1246819-58-8

Mabuterol-d<sub>9</sub> Chemical Structure
1246819-58-8

Chemical Structure

Mabuterol-d9

  • CAS No.: 1246819-58-8
  • Formula:C13H9D9ClF3N2O
  • Molecular Weight:319.80

IUPAC Name: 1-(4-amino-3-chloro-5-(trifluoromethyl)phenyl)-2-((2-(methyl-d3)propan-2-yl-1,1,1,3,3,3-d6)amino)ethan-1-ol

InChIKey: JSJCTEKTBOKRST-GQALSZNTSA-N

SMILES: OC(CNC(C([2H])([2H])[2H])(C([2H])([2H])[2H])C([2H])([2H])[2H])C1=CC(C(F)(F)F)=C(N)C(Cl)=C1

Biological Activity: Mabuterol-d9 is a deuterium labeled Mabuterol. Mabuterol is an agonist of the β2-adrenergic receptor[1].

Cat. No. Product Name Purity Description Pricing
HY-13338S
Mabuterol-d9 Mabuterol-d9 is a deuterium labeled Mabuterol. Mabuterol is an agonist of the β2-adrenergic receptor.
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HY-13338R
Mabuterol (Standard) ≥98% Mabuterol (Standard) is the analytical standard of Mabuterol. This product is intended for research and analytical applications. Mabuterol is a selective and orally active beta-2 adrenergic receptor (ADRB2) agonist. Mabuterol inhibits the proliferation and suppresses the increase of intracellular Ca2+ induced by PDGF-BB. Mabuterol suppresses the protein expressions of Drp-1, cyclinD1 and PCNA and enhanced the expression of Mfn-2 induced by PDGF-BB.
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HY-13338
Mabuterol 99.96% Mabuterol is a selective and orally active beta-2 adrenergic receptor (ADRB2) agonist. Mabuterol inhibits the proliferation and suppresses the increase of intracellular Ca2+ induced by PDGF-BB. Mabuterol suppresses the protein expressions of Drp-1, cyclinD1 and PCNA and enhanced the expression of Mfn-2 induced by PDGF-BB.
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References