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RS 102895

Basic information Safety Supplier Related

RS 102895 Basic information

Product Name:
RS 102895
Synonyms:
  • 1'-(4-(TrifluoroMethyl)phenethyl)spiro[benzo[d][1,3]oxazine-4,4'-piperidin]-2(1H)-one hydrochloride
  • 1'-[2-[4-(trifluoromethyl)phenyl]ethyl]spiro[1H-3,1-benzoxazine-4,4'-piperidine]-2-one,hydrochloride
  • RS 102895 HYDROCHLORIDE
  • 1'-[2-[4-(trifluoromethyl)phenyl]ethyl]-spiro[4h-3,1-benzoxazine-4,4'-peperidin]-2(1h)-one
  • 1'-[2-[4-(TRIFLUOROMETHYL)PHENYL]ETHYL]-SPIRO[4H-3,1-BENZOXAZINE-4,4'-PIPERIDIN]-2(1H)-ONE HYDROCHLORIDE
  • Spiro[4H-3,1-benzoxazine-4,4'-piperidin]-2(1H)-one, 1'-[2-[4-(trifluoromethyl)phenyl]ethyl]-
  • 1'-(4-(trifluoromethyl)phenethyl)spiro[benzo[d][1,3]oxazine-4,4'-piperidin]-2(1H)-one
  • CC chemokine receptor,CCR,Inhibitor,RS102895,inhibit,RS-102895,RS 102895
CAS:
300815-41-2
MF:
C21H21F3N2O2
MW:
390.4
Product Categories:
  • RS 102895 CCR2-selective chemokine receptor antagonist.
  • Cytokine signaling
Mol File:
300815-41-2.mol
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RS 102895 Chemical Properties

Boiling point:
446.1±45.0 °C(Predicted)
Density 
1.33±0.1 g/cm3 (20 ºC 760 Torr)
storage temp. 
Desiccate at RT
solubility 
DMSO: 18 mg/mL, clear, colorless
form 
powder
pka
13.46±0.20(Predicted)
color 
white
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
SMILES
Cl.FC(F)(F)c1ccc(CCN2CCC3(CC2)OC(=O)Nc4ccccc34)cc1
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
Storage Class
11 - Combustible Solids
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RS 102895 Usage And Synthesis

Uses

RS 102895 is a CCR2-selective chemokine receptor inhibitor.

Biological Activity

CCR2-selective chemokine receptor antagonist (IC 50 values are 0.36 and 17.8 μ M for inhibition of human recombinant CCR2b and CCR1 receptors respectively). Blocks MCP-1-stimulated calcium influx and chemotaxis with IC 50 values of 32 nM and 1.7 μ M respectively. Also inhibits α 1A , α 1D and 5-HT 1A receptors.

in vivo

RS102895 (3 g/L) causes progressive decrease in pain threshold in rats with bone cancer pain (BCP) at day 3-9 after surgery via intrathecal injection, but the pain threshold increases after 12 days. RS102895 also potently reverses the pattern of NR2B, nNOS, and SIGIRR expression in spinal cord[3].

IC 50

CCR2: 360 nM (IC50); CCR1: 17800 nM (IC50); Human α1a receptor: 130 nM (IC50); Human α1d receptor: 320 nM (IC50); 5HT-1a receptor: 470 nM (IC50)

RS 102895Supplier

Shanghai Boyle Chemical Co., Ltd.
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Email
sales@boylechem.com
3B Pharmachem (Wuhan) International Co.,Ltd.
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821-50328103-801 18930552037
Email
3bsc@sina.com
VDM Biochemicals
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0330-2528181
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sales@vdmbio.com
MedChemexpress LLC
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021-58955995
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sales@medchemexpress.cn
Quality Control Solutions Ltd.
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66853366 13670046396
Email
sales@chem-strong.com