VDM11

CAT: 0804-HY-103339-01Size: 5 mgDry Ice: NoHazardous: No

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CAT#:0804-HY-103339-01Size:5 mg

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24/48H Stock Items & 2 to 6 Weeks non Stock Items.

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Description

VDM11 is a potent and selective anandamide membrane transporter (AMT) inhibitor[1]. VDM11 inhibits FAAH and MAGL and may act as an alternative FAAH substrate[2].

CAS Number

313998-81-1

UNSPSC

12352005

Hazard Statement

H302-H312-H332-H334

Target

FAAH; MAGL

Type

Reference compound

Related Pathways

Metabolic Enzyme/Protease; Neuronal Signaling

Field of Research

Neurological Disease

Assay Protocol

https://www.medchemexpress.com/vdm11.html

Solubility

10 mM in DMSO

Smiles

CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(NC1=CC=C(O)C=C1C)=O

Molecular Formula

C27H39NO2

Molecular Weight

409.60

Precautions

P261-P264-P270-P271-P280-P284-P302+P352-P304+P340-P330-P362+P364-P501

References & Citations

[1]De Petrocellis L, et al. Overlap between the ligand recognition properties of the anandamide transporter and the VR1 vanilloid receptor: inhibitors of anandamide uptake with negligible capsaicin-like activity. FEBS Lett. 2000 Oct 13;483 (1) :52-6. |[2]Vandevoorde S, Fowler CJ. Inhibition of fatty acid amide hydrolase and monoacylglycerol lipase by the anandamide uptake inhibitor VDM11: evidence that VDM11 acts as an FAAH substrate. Br J Pharmacol. 2005 Aug;145 (7) :885-93.

Shipping Conditions

Room temperature

Scientific Category

Reference compound1

Clinical Information

No Development Reported

VDM11

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