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Lificiguat

Base Information
  • Chemical Name:Lificiguat
  • CAS No.:170632-47-0
  • Molecular Formula:C19H16 N2 O2
  • Molecular Weight:304.348
  • Hs Code.:
  • NSC Number:728165
  • UNII:515CC1WPTE
  • DSSTox Substance ID:DTXSID70165635
  • Nikkaji Number:J651.601G
  • Wikidata:Q27089256
  • NCI Thesaurus Code:C82248
  • ChEMBL ID:CHEMBL333985
  • Mol file:170632-47-0.mol
Lificiguat

Synonyms:3-(5'-hydroxymethyl-2'-furyl)-1-benzylindazole;YC -1 compound;YC 1 compound;YC-1 compound

Suppliers and Price of Lificiguat
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • YC-1
  • 5mg
  • $ 273.00
  • Usbiological
  • YC-1
  • 1mg
  • $ 265.00
  • Usbiological
  • YC 1
  • 10mg
  • $ 495.00
  • Tocris
  • YC-1 ≥99%(HPLC)
  • 50
  • $ 870.00
  • Tocris
  • YC-1 ≥99%(HPLC)
  • 10
  • $ 212.00
  • Sigma-Aldrich
  • YC-1
  • 5mg
  • $ 173.90
  • Sigma-Aldrich
  • YC-1 powder
  • 5mg
  • $ 155.00
  • Sigma-Aldrich
  • YC-1 powder
  • 25mg
  • $ 673.00
  • DC Chemicals
  • YC-1(Lificiguat) >98%
  • 1 g
  • $ 1500.00
  • DC Chemicals
  • YC-1(Lificiguat) >98%
  • 100 mg
  • $ 375.00
Total 27 raw suppliers
Chemical Property of Lificiguat
Chemical Property:
  • Melting Point:110-112℃ 
  • Boiling Point:522.2±50.0 °C(Predicted) 
  • PKA:13.83±0.10(Predicted) 
  • PSA:51.19000 
  • Density:1.24±0.1 g/cm3(Predicted) 
  • LogP:3.83690 
  • Storage Temp.:-20C 
  • Solubility.:DMSO: 12 mg/mL 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:304.121177757
  • Heavy Atom Count:23
  • Complexity:386
Purity/Quality:

99%, *data from raw suppliers

YC-1 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CN2C3=CC=CC=C3C(=N2)C4=CC=C(O4)CO
  • Description YC-1 (170632-47-0) is a nitric oxide-independent activator of soluble guanylyl cyclase (sGC). Significantly elevates cGMP levels and inhibits collagen-stimulated aggregation of rabbit platelets (IC50?= 14.6 μM).1?Induces human endometrial cancer cell senescence via modulation of HIF1α activity.2?Induces degradation of HIF1α.3?Protects against glutamate-induced neuronal damage4?and β-amyloid-induced toxicity in differentiated PC12 cells5.
  • Uses YC-1 has been used as a hypoxia-inducible factor 1α (HIF-1α) inhibitor:to reduce hypoxia induced Jagged1 expression in cardiomyocytes (CMs)to study its effect on progenitor expansion and CD34+ and side population (SP) cell phenotype and on the proliferation rate of cells with an ability to form long term colony forming unitsto study its effect on regulating sphingosine 1-phosphate (S1P) bound to albumin induced plasminogen activator inhibitor 1 (PAI-1) expression by activating Rho/ Rho-associated protein kinase (ROCK) pathway.
Technology Process of Lificiguat

There total 32 articles about Lificiguat which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With diisobutylaluminium hydride; In tetrahydrofuran; hexane; at -10 - 20 ℃; Inert atmosphere;
DOI:10.1039/c0cc01097a
Guidance literature:
With sodium tetrahydroborate; In methanol; at 20 ℃; for 1h;
DOI:10.1039/c5ob00710k
Guidance literature:
With calcium borohydride; In tetrahydrofuran; for 6h; Heating;
DOI:10.1021/jm020070b
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