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Catalog: | HY-N10113 |
Brand: | MCE |
CAS: | 4643-58-7 |
MDL | - |
---|---|
Molecular Weight | 484.54 |
Molecular Formula | C27H32O8 |
SMILES | CC1=C[C@@H]2[C@]3(COC(/C=C(C)/CCOC(/C=C/C=C\C(OC4[C@]3(C)[C@@]5([C@H](O2)C4)CO5)=O)=O)=O)CC1 |
Verrucarin J (Muconomycin B) is a metabolite of the Myrothecium fungus family. Verrucarin J generates reactive oxygen species ( ROS ) and induces apoptosis of cancer cell lines, such as A549, HCT 116 and SW-620 cells. Verrucarin J shows activities against Candida albicans and Mucor miehei . Verrucarin J inhibits arenavirus Junin (JUNV) yield with an IC 50 of 1.2 ng/mL [1] [2] [3] [4] [5] .
Verrucarin J (0, 5, 10, 20, 50 nM; 24 hours) induces the
apoptosis
of A549 cells
[1]
.
Verrucarin J (0, 1, 2, 5, 10, 20, 50 nM; 24, 48, 72 hours) significantly inhibits cell proliferation of A549 and H1793 cells with IC
50
values of approximately 10 nM and 20 nM after 48 h of treatment, respectively
[1]
.
Verrucarin J (0, 0.1, 0.2, 0.3, 0.4, 0.5 μM; 24 hours) has an IC
50
of 300 nM for HCT 116 and SW-620 cell proliferation
[2]
.
Verrucarin J (0, 10, 20 nM, 48 hours) inhibits
cancer
stem cell (CSC) self-renewal pathways Wnt1/β-catenin and Notch1 and down-regulates the expression of key CSC specific genes (ALDH1, LGR5, OCT4 and CD133) of A549 cells
[1]
.
Verrucarin J (compound 2; 50 μg/disk) shows noteworthy activities against
Candida albicans
and
Mucor miehei
[3]
.
Verrucarin J reduces JUNV yield more than 2 log units and has a similar effect against the
arenavirus
Tacaribe
[4]
.
Verrucarin J reduces the cell viability of Vero cells with a cytotoxic concentration 50%
(CC
50
) of 8.2 ng/mL
[4]
.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Verrucarin J (0.5 mg/kg; i.p. for 4 weeks) suppresses AKT-induced tumor growth in a xenograft model
[2]
.
Verrucarin J (0.1, 0.5, 2.0 mg/kg; i.p. for three weeks) is a highly potent
anticancer
drug and suppresses tumor growth and metastasis
[5]
.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | 6-8 weeks old BALB/c athymic nude mice (nu/nu) with pCMV/HCT 116 and AKT/HCT 116 xenografts [2] |
Dosage: | 0.5 mg/kg body weight |
Administration: | i.p. for 4 weeks |
Result: | Reduced the expression of prosurvival markers pAKT, Notch1, p65, and Ki67 in all tumors. |
Animal Model: | Female nude nu/nu (5 to 6 weeks old) mice with A2780 xenografts [5] |
Dosage: | 0.1, 0.5, 2.0 mg/kg (vehicle: 10% DMSO, 90% glyceryl trioctanoate) |
Administration: | i.p. for three weeks after 10 days of injection of A2780 cells |
Result: |
Reduced tumor weight (32% lower compared to control), and reduced visible metastasis in 0.1 mg/kg.
Showed a significant reduction in visible peritoneal tumors (61% lower compared to control group) and highly reduced visible metastasis in 0.5 mg/kg. Reduced ovarian tumor weight by 71% compared to vehicle in 0.5 mg/kg. In lethal dose 2 mg/kg, mice sick with a swollen belly, body fluid and subsequently died within 3 treatments. |
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
4°C | 2 years | |
In solvent | -80°C | 6 months |
-20°C | 1 month |
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