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VU 0364439
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
VU 0364439图片
CAS NO:1246086-78-1
规格:≥98%
包装与价格:
包装价格(元)
2mg电议
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
250mg电议
500mg电议

产品介绍
理化性质和储存条件
Molecular Weight (MW)422.29
FormulaC18H13Cl2N3O3S
CAS No.1246086-78-1
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 85 mg/mL (201.3 mM)
Water: <1 mg/mL
Ethanol: <1 mg/mL
SMILES CodeO=C(C1=NC=CC=C1)NC2=CC=C(S(=O)(NC3=CC=CC=C3Cl)=O)C(Cl)=C2
SynonymsVU0364439, VU-0364439, VU 0364439
实验参考方法
In Vitro

In vitro activity: VU 0364439 is a mGlu4 (metabotropic glutamate receptor 4) positive allosteric modulator (PAM) with EC50 value of 19.8 nM. VU 0364439 possessed less favorable pharmacokinetic properties. The properties of VU 0364439 prevents VU 0364439 itself from being used as an in vivo tool, but VU 0364439 might inform the mGlu4 community with more in vitro tool compounds. The activation of the mGlu4 receptor, either with an orthosteric agonist or a positive allosteric modulator (PAM), provides impactful interventions in diseases such as Parkinson's disease, anxiety, and pain. mGlu4 PAMs may have several advantages over mGlu4 agonists for a number of reasons.


Kinase Assay: VU 0364439 is a mGlu4 (metabotropic glutamate receptor 4) positive allosteric modulator (PAM) with EC50 value of 19.8 nM.


Cell Assay: VU 0364439 exhibited excellent in vitro maximal response and potency relative to another PAM, (–)-PHCCC (a partially selective mGlu4 potentiator, its chemical structure could be found in reference 4). Starting at 30μM, using a 1:3 serial dilutions, VU 0364439 was tested in triplicate. The entire test was performed on one day. Finally, the % (–)-PHCCC value of VU 0364439 was 102.3. The value of % (–)-PHCCC was computed through dividing the maximal response elicited by VU 0364439 by the response of the control PAM, (–)-PHCCC, on the same day. It was also found that the EC50 value of VU 0364439 was 19.8 nM at human mGlu4

In VivoVU 0364439 possess less than ideal PK properties preventing their use as in vivo tools. It shows better stability in HLM (63% remaining) than RLM (2% remaining).
Animal modelN/A
Formulation & DosageN/A
ReferencesBioorg Med Chem Lett. 2010 Sep 1;20(17):5175-8; J Med Chem. 2011 Jul 28;54(14):5070-81.