
BI 6901
CAS No. 2040401-92-9
BI 6901( BI6901 )
Catalog No. M13172 CAS No. 2040401-92-9
BI 6901 is a potent, selective CCR10 antagonist with Aequorin Ca2+ flux pIC50 of 9.0.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 338 | Get Quote |
![]() ![]() |
50MG | 1341 | Get Quote |
![]() ![]() |
100MG | 2124 | Get Quote |
![]() ![]() |
200MG | Get Quote | Get Quote |
![]() ![]() |
500MG | Get Quote | Get Quote |
![]() ![]() |
1G | Get Quote | Get Quote |
![]() ![]() |
Biological Information
-
Product NameBI 6901
-
NoteResearch use only, not for human use.
-
Brief DescriptionBI 6901 is a potent, selective CCR10 antagonist with Aequorin Ca2+ flux pIC50 of 9.0.
-
DescriptionBI 6901 is a potent, selective CCR10 antagonist with Aequorin Ca2+ flux pIC50 of 9.0, shows high selectivity over other GPCRs; inhibits the CCL27 dependent chemotaxis of Ba/F3 cells stably transfected with human CCR10 with pIC50 of 9.0, BI 6901 is efficacious in a murine model of DNFB contact hypersensitivity, inhibits DNFB stimulated inflammatory response in sensitized Balb-C mice.
-
In Vitro——
-
In VivoAnimal Model:Balb-C mice with a DNFB model of contact hypersensitivity.Dosage:100 mg/kg Administration:Intraperitoneal?injection Result:Had a inhibitory effect on the DNFB stimulated inflammatory response in sensitized Balb-c mice.
-
SynonymsBI6901
-
PathwayGPCR/G Protein
-
TargetChemokine Receptor
-
RecptorChemokine Receptor
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2040401-92-9
-
Formula Weight453.561
-
Molecular FormulaC23H27N5O3S
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 160 mg/mL (352.76 mM)
-
SMILESO=S(C1=CC=CC2=C1C=CN2)(N[C@H](CCN3C(C#N)=CC=C3)C(N4CCC(C)CC4)=O)=O
-
Chemical NameN-[(2R)-4-(2-cyanopyrrol-1-yl)-1-(4-methylpiperidin-1-yl)-1-oxobutan-2-yl]-1H-indole-4-sulfonamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Abeywardane A, et al. Bioorg Med Chem Lett. 2016 Nov 1;26(21):5277-5283.
molnova catalog



related products
-
SX-517
A potent, specific, noncompetitive dual CXCR1 and CXCR2 antagonist with IC50 of 38 nM (vs. CXCL1) and 36 nM (vs. CXCL8), respectively.
-
POL3026
A highly potent, selective beta-hairpin mimetic CXCR4 inhibitor with IC50 of 1.2 nM in Ca2+ flux assay.
-
Chalcone 4 hydrate
Chalcone 4 hydrate is a potent, selective inhibitor of CXCL12 binding to CXCR4 and CXCR7 with IC50 of 200 nM.