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VUF 11222 - 98%, high purity , CAS No.1414376-84-3

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VUF 11222 - 98%, high purity , CAS No.1414376-84-3

COA

Grade & Purity:

≥98%

Cas Number: 1414376-84-3
Molecular Weight: 552.33
PubChem CID: 71459294

In stock

Item Number

V288506

Grouped product items
SKU	Size	Availability	Price
V288506-10mg	10mg	2	$649.90
V288506-50mg	50mg	2	$1,669.90
V288506-25mg	25mg	2	$1,129.90
V288506-100mg	100mg	1	$2,669.90

High affinity non-peptide CXCR3 agonist

View related series

Chemokine CXC Receptor Agonists (1) Class A GPCR (4138)

Basic Description

Synonyms	2'-Bromo-N-[[(1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl]methyl]-N,N-dimethyl-[1,1'-biphenyl]-4-methanaminium iodide
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	High affinity non-peptide CXCR3 agonist (pKi= 7.2).
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	High affinity non-peptide CXCR3 agonist.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Biphenyls and derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Biphenyls and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Brominated biphenyls
Alternative Parents	Bicyclic monoterpenoids Aromatic monoterpenoids Phenylmethylamines Benzylamines Bromobenzenes Aralkylamines Aryl bromides Tetraalkylammonium salts Organobromides Organic iodide salts Hydrocarbon derivatives Organic cations
Molecular Framework	Aromatic homopolycyclic compounds
Substituents	Brominated biphenyl - Aromatic monoterpenoid - Bicyclic monoterpenoid - Pinane monoterpenoid - Monoterpenoid - Benzylamine - Phenylmethylamine - Aralkylamine - Bromobenzene - Halobenzene - Aryl bromide - Aryl halide - Tetraalkylammonium salt - Quaternary ammonium salt - Amine - Organic nitrogen compound - Organohalogen compound - Organobromide - Organonitrogen compound - Organic salt - Organic iodide salt - Hydrocarbon derivative - Organic cation - Aromatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as brominated biphenyls. These are organic compounds containing a biphenyl moiety substituted at one or more positions by a bromine atom.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

CXCR3 Tchem C-X-C chemokine receptor type 3 (1 Activities)

Discover Target: CXCR3

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

IUPAC Name	[4-(2-bromophenyl)phenyl]methyl-[[(1R,5S)-6,6-dimethyl-2-bicyclo[3.1.1]hept-2-enyl]methyl]-dimethylazanium;iodide
INCHI	InChI=1S/C25H31BrN.HI/c1-25(2)21-14-13-20(23(25)15-21)17-27(3,4)16-18-9-11-19(12-10-18)22-7-5-6-8-24(22)26;/h5-13,21,23H,14-17H2,1-4H3;1H/q+1;/p-1/t21-,23-;/m0./s1
InChIKey	IXXWHYDKYNWDKJ-IUQUCOCYSA-M
Smiles	CC1(C2CC=C(C1C2)C[N+](C)(C)CC3=CC=C(C=C3)C4=CC=CC=C4Br)C.[I-]
Isomeric SMILES	CC1([C@H]2CC=C([C@@H]1C2)C[N+](C)(C)CC3=CC=C(C=C3)C4=CC=CC=C4Br)C.[I-]
PubChem CID	71459294
Molecular Weight	552.33

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

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

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot Number	Certificate Type	Date	Item
H2427377	Certificate of Analysis	May 16, 2024	V288506
H2427378	Certificate of Analysis	May 16, 2024	V288506
H2427379	Certificate of Analysis	May 16, 2024	V288506
H2427383	Certificate of Analysis	May 16, 2024	V288506
H2427386	Certificate of Analysis	May 16, 2024	V288506
H2427387	Certificate of Analysis	May 16, 2024	V288506
H2427388	Certificate of Analysis	May 16, 2024	V288506
H2427406	Certificate of Analysis	May 16, 2024	V288506

Chemical and Physical Properties

Solubility	Solvent:DMSO, Max Conc. mg/mL: 55.23, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 5.52, Max Conc. mM: 10 with gentle warming

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