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Synonyms | XE178590 | AS-15078 | HY-N0114A | NCGC00163553-02 | SureCN682158 | FT-0651829 | Evodiamine, Evodia rutaecarpa | NSC258314 | NSC-258314 | Evodiamine; | NCGC00163553-03 | Q5418554 | PubChem18244 | (1S)-21-methyl-3,13,21-triazapentacyclo[11.8.0.0^{2,10.0^{4, |
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Specifications & Purity | ≥98% |
Biochemical and Physiological Mechanisms | The interferon-γ priming signal regulating the transcriptional activation of the iNOS gene is blocked by Evodiamine, suppressing iNOS protein synthesis but not affecting iNOS function. Evodiamine also demonstrates antiangiogenesis through inhibition of va |
Storage Temp | Store at 2-8°C |
Shipped In | Wet ice |
Product Description | Evodiamine is a quinozole alkaloid isolated from Evodia rutaecarpa, described as an agonist of the VR1 (vanilloid receptor subtype 1, TRPV1) with affinity (Ki = 5.95 microM) comparable to that of the prototypical VR1 chemical activator Capsaicin .Evodiamine induction of 45Ca2+ uptake was competitively antagonized by the Capsaicin antagonist Capsazepine .Evodiamine is described to inhibit prostaglandin E2 synthesis, cyclooxygenase-2 induction and NF-κB activation, producing antiinflammatory effects. |
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IUPAC Name | 21-methyl-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15,17,19-heptaen-14-one |
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INCHI | InChI=1S/C19H17N3O/c1-21-16-9-5-3-7-14(16)19(23)22-11-10-13-12-6-2-4-8-15(12)20-17(13)18(21)22/h2-9,18,20H,10-11H2,1H3 |
InChi Key | TXDUTHBFYKGSAH-UHFFFAOYSA-N |
Canonical SMILES | CN1C2C3=C(CCN2C(=O)C4=CC=CC=C41)C5=CC=CC=C5N3 |
Isomeric SMILES | CN1C2C3=C(CCN2C(=O)C4=CC=CC=C41)C5=CC=CC=C5N3 |
PubChem CID | 151289 |
Molecular Weight | 303.37 |
Reaxy-Rn | 94484 |
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Solubility | Soluble in DMSO (5 mg/mL,warm to 40°C), water (<1 mg/mL) at 25 °C, and ethanol (<1 mg/mL) at 25 °C |
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Sensitivity | Light sensitive. |
Melt Point(°C) | 272°C(lit.) |
Reaxy-Rn | 94484 |
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