SB 328437 (DMSO solution) , CAS No.247580-43-4, Antagonist of CCR3

Item Number
S275358
Grouped product items
SKUSizeAvailabilityPrice Qty
S275358-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$187.90
S275358-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$612.90

Highly potent selective CCR3 antagonist

Basic Description

SynonymsF81757 | AKOS040745353 | HMS3414E05 | SCHEMBL3930225 | MS-26166 | SB 328437 | L-Phenylalanine, N-(1-naphthalenylcarbonyl)-4-nitro-, methyl ester | BDBM50100021 | DTXSID30440571 | N-(1-NAPHTHALENYLCARBONYL)-4-NITRO-L-PHENYLALANINE METHYL ESTER | methyl (2S
Specifications & PurityMoligand™
Storage TempProtected from light,Store at -20°C,Desiccated
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionAntagonist of CCR3
Product Description

Shipped at Room Temperature. Store at -20°C. Store In the Dark. Store under desiccating conditions.

Associated Targets(Human)

CCR3 Tchem C-C chemokine receptor type 3 (11 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CCR3 Tchem C-C chemokine receptor type 3 (1666 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name methyl (2S)-2-(naphthalene-1-carbonylamino)-3-(4-nitrophenyl)propanoate
INCHI InChI=1S/C21H18N2O5/c1-28-21(25)19(13-14-9-11-16(12-10-14)23(26)27)22-20(24)18-8-4-6-15-5-2-3-7-17(15)18/h2-12,19H,13H2,1H3,(H,22,24)/t19-/m0/s1
InChi Key VMFGCGRAIBLAFY-IBGZPJMESA-N
Canonical SMILES COC(=O)C(CC1=CC=C(C=C1)[N+](=O)[O-])NC(=O)C2=CC=CC3=CC=CC=C32
Isomeric SMILES COC(=O)[C@H](CC1=CC=C(C=C1)[N+](=O)[O-])NC(=O)C2=CC=CC3=CC=CC=C32
PubChem CID 10474776
Molecular Weight 378.38

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Safety and Hazards(GHS)

Pictogram(s) GHS09,   GHS07
Signal Warning
Hazard Statements

H302:Harmful if swallowed

H400:Very toxic to aquatic life

Precautionary Statements

P273:Avoid release to the environment.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P391:Collect spillage.

P330:Rinse mouth.

P301+P317:IF SWALLOWED: Get medical help.

Related Documents

References

1. Abonyo BO et al..  (2005)  Autoregulation of CCL26 synthesis and secretion in A549 cells: a possible mechanism by which alveolar epithelial cells modulate airway inflammation..  Am J Physiol Lung Cell Mol Physiol,  289  (3): (L478-88).  [PMID:15863444]
2. White JR et al..  (2000)  Identification of potent, selective non-peptide CC chemokine receptor-3 antagonist that inhibits eotaxin-, eotaxin-2-, and monocyte chemotactic protein-4-induced eosinophil migration..  J Biol Chem,  275  (47): (36626-31).  [PMID:10969084]
3. Mori A et al..  (2007)  Selective suppression of Th2-mediated airway eosinophil infiltration by low-molecular weight CCR3 antagonists..  Int Immunol,  19  (8): (913-21).  [PMID:17804691]

Solution Calculators