Apogossypolone
Based on 1 Customer Validation
Apogossypolone (ApoG2) is an orally active Bcl-2 family proteins inhibitor with Ki values of 35, 25 and 660 nM for Bcl-2, Mcl-1 and Bcl-XL, respectively. Apogossypolone shows antitumor activities, induces cell apoptosis and autophagy. Apogossypolone also has antifungal activity.
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- Pureté: 98.58%
- CAS No.: 886578-07-0
- Formule: C28H26O8
- Masse moléculaire:490.50
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Stockage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
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Activité biologique
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Chemical Information
- Pureté et documentation
- Références
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Help & FAQs
Activité biologique
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Mcl-1 25 nM (Ki) |
Bcl-2 35 nM (Ki) |
Bcl-xL 660 nM (Ki) |
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Cell Line
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Type | Value | Description | References |
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| NCI-H1299 | EC50 |
2.76 μM
Compound: 6a
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Cytotoxicity against human H1299 cells expressing high level of Mcl-1 after 72 hrs by ATP-LITE assay
Cytotoxicity against human H1299 cells expressing high level of Mcl-1 after 72 hrs by ATP-LITE assay
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[PMID: 21033669] |
| NCI-H460 | EC50 |
0.4 μM
Compound: 6a
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Cytotoxicity against human H460 cells expressing high level of Bcl-2 after 72 hrs by ATP-LITE assay
Cytotoxicity against human H460 cells expressing high level of Bcl-2 after 72 hrs by ATP-LITE assay
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[PMID: 21033669] |
| PC-3 | EC50 |
1.46 μM
Compound: 6a
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Cytotoxicity against human PC3 cells expressing high level of Bcl-xL after 72 hrs by ATP-LITE assay
Cytotoxicity against human PC3 cells expressing high level of Bcl-xL after 72 hrs by ATP-LITE assay
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[PMID: 21033669] |
| RS4-11 | EC50 |
7.4 μM
Compound: 6a
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Induction of apoptosis in human RS4:11 cells expressing high level of Bcl-2 and Bcl-xL after 24 hrs by annexin V-FITC and propidium iodide staining
Induction of apoptosis in human RS4:11 cells expressing high level of Bcl-2 and Bcl-xL after 24 hrs by annexin V-FITC and propidium iodide staining
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[PMID: 21033669] |
| RS4-11 | EC50 |
7.47 μM
Compound: 6a
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Cytotoxicity against human RS4:11 cells expressing high level of Bcl-2 and Bcl-xL after 72 hrs by annexin V-FITC and propidium iodide staining
Cytotoxicity against human RS4:11 cells expressing high level of Bcl-2 and Bcl-xL after 72 hrs by annexin V-FITC and propidium iodide staining
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[PMID: 21033669] |
Apogossypolone (ApoG2) shows improved stability under stressed conditions[1].
Apogossypolone (0-1 μM, 72 or 96 h) inhibits WSU-DLCL2 cells growth in a dose-dependent manner[1].
Apogossypolone (0-5 μM, 24 or 48 h) interferes with the formation of heterodimers between anti-apoptotic and pro-apoptotic Bcl-2 family members, and leads to cleavage of caspase-3, caspase-9 and PARP[1].
Apogossypolone (0-8 μM, 0-72 h) induces apoptotic WSU-DLCL2 cell death in a time- and dose-dependent manner[1].
Apogossypolone (0-10 μM, 0-24 h) induces autophagy and promotes ROS generation in HCC cells[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:WSU-DLCL2
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Concentration:250, 350, 500 and 1000 nM
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Incubation Time:96 h for cell counting, 72 h for MTT
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Result:Inhibited growth in a dose-dependent manner. The 50% growth inhibition concentration (IC50) was approximately 350 nM.
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Cell Line:WSU-DLCL2
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Concentration:0.35, 0.5, 1 and 5 µM
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Incubation Time:24 or 48 h
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Result:Blocked the formation of heterodimers between Bcl-XL and Bim in a concentration-dependent manner. Resulted in the activation of cleavages of caspase-3, caspase-9 and PARP.
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Cell Line:WSU-DLCL2
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Concentration:0, 1, 2, 4 and 8 µM
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Incubation Time:24, 48 and 72 h
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Result:Induced cell apoptosis in a time- and dose-dependent manner.
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Cell Line:HepG2 and Hep3B
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Concentration:1.25, 2.5, 5 and 10 µM
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Incubation Time:6, 12, 18 and 24 h
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Result:Induced LC3 (Light chain 3)-II conversion in a dose- and time-dependent manner.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Four-week-old female ICR-SCID mice, each mouse received 107 WSU-DLCL2 cells (in serum-free RPMI 1640) subcutaneously (sc) in each flank area[1]
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Dosage:120 mg/kg
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Administration:Intravenous or administration per day for five days
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Result:Inhibited the growth of WSU-DLCL2 and significantly decreased the tumor weight.
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Animal Model:Non-tumor-bearing SCID mice[1]
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Dosage:160 mg/kg
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Administration:Intravenous or administration per day for five days
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Result:Was well tolerated in mice up to 800 mg/kg. Displayed no gross signs of toxicity.
Chemical Information
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CAS No. 886578-07-0
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Appearance Solid
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Masse moléculaire 490.50
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Formule C28H26O8
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Color Orange to reddish brown
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SMILES
O=C1C(C(C2=O)=C(C)C(C3=C2C=C(O)C(O)=C3C(C)C)=O)=C(C)C(C4=C1C=C(O)C(O)=C4C(C)C)=O
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Synonyms
ApoG2
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Pureté et documentation
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Fiche technique (279 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Instruction de manipulation (2659 KB)
Références
[1]. Yuan Sun, et al. Apogossypolone, a nonpeptidic small molecule inhibitor targeting Bcl-2 family proteins, effectively inhibits growth of diffuse large cell lymphoma cells in vitro and in vivo. Cancer Biol Ther. 2008 Sep;7(9):1418-26. [Content Brief]
[2]. Cheng P, et al. The novel BH-3 mimetic apogossypolone induces Beclin-1- and ROS-mediated autophagy in human hepatocellular carcinoma [corrected] cells. Cell Death Dis. 2013 Feb 7;4(2):e489. [Content Brief]
[3]. Jay E Mellon, et al. Inhibitory effects of gossypol, gossypolone, and apogossypolone on a collection of economically important filamentous fungi. J Agric Food Chem. 2012 Mar 14;60(10):2740-5. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Apogossypolone Related Classifications
HY-19551 Related Classifications
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