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Fasudil

Base Information Edit
  • Chemical Name:Fasudil
  • CAS No.:103745-39-7
  • Molecular Formula:C14H17N3O2S
  • Molecular Weight:291.374
  • Hs Code.:29334900
  • European Community (EC) Number:816-154-4
  • NSC Number:759827
  • UNII:Q0CH43PGXS
  • DSSTox Substance ID:DTXSID4048569
  • Nikkaji Number:J227.600C
  • Wikipedia:Fasudil
  • Wikidata:Q5437132
  • NCI Thesaurus Code:C65624
  • Pharos Ligand ID:PR7RKZVNN5TC
  • Metabolomics Workbench ID:151310
  • ChEMBL ID:CHEMBL38380
  • Mol file:103745-39-7.mol
Fasudil

Synonyms:1H-1,4-Diazepine,hexahydro-1-(5-isoquinolinylsulfonyl)- (9CI);1-(5-Isoquinolinesulphonyl)homopiperazine;AT 877;Hexahydro-1-(5-isoquinolinylsulfonyl)-1H-1,4-diazepine;HA 1077;

Suppliers and Price of Fasudil
Supply Marketing:Edit
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
  • TRC
  • Fasudil
  • 100mg
  • $ 165.00
  • Sigma-Aldrich
  • HA 1077, Dihydrochloride - CAS 103745-39-7 - Calbiochem
  • 1mg
  • $ 124.00
  • Labseeker
  • (5-ISOQUINOLINESULFONYL)HOMOPIPERAZINE,2HCL 95
  • 100g
  • $ 923.00
  • DC Chemicals
  • Fasudil
  • 1g
  • $ 350.00
  • CSNpharm
  • Fasudil
  • 250mg
  • $ 67.00
  • Crysdot
  • Fasudil 98+%
  • 250mg
  • $ 63.00
  • AvaChem
  • Fasudil
  • 10g
  • $ 590.00
  • AvaChem
  • Fasudil
  • 100mg
  • $ 49.00
  • AvaChem
  • Fasudil
  • 1g
  • $ 109.00
  • ApexBio Technology
  • Fasudil
  • 200mg
  • $ 70.00
Total 113 raw suppliers
Chemical Property of Fasudil Edit
Chemical Property:
  • Appearance/Colour:White crystalline solid 
  • Vapor Pressure:2.55E-12mmHg at 25°C 
  • Boiling Point:506.2 °C at 760 mmHg 
  • PKA:9.73±0.20(Predicted) 
  • Flash Point:259.9 °C 
  • PSA:70.68000 
  • Density:1.289 g/cm3 
  • LogP:4.17030 
  • Storage Temp.:Store at RT 
  • Solubility.:H2O: >200 mg/mL 
  • Water Solubility.:Soluble in water or DMSO 
  • XLogP3:1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:2
  • Exact Mass:291.10414797
  • Heavy Atom Count:20
  • Complexity:421
Purity/Quality:

99% *data from raw suppliers

Fasudil *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:C1CNCCN(C1)S(=O)(=O)C2=CC=CC3=C2C=CN=C3
  • Recent ClinicalTrials:Inhibition of Rho Kinase (ROCK) With Fasudil as Disease-modifying Treatment for ALS
  • Recent NIPH Clinical Trials:Clinical trial of prevention for PCI-related myocardial infarction evaluating index of microvascular resistance in stable coronary artery disease. -Effect of Fasudil, a selective Rho-kinase inhibitor-
  • Uses vasodilator (cerebral), Ca antagonist A potent calcium antagonist vasodilator which is considered to act by employing different mechanisms from the usual calcium channel blockers since it inhibits (1) calcium ionophore A23187 induced co ntraction in arterial strips and (2) phenylephrine induced contraction in calcium free media suggesting that its site of action is in the intracellular space. Also reported to potently inhibit Rho- associated Kinase (ROCK IC50= 10.7 uM). Fasudil is a protein kinase A inhibitor and may be used in medicinal combinations for hepatitis treatment.
Technology Process of Fasudil

There total 6 articles about Fasudil 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:
In dichloromethane; at 0 ℃; for 2h;
DOI:10.14233/ajchem.2014.17658
Guidance literature:
In (2S)-N-methyl-1-phenylpropan-2-amine hydrate; dichloromethane;
Guidance literature:
In (2S)-N-methyl-1-phenylpropan-2-amine hydrate; dichloromethane;
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