RS 102895 hydrochloride - 98%, high purity , CAS No.1173022-16-6

  • ≥98%
Item Number
R274707
Grouped product items
SKUSizeAvailabilityPrice Qty
R274707-5mg
5mg
2
$79.90
R274707-10mg
10mg
2
$127.90
R274707-25mg
25mg
2
$288.90
R274707-50mg
50mg
2
$495.90
R274707-100mg
100mg
2
$892.90

Selective CCR2 receptor antagonist

Basic Description

Synonyms1'-[2-[4-(Trifluoromethyl)phenyl]ethyl]-spiro[4H-3,1-benzoxazine-4,4'-piperidin]-2(1H)-one HCl | AKOS024456940 | 1'-{2-[4-(Trifluoromethyl)phenyl]ethyl}spiro[3,1-benzoxazine-4,4'-piperidin]-2(1H)-one--hydrogen chloride (1/1) | BCP18408 | RS-102895 HCl | 1
Specifications & Purity≥98%
Biochemical and Physiological MechanismsSelective CCR2 receptor antagonist (IC 50 values are 360 nM and 17.8 μM at CCR2 and CCR1 receptors, respectively). Inhibits MCP-1 and MCP-3 stimulated calcium influx (IC 50 values are 32 and 130 nM, respectively). Active in vivo .
Storage TempStore at -20°C,Argon charged,Desiccated
Shipped InIce chest + Ice pads
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

 

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Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

Pubchem Sid504768521
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504768521
IUPAC Name 1'-[2-[4-(trifluoromethyl)phenyl]ethyl]spiro[1H-3,1-benzoxazine-4,4'-piperidine]-2-one;hydrochloride
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
InChi Key KRRISOFSWVKYBF-UHFFFAOYSA-N
Canonical SMILES C1CN(CCC12C3=CC=CC=C3NC(=O)O2)CCC4=CC=C(C=C4)C(F)(F)F.Cl
Isomeric SMILES C1CN(CCC12C3=CC=CC=C3NC(=O)O2)CCC4=CC=C(C=C4)C(F)(F)F.Cl
PubChem CID 16759153
Molecular Weight 426.9

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
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5 results found

Lot NumberCertificate TypeDateItem
C23021029Certificate of AnalysisDec 20, 2023 R274707
C23021033Certificate of AnalysisDec 20, 2023 R274707
C23021186Certificate of AnalysisDec 20, 2023 R274707
C23021187Certificate of AnalysisDec 20, 2023 R274707
C23021192Certificate of AnalysisDec 20, 2023 R274707

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References

1. Wang JB et al..  (2022)  CDK5RAP3 acts as a tumour suppressor in gastric cancer through the infiltration and polarization of tumour-associated macrophages..  Cancer Gene Ther,      [PMID:35999359]
2. Han S et al..  (2019)  High CCL7 expression is associated with migration, invasion and bone metastasis of non-small cell lung cancer cells..  Am J Transl Res,  11  (442-452).  [PMID:30788000]
3. Zhan X et al..  (2020)  Monocyte Chemoattractant Protein-1 stimulates the differentiation of rat stem and progenitor Leydig cells during regeneration..  BMC Dev Biol,  20  (20).  [PMID:33023470]
4. Maolake A et al..  (2017)  Tumor-associated macrophages promote prostate cancer migration through activation of the CCL22-CCR4 axis..  Oncotarget,  (6): (9739-9751).  [PMID:28039457]

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