Drug intelligence / Profile preview

1(R)-1-ACETAMIDO-2-(3-CARBOXY-2-HYDROXYPHENYL)ETHYL BORONIC ACID

Development stage
Unknown
Modality
Small Molecules
01

Overview

This compound is a small molecule inhibitor designed to mimic the transition state of deacylation in beta-lactamase enzymes. It is specifically effective against TEM-1 beta-lactamase, with an inhibition constant of 13 nM, making it a potent competitive inhibitor[6][7].

Other names
3-[(2R)-2-Acetamido-2-(dihydroxyboryl)ethyl]-2-hydroxybenzoic acidAcide 3-[(2R)-2-acétamido-2-(dihydroxyboryl)éthyl]-2-hydroxybenzoïqueBenzoic acid, 3-[(2R)-2-(acetylamino)-2-boronoethyl]-2-hydroxy-
02

Targets

CD248 (Endosialin)

Beyond the preview

Go deeper on 1(R)-1-ACETAMIDO-2-(3-CARBOXY-2-HYDROXYPHENYL)ETHYL BORONIC ACID.

Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.

Clinical trials

Follow clinical development from study design and recruitment through results.

  • Trial phase
  • Status
  • Readouts

Indications & development

Explore development by indication, patient population, and geography.

  • Indications
  • Development status
  • Countries

Licensing & deals

Trace asset ownership, licensing agreements, and commercial partnerships.

  • Partners
  • Deal terms
  • Milestones

Patents & exclusivity

Explore the patent landscape and regulatory exclusivity around an asset.

  • Patents
  • Expiration dates
  • Exclusivity

Competitive landscape

Compare development programs by target, modality, and indication.

  • Competing assets
  • Targets
  • Development stage

Research & analysis

Connect source evidence and development news to your research questions.

  • Publications
  • News
  • Analysis

Bring the full picture into focus.

See how Gosset can support your research on 1(R)-1-ACETAMIDO-2-(3-CARBOXY-2-HYDROXYPHENYL)ETHYL BORONIC ACID.

Gosset Free

Get started with Gosset.

Enter your corporate email.

Work email preferred.

Book a call