Ubiquitination-IN-1
CAS No. 1819330-15-8
Ubiquitination-IN-1 ( —— )
Catalog No. M26494 CAS No. 1819330-15-8
Ubiquitination-IN-1 is an inhibitor of ubiquitination and Cksl-Skp2 protein-protein interaction (IC50: 0.17 μM).
Purity : >98% (HPLC)
Size | Price / USD | Stock | Quantity |
5MG | 58 | Get Quote |
|
10MG | 87 | Get Quote |
|
25MG | 159 | Get Quote |
|
50MG | 264 | Get Quote |
|
100MG | 395 | Get Quote |
|
500MG | 888 | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameUbiquitination-IN-1
-
NoteResearch use only, not for human use.
-
Brief DescriptionUbiquitination-IN-1 is an inhibitor of ubiquitination and Cksl-Skp2 protein-protein interaction (IC50: 0.17 μM).
-
DescriptionUbiquitination-IN-1 is an inhibitor of ubiquitination and Cksl-Skp2 protein-protein interaction (IC50: 0.17 μM).(In Vitro):Ubiquitination-IN-1 inhibits A549 and HT1080 cells (IC50s: 0.91 and 0.4 μM).
-
Synonyms——
-
PathwayOthers
-
TargetOther Targets
-
RecptorPim2
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1819330-15-8
-
Formula Weight429.4
-
Molecular FormulaC21H14F3N3O2S
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESFC(F)(F)c1cccc(c1)S(=O)(=O)Nc1ccc(-c2cccnc2)c2cccnc12
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
ELA-32 (human)
Potent, high affinity apelin receptor agonist (IC50 = 0.27 nM; Kd = 0.51 nM). Exhibits no binding GPR15 and GPR25. Activates the PI3K/AKT pathway and promotes self-renewal of hESCs via cell-cycle progression and protein translation. Also potentiates the TGFβ pathway, priming hESCs toward the endoderm lineage. Stimulates angiogenesis in HUVEC cells. Relaxes mouse aortic vessels. Functions as an anorexigenic hormone through activation of the AVP and CRH neurons in the PVN.
-
Cyclo(Tyr-Pro)
Cyclo(Tyr-Pro) shows antibacterial activity towards several marine bacterial species, it also shows weak antagonistic activity against VEGFR2 -CD. Cyclo(Tyr-Pro) and cyclo(Pro-Val) are toxic to both suspension cells and seedlings of Pinus thunbergii, which may offer some clues to research the mechanism of pine wilt disease caused by pine wood nematode.
-
Homo-VK-II-36
Homo-VK-II-36 is a carvedilol analogue that acts by inhibiting store-?overload-induced calcium release through the RyR2 channel.