(3S,4S)-A2-32-01

For research use only. Not for therapeutic Use.

  • CAT Number: I045627
  • Molecular Formula: C19H27NO2
  • Molecular Weight: 301.42
  • Purity: ≥95%
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(3S,4S)-A2-32-01 (Cat No.: I045627) is a stereochemically defined synthetic compound designed for research applications in biomedical science. Its chiral configuration, indicated by the (3S,4S) designation, suggests specificity in binding interactions with molecular targets, enabling exploration of structure–activity relationships. This compound is studied as a potential modulator of biological pathways, supporting investigations into drug discovery, disease mechanisms, and pharmacological profiling. While therapeutic uses remain experimental, (3S,4S)-A2-32-01 provides researchers with a valuable tool for probing stereoselective effects in biochemical and cellular systems.


Synonyms

(3S,4S)-3-non-8-enyl-4-(2-pyridin-3-ylethyl)oxetan-2-one

Molecular Formula C19H27NO2
Purity ≥95%
InChI InChI=1S/C19H27NO2/c1-2-3-4-5-6-7-8-11-17-18(22-19(17)21)13-12-16-10-9-14-20-15-16/h2,9-10,14-15,17-18H,1,3-8,11-13H2/t17-,18-/m0/s1
InChIKey WBHVHPLFRGISDD-ROUUACIJSA-N
SMILES C=CCCCCCCCC1C(OC1=O)CCC2=CN=CC=C2
Reference

[1]. Malte Gersch, et al. The mechanism of caseinolytic protease (ClpP) inhibition. Angew Chem Int Ed Engl. 2013 Mar 4;52(10):3009-14.
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