YS-49
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


YS-49
Description:
YS-49 is a PI3K/Akt (a downstream target of RhoA) activator, to reduce RhoA/PTEN activation in the 3-methylcholanthrene-treated cells. YS-49 inhibits angiotensin II (Ang II) -stimulated proliferation of VSMCs via induction of heme oxygenase (HO) -1. YS-49 is also an isoquinoline compound alkaloid, has a strong positive inotropic action through activation of cardiac β-adrenoceptors[1][2][3].UNSPSC:
12352005Hazard Statement:
H302Target:
Adrenergic Receptor; Akt; Angiotensin Receptor; PI3KType:
Reference compoundRelated Pathways:
GPCR/G Protein; Neuronal Signaling; PI3K/Akt/mTORApplications:
COVID-19-immunoregulationField of Research:
Cardiovascular Disease; EndocrinologyAssay Protocol:
https://www.medchemexpress.com/ys-49.htmlPurity:
99.98Solubility:
DMSO : 100 mg/mL (ultrasonic) |H2O : 10 mg/mL (ultrasonic; warming; heat to 60°C)Smiles:
OC1=CC2=C(C(CC3=C4C=CC=CC4=CC=C3)NCC2)C=C1O.[H]BrMolecular Formula:
C20H20BrNO2Molecular Weight:
386.28Precautions:
H302References & Citations:
[1]Sun JJ, Kim HJ, Seo HG, et al. YS49,1- (alpha-naphtylmethyl) -6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline, regulates angiotensin II-stimulated ROS production, JNK phosphorylation and vascular smooth muscle cell proliferation via the induction of heme oxygenase-1. Life Sci. 2008;82 (11-12) :600-7.|[2]Kang YJ, et al. Prevention of the expression of inducible nitric oxide synthase by a novel positive inotropic agent, YS 49, in rat vascular smooth muscle and RAW 264.7 macrophages. Br J Pharmacol. 1999 Sep;128 (2) :357-64.|[3]Hsu YH, et al. RhoA-mediated inhibition of vascular endothelial cell mobility: positive feedback through reduced cytosolic p21 and p27. J Cell Physiol. 2014 Oct;229 (10) :1455-65.Shipping Conditions:
Room TemperatureStorage Conditions:
4°C (Powder, stored under nitrogen)Scientific Category:
Reference compound1Clinical Information:
No Development ReportedCAS Number:
[132836-42-1]
