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AB120812

RS 102895 hydrochloride, CCR2 receptor antagonist

RS 102895 hydrochloride, CCR2 receptor antagonist

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(5 Publications)

MW 426.9 Da, Purity >99%. Selective CCR2 receptor antagonist (IC50 values are 360 nM and 17.8 μM at CCR2 and CCR1 receptors, respectively). Inhibits MCP-1 and MCP-3 stimulated calcium influx (IC50 values are 32 and 130 nM, respectively). Active in vivo.
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Chemical Structure - RS 102895 hydrochloride, CCR2 receptor antagonist (AB120812)
  • Chemical Structure

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Chemical Structure - RS 102895 hydrochloride, CCR2 receptor antagonist (AB120812)

2D chemical structure image of ab120812, RS 102895 hydrochloride, CCR2 receptor antagonist

关键信息

CAS 号

300815-41-2

纯度

>99%

形式

Solid

form

分子量

426.9 Da

分子式

C<sub>2</sub><sub>1</sub>H<sub>2</sub><sub>2</sub>ClF<sub>3</sub>N<sub>2</sub>O<sub>2</sub>

PubChem

16759153

属性

Synthetic

溶解度

Soluble in DMSO to 50 mM

生化试剂名称

RS 102895 hydrochloride

生物学描述

Selective CCR2 receptor antagonist (IC50 values are 360 nM and 17.8 μM at CCR2 and CCR1 receptors, respectively). Inhibits MCP-1 and MCP-3 stimulated calcium influx (IC50 values are 32 and 130 nM, respectively). Active in vivo.

经典 SMILES

C1CN(CCC12C3=CC=CC=C3NC(=O)O2)CCC4=CC=C(C=C4)C(F)(F)F.Cl

InChi

InChI=1S/C21H21F3N2O2.ClH/c22-21(23,24)16-7-5-15(6-8-16)9-12-26-13-10-20(11-14-26)17-3-1-2-4-18(17)25-19(27)28-20;/h1-8H,9-14H2,(H,25,27);1H

InChiKey

KRRISOFSWVKYBF-UHFFFAOYSA-N

IUPAC 名

1'-[2-[4-(trifluoromethyl)phenyl]ethyl]spiro[1H-3,1-benzoxazine-4,4'-piperidine]-2-one;hydrochloride

性能和储存信息

运输条件
Ambient - Can Ship with Ice
推荐的短期储存条件
Ambient
推荐的长期储存条件
Ambient
储存信息
Store under desiccating conditions|The product can be stored for up to 12 months

产品实验方案

文献 (5)

Recent publications for all applications. Explore the full list and refine your search

Molecular medicine (Cambridge, Mass.) 30:21 PubMed38317079

2024

Platelet-derived growth factor signaling in pericytes promotes hypothalamic inflammation and obesity.

Applications

Unspecified application

Species

Unspecified reactive species

Akira Okekawa,Tsutomu Wada,Yasuhiro Onogi,Yuki Takeda,Yuichiro Miyazawa,Masakiyo Sasahara,Hiroshi Tsuneki,Toshiyasu Sasaoka

Cancer gene therapy 30:22-37 PubMed35999359

2022

CDK5RAP3 acts as a tumour suppressor in gastric cancer through the infiltration and polarization of tumour-associated macrophages.

Applications

Unspecified application

Species

Unspecified reactive species

Jia-Bin Wang,You-Xin Gao,Yin-Hua Ye,Tong-Xing Lin,Ping Li,Jian-Xian Lin,Qi-Yue Chen,Long-Long Cao,Mi Lin,Ru-Hong Tu,Ju-Li Lin,Ze-Ning Huang,Hua-Long Zheng,Jian-Wei Xie,Chao-Hui Zheng,Chang-Ming Huang

BMC developmental biology 20:20 PubMed33023470

2020

Monocyte Chemoattractant Protein-1 stimulates the differentiation of rat stem and progenitor Leydig cells during regeneration.

Applications

Unspecified application

Species

Unspecified reactive species

Xiangcheng Zhan,Jingwei Zhang,Saiyang Li,Xiaolu Zhang,Linchao Li,Tiantian Song,Qunlong Liu,Jun Lu,Yunfei Xu,Ren-Shan Ge

American journal of translational research 11:442-452 PubMed30788000

2019

High CCL7 expression is associated with migration, invasion and bone metastasis of non-small cell lung cancer cells.

Applications

Unspecified application

Species

Unspecified reactive species

Shuai Han,Ting Wang,Yuanming Chen,Zhitao Han,Lihan Guo,Zhipeng Wu,Wangjun Yan,Haifeng Wei,Tielong Liu,Jian Zhao,Wang Zhou,Xinghai Yang,Jianru Xiao

Oncotarget 8:9739-9751 PubMed28039457

2017

Tumor-associated macrophages promote prostate cancer migration through activation of the CCL22-CCR4 axis.

Applications

Unspecified application

Species

Unspecified reactive species

Aerken Maolake,Kouji Izumi,Kazuyoshi Shigehara,Ariunbold Natsagdorj,Hiroaki Iwamoto,Suguru Kadomoto,Yuta Takezawa,Kazuaki Machioka,Kazutaka Narimoto,Mikio Namiki,Wen-Jye Lin,Guzailinuer Wufuer,Atsushi Mizokami
View all publications

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