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Motolimod

Base Information
  • Chemical Name:Motolimod
  • CAS No.:926927-61-9
  • Deprecated CAS:1345249-66-2,1370046-37-9
  • Molecular Formula:C28H34N4O2
  • Molecular Weight:458.604
  • Hs Code.:
  • UNII:WP6PY72ZH3
  • ChEMBL ID:CHEMBL3301618
  • DSSTox Substance ID:DTXSID10239107
  • Metabolomics Workbench ID:153317
  • NCI Thesaurus Code:C80521
  • Nikkaji Number:J3.657.311B
  • Pharos Ligand ID:S4U69UGB54G8
  • Wikidata:Q27087722
  • Wikipedia:Motolimod
  • Mol file:926927-61-9.mol
Motolimod

Synonyms:motolimod;VTX-2337

Suppliers and Price of Motolimod
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
  • DC Chemicals
  • Motolimod(VTX-2337) >98%
  • 1 g
  • $ 1800.00
  • DC Chemicals
  • Motolimod(VTX-2337) >98%
  • 250 mg
  • $ 900.00
  • DC Chemicals
  • Motolimod(VTX-2337) >98%
  • 100 mg
  • $ 500.00
  • Crysdot
  • Motolimod 98+%
  • 50mg
  • $ 718.00
  • Crysdot
  • Motolimod 98+%
  • 25mg
  • $ 453.00
  • Crysdot
  • Motolimod 98+%
  • 10mg
  • $ 256.00
  • ChemScene
  • Motolimod 98.58%
  • 5mg
  • $ 204.00
  • ChemScene
  • Motolimod 98.58%
  • 10mg
  • $ 324.00
  • ChemScene
  • Motolimod 98.58%
  • 50mg
  • $ 840.00
  • ChemScene
  • Motolimod 98.58%
  • 25mg
  • $ 588.00
Total 27 raw suppliers
Chemical Property of Motolimod
Chemical Property:
  • Appearance/Colour:Solid 
  • Boiling Point:718.7±70.0 °C(Predicted) 
  • PKA:2.47±0.40(Predicted) 
  • PSA:76.50000 
  • Density:1.19±0.1 g/cm3 (20 oC 760 Torr) 
  • LogP:5.59010 
  • Storage Temp.:-20°C 
  • Solubility.:Soluble in DMSO (up to at least 25 mg/ml) 
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:7
  • Exact Mass:458.26817634
  • Heavy Atom Count:34
  • Complexity:771
Purity/Quality:

99%, *data from raw suppliers

Motolimod(VTX-2337) >98% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCN(CCC)C(=O)C1=CC2=C(C=C(C=C2)C3=CC=C(C=C3)C(=O)N4CCCC4)N=C(C1)N
  • Recent ClinicalTrials:A Study to Evaluate Immune Biomarker Modulation in Response to VTX-2337 in Combination With an Anti- PD-1 Inhibitor in Head and Neck Cancer
  • Description Motolimod is an agonist of toll-like receptor 8 (TLR8). It increases the production of TNF-α and IL-12 in human peripheral blood mononuclear cells (PBMCs; EC50s = 140 and 120 nM, respectively), monocytes, and myeloid dendritic cells. Motolimod also increases IFN-γ production in natural killer (NK) cells and increases cytolysis in K562 NK cell-sensitive leukemia cells when used at concentrations of 167 and 500 nM for 48 hours. It increases plasma levels of a group of human cytokines, including IL-6, IL-12p70, TNF-α, MCP-1, and MIP-1β, in NOD-scid IL2rynull (NSG) mice reconstituted with human immune system (NSG-HIS) when administered at doses of 1.5 and 15 mg/m2. Motolimod, when used in combination with pegylated liposomal doxorubicin (PLD), reduces tumor growth and increases tumor infiltration of monocytes and T cells in an ovarian cancer NSG-HIS mouse model.
  • Uses Motolimod is an agonist of toll-like receptor 8 (TLR8) with potential immune-stimulating and antineoplastic properties. Motolimod is used in combination with PLD for the treatment of ovarian cancer.
Technology Process of Motolimod

There total 2 articles about Motolimod 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:
(tert-butoxy)-N-{4-(N,N-dipropylcarbamoyl)-8-[4-(pyrrolidinylcarbonyl)phenyl](3H-benzo[f]azepin-2-yl)}carboxamide; With trifluoroacetic acid; In dichloromethane; at -25 - 20 ℃;
With sodium hydrogencarbonate; In water;
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