4-methoxy-6-styryl-pyran-2-one

chemical compound
ChemicalSubstance group_of_stereoisomers Q104983396
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4-methoxy-6-styryl-pyran-2-one

Summary

4-methoxy-6-styryl-pyran-2-one is a group of stereoisomers[1].

Key Facts

  • 4-methoxy-6-styryl-pyran-2-one's instance of is recorded as group of stereoisomers[2].
  • 4-methoxy-6-styryl-pyran-2-one's CAS Registry Number is recorded as 1952-41-6[3].
  • 4-methoxy-6-styryl-pyran-2-one's canonical SMILES is recorded as O=C1OC(C=CC=2C=CC=CC2)=CC(OC)=C1[4].
  • 4-methoxy-6-styryl-pyran-2-one's InChI is recorded as InChI=1S/C14H12O3/c1-16-13-9-12(17-14(15)10-13)8-7-11-5-3-2-4-6-11/h2-10H,1H3[5].
  • 4-methoxy-6-styryl-pyran-2-one's InChIKey is recorded as DKKJNZYHGRUXBS-UHFFFAOYSA-N[6].
  • 4-methoxy-6-styryl-pyran-2-one's chemical formula is recorded as C₁₄H₁₂O₃[7].
  • 4-methoxy-6-styryl-pyran-2-one's subclass of is recorded as chemical compound[8].
  • 4-methoxy-6-styryl-pyran-2-one's PubChem CID is recorded as 164901[9].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Alpinia blepharocalyx[10].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Alpinia mutica[11].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Alpinia rafflesiana[12].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Aniba firmula[13].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Aniba permollis[14].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Boesenbergia rotunda[15].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Lindera umbellata[16].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Piper cubeba[17].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Piper lolot[18].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Piper sarmentosum[19].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Piper methysticum[20].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Piper sanctum[21].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Piper auritum[22].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Piper majusculum[23].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Alpinia roxburghii[24].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Alpinia zerumbet[25].
  • 4-methoxy-6-styryl-pyran-2-one's found in taxon is recorded as Etlingera elatior[26].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Chemical Abstracts Service. Retrieved . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . wikidata.org.
  9. [10] . A New Antiplatelet Diarylheptanoid from Alpinia blepharocalyx. wikidata.org.
  10. [11] . Phytochemical and cytotoxic investigations of Alpinia mutica rhizomes.. wikidata.org.
  11. [12] . Constituents of the rhizomes of two Alpinia species of Malaysia. wikidata.org.
  12. [13] . The Chemistry of Rosewood. III. Isolation of 5,6-Dehydrokavain and 4-Methoxyparacotoin from Aniba firmula Mez. wikidata.org.
  13. [14] . The 2-pyrones of Aniba species. wikidata.org.
  14. [15] . Bioactive secondary metabolites from Boesenbergia pandurata of Myanmar and their preferential cytotoxicity against human pancreatic cancer PANC-1 cell line in nutrient-deprived medium.. wikidata.org.
  15. [16] . A lignan from Lindera praecox. wikidata.org.
  16. [17] . Radical scavenging ability of some compounds isolated from Piper cubeba towards free radicals. wikidata.org.
  17. [18] . Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot. wikidata.org.
  18. [19] . Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot. wikidata.org.
  19. [20] . Kavalactones from Piper methysticum, and their 13C NMR spectroscopic analyses. wikidata.org.
  20. [21] . Antimycobacterial compounds from Piper sanctum. wikidata.org.
  21. [22] . Antimycobacterial compounds from Piper sanctum. wikidata.org.
  22. [23] . Extracts and kavalactones of Piper methysticum G. Forst (kava-kava) inhibit P-glycoprotein in vitro. wikidata.org.
  23. [24] . Calyxin H, Epicalyxin H, and Blepharocalyxins A and B, Novel Diarylheptanoids from the Seeds of Alpinia blepharocalyx. wikidata.org.
  24. [25] . Death receptor 5 promoter-enhancing compounds isolated from Catimbium speciosum and their enhancement effect on TRAIL-induced apoptosis.. wikidata.org.
  25. [26] . Phenolic compounds from the rhizomes of Alpinia speciosa. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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