BEC hydrochloride
Cat. No.: DC9964
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Chemical Structure
222638-67-7
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Field of application
BEC is a boronic acid-based arginine analog that acts as a slow-binding, competitive transition state inhibitor of arginase I and II (Ki = 310 nM for human recombinant type II arginase, pH 7.5).
Cas No.: |
222638-67-7 |
Chemical Name: |
BEC HCl |
Synonyms: |
L-Cysteine,S-(2-boronoethyl)-, hydrochloride (1:1);L-Cysteine,S-(2-boronoethyl)-, hydrochloride (9CI);BEC HCl;(R)-2-amino-3-((2-boronoethyl)thio)propanoic acid hydrochloride;BEC (hydrochloride);S-(2-BORONOETHYL)-L-CYSTEINE HYDROCHLORIDE;BEC hydrochloride;(2R)-2-amino-3-(2-boronoethylsulfanyl)propanoic acid hydrochloride;bec-hydrochloride;BCP25043;S-(2-Boronoethyl)-l-cysteine, HCl;(R)-2-Amino-3-(2-boronoethylthio)propanoic acid hydrochloride;(2R)-2-amino-3-{[2-(dihydroxyboranyl)ethyl]sulfanyl}propanoic acid hydrochloride |
SMILES: |
Cl[H].S(C([H])([H])C([H])([H])B(O[H])O[H])C([H])([H])[C@@]([H])(C(=O)O[H])N([H])[H] |
Formula: |
C5H13BClNO4S |
M.Wt: |
229.49 |
Sotrage: |
4°C for 1 year, -20°C for more than 2 years |
Description: |
BEC HCl is a slow-binding and competitive Arginase II inhibitor with Ki of 0.31 μM (ph 7.5). |
In Vitro: |
BEC HCl causes significant enhancement of NO-dependent smooth muscle relaxation in this tissue. [2] BEC HCl enhances perivascular and peribronchiolar lung inflammation, mucus metaplasia, NF-κB DNA binding, and mRNA expression of the NF-κB-driven chemokine genes CCL20 and KC, and lead to further increases in airways hyperresponsiveness. [3] In vivo: BEC HCl increased contractility in isolated myocytes from WT and NOS3 but not NOS1 knockout mice. [4] |
MSDS
COA
LOT NO. |
DOWNLOAD |
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2018-0101 |
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2018-0101 |
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