BEC hydrochloride

For research use only. Not for therapeutic Use.

  • CAT Number: I002706
  • CAS Number: 222638-67-7
  • Molecular Formula: C5H12BNO4S • HCl
  • Molecular Weight: 229.5
  • Purity: ≥95%
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BEC HCl is a slow-binding, competitive arginase inhibitor with Ki values of 0.31 μM (pH7.5) and 0.4-0.6 μM for Arginase II and rat Arginase I, respectively. BEC resulted in a significant enhancement of NO-dependent smooth muscle contraction. In cardiomyocytes, BECs enhanced Ca(2+)-dependent NOS activity and NO production while increasing their basal contractility.


Catalog Number I002706
CAS Number 222638-67-7
Synonyms

S-(2-boronoethyl)-L-cysteine, monohydrochloride

Molecular Formula C5H12BNO4S • HCl
Purity ≥95%
Target Metabolic Enzyme/Protease
Solubility 45 mg/mL in H2O; 45 mg/mL in DMSO.
Storage -20°C
IUPAC Name (2R)-2-amino-3-(2-boronoethylsulfanyl)propanoic acid;hydrochloride
InChI InChI=1S/C5H12BNO4S.ClH/c7-4(5(8)9)3-12-2-1-6(10)11;/h4,10-11H,1-3,7H2,(H,8,9);1H/t4-;/m0./s1
InChIKey GHPYJLCQYMAXGG-WCCKRBBISA-N
SMILES B(CCSCC(C(=O)O)N)(O)O.Cl
Reference

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<br>[1]. Colleluori DM et al. Classical and slow-binding inhibitors of human type II arginase. Biochemistry. 2001 Aug 7;40(31):9356-62.

<br>[2]. Kim NN et al. Probing erectile function: S-(2-boronoethyl)-L-cysteine binds to arginase as a transition state analogue and enhances smooth muscle relaxation in human penile corpus cavernosum. Biochemistry. 2001 Mar 6;40(9):2678-88.

<br>[3]. Karina Ckless et al. Inhibition of Arginase Activity Enhances Inflammation in Mice with Allergic Airway Disease, in Association with Increases in Protein S-Nitrosylation and Tyrosine Nitration. J Immunol. Author manuscript; available in PMC 2010 Jun 28.

<br>[4]. Steppan J et al. Arginase modulates myocardial contractility by a nitric oxide synthase 1-dependent mechanism. Proc Natl Acad Sci U S A. 2006 Mar 21;103(12):4759-64.

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