CGK-1026
CAS No. 287383-59-9
CGK-1026( CGK 1026 | CGK1026 )
Catalog No. M13877 CAS No. 287383-59-9
A small molecule that inhibits human telomerase reverse transcriptase (hTERT) expression.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 59 | In Stock |
|
| 10MG | 88 | In Stock |
|
| 25MG | 194 | In Stock |
|
| 50MG | 357 | In Stock |
|
| 100MG | 537 | In Stock |
|
| 500MG | 1134 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameCGK-1026
-
NoteResearch use only, not for human use.
-
Brief DescriptionA small molecule that inhibits human telomerase reverse transcriptase (hTERT) expression.
-
DescriptionA small molecule that inhibits human telomerase reverse transcriptase (hTERT) expression; inhibits the recruitment of HDAC into E2F-pocket protein complexes assembled on the hTERT promoter, inhibits HDAC activity with IC50 of 100 nM; induces G1 arrest of IMR90 cells.
-
In Vitro——
-
In Vivo——
-
SynonymsCGK 1026 | CGK1026
-
PathwayCell Cycle/DNA Damage
-
TargetHDAC
-
RecptorHDAC
-
Research AreaCancer
-
Indication——
Chemical Information
-
CAS Number287383-59-9
-
Formula Weight326.352
-
Molecular FormulaC18H18N2O4
-
Purity>98% (HPLC)
-
SolubilityDMSO: 32.6 mg/mL (100 mM) ( < 1 mg/ml refers to the product slightly soluble or insoluble )
-
SMILESO=C(NO)CCCCCN(C(C1=CC=CC2=CC=CC3=C12)=O)C3=O
-
Chemical NameN-Hydroxy-1,3-dioxo-1H-benz[de]isoquinoline-2(3H)-hexanamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Won J, et al. Proc Natl Acad Sci U S A. 2004 Aug 3;101(31):11328-33.
2. Alimirah F, et al. Mol Cancer Res. 2007 Mar;5(3):251-9.
3. Song LL, et al. PLoS One. 2010 Jan 5;5(1):e8569.
molnova catalog
related products
-
YPX-C-05
YPX-C-05 is an isohydroxamic acid derivative and HDAC inhibitor with vasodilatory and antihypertensive activity.YPX-C-05 is used in the study of hypertension and vascular related disorders.
-
SIS17
SIS17 is a potent and selective HDAC 11 inhibitor with an IC50 value of 0.83 μM. SIS17 is active in cells and inhibited the demyristoylation of a known HDAC11 substrate serine hydroxymethyl transferase 2 without inhibiting other HDACs.
-
SKLB-23bb
SKLB-23bb is an orally bioavailable HDAC6-selective inhibitor and also has microtubule-disrupting ability.
Cart
sales@molnova.com