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YC-1 (CAS 170632-47-0)

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Synonym:3-(5′-Hydroxymethyl-2′-furyl)-1-benzylindazole
Application:An agent that can activate sGC independent of nitric oxide activation
CAS Number:170632-47-0
Purity:>99%
Molecular Weight:304.3
Molecular Formula:C19H16N2O2
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Product NameCatalog #UnitPriceQtyAdd 
YC-1 sc-202856 1 mg $30
Description
YC-1 can activate platelet soluble guanylate cylcase (sGC) indepedent of nitric oxide activation. It has the ability to inhibit aggregation of platelets and increase the platelets cAMP and cGMP content, as well as act as an antithrombotic compound. Data shows that the highest activation of sGC is observed in the presence of YC-1. The compound can suppress HIF-1 alpha activity in neonatal rat ventricular myocytes. Research shows that YC-1 might have the ability to activate the sGC/cGMP/PKG pathway and influence the activation of Ras/Raf-1/p44/42 MAPK.
Technical Information
Appearance:Off-white to pale yellow solid
Physical State:Solid
Solubility:Soluble in DMSO (12 mg/ml), methanol (5 mg/ml), ethanol (50 mM), DMF (~20 mg/ml), 5:2 DMSO:PBS(pH 7.2) (~10 ug/ml), and dichloromethane. Insoluble in water.
Storage:Store at -20° C
Melting Point:110 to 113°C
Boiling Point:522.17 °C at 760 mmHg (Predicted)
Density:1.25 g/cm3 (Predicted)
Refractive Index:n20D 1.65 (Predicted)
IC50:soluble guanylyl cyclase: EC5050 = 18.6 µM; collagen (10 µg/ml) induced platelet aggregation: IC50 = 11.7-14.6 µM; thrombin (0.1 U/ml) induced platelet aggregation: IC50 = 57.3-59.3 µM; Guanylate cyclase soluble alpha-1 chain: EC5050 = 4.11 µM (Bos taurus); ACHN: IC50 = 300 nM (human); hypoxia-induced HIF-1 transcriptional activity: IC50 = 1.2 µM; NCI-H226: IC50 = 1.9 µM (human); Hypoxia-inducible factor 1 alpha: IC50 = 2 µM (human); AGS: IC50 = 2 µM (human)
Safety and Reference Information
WGK Germany:3
RTECS:LU2370000
PubChem CID:5712
MDL Number:MFCD06407798
SMILES:OCC1=CC=C(O1)C1=NN(CC2=CC=CC=C2)C2=CC=CC=C12
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
References
1. Ko, F.N., et al. 1994. Blood. 84: 4226-4233. PMID: 7527671
2. Wu, C.C., et al. 1995. Br. J. Pharmacol. 116: 1973-1978. PMID: 8640334
3. Stone, J.R. and Marletta, M.A. 1998. Chem. Biol. 5: 255-261. PMID: 9646941
4. Chang, M.S., et al. 2009. Pharmacol. Res. 60: 247-253. PMID: 19717011
5. Zhou, Y.F., et al. 2010. Cardiovasc J Afr. 21: 37-41. PMID: 20224844
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