An inhibitor of DAGLα and DAGLβ
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Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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A1480LS

Item No. 45340

Product Insert (PDF)
Technical Information
Formal Name
(S)-(2-benzyl-4-(6-(trifluoromethyl)pyrazin-2-yl)piperazin-1-yl)(5-phenyl-2H-indazol-2-yl)methanone
Molecular Formula
C30H25F3N6O
Formula Weight
Purity
≥98%
A solid
DMSO: Soluble: ≥ 10 mg/ml
SMILES
O=C(N1N=C2C=CC(C3=CC=CC=C3)=CC2=C1)N4CCN(C[C@@H]4CC5=CC=CC=C5)C6=NC(C(F)(F)F)=CN=C6
InChi Code
InChI=1S/C30H25F3N6O/c31-30(32,33)27-17-34-18-28(35-27)37-13-14-38(25(20-37)15-21-7-3-1-4-8-21)29(40)39-19-24-16-23(11-12-26(24)36-39)22-9-5-2-6-10-22/h1-12,16-19,25H,13-15,20H2/t25-/m0/s1
InChi Key
LULPTIBVONZWPH-VWLOTQADSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    A1480LS is a peripherally biased inhibitor of diacylglycerol lipase α (DAGLα) and DAGLβ (IC50s = 6 and 4 nM, respectively, in human brain membrane homogenates).1 It reduces levels of the DAGL-derived endocannabinoid 2-arachidonoyl glycerol (2-AG) in peripheral tissue but not in the brain in mice when administered at 20 mg/kg. A1480LS (20 mg/kg, p.o.) reduces mechanical allodynia in rat models of inflammatory pain and chemotherapy-induced neuropathy without inducing CNS adverse effects in the Irwin primary observation test.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Tufail, Y.Z., Guijas, C., Kummer, D.A., et alSuppression of pain transmission and behavior by inhibition of peripheral diacylglycerol metabolism. Cell Chem. Bio. 33(1), 74-90.e19 (2025).