2. Immunology/Inflammation NF-κB Metabolic Enzyme/Protease
  3. Reactive Oxygen Species
  4. Fusarochromanone

Fusarochromanone (FC-101) is a fungal metabolite with potent anti-angiogenic and anti-cancer activity. Fusarochromanone-activated JNK pathway is attributed to induction of reactive oxygen species (ROS).

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Fusarochromanone Chemical Structure

Fusarochromanone Chemical Structure

CAS No. : 802915-53-3

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Fusarochromanone Related Antibodies

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Description

Fusarochromanone (FC-101) is a fungal metabolite with potent anti-angiogenic and anti-cancer activity[1]. Fusarochromanone-activated JNK pathway is attributed to induction of reactive oxygen species (ROS)[2].

In Vitro

Fusarochromanone (FC101; 10 μM; 24 hours) induces apoptosis and an increase in proportion of cells in the sub-G1 phase in both HaCat and P9-WT cell lines[1].
Fusarochromanone (FC101; 0-1 μM; 24 h) induces the cleavage of both caspase-3 and PARP, a well-known substrate for activated caspases. FC101 does not affect the expression of the anti-apoptotic proteins, Bcl-2, Bcl-XL, Mcl-1, or the pro-apoptotic proteins BAD, BAK, BAX[1].
Fusarochromanone (FC101) exhibits very potent in-vitro growth inhibitory effects (IC50 ranging from 10 nM-2.5 μM) against HaCat (pre-malignant skin), P9-WT (malignant skin), MCF-7 (low malignant breast), MDA-231 (malignant breast), SV-HUC (premalignant bladder), UM-UC14 (malignant bladder), and PC3 (malignant prostate) in a time-course and dose-dependent manner, with the UM-UC14 cells being the most sensitive.

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Fusarochromanone Related Antibodies

Cell Cycle Analysis[1]

Cell Line: HaCat and P9-WT cell lines
Concentration: 10 μM
Incubation Time: 24 hours
Result: Showed cells in the G2 and M phases of the cell cycle for both cell lines.

Western Blot Analysis[1]

Cell Line: MDA-MB-231 cells
Concentration: 0.05 μM, 0.1 μM, 0.2 μM, 0.5 μM, 1 μM
Incubation Time: 24 hours
Result: Induced the cleavage of both caspase-3 and PARP.
In Vivo

Fusarochromanone (8 mg/kg; IP; 5 days per week; for 3.5 weeks) Is well tolerated, non-toxic, and achieved a 30% reduction in tumor size at a dose of 8 mg/kg/day[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: SCID Beige mice (CB17/Icr.Cg-PrkdcscidLystbg/Crl) injected with SRB12-p9 cells[1]
Dosage: 8 mg/kg
Administration: IP; 5 days per week; for 3.5 weeks
Result: Achieved a 30% reduction in tumor size at a dose of 8 mg/kg/day.
Molecular Weight

292.33

Formula

C15H20N2O4
CAS No.
SMILES

O=C1CC(C)(C)OC2=CC=C(C(C[C@@H](N)CO)=O)C(N)=C12
Structure Classification
Initial Source

Fusarium equiseti
Shipping

Room temperature in continental US; may vary elsewhere.
Storage

Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
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Fusarochromanone Related Classifications

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Fusarochromanone802915-53-3FC-101FC101FC 101Reactive Oxygen Speciesfungal metaboliteanti-angiogenicanti-cancer activitycell cycle arrestInhibitorinhibitorinhibit

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