Cart
sales@molnova.com
USP30 inhibitor 18
CAS No. 2242582-40-5
USP30 inhibitor 18( —— )
Catalog No. M28079 CAS No. 2242582-40-5
USP30 inhibitor 18 is a selective inhibitor of USP30 (IC50 = 0.02 μM). USP30 inhibitor 18 is able to accelerate mitophagy and increase protein ubiquitination.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 326 | In Stock |
|
| 5MG | 297 | In Stock |
|
| 10MG | 472 | In Stock |
|
| 25MG | 753 | In Stock |
|
| 50MG | 1051 | In Stock |
|
| 100MG | 1414 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 2762 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameUSP30 inhibitor 18
-
NoteResearch use only, not for human use.
-
Brief DescriptionUSP30 inhibitor 18 is a selective inhibitor of USP30 (IC50 = 0.02 μM). USP30 inhibitor 18 is able to accelerate mitophagy and increase protein ubiquitination.
-
DescriptionUSP30 inhibitor 18 is a selective inhibitor of USP30 (IC50 = 0.02 μM). USP30 inhibitor 18 is able to accelerate mitophagy and increase protein ubiquitination.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayProteasome/Ubiquitin
-
TargetDUB
-
RecptorhTRPV1
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2242582-40-5
-
Formula Weight497.58
-
Molecular FormulaC26H28FN3O4S
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 100 mg/mL (200.97 mM)
-
SMILESN/A
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Ortar G, et al. New N-arachidonoylserotonin analogues with potential "dual" mechanism of action against pain. J Med Chem. 2007 Dec 27;50(26):6554-69.
molnova catalog
related products
-
USP8-IN-22d
A potent, selective ubiquitin-specific protease USP8 inhibitor with IC50 of 0.85 uM.
-
USP1-IN-2
USP1-IN-2 is a potent USP1 inhibitor with potential anti-tumor activity for the study of cancer.
-
USP30 inhibitor 11
USP30 inhibitor 11 (USP30-IN-11) is a selective USP30 inhibitor (IC50: 0.01 μΜ) that inhibits SVA and can be used in studies of cancer, mitochondrial dysfunction and Parkinson's.
