ChemicalBook--->CAS DataBase List--->85801-02-1

85801-02-1

85801-02-1 Structure

85801-02-1 Structure
IdentificationBack Directory
[Name]

indomethacin farnesil
[CAS]

85801-02-1
[Synonyms]

IM-F
E-0710
Infree
Infree S
indomethacin farnesil
-5-methoxy-2-methyl-1H-indol-3-yl)
3,7,11-Trimethyldodeca-2,6,10-trien-1-yl 2-(1-(4-chlorobenzoyl)
3,7,11-TriMethyldodeca-2,6,10-trien-1-yl 2-(1-(4-chlorobenzoyl)-5-Methoxy-2-Methyl-1H-indol-3-yl)acetate
1-(4-Chlombenzoyl)-5-methoxy-2-methyl-1-indole-3-acetic acid3,7,11-trimethyl-2,6,10-dodecanetriene ester
1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic acid 3,7,11-trimethyl-2,6,10-dodecatrienyl ester
1H-Indole-3-acetic acid, 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-, 3,7,11-trimethyl-2,6,10-dodecatrien-1-yl ester
[Molecular Formula]

C34H40CINO4
[MDL Number]

MFCD00870661
[MOL File]

85801-02-1.mol
[Molecular Weight]

562.14
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Water Solubility ]

Insoluble in water
[form ]

clear liquid
[color ]

Light yellow to Yellow to Orange
[CAS DataBase Reference]

85801-02-1
Safety DataBack Directory
[RTECS ]

NL3522820
[HS Code ]

2933.79.1500
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Thionyl chloride-->Triethylamine-->Indometacin
Hazard InformationBack Directory
[Chemical Properties]

Acute toxicity LD50 mice, rats, dogs (mg/kg): 6800~7800, 1680~2000, >3000 orally.
[Uses]

Indomethacin farnesil is a new type of non-steroidal anti-inflammatory analgesic that is well distributed in inflammatory tissues. It is suitable for rheumatoid arthritis, osteoarthritis, low back pain, periarthritis of the shoulder and shoulder and neck, shoulder and arm syndrome.
[Definition]

ChEBI:Indomethacin farnesil is a N-acylindole.
[Synthesis]

After indomethacin is chlorinated with thionyl chloride, it reacts with 3,7,1-trimethyl-2,6,10-dodecatrienol in tetrahydrofuran solution in the presence of triethylamine to form indomethacin farnesil.
[in vivo]

Indomethacin farnesil (IMF) can effectively release indomethacin when administered locally[1].

Animal Model:Rats[1].
Dosage:50 nmol a rat paw.
Administration:Once.
Result:Reduced the level of PGE2 in a dose dependent manner.
Spectrum DetailBack Directory
[Spectrum Detail]

indomethacin farnesil(85801-02-1)1HNMR
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