Atg4B-IN-2
CAS No. 2765008-88-4
Atg4B-IN-2( —— )
Catalog No. M35497 CAS No. 2765008-88-4
Atg4B-IN-2. A potent, selective Atg4B inhibitor with anticancer activity, inhibits both Atg4B and PLA2, enabling autophagy that counteracts the anticancer activity of anti-desiccation-resistant prostate cancer drugs.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 175 | Get Quote |
|
| 5MG | 217 | Get Quote |
|
| 10MG | 361 | Get Quote |
|
| 25MG | 630 | Get Quote |
|
| 50MG | 918 | Get Quote |
|
| 100MG | 1350 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameAtg4B-IN-2
-
NoteResearch use only, not for human use.
-
Brief DescriptionAtg4B-IN-2. A potent, selective Atg4B inhibitor with anticancer activity, inhibits both Atg4B and PLA2, enabling autophagy that counteracts the anticancer activity of anti-desiccation-resistant prostate cancer drugs.
-
DescriptionAtg4B-IN-2 is a potent competitive Atg4B inhibitor with Ki value of 3.1 μM, also possesses declining PLA2 inhibitory potency, IC50s of 11 μM and 3.5 μM for Atg4B and PLA2, respectively. Atg4B-IN-2 enhances the anticancer activity of anti-castration-resistant prostate cancer agents via autophagy inhibition.
-
In VitroAtg4B-IN-2 (compound 21f) (1-10 μM; 2 hours) restores the p62 expression in cells treated with AF (amino acid-free) in a dose-dependent manner.Atg4B-IN-2 (1 and 5 μM; 2 hours) decreases moderately autophagic vesicles at 1 μM, and almost completely inhibits autophagy at 5 μM.Atg4B-IN-2 (5 μM; 2 hours) inhibits Abi-induced autophagy and significantly augments apoptotic cell death and sensitivity to Abi.Western Blot AnalysisCell Line:LNCaP cells (incubated in AF medium)Concentration:1, 2, 5, 10 μM Incubation Time:2 hours (then incubated in AFM for 24 or 3 hours) Result:Restored the p62 expression in cells treated with AF in a dose-dependent manner.Cell Autophagy Assay Cell Line:LNCaP cells (incubated in AF medium) Concentration:1 and 5 μM Incubation Time:2 hours (then incubated in AFM for 24 or 3 hours)Result:Decreased moderately autophagic vesicles at 1 μM, and almost completely inhibited autophagy at 5 μM.
-
In Vivo——
-
Synonyms——
-
PathwayMetabolic Enzyme/Protease
-
TargetPhospholipase
-
RecptorPhospholipase | Autophagy
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2765008-88-4
-
Formula Weight330.46
-
Molecular FormulaC21H30O3
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (302.61 mM; Ultrasonic )
-
SMILESC(/C=C/C(O)=O)(=O)C1=CC=C(CCCCCCCCCCC)C=C1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Kudo Y, Endo S, Fujita M, et al. Discovery and Structure-Based Optimization of Novel Atg4B Inhibitors for the Treatment of Castration-Resistant Prostate Cancer. J Med Chem. 2022;65(6):4878-4892.?
molnova catalog
related products
-
GW 4869
A cell-permeable, symmetrical dihydroimidazolo-amide compound that acts as a potent, specific, non-competitive inhibitor of N-SMase (neutral sphingomyelinase) [IC50?= ~ 1 μM, rat brain; Km?for sphingomyelin ~13 μM].
-
D-Erythro-dihydrosph...
D-Erythro-dihydrosphingosine inhibits arachidonic acid release and cPLA2α activity.
-
Sodium stibogluconat...
Sodium stibogluconate is a potent protein tyrosine phosphatase inhibitor.
Cart
sales@molnova.com