Pinokembrin

Pinokembrin
Nama
Nama IUPAC
5,7-Dihidroksi-2-fenil-2,3-dihidro-4H-kromen-4-ona
Nama lain
Dihidrokrisin
Galangin flavanona
5,7-Dihidroksiflavanona
5,7-Dihidroksi-2-fenil-2,3-dihidro-4H-kromen-4-ona
4H-1-Benzopiran-4-ona, 2,3-dihidro-5,7-dihidroksi-2-fenil-
5,7-Dihidroksi-2-fenil-kroman-4-ona
Penanda
Model 3D (JSmol)
ChEBI
ChEMBL
ChemSpider
Nomor EC
KEGG
Nomor RTECS {{{value}}}
UNII
  • InChI=1S/C15H12O4/c16-10-6-11(17)15-12(18)8-13(19-14(15)7-10)9-4-2-1-3-5-9/h1-7,13,16-17H,8H2 checkY
    Key: URFCJEUYXNAHFI-UHFFFAOYSA-N checkY
  • InChI=1/C15H12O4/c16-10-6-11(17)15-12(18)8-13(19-14(15)7-10)9-4-2-1-3-5-9/h1-7,13,16-17H,8H2
    Key: URFCJEUYXNAHFI-UHFFFAOYAA
  • O=C2c3c(OC(c1ccccc1)C2)cc(O)cc3O
Sifat
C15H12O4
Massa molar 256,26 g·mol−1
Densitas 1,386 g/mL
Kecuali dinyatakan lain, data di atas berlaku pada suhu dan tekanan standar (25 °C [77 °F], 100 kPa).
N verifikasi (apa ini checkYN ?)
Referensi

Pinokembrin adalah suatu flavanona, sejenis flavonoid. Flavanona ini adalah antioksidan yang ditemukan dalam damiana,[1] madu, temu kunci,[2] dan propolis.[3] Pinokembrin dapat diubah secara biosintetik menjadi pinobanksin melalui hidroksilasi.

Referensi

  1. ^ Zhao, J; Dasmahapatra AK; Khan SI; Khan IA (Dec 2008). "Anti-aromatase activity of the constituents from damiana (Turnera diffusa)". J Ethnopharmacol. 120 (3): 387–393. doi:10.1016/j.jep.2008.09.016. PMID 18948180.
  2. ^ Punvittayagul, C; Wongpoomchai R; Taya S; Pompimon W. (January 2011). "Effect of pinocembrin isolated from Boesenbergia pandurata on xenobiotic-metabolizing enzymes in rat liver". Drug Metabolism Letters. 5 (1): 1–5. doi:10.2174/187231211794455226. PMID 20942797.
  3. ^ Bosio K; Avanzini C; D’Avolio A; Ozino O; Savoia D (2000). "In vitro activity of propolis against Streptococcus pyogenes". Letters in Applied Microbiology. 31 (2): 174–177. doi:10.1046/j.1365-2672.2000.00785.x. PMID 10972723. S2CID 1622868.

Pranala luar

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