Introduction:Basic information about CAS 41060-16-6|Panicolin, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Panicolin |
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| CAS Number | 41060-16-6 | Molecular Weight | 314.29 |
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| Density | 1.4±0.1 g/cm3 | Boiling Point | 573.6±50.0 °C at 760 mmHg |
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| Molecular Formula | C17H14O6 | Melting Point | 254-256℃ |
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| MSDS | / | Flash Point | 215.5±23.6 °C |
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Names
| Name | Skullcapflavone I |
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| Synonym | More Synonyms |
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Panicolin BiologicalActivity
| Description | Skullcapflavone I can be isolated from A. nallamalayana. Skullcapflavone I inhibits collagenase and elastase enzyme with IC50s of 106.74 μM and 186.70 μM. Skullcapflavone I has anticancer activities by down-regulating miR-23a[1]. |
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| Related Catalog | Research Areas >>CancerSignaling Pathways >>Epigenetics >>MicroRNASignaling Pathways >>Metabolic Enzyme/Protease >>Elastase |
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| References | [1]. Yang B, et al. Anti-cancer, Anti-collagenase and Anti-elastase Potentials of Some Natural Derivatives: In vitro and in silico Studies. J Oleo Sci. 2023;72(5):557-570. [2]. Cui J, et al. Skullcapflavone I has a potent anti-pancreatic cancer activity by targeting miR-23a. Biofactors. 2020 Sep;46(5):821-830. |
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Chemical & Physical Properties
| Density | 1.4±0.1 g/cm3 |
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| Boiling Point | 573.6±50.0 °C at 760 mmHg |
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| Melting Point | 254-256℃ |
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| Molecular Formula | C17H14O6 |
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| Molecular Weight | 314.29 |
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| Flash Point | 215.5±23.6 °C |
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| Exact Mass | 314.079041 |
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| PSA | 89.13000 |
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| LogP | 2.06 |
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| Vapour Pressure | 0.0±1.6 mmHg at 25°C |
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| Index of Refraction | 1.646 |
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| InChIKey | CZRGNFVQUYWGKP-UHFFFAOYSA-N |
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| SMILES | COc1cc(O)c2c(=O)cc(-c3ccccc3O)oc2c1OC |
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Safety Information
| Hazard Codes | T+ |
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| HS Code | 2914509090 |
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Customs
| HS Code | 2914509090 |
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| Summary | HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
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Synonyms
| SKULLCAPFLAVONE I |
| 5-Hydroxy-2-(2-hydroxyphenyl)-7,8-dimethoxy-4H-chromen-4-one |
| 4H-1-Benzopyran-4-one, 5-hydroxy-2-(2-hydroxyphenyl)-7,8-dimethoxy- |
| Panicolin |