ChemicalBook--->CAS DataBase List--->53760-20-6

53760-20-6

53760-20-6 Structure

53760-20-6 Structure
IdentificationBack Directory
[Name]

CYTOCHALASIN J
[CAS]

53760-20-6
[Synonyms]

CYTOCHALASIN J
deacetylcytochalasin H
cytochalasin J from A phomopsis species
1H-Cycloundec[d]isoindol-1-one, 2,3,3a,4,5,6,6a,9,10,11,12,15-dodecahydro-6,12,15-trihydroxy-4,10,12-trimethyl-5-methylene-3-(phenylmethyl)-, (3S,3aR,4S,6S,6aR,7E,10S,12R,13E,15R,15aR)-
[Molecular Formula]

C28H37NO4
[MDL Number]

MFCD00077708
[MOL File]

53760-20-6.mol
[Molecular Weight]

451.6
Chemical PropertiesBack Directory
[Melting point ]

138°C (dec.)
[Boiling point ]

679.5±55.0 °C(Predicted)
[density ]

1.20±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

Soluble in ethanol;Soluble in methanol;Soluble in DMSO;Soluble in dimethyl formamide
[form ]

white lyophilisate
[pka]

13.03±0.70(Predicted)
[color ]

White
[Stability:]

Light Sensitive
Safety DataBack Directory
[Hazard Codes ]

T+
[Risk Statements ]

26/27/28-63-40
[Safety Statements ]

28-36/37-45-36/37/39-22
[RIDADR ]

UN 3462 6.1/PG 2
[WGK Germany ]

3
[RTECS ]

HA5306500
[F ]

10
Hazard InformationBack Directory
[Uses]

Cytochalasin J is a cell-permeable fungal toxin used in actin polymerization studies and cytological research.
[Biological Activity]

cytochalasin j can alter mitotic spindle microtubule organization and kinetochore structure.the cytochalasins are cell-permeable fungal metabolites inhibiting actin polymerization, which can alter diverse processes including cell movement, growth, phagocytosis, degranulation, and secretion.
[in vitro]

cytochalasin j was identified as a deacetylated analog of cytochalasin h that weakly inhibited actin assembly but significantly altered mitotic spindle microtubule organization and kinetochore structure [1]. in a previous study, cytochalasin j treatment of prometaphase cells reduced the number of kmts and the size and organization of the kinetochore lamina. moreover, in approximately 30% of cells treated with cytochalasin j, the failure of a small number of chromosomes to attach to spindle fibers could be documented. these chromosomes showed a significant change in the organization of the kinetochore laminae. light microscopic analyses of cells treated with cytochalasin j revealed loss of chromosome congression, with chromsomes usually located at the periphery of the spindle. cells treated with 10 microg/ml cytochalasin j for 10 min and released into tissue culture medium showed a resumption of chromosome motion within a few minutes, both during congression and anaphase [2].
[storage]

Store at -20°C
[References]

[1] walling, e. a.,krafft, g.a. and ware, b.r. actin assembly activity of cytochalasins and cytochalasin analogs assayed using fluorescence photobleaching recovery. archives of biochemistry and biophysics 264(1), 321-332 (1988).
[2] wrench, g. a. and snyder, j.a. cytochalasin j treatment significantly alters mitotic spindle microtubule organization and kinetochore structure in ptk1 cells. cell motility and the cytoskeleton 36(2), 112-124 (1997).
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