SBP-9330

Possible drug for treating drug dependence From Wikipedia, the free encyclopedia

SBP 9330 is an investigational small-molecule drug and a positive allosteric modulator (PAM) of the Metabotropic glutamate receptor 2 (mGluR2), being developed as a potential treatment for nicotine dependence and other substance-use disorders.

Other names4-chloro-3′-((2-cyclopentyl-1-oxoisoindolin-5-yloxy)methyl)biphenyl-3-carboxylic acid
Drug classPositive allosteric modulator of mGluR2
Legal status
  • Investigational
Quick facts Clinical data, Other names ...
SBP-9330
Clinical data
Other names4-chloro-3′-((2-cyclopentyl-1-oxoisoindolin-5-yloxy)methyl)biphenyl-3-carboxylic acid
Routes of
administration
Oral
Drug classPositive allosteric modulator of mGluR2
Legal status
Legal status
  • Investigational
Identifiers
  • 4-chloro-3′-((2-cyclopentyl-1-oxoisoindolin-5-yloxy)methyl)biphenyl-3-carboxylic acid
CAS Number
PubChem CID
ChemSpider
ChEMBL
Chemical and physical data
FormulaC27H24ClNO4
Molar mass455.94 g/mol
3D model (JSmol)
  • OC(=O)c1cc(ccc1Cl)-c1cccc(COc2ccc3C(=O)N(Cc3c2)C2CCCC2)c1
  • InChI=InChI=1S/C27H24ClNO4/c28-24-9-7-22(19-4-2-3-5-20(19)24)18-31-21-6-8-25-23(16-31)27(32)29(26(25)17-21)14-11-12-15-27/h2-9,16,18,21H,11-15,17H2,1H3,(H,32,27)
  • Key:DWTYHCYVKJONSP-UHFFFAOYSA-N
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Chemistry

SBP 9330 is chemically named 4-chloro-3′-((2-cyclopentyl-1-oxoisoindolin-5-yloxy)methyl)biphenyl-3-carboxylic acid. It consists of a biphenyl-3-carboxylic acid core bearing a chloro substituent and an isoindolinone-derived ether moiety.[1]

Pharmacology

Pharmacokinetics

Pharmacokinetic analyses showed oral bioavailability, dose-dependent increases in plasma exposure, and parameters compatible with once-daily dosing.[2]

Pharmacodynamics

SBP 9330 acts as a positive allosteric modulator of mGluR2, a presynaptic G-protein-coupled receptor involved in regulating glutamatergic neurotransmission. Rather than activating the receptor directly, PAMs enhance the receptor's response to endogenous glutamate. Activation of mGluR2 reduces glutamate release in brain regions implicated in reward processing and addiction, including the prefrontal cortex and nucleus accumbens.[3]

History

SBP 9330 was discovered in medicinal chemistry programs aimed at identifying orally bioavailable mGluR2 PAMs. Early structure–activity relationship studies optimized potency, brain penetration, and pharmacokinetic properties.

It was disclosed in the following patents:

  • US13051798 – Positive allosteric modulators of group II mGluRs[4]
  • WO2025019598A1 – Positive allosteric modulator of the metabotropic glutamate receptor subtype 2 receptor, synthesis and solid forms thereof[5]

Research

Addiction models

Preclinical studies demonstrated that SBP 9330 decreased cocaine self-administration in rats, suggesting attenuation of drug-reinforcing effects.[1] Additional experiments within the same paper showed reductions in drug-seeking behavior, attenuation of cue-induced reinstatement, and decreased reward-associated responding.[1]

Nicotine dependence

SBP 9330 has been evaluated as a potential aid to smoking cessation. In animal models of nicotine reinforcement, mGluR2 positive allosteric modulation was associated with reduced nicotine self-administration and decreased nicotine-seeking behavior.[6]

Clinical development

Phase I

A randomized, double-blind, placebo-controlled Phase I study evaluated the safety, tolerability, and pharmacokinetics of SBP 9330 following single and multiple ascending oral doses in healthy volunteers.[7][8]

References

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