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Carmofur

Base Information Edit
  • Chemical Name:Carmofur
  • CAS No.:61422-45-5
  • Molecular Formula:C11H16FN3O3
  • Molecular Weight:257.265
  • Hs Code.:29335990
  • European Community (EC) Number:689-431-9
  • NSC Number:758963
  • UNII:HA82M3RAB2
  • DSSTox Substance ID:DTXSID2045941
  • Nikkaji Number:J1.101K
  • Wikipedia:Carmofur
  • Wikidata:Q5043732
  • NCI Thesaurus Code:C955
  • Pharos Ligand ID:WN3HDW538SSQ
  • Metabolomics Workbench ID:152083
  • ChEMBL ID:CHEMBL460499
  • Mol file:61422-45-5.mol
Carmofur

Synonyms:1(2H)-pyrimidinecarboxamide, 5-fluoro-N-hexyl-3,4-dihydro-2,4-dioxo-;1-hexylcarbamoyl-5-fluorouracil;carmofur;HCFU;Mifurol;N-hexylcarbamoyl-5-fluorouracil

Suppliers and Price of Carmofur
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
  • Carmofur
  • 500mg
  • $ 110.00
  • TCI Chemical
  • Carmofur >98.0%(HPLC)(T)
  • 5g
  • $ 233.00
  • SynQuest Laboratories
  • 1-(n-Hexylcarbamoyl)-5-fluorouracil 98%
  • 5 g
  • $ 95.00
  • SynQuest Laboratories
  • 1-(n-Hexylcarbamoyl)-5-fluorouracil 98%
  • 1 g
  • $ 45.00
  • Sigma-Aldrich
  • Carmofur ≥98% (HPLC), powder
  • 50mg
  • $ 324.00
  • Sigma-Aldrich
  • Carmofur ≥98% (HPLC), powder
  • 10mg
  • $ 79.80
  • Crysdot
  • Carmofur 98+%
  • 100mg
  • $ 92.00
  • ChemScene
  • Carmofur 99.95%
  • 500mg
  • $ 84.00
  • ChemScene
  • Carmofur 99.95%
  • 100mg
  • $ 60.00
  • Chem-Impex
  • Carmofur,98%(Assaybytitration,HPLC) 98%(Assaybytitration,HPLC)
  • 5G
  • $ 189.28
Total 70 raw suppliers
Chemical Property of Carmofur Edit
Chemical Property:
  • Melting Point:110-111 °C 
  • Refractive Index:1.525 
  • PKA:6.94±0.10(Predicted) 
  • PSA:83.96000 
  • Density:1.26 g/cm3 
  • LogP:1.20460 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO: >15mg/mL 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:257.11756954
  • Heavy Atom Count:18
  • Complexity:382
Purity/Quality:

99% *data from raw suppliers

Carmofur *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi,T 
  • Statements: 60-61-25 
  • Safety Statements: 45 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CCCCCCNC(=O)N1C=C(C(=O)NC1=O)F
  • Description Carmofur is an inhibitor of acid ceramidase (IC50 = 79 nM for the rat enzyme) and a derivative of 5-flurouracil . It reduces acid ceramidase activity in a dose- and time-dependent manner and induces intracellular accumulation of various ceramide species, including C18 ceramide , C16 ceramide , and C14 ceramide in SW403 colon and LNCaP prostate cancer cells. Carmofur induces apoptosis in SW403 cells without inhibiting DNA synthesis (IC50 = 1,212 mM for human thymidylate synthetase). It also reduces acid ceramidase activity and increases ceramide accumulation in mouse lung and brain when administered at doses of 10 and 30 mg/kg.
  • Uses antineoplastic Carmofur has been used as an inhibitor of acid ceramidase to study its effects on glucosylsphingosine (GlcSph) production in human embryonic kidney 293T (HEK293T) cells. It has also been used as an inhibitor of acid ceramidase to study its effects on acid‐mediated hydrolysis of ceramide which kicks-in consumption and the generation of sphingosine .
  • Therapeutic Function Antineoplastic
Technology Process of Carmofur

There total 2 articles about Carmofur 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 pyridine; dmap; at 60 ℃;
DOI:10.1039/c7ra02237a

Reference yield:

Guidance literature:
DOI:10.1246/bcsj.50.2406
Guidance literature:
With pyridine; at 20 ℃; for 2h; Inert atmosphere;
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