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L755507

Chemical Structure : L755507

CAS No.: 159182-43-1

L755507 (L 755507)

Catalog No.: PC-38661Not For Human Use, Lab Use Only.

L755507 is a potent, selective β3-adrenoceptor (β3-AR) agonist, exhibits robust concentration-dependent increase in cAMP accumulation in CHO-K1 cells expressing human β3-adrenoceptors (pEC50=12.3), also effectively inhibits the c-Myc-MAX heterodimerization.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

L755507 is a potent, selective β3-adrenoceptor (β3-AR) agonist, exhibits robust concentration-dependent increase in cAMP accumulation in CHO-K1 cells expressing human β3-adrenoceptors (pEC50=12.3), also effectively inhibits the c-Myc-MAX heterodimerization.
L755507 increases phosphorylation of extracellular signal-regulated kinase 1/2 (Erk1/2) with pEC50 of 11.7, couples to both Gs and Gi to activate adenylate cyclase and MAPK signaling.
L755507 efficiently restricts the growth of diverse Myc-expressing cells with low micromolar IC50 values, decreases expression of c-Myc target genes.
L755507 binds to the c-Myc peptide and thereby stabilizes the helix–loop–helix conformation of the c-Myc transcription factor.

Physicochemical Properties

M.Wt 584.732
Formula C30H40N4O6S
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(S)-4-(3-hexylureido)-N-(4-(2-((2-hydroxy-3-(4-hydroxyphenoxy)propyl)amino)ethyl)phenyl)benzenesulfonamide

References

1. Sato M, et al. Mol Pharmacol. 2008 Nov;74(5):1417-28.

2. Hutchinson DS, et al. Br J Pharmacol. 2002 Apr;135(8):1903-14.

3. Singh A, et al. J Biol Chem. 2021 Jul;297(1):100903.

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