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Pyroxamide

Base Information
  • Chemical Name:Pyroxamide
  • CAS No.:382180-17-8
  • Molecular Formula:C13H19N3O3
  • Molecular Weight:265.312
  • Hs Code.:2933399090
  • European Community (EC) Number:803-756-7
  • NSC Number:696085
  • UNII:12N86DSS23
  • DSSTox Substance ID:DTXSID70191595
  • Nikkaji Number:J1.444.219G
  • Wikidata:Q27165709
  • NCI Thesaurus Code:C2801
  • Pharos Ligand ID:3JXC3AAN32QF
  • Metabolomics Workbench ID:153751
  • ChEMBL ID:CHEMBL353581
  • Mol file:382180-17-8.mol
Pyroxamide

Synonyms:pyroxamide;suberoyl-3-aminopyridineamide hydroxamic acid

Suppliers and Price of Pyroxamide
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
  • Pyroxamide
  • 25mg
  • $ 496.00
  • Usbiological
  • Pyroxamide
  • 10mg
  • $ 438.00
  • Usbiological
  • Pyroxamide
  • 5mg
  • $ 252.00
  • TRC
  • Pyroxamide
  • 25mg
  • $ 175.00
  • Tocris
  • Pyroxamide ≥98%(HPLC)
  • 25
  • $ 272.00
  • Tocris
  • Pyroxamide ≥98%(HPLC)
  • 5
  • $ 72.00
  • Sigma-Aldrich
  • Pyroxamide ≥97% (HPLC)
  • 5mg
  • $ 94.80
  • Sigma-Aldrich
  • Pyroxamide ≥97% (HPLC)
  • 25mg
  • $ 384.00
  • Medical Isotopes, Inc.
  • Pyroxamide
  • 250 mg
  • $ 2200.00
  • DC Chemicals
  • Pyroxamide >98%
  • 100 mg
  • $ 450.00
Total 35 raw suppliers
Chemical Property of Pyroxamide
Chemical Property:
  • PSA:91.32000 
  • Density:1.215 g/cm3 
  • LogP:2.33000 
  • Storage Temp.:?20°C 
  • Solubility.:DMSO: soluble10mg/mL (clear solution) 
  • XLogP3:0.9
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:8
  • Exact Mass:265.14264148
  • Heavy Atom Count:19
  • Complexity:284
Purity/Quality:

99%, *data from raw suppliers

Pyroxamide *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xn 
  • Hazard Codes:Xn 
  • Statements: 22 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=CN=C1)NC(=O)CCCCCCC(=O)NO
  • Recent ClinicalTrials:Pyroxamide in Treating Patients With Advanced Cancer
  • Description Pyroxamide is an inhibitor of histone deacetylases (HDACs), including HDAC1 (IC50 = 0.1-0.2 μM). It induces growth suppression and cell death of certain types of cancer cells in culture.
  • Uses Pyroamide is a histone decetylase inhibitor (HDCi), a novel class of anti-neoplastic agent that acts by enhancing acetylation of histones, promoting uncoiling of chromatin and activation of genes imp licated in the regulation of cell survival such as poliferation, differentiation and apoptosis. Pyroamide is known to potently inhibits affinity purified HDAC1. Also inhibits the growth of tumor cells in vitro and in vivo. Induces p21/WAF1 expression in tumor cells. Pyroxamide is an inhibitor of histone deacetylases (HDACs), including HDAC1 (IC50 = 0.1-0.2 μM). It induces growth suppression and cell death of certain types of cancer cells in culture. Pyroamide is a histone decetylase inhibitor (HDCi), a novel class of anti-neoplastic agent that acts by enhancing acetylation of histones, promoting uncoiling of chromatin and activation of genes implicated in the regulation of cell survival such as poliferation, differentiation and apoptosis. Pyroamide is known to potently inhibits affinity purified HDAC1. Also inhibits the growth of tumor cells in vitro and in vivo. Induces p21/WAF1 expression in tumor cells.
Technology Process of Pyroxamide

There total 3 articles about Pyroxamide 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 potassium hydroxide; hydroxylamine hydrochloride; In methanol;
DOI:10.1021/jm015568c
Guidance literature:
Multi-step reaction with 3 steps
1: N-methylmorpholine / tetrahydrofuran
2: 1.99 g / N-methylmorpholine / tetrahydrofuran
3: 47 percent / HONH3Cl; KOH / methanol
With 4-methyl-morpholine; potassium hydroxide; hydroxylamine hydrochloride; In tetrahydrofuran; methanol;
DOI:10.1021/jm015568c
Guidance literature:
Multi-step reaction with 2 steps
1: 1.99 g / N-methylmorpholine / tetrahydrofuran
2: 47 percent / HONH3Cl; KOH / methanol
With 4-methyl-morpholine; potassium hydroxide; hydroxylamine hydrochloride; In tetrahydrofuran; methanol;
DOI:10.1021/jm015568c
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