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Ki16425 - ≥98%, high purity , CAS No.355025-24-0, Antagonist of GPR87;Antagonist of LPA 1 receptor;Antagonist of LPA 2 receptor;Antagonist of LPA 3 receptor

  • Moligand™
  • ≥98%
Item Number
K126742
Grouped product items
SKUSizeAvailabilityPrice Qty
K126742-1mg
1mg
In stock
$15.90
K126742-5mg
5mg
In stock
$64.90
K126742-25mg
25mg
In stock
$292.90
K126742-100mg
100mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,053.90

LPA1and LPA3receptor antagonist

Basic Description

SynonymsKi16425|355025-24-0|Ki-16425|Ki 16425|3-((4-(4-(((1-(2-Chlorophenyl)ethoxy)carbonyl)amino)-3-methylisoxazol-5-yl)benzyl)thio)propanoic acid|3-[({4-[4-({[1-(2-chlorophenyl)ethoxy]carbonyl}amino)-3-methyl-1,2-oxazol-5-yl]phenyl}methyl)sulfanyl]propanoic aci
Specifications & PurityMoligand™, ≥98%
Biochemical and Physiological MechanismsAntagonist of the lysophosphatidic acid receptors LPA1and LPA3(Kivalues are 0.25 and 0.36μM respectively, in a GTPγS binding assay). Blocks LPA-induced dephosphorylation of Yes-associated protein (YAP) and WW domain-containing transcription regulator prot
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionAntagonist of GPR87;Antagonist of LPA 1 receptor;Antagonist of LPA 2 receptor;Antagonist of LPA 3 receptor
Product Description

Ki16425 is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA3 with Ki of 0.34 μM, 6.5 μM and 0.93 μM in RH7777 cell lines, respectively, shows no activity at LPA4, LPA5, LPA6.
A competitive inhibitor of EDG-2, EDG-4, and EDG-7.

Associated Targets

GPR87 Tchem G-protein coupled receptor 87 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ENPP2 Tchem Ectonucleotide pyrophosphatase/phosphodiesterase family member 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

VDR Tclin Vitamin D3 receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

LPAR3 Tchem Lysophosphatidic acid receptor 3 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

LPAR1 Tchem Lysophosphatidic acid receptor 1 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

LPAR5 Tchem Lysophosphatidic acid receptor 5 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

LPAR2 Tchem Lysophosphatidic acid receptor 2 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 3-[[4-[4-[1-(2-chlorophenyl)ethoxycarbonylamino]-3-methyl-1,2-oxazol-5-yl]phenyl]methylsulfanyl]propanoic acid
INCHI InChI=1S/C23H23ClN2O5S/c1-14-21(25-23(29)30-15(2)18-5-3-4-6-19(18)24)22(31-26-14)17-9-7-16(8-10-17)13-32-12-11-20(27)28/h3-10,15H,11-13H2,1-2H3,(H,25,29)(H,27,28)
InChi Key LLIFMNUXGDHTRO-UHFFFAOYSA-N
Canonical SMILES CC1=NOC(=C1NC(=O)OC(C)C2=CC=CC=C2Cl)C3=CC=C(C=C3)CSCCC(=O)O
Isomeric SMILES CC1=NOC(=C1NC(=O)OC(C)C2=CC=CC=C2Cl)C3=CC=C(C=C3)CSCCC(=O)O
WGK Germany 3
PubChem CID 10367662
Molecular Weight 474.96

Certificates

Certificate of Analysis(COA)

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4 results found

Lot NumberCertificate TypeDateItem
H2112135Certificate of AnalysisMay 12, 2023 K126742
H2112145Certificate of AnalysisMay 12, 2023 K126742
H2112146Certificate of AnalysisMay 12, 2023 K126742
H2112149Certificate of AnalysisMay 12, 2023 K126742

Chemical and Physical Properties

SolubilitySolvent:DMSO, Max Conc. mg/mL: 47.5, Max Conc. mM: 100; Solvent:1eq. NaOH, Max Conc. mg/mL: 9.5, Max Conc. mM: 20
Refractive Index1.63
Boil Point(°C)623.7° C at 760 mmHg
Melt Point(°C)59.5-60.5°C

Safety and Hazards(GHS)

WGK Germany 3

Related Documents

Solution Calculators