Determine the necessary mass, volume, or concentration for preparing a solution.
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SKU | Size | Availability | Price | Qty |
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H421649-1ml | 1ml | Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience! | $241.90 |
Partial positive allosteric modulator at the benzodiazepine site
Synonyms | Hispidulin | 1447-88-7 | Dinatin | Scutellarein 6-methyl ether | 4',5,7-Trihydroxy-6-methoxyflavone | 4H-1-BENZOPYRAN-4-ONE, 5,7-DIHYDROXY-2-(4-HYDROXYPHENYL)-6-METHOXY- | Salvitin | 5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-4H-chromen-4-one | 6-O-Methylapigenin | NSC 12 |
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Specifications & Purity | 10mM in DMSO |
Biochemical and Physiological Mechanisms | Partial positive allosteric modulator at the benzodiazepine receptor (IC50= 1.3μM for inhibition of flumazenil binding); natural sage flavone. Stimulates GABA-induced chloride currents in Xenopus oocytes expressingα1-,α2-,α3-,α5- orα6-β2γ2S GABAAreceptors |
Storage Temp | Store at -80°C |
Shipped In | Ice chest + Ice pads |
Product Description | Hispidulin has been used as a calibration standard:
in high-performance liquid chromatography (HPLC) for quantification of Clerodendrum petasites flavonoids
in liquid chromatography/electrospray ionization mass spectrometry (LC/ESI-MS) analysis
in reverse-phase high-performance liquid chromatography with a diode-array detector (HPLC-DAD) and high-performance thin-layer chromatography (HPTLC) |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | 5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxychromen-4-one |
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INCHI | InChI=1S/C16H12O6/c1-21-16-11(19)7-13-14(15(16)20)10(18)6-12(22-13)8-2-4-9(17)5-3-8/h2-7,17,19-20H,1H3 |
InChi Key | IHFBPDAQLQOCBX-UHFFFAOYSA-N |
Canonical SMILES | COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O |
Isomeric SMILES | COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O |
WGK Germany | 3 |
RTECS | DJ2996000 |
PubChem CID | 5281628 |
Molecular Weight | 300.26 |
Enter Lot Number to search for COA:
Pictogram(s) | GHS07 |
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Signal | Warning |
Hazard Statements | H302:Harmful if swallowed |
Precautionary Statements | P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P270:Do not eat, drink or smoke when using this product. P330:Rinse mouth. P301+P317:IF SWALLOWED: Get medical help. |
WGK Germany | 3 |
RTECS | DJ2996000 |
1. Zhihua Chen, Guofeng Zhu, Chunpeng Sheng, Jianwei Lei, Sihui Song, Jianming Zhu. (2022) Hispidulin Enhances Temozolomide (TMZ)-Induced Cytotoxicity against Malignant Glioma Cells In Vitro by Inhibiting Autophagy. Computational Intelligence and Neuroscience, 2022 (5266770). [PMID:35800695] [10.1155/2022/5266770] |
2. Xiaoli Wang, Jichen Yang, Huan Li, Se Shi, Xin Peng. (2022) Mechanistic study and synergistic effect on inhibition of α-amylase by structurally similar flavonoids. JOURNAL OF MOLECULAR LIQUIDS, 360 (119485). [PMID:] [10.1016/j.molliq.2022.119485] |
3. Li Lv, Wenhui Zhang, Tingting Li, Lifeng Jiang, Xinyan Lu, Jie Lin. (2020) Hispidulin exhibits potent anticancer activity in vitro and in vivo through activating ER stress in non‑small‑cell lung cancer cells. ONCOLOGY REPORTS, 43 (6): (1995-2003). [PMID:32236602] [10.3892/or.2020.7568] |
1. Zhihua Chen, Guofeng Zhu, Chunpeng Sheng, Jianwei Lei, Sihui Song, Jianming Zhu. (2022) Hispidulin Enhances Temozolomide (TMZ)-Induced Cytotoxicity against Malignant Glioma Cells In Vitro by Inhibiting Autophagy. Computational Intelligence and Neuroscience, 2022 (5266770). [PMID:35800695] [10.1155/2022/5266770] |
2. Xiaoli Wang, Jichen Yang, Huan Li, Se Shi, Xin Peng. (2022) Mechanistic study and synergistic effect on inhibition of α-amylase by structurally similar flavonoids. JOURNAL OF MOLECULAR LIQUIDS, 360 (119485). [PMID:] [10.1016/j.molliq.2022.119485] |
3. Li Lv, Wenhui Zhang, Tingting Li, Lifeng Jiang, Xinyan Lu, Jie Lin. (2020) Hispidulin exhibits potent anticancer activity in vitro and in vivo through activating ER stress in non‑small‑cell lung cancer cells. ONCOLOGY REPORTS, 43 (6): (1995-2003). [PMID:32236602] [10.3892/or.2020.7568] |