Chondramide C
Chondramide C has anti-candida, Henson yeast, lipids yeast, ball-like yeast and other fungal activities, but has no anti-Gram positive and negative bacteria activities.
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- CAS No.: 172430-62-5
- Formule: C35H44N4O6
- Masse moléculaire:616.75
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Activité biologique
Description
Cellular Effect
|
Cell Line
|
Type | Value | Description | References |
|---|---|---|---|---|
| MCF7 | IC50 |
23 nM
|
Cytotoxicity against human MCF-7 cells by cell viability assay.
Cytotoxicity against human MCF-7 cells by cell viability assay.
|
22475347 |
| HT-29 | IC50 |
21 nM
|
Cytotoxicity against human HT-29 cells by cell viability assay.
Cytotoxicity against human HT-29 cells by cell viability assay.
|
22475347 |
| MCF7 | IC50 |
0.023 μM
|
Cytotoxicity of natural Chondramide C against human MCF-7 breast cancer cells.
Cytotoxicity of natural Chondramide C against human MCF-7 breast cancer cells.
|
20148556 |
| HT-29 | IC50 |
0.021 μM
|
Cytotoxicity of natural Chondramide C against human HT-29 colorectal cancer cells.
Cytotoxicity of natural Chondramide C against human HT-29 colorectal cancer cells.
|
20148556 |
| MCF7 | IC50 |
0.083 μM
|
Cytotoxicity of Synthetic Chondramide C against human MCF-7 breast cancer cells.
Cytotoxicity of Synthetic Chondramide C against human MCF-7 breast cancer cells.
|
20148556 |
| HT-29 | IC50 |
0.031 μM
|
Cytotoxicity of Synthetic Chondramide C against human HT-29 colorectal cancer cells.
Cytotoxicity of Synthetic Chondramide C against human HT-29 colorectal cancer cells.
|
20148556 |
In Vitro
Chondramide C (compound 3c) (24 h) disrupts actin organization in BSC-1 cells, leading to loss of stress fibers and formation of perinuclear actin aggregates[3].
Chondramide C can serve as an intermediate for the synthesis of derivatives with anticancer activity[4].
Chondramide C shows strong binding affinity to the spike proteins of SARS-CoV-2 wild-type, N501Y, E484K, and D614G-I472V variants in molecular docking simulations, and can bind to key amino acid sites of the spike protein through molecular interactions such as hydrogen bonds and π-π stacking[5].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 172430-62-5
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Masse moléculaire 616.75
-
Formule C35H44N4O6
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SMILES
O=C(C[C@H](C1=CC=C(O)C=C1)NC([C@@H](CC2=CNC3=C2C=CC=C3)N4C)=O)O[C@H](C)[C@H](C)/C=C(C)\C[C@H](C)C(N[C@@H](C)C4=O)=O
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Structure Classification
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Initial Source
Myxobacterium Chondromyces crocatus
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)