239824 Sigma-AldrichCXCR7 Agonist, VUF11207 - CAS 1378524-41-4 - Calbiochem
CXCR7 Agonist, VUF11207, CAS 1378524-41-4, is a high affinity and high potency ligand of CXCR7 (pKi = 8.1). Induces the recruitment of β-arrestin2 and subsequent interenalization of CXCR7.
More>> CXCR7 Agonist, VUF11207, CAS 1378524-41-4, is a high affinity and high potency ligand of CXCR7 (pKi = 8.1). Induces the recruitment of β-arrestin2 and subsequent interenalization of CXCR7. Less<<Synonyms: (E)-N-(3-(2-fluorophenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide, RDC1 agonist, CMKOR1 Agonist, CXCR-7 Agonist, CXC-R7 Agonist, RDC-1 Agonist, GPR159 Agonist
Recommended Products
Overview
Replacement Information |
---|
Key Specifications Table
CAS # | Empirical Formula |
---|---|
1378524-41-4 | C₂₇H₃₅FN₂O₄ |
Products
Catalog Number | Packaging | Qty/Pack | |
---|---|---|---|
239824-10MG | Glass bottle | 10 mg |
References | |
---|---|
References | Wijtmans, M., et al. 2011, Eur J Med Chem 51, 184. |
Product Information | |
---|---|
CAS number | 1378524-41-4 |
Form | Light yellow oil |
Hill Formula | C₂₇H₃₅FN₂O₄ |
Reversible | Y |
Structure formula Image | |
Quality Level | MQ100 |
Biological Information | |
---|---|
Primary Target | CXCR7 |
Purity | ≥95% by HPLC |
Physicochemical Information | |
---|---|
Cell permeable | Y |
Dimensions |
---|
Materials Information |
---|
Toxicological Information |
---|
Safety Information according to GHS |
---|
Safety Information |
---|
Product Usage Statements |
---|
Packaging Information | |
---|---|
Packaged under inert gas | Packaged under inert gas |
Transport Information |
---|
Supplemental Information |
---|
Specifications |
---|
Global Trade Item Number | |
---|---|
Catalog Number | GTIN |
239824-10MG | 04055977198980 |
Documentation
CXCR7 Agonist, VUF11207 - CAS 1378524-41-4 - Calbiochem SDS
Title |
---|
CXCR7 Agonist, VUF11207 - CAS 1378524-41-4 - Calbiochem Certificates of Analysis
Title | Lot Number |
---|---|
239824 |
References
Reference overview |
---|
Wijtmans, M., et al. 2011, Eur J Med Chem 51, 184. |