1947313-60-1

Buloxibutid hydrochloride Chemical Structure
1947313-60-1

Chemical Structure

Buloxibutid hydrochloride

Synonym(s): AT2 receptor agonist C21 hydrochloride

  • CAS No.: 1947313-60-1
  • Formula:C23H30ClN3O4S2
  • Molecular Weight:512.09

InChIKey: BIIVOXDZWDUHOO-UHFFFAOYSA-N

SMILES: O=C(NS(=O)(C1=C(C2=CC=C(CN3C=NC=C3)C=C2)C=C(CC(C)C)S1)=O)OCCCC.Cl

Biological Activity: Buloxibutid (AT2 receptor agonist C21) hydrochloride is an orally active, selective angiotensin II type 2 receptor (AT2R) agonist, with a Ki value of 0.4 nM for porcine AT2R. Buloxibutid hydrochloride exerts vasodilatory, anti-inflammatory, antifibrotic (promoting the expression of collagenase MMP-13) and tissue repair effects mainly by activating the NO/cGMP pathway, inhibiting the pro-proliferative MAPK signaling, and suppressing the pro-fibrotic TGF-β/Smad pathway and inflammatory NF-κB pathway. Buloxibutid hydrochloride can be used in research related to idiopathic pulmonary fibrosis, hypertension, systemic sclerosis and other conditions[1][2][3][4].

Cat. No. Product Name Purity Description Pricing
HY-100113A
Buloxibutid hydrochloride Buloxibutid (AT2 receptor agonist C21) hydrochloride is an orally active, selective angiotensin II type 2 receptor (AT2R) agonist, with a Ki value of 0.4 nM for porcine AT2R. Buloxibutid hydrochloride exerts vasodilatory, anti-inflammatory, antifibrotic (promoting the expression of collagenase MMP-13) and tissue repair effects mainly by activating the NO/cGMP pathway, inhibiting the pro-proliferative MAPK signaling, and suppressing the pro-fibrotic TGF-β/Smad pathway and inflammatory NF-κB pathway. Buloxibutid hydrochloride can be used in research related to idiopathic pulmonary fibrosis, hypertension, systemic sclerosis and other conditions.
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