cancer and solid tumors.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 179 | Get Quote |
|
| 5MG | 278 | Get Quote |
|
| 10MG | 451 | Get Quote |
|
| 25MG | 877 | Get Quote |
|
| 50MG | 1408 | Get Quote |
|
| 100MG | 1782 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameThymectacin
-
NoteResearch use only, not for human use.
-
Brief DescriptionThymectacin (NB 1011) is a selective thymidine synthase (TS) inhibitor with anticancer activity for the study of colon cancer and solid tumors.
-
DescriptionThymectacin (NB1011) is an agent selectively targeting tumor cells that have a high expression of thymidylate synthase (TS). Thymectacin is an aryloxy phosphoramidate derivative of BVdU (brivudin).
-
In VitroThymectacin (NB1011) is an agent selectively targeting tumor cells that have a high expression of thymidylate synthase (TS).
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetDNA/RNA Synthesis
-
RecptorDNA/RNA Synthesis
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number232925-18-7
-
Formula Weight574.32
-
Molecular FormulaC21H25BrN3O9P
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C1N(C=C(/C=C/Br)C(=O)N1)[C@@H]2O[C@H](COP(OC3=CC=CC=C3)(N[C@H](C(OC)=O)C)=O)[C@@H](O)C2
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Wilson RH. Novel therapeutic developments other than EGFR and VEGF inhibition in colorectal cancer. Oncologist. 2006;11(9):1018-1024.?
molnova catalog
related products
-
ART812
ART812 is an orally active inhibitor of DNA polymerase Polθ, possessing an IC50 value of 7.6 nM. Additionally, ART812 exhibits a cell-based microhomology-mediated end joining (MMEJ) IC50 value of 240 nM.
-
CBFβ Inhibitor
CBFβ Inhibitor is a cell-permeable CBFβ inhibitor and inhibits its association with Runx1.
-
Mefenidil
Mefenidil (McN-2378), a selective cerebral vasodilator, was shown to increase CBF in healthy brains without stimulating O2 uptake in a dog anesthesia model.
