NIBR189
CAS No. 1599432-08-2
NIBR189( —— )
Catalog No. M20651 CAS No. 1599432-08-2
NIBR189 is a potent and selective antagonist of EBI2 (GPR183) receptor (IC50 of 11 and 15 nM for human and mouse EBI2 receptors respectively).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 72 | In Stock |
|
| 10MG | 125 | In Stock |
|
| 25MG | 232 | In Stock |
|
| 50MG | 410 | In Stock |
|
| 100MG | 605 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameNIBR189
-
NoteResearch use only, not for human use.
-
Brief DescriptionNIBR189 is a potent and selective antagonist of EBI2 (GPR183) receptor (IC50 of 11 and 15 nM for human and mouse EBI2 receptors respectively).
-
DescriptionNIBR189 is a potent and selective antagonist of EBI2 (GPR183) receptor (IC50 of 11 and 15 nM for human and mouse EBI2 receptors respectively).
-
In VitroNIBR189 (0-1 μM; 3 h) blocks migration of U937 cells.NIBR189 (0-10 μM) blocks oxysterol-dependent activation with an IC50 value of 9 nM. Cell Migration Assay Cell Line:U937 cell lines Concentration:0-1 μM Incubation Time:3 hours Result:Blocked the direct migration of U937 cells with an IC50 value of 0.3 nM.
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetGPR
-
RecptorGPR183
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1599432-08-2
-
Formula Weight429.31
-
Molecular FormulaC21H21BrN2O3
-
Purity>98% (HPLC)
-
SolubilityDMSO:47 mg/mL (109.48 mM)
-
SMILESCOc1ccc(cc1)C(=O)N1CCN(CC1)C(=O)\C=C\c1ccc(Br)cc1
-
Chemical Name(E)-3-(4-bromophenyl)-1-(4-(4-methoxybenzoyl)piperazin-1-yl)prop-2-en-1-one
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Gessier F Preuss I Yin H et al. Identification and Characterization of Small Molecule Modulators of the Epstein–Barr Virus-Induced Gene 2 (EBI2) Receptor[J]. Journal of Medicinal Chemistry 2014 57(8):3358-3368.
molnova catalog
related products
-
ZK 756326
ZK 756326 is a selective, non-peptide CCR8 chemokine receptor agonist (IC50: 1.8 μM, in human; 2.6?μM, in mouse).
-
Pamoic acid
Pamoic acid is the orphan G protein-coupled receptor GPR35?agonist. Pamoic acid activates ERK and beta-arrestin2 and causes antinociceptive activity.
-
CRTh2 antagonist 2
CRTh2 antagonist 2 is a selective and potent CRTH2 antagonist, IC50≤10 nM. CRTh2 antagonist 2 can be used to study the direction of androgenic alopecia.
Cart
sales@molnova.com