Contact us: +91 9550333722 040 - 40102781
Structured search
India
Choose your country
Different countries will display different contents
Try our best to find the right business for you.
My chemicalbook

Welcome back!

HomeProduct name listFERULENOL

FERULENOL

FERULENOL Structural

What is FERULENOL?

The Uses of FERULENOL

Ferulenol is antibiotic useful against mycobacteria similar to taxol.

What are the applications of Application

Ferulenol is antibiotic useful against mycobacteria similar to taxol

Biological Activity

ferulenol is a prenylated 4-hydroxycoumarin derivative from ferula communis var. genuine with haemorrhagic action [1]. it has been demonstrated that ferulenol exihibits potent antimycobacterial activity [2].

in vitro

ferulenol stimulated tubulin polymerization in the absence of gtp, with a less extensive polymerization profile at 100 pm concentration. ferulenol decreased radiolabeled colchicine bound by tubulin in a dose-dependent manner. ferulenol altered the normal nuclear morphology of mcf-7 cells. treatment with ferulenol (100 nm and 1 μm) for 24h induced a dose-dependent reduction of cell viability [3]

in vivo

in albino mice, the acute ld50s of ferulenol by single po or ip were 2,100 and 319 mg/kg bw, respectively. three days after ferulenol administration, dosed animals showed hypoprothrombinemia with internal and external hemorrhages. male mice were more sensitive to intoxication than females [4].

Storage

+4°C

References

[1] lamnaouer d, bodo b, martin m t, et al. ferulenol and ω-hydroxyferulenol, toxic coumarins from ferula communis var. genuina[j]. phytochemistry, 1987, 26(6): 1613-1615.
[2] e. mamoci, i. cavoski, v. simone, et al. chemical composition and in vitro activity of plant extracts from ferula communis and dittrichia viscosa against postharvest fungi. molecules 16(3), 2609-2625 (2011).
[3] bocca c, gabriel l, bozzo f, et al. microtubule-interacting activity and cytotoxicity of the prenylated coumarin ferulenol[j]. planta medica, 2002, 68(12): 1135-1137.
[4] fraigui o, lamnaouer d, faouzi m y. acute toxicity of ferulenol, a 4-hydroxycoumarin isolated from ferula communis l[j]. veterinary and human toxicology, 2002, 44(1): 5-7.

Properties of FERULENOL

Melting point: 55-56℃
Boiling point: 525.3±50.0 °C(Predicted)
Density  1.070±0.06 g/cm3(Predicted)
storage temp.  Store at -20°C
solubility  Soluble in DMSO
pka 4.50±1.00(Predicted)
form  Off-white solid.
color  White to off-white

Safety information for FERULENOL

Computed Descriptors for FERULENOL

Related products of tetrahydrofuran

You may like

  • Deuterated Styrene-d8 19361-62-7 97-99%
    Deuterated Styrene-d8 19361-62-7 97-99%
    19361-62-7
    View Details
  • 1187989-89-4 97-99%
    1187989-89-4 97-99%
    1187989-89-4
    View Details
  • (S)-2-Bromobutanoic acid 97-99%
    (S)-2-Bromobutanoic acid 97-99%
    32659-49-7
    View Details
  • 665020-24-6 ethyl 1-(2,4-dichlorophenyl)-4,5-dihydro-1H-benzo[g]indazole-3-carboxylate 97-99%
    665020-24-6 ethyl 1-(2,4-dichlorophenyl)-4,5-dihydro-1H-benzo[g]indazole-3-carboxylate 97-99%
    665020-24-6
    View Details
  • methyl 3-amino-4-formylbenzoate 97-99%
    methyl 3-amino-4-formylbenzoate 97-99%
    212322-17-3
    View Details
  • 3-bromo-[1,1'-biphenyl]-2-amine 1620885-59-7 97-99%
    3-bromo-[1,1'-biphenyl]-2-amine 1620885-59-7 97-99%
    1620885-59-7
    View Details
  • (13S,17S)-13-methyl-3-oxo-2,3,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl acetate 2590-41-2 97-99%
    (13S,17S)-13-methyl-3-oxo-2,3,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl acetate 2590-41-2 97-99%
    2590-41-2
    View Details
  • 1503408-77-2 6-Chloro-3,4-dimethylpyridin-2-amine 97-99%
    1503408-77-2 6-Chloro-3,4-dimethylpyridin-2-amine 97-99%
    1503408-77-2
    View Details
Statement: All products displayed on this website are only used for non medical purposes such as industrial applications or scientific research, and cannot be used for clinical diagnosis or treatment of humans or animals. They are not medicinal or edible.