CID 5951923
CAS No. 749872-43-3
CID 5951923( —— )
Catalog No. M27613 CAS No. 749872-43-3
CID 5951923 is an inhibitor of KLF5 transcription factor with an IC50 of 603 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 80 | Get Quote |
|
10MG | 102 | Get Quote |
|
25MG | 196 | Get Quote |
|
50MG | 350 | Get Quote |
|
100MG | 524 | Get Quote |
|
500MG | 1143 | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameCID 5951923
-
NoteResearch use only, not for human use.
-
Brief DescriptionCID 5951923 is an inhibitor of KLF5 transcription factor with an IC50 of 603 nM.
-
DescriptionCID 5951923 is an inhibitor of KLF5 transcription factor with an IC50 of 603 nM.(In Vitro):CID 5951923 (10 μM) inhibits the proliferation of cancer cell lines mainly in highly expressing KLF5 cells. CID 5951923 (0.001, 0.01, 0.1, 1, 10, 100 μM) inhibits proliferation of DLD-1 cells in a dose-dependent manner. CID 5951923 (10 μM) significantly decreases endogenous KLF5 levels in the DLD-1 cells, downregulates EGR1, and increases phosphorylation levels of pEGFFpY1068.
-
In VitroCID 5951923 (1 nM-100 μM; 48 h) inhibits proliferation of DLD-1 cells in a dose-dependent manner.CID 5951923 (10 μM; 24 h) significantly decreases endogenous KLF5 levels in the DLD-1 cells, increases phosphorylation levels of pEGFFpY1068, and downregulated EGR1.CID 5951923 (10 μM) inhibits proliferation of cancer cell lines mainly in highly express KLF5 cells. Cell Viability Assay Cell Line:DLD-1 and IEC-6 cells Concentration:0.001, 0.01, 0.1, 1, 10, 100 μM Incubation Time:48 h Result:Inhibited proliferation of DLD-1 cells with an IC50 of 1.6 μM.
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetDNA/RNA Synthesis
-
RecptorROCK2
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number749872-43-3
-
Formula Weight382.39
-
Molecular FormulaC16H18N2O7S
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 10 mg/mL (26.15 mM)
-
SMILESCN([C@H]1CCS(=O)(=O)C1)C(=O)COC(=O)\C=C\c1cccc(c1)[N+]([O-])=O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Aicher, Thomas Daniel, et al. INDAZOLYL THIADIAZOLAMINES AND RELATED COMPOUNDS FOR INHIBITION OF RHO-ASSOCIATED PROTEIN KINASE AND THE TREATMENT OF DISEASE. US20180093978A1.
molnova catalog
related products
-
Shanzhiside methyl e...
Shanzhiside methylester reduces neuropathic pain by activating spinal GLP-1 receptors and subsequently stimulating microglial β-endorphin expression via the p38 MAPK signaling.
-
Tetrahydrouridine
Tetrahydrouridine (THU) is a multidrug resistance modulator. It can be used in cancer treatment to make tumor cells more sensitive to radiation therapy.
-
Fludarabine Phosphat...
Fludarabine Phosphate is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis.