ChemicalBook--->CAS DataBase List--->11078-21-0

11078-21-0

11078-21-0 Structure

11078-21-0 Structure
IdentificationBack Directory
[Name]

FILIPIN COMPLEX
[CAS]

11078-21-0
[Synonyms]

FILIPIN
filmirisin
filimirasin
14-deoxylagosin
FILIPIN COMPLEX
FILIPIN COMPLEX USP/EP/BP
FILIPIN COMPLEX FROM STREPTOMYCES &
filipin complex from streptomyces filipinensis
[Molecular Formula]

C35H58O11
[MDL Number]

MFCD00131073
[MOL File]

11078-21-0.mol
[Molecular Weight]

654.828
Chemical PropertiesBack Directory
[Melting point ]

195-205°
[alpha ]

D22 -148.3° (c = 0.89 in methanol)
[storage temp. ]

−20°C
[solubility ]

methanol: 10 mg/mL, clear, very dark yellow
[form ]

powder
[color ]

yellow
[Merck ]

13,4111
Safety DataBack Directory
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[RTECS ]

LK4400000
[F ]

10
[HS Code ]

2941900000
Hazard InformationBack Directory
[Uses]

Filipin complex comprises a family of pentaene macrocyclic lactones first isolated from Streptomyces filipinensis and reported by researchers at Upjohn in 1955. Filipin complex consists of four analogues, with filipin III comprising the bulk (>70%) of the complex. Filipin complex is a potent broad spectrum antifungal agent that also exhibits antitumor and antiviral activities. Filipin complex acts by binding cell membrane sterols, disrupting membrane integrity.
[Definition]

ChEBI: Filipin III is a macrolide that is the major component of a mixture of four isomeric polyene macrolides isolated from Streptomyces filipinensis. It has a role as a bacterial metabolite and a fluorescent probe. It is a macrolide, a polyol and an olefinic compound.
[General Description]

Chemical structure: macrolide
[Biochem/physiol Actions]

Filipin is a polyene macrolide antibiotic and antifungal. The antifungal mechanism of action is unclear but may be due to altering membrane permeability. Filipin binds to model crystalline phase lipid bilayers containing cholesterol, and to liquid phase bilayers with or without cholesterol, in an orientation that forms membrane pores.It both inhibits prion protein (PrP) endocytosis and causes the release of PrP from the plasma membrane.
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