HDAC8-IN-22d
CAS No. 1417997-93-3
HDAC8-IN-22d( HDAC8-IN-1 | MDK-7933 | MDK 7933 | MDK7933 )
Catalog No. M11745 CAS No. 1417997-93-3
HDAC8-IN-22d is a potent, selective HDAC8 inhibitor with IC50 of 27.2 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 64 | In Stock |
|
| 5MG | 58 | In Stock |
|
| 10MG | 87 | In Stock |
|
| 25MG | 176 | In Stock |
|
| 50MG | 267 | In Stock |
|
| 100MG | 341 | In Stock |
|
| 200MG | 483 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameHDAC8-IN-22d
-
NoteResearch use only, not for human use.
-
Brief DescriptionHDAC8-IN-22d is a potent, selective HDAC8 inhibitor with IC50 of 27.2 nM.
-
DescriptionHDAC8-IN-22d is a potent, selective HDAC8 inhibitor with IC50 of 27.2 nM, exhibits no activity against other HDACs and limited activity against HDAC1 and 3; shows antiproliferative effects toward several human lung cancer cell lines (A549, H1299, and CL1-5); exhibits cytotoxicity against human lung CL1-5 cells (IC50=7.0 uM) similar to that of SAHA yet without significant cytotoxicity for normal IMR-90 cells.
-
In VitroHDAC8-IN-1 is a HDAC8 inhibitor with an IC50 of 27.2 nM in cancer cell lines. HDAC8-IN-1 (compound 22 d) shows antiproliferative effects toward several human lung cancer cell lines (A549, H1299, and CL1-5); HDAC8-IN-1 exhibits cytotoxicity against human lung CL1-5 cells without significant cytotoxicity for normal IMR-90 cells.
-
In Vivo——
-
SynonymsHDAC8-IN-1 | MDK-7933 | MDK 7933 | MDK7933
-
PathwayCell Cycle/DNA Damage
-
TargetHDAC
-
RecptorHDAC8
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1417997-93-3
-
Formula Weight345.398
-
Molecular FormulaC22H19NO3
-
Purity>98% (HPLC)
-
SolubilityDMSO: 130 mg/mL ( < 1 mg/ml refers to the product slightly soluble or insoluble )
-
SMILESONC(/C=C/C1=CC=C(C=C1C2=CC=C(C=C2)C3=CC=CC=C3)OC)=O
-
Chemical Name(2E)-N-Hydroxy-3-(5-methoxy[1,1':4',1''-terphenyl]-2-yl)-2-propenamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Huang WJ, et al. ChemMedChem. 2012 Oct;7(10):1815-24.
molnova catalog
related products
-
ACY-738
ACY-738 (ACY738) is a potent and specific HDAC6 inhibitor (IC50=1.7 nM) with improved brain bioavailability; displays 60-1500 fold selectivity over class I HDACs.
-
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.
-
NVP-BSK805 2HCl
NVP-BSK805 2HCl(IC50=0.5 nM), a specific and effective ATP-competitive JAK2 inhibitor, is more than 20-fold specificity over JAK1, JAK3 and TYK2.
Cart
sales@molnova.com