An MRGPRX1 positive allosteric modulator
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ML-382

Item No. 36668

Technical Information
Formal Name
2-[(cyclopropylsulfonyl)amino]-N-(2-ethoxyphenyl)-benzamide
CAS Number
1646499-97-9
Synonyms
  • VU0485891
Molecular Formula
C18H20N2O4S
Formula Weight
Purity
≥98%
Formulation
A solid
DMF: 5 mg/mlDMSO: 2 mg/mlEthanol: 3 mg/ml
SMILES
O=S(NC1=C(C=CC=C1)C(NC2=CC=CC=C2OCC)=O)(C3CC3)=O
InChi Code
InChI=1S/C18H20N2O4S/c1-2-24-17-10-6-5-9-16(17)19-18(21)14-7-3-4-8-15(14)20-25(22,23)13-11-12-13/h3-10,13,20H,2,11-12H2,1H3,(H,19,21)
InChi Key
RCSLEKLNDJJJLF-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    ML-382 is a positive allosteric modulator of MAS-related G protein-coupled receptor family member X1 (MRGPRX1).1 It potentiates activation of MRGPRX1 induced by the MRGPRX1 agonist BAM 22P (8-22) (Item No. 35263) in HEK293 cells expressing the human receptor (EC50 = 0.19 µM) but does not potentiate activation of MRGPRX2 induced by the MRGPRX2 agonist proadrenomedullin (PAMP) in HEK293 cells expressing the human receptor at 5 µM. ML-382 is also selective for MRGPRX1 over a panel of 68 G protein-coupled receptors (GPCRs), ion channels, and transporters at 10 µM. It enhances inhibition of high-voltage-activated calcium currents (ICa ) induced by BAM 22P (8-22) in dorsal root ganglion neurons isolated from transgenic mice expressing human MRGPRX1 when used at a concentration of 5 µM.2 Intrathecal administration of ML-382 (5 µl of a 25 µM solution) decreases formalin-induced paw licking and shaking in MRGPRX1 transgenic mice.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Wen, W., Wang, Y., Li, Z., et alDiscovery and characterization of 2-(cyclopropanesulfonamido)-N-(2-ethoxyphenyl)benzamide, ML382: A potent and selective positive allosteric modulator of MrgX1. ChemMedChem 10(1), 57-61 (2015).

    2. Li, Z., Tseng, P.-Y., Tiwari, V., et alTargeting human Mas-related G protein-coupled receptor X1 to inhibit persistent pain. Proc. Natl. Acad. Sci. USA 114(10), E1996-E2005 (2017).