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Lonafarnib

Base Information Edit
  • Chemical Name:Lonafarnib
  • CAS No.:193275-84-2
  • Molecular Formula:C27H31Br2ClN4O2
  • Molecular Weight:638.83
  • Hs Code.:
  • European Community (EC) Number:679-527-9
  • NSC Number:719467
  • UNII:IOW153004F
  • DSSTox Substance ID:DTXSID90172927
  • Nikkaji Number:J1.013.643A
  • Wikipedia:Lonafarnib
  • Wikidata:Q3258910
  • NCI Thesaurus Code:C1829
  • RXCUI:2467553
  • Pharos Ligand ID:B4VX44PMPXKJ
  • Metabolomics Workbench ID:130085
  • ChEMBL ID:CHEMBL298734
  • Mol file:193275-84-2.mol
Lonafarnib

Synonyms:(+)4-(2-(4-(8-chloro-3,10-dibromo-6,11-dihydro-5H-benzo(5,6)cyclohepta(1,2-b)pyridin-11-yl)-1-piperidinyl)-2-oxoethyl)-1-piperidinecarboxamide;1-piperidinecarboxamide, 4(2-(4-(11R-3,10-dibromo-8-chloro-6,11-dihydro-5H-benzo(5,6)cyclohepta(1,2-b)pyridine-11-yl)-1-piperidinyl)-2-oxoethyl)-;4-(2-(4-(8-chloro-3,10-dibromo-6,11-dihydro-5H-benzo-(5,6)-cyclohepta(1,2-b)-pyridin-11(R)-yl)-1-piperidinyl)-2-oxo-ethyl)-1-piperidinecarboxamide;lonafarnib;Sarasar;SCH 66336;SCH-66336;SCH66336;zokinvy

Suppliers and Price of Lonafarnib
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
  • Lonafarnib
  • 1mg
  • $ 50.00
  • TRC
  • Lonafarnib
  • 50mg
  • $ 375.00
  • Tocris
  • Lonafarnib ≥98%(HPLC)
  • 10
  • $ 135.00
  • Tocris
  • Lonafarnib ≥98%(HPLC)
  • 50
  • $ 563.00
  • DC Chemicals
  • Lonafarnib >98%
  • 1 g
  • $ 2900.00
  • DC Chemicals
  • Lonafarnib >98%
  • 250 mg
  • $ 1500.00
  • CSNpharm
  • Lonafarnib
  • 5mg
  • $ 68.00
  • CSNpharm
  • Lonafarnib
  • 10mg
  • $ 116.00
  • ChemScene
  • Lonafarnib 98.67%
  • 5mg
  • $ 146.00
  • ChemScene
  • Lonafarnib 98.67%
  • 10mg
  • $ 264.00
Total 64 raw suppliers
Chemical Property of Lonafarnib Edit
Chemical Property:
  • Melting Point:214.5-215.9° (monohydrate); mp 222-223° 
  • Boiling Point:710.432 °C at 760 mmHg 
  • PKA:15.76±0.40(Predicted) 
  • Flash Point:383.455 °C 
  • PSA:79.53000 
  • Density:1.537 g/cm3 
  • LogP:6.48600 
  • Storage Temp.:-20°C 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
  • XLogP3:4.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:638.04818
  • Heavy Atom Count:36
  • Complexity:790
Purity/Quality:

98%,99%, *data from raw suppliers

Lonafarnib *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Drug Classes:Genetic Disease Agents, Small Molecule Enzyme Inhibitors
  • Canonical SMILES:C1CN(CCC1CC(=O)N2CCC(CC2)C3C4=C(CCC5=C3N=CC(=C5)Br)C=C(C=C4Br)Cl)C(=O)N
  • Isomeric SMILES:C1CN(CCC1CC(=O)N2CCC(CC2)[C@@H]3C4=C(CCC5=C3N=CC(=C5)Br)C=C(C=C4Br)Cl)C(=O)N
  • Recent ClinicalTrials:Once Daily Dosing of Lonafarnib Co-administered With Ritonavir for Treatment of Chronic Hepatitis D Virus Infection
  • Recent EU Clinical Trials:A Phase 3, Matrix Design, Partially Double-Blind, Randomized Study of the Efficacy and Safety of 50 mg Lonafarnib/100 mg Ritonavir BID with and without 180 mcg PEG IFN-alfa-2a for 48 Weeks Compared with PEG IFN-alfa-2a Monotherapy and Placebo Treatment in Patients Chronically Infected with Hepatitis Delta Virus Being Maintained on Anti-HBV Nucleos(t)ide Therapy (D-LIVR)
  • Uses Chemotherapeutic (farnesyl transfer ase inhibitor). Lonafarnib is an orally bioavailable tricyclic inhibitor of farnesyl protein transferase. It inhibits Rheb farnesylation and mTOR signaling and enhances taxane and tamoxifen antitumor activity. Studies show that it induces CCAAT/enhancer-binding protein homologous protein-dependent expression of death receptor 5, leading to induction of apoptosis in human cancer cells
Technology Process of Lonafarnib

There total 16 articles about Lonafarnib 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 tetrahydrofuran; water; ethyl acetate; at 20 - 65 ℃; for 2h; Purification / work up;
Guidance literature:
With sodium carbonate; In tetrahydrofuran; water; at 20 - 50 ℃; for 4h;
Refernces Edit
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