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Merck
CN
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文件

SML0669

Sigma-Aldrich

VUF11207 trifluoroacetate salt

≥98% (HPLC)

别名:

(E)-N-(3-(2-Fluorophenyl)-2-methylallyl)-3,4,5-trimethoxy-N-(2-(1-methylpyrrolidin-2-yl)ethyl)benzamide trifluoroacetate salt, N-[(2E)-3-(2-Fluorophenyl)-2-methyl-2-propen-1-yl]-3,4,5-trimethoxy-N-[2-(1-methyl-2-pyrrolidinyl)ethyl]-benzamide trifluoroacetate salt

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About This Item

经验公式（希尔记法）:
C27H35FN2O4 · C2HF3O2
CAS号:
1378524-41-4
分子量:
584.60
MDL编号:
MFCD26961112
UNSPSC代码:
51111800
PubChem化学物质编号:
329825579
NACRES:
NA.77

质量水平

100

检测方案

≥98% (HPLC)

储存条件

desiccated
protect from light

颜色

white to beige

溶解性

H2O: 5 mg/mL, clear (warmed)

储存温度

−20°C

SMILES字符串

O=C(N(CCC1N(C)CCC1)C/C(C)=C/C2=C(F)C=CC=C2)C3=CC(OC)=C(OC)C(OC)=C3.OC(C(F)(F)F)=O

InChI

1S/C27H35FN2O4.C2HF3O2/c1-19(15-20-9-6-7-11-23(20)28)18-30(14-12-22-10-8-13-29(22)2)27(31)21-16-24(32-3)26(34-5)25(17-21)33-4;3-2(4,5)1(6)7/h6-7,9,11,15-17,22H,8,10,12-14,18H2,1-5H3;(H,6,7)/b19-15+;

InChI key

GZXNWMFPSYCITC-QTCZRQAZSA-N

生化/生理作用

VUF11207 is a highly potent CXCR7 agonist. VUF11207 induces recruitment of β-arrestin2 to the CXCR7 followed by internalization of the receptor.
VUF11207 is considered as a selective inhibitor of CXCR4 (C-X-C motif chemokine receptor 4).

其他说明

Hygroscopic and light sensitive

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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Breast Cancer: An Examination of the Potential of ACKR3 to Modify the Response of CXCR4 to CXCL12
del Molino del Barrio I, et al.
International Journal of Molecular Sciences, 19(11), 3592-3592 (2018)

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