ENSIKLOPEDIA Cari Tekan Enter untuk memulai pencarian cepat. Kembali ke Ensiklopedia Arsip Wikipedia Indonesia Foeniculoside I Foeniculoside I Foeniculoside I Chemical structure of foeniculoside I Names IUPAC name 3-{(2S,2′R,3S,3′R)-6,6′-Dihydroxy-2,2′-bis(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethen-1-yl]-2,2′,3,3′-tetrahydro[3,4′-bi-1-benzofuran]-3′-yl}-5-hydroxyphenyl β-D-glucopyranoside Systematic IUPAC name (12S,13R,14S,15S,16R,42R,43R,52S,53S,6E)-16-(Hydroxymethyl)-42,52-bis(4-hydroxyphenyl)-42,43,52,53-tetrahydro-4,5(3,4)-bis([1]benzofurana)-1(2)-oxana-3(1,3),8(1)-dibenzenaoctaphan-6-ene-13,14,15,35,46,56,84-heptol Other names cis-Miyabenol C 11a-O-β-D-glucopyranoside Identifiers CAS Number 168010-10-4 3D model (JSmol) Interactive image PubChem CID 101924276 InChI InChI=1S/C48H42O14/c49-22-38-43(56)44(57)45(58)48(62-38)59-34-17-27(16-31(53)18-34)40-41-35(19-33(55)21-37(41)61-46(40)24-5-11-29(51)12-6-24)42-39-26(4-1-23-2-9-28(50)10-3-23)15-32(54)20-36(39)60-47(42)25-7-13-30(52)14-8-25/h1-21,38,40,42-58H,22H2/b4-1+/t38-,40-,42+,43-,44+,45-,46+,47-,48-/m1/s1Key: SZKVNSODIJRAET-AKFYMKAISA-N SMILES OCC1OC(OC2=CC(=CC(O)=C2)C2C(OC3=CC(O)=CC(C4C(OC5=C4C(\C=C\C4=CC=C(O)C=C4)=CC(O)=C5)C4=CC=C(O)C=C4)=C23)C2=CC=C(O)C=C2)C(O)C(O)C1O Properties Chemical formula C48H42O14 Molar mass 842.850 g·mol−1 Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references Chemical compound Foeniculoside I is a stilbenoid. It is a glucoside of the stilbene trimer cis-miyabenol C. It can be found in Foeniculi fructus (fruit of Foeniculum vulgare).[1] References ↑ Ono, Masateru; Ito, Yasuyuki; Kinjyo, Junei; Yahara, Shoji; Nohara, Toshihiro; Niiho, Yujiro (1995). "Four New Glycosides of Stilbene Trimer from Foeniculi Fructus (Fruit of Foeniculum vulgare MILLER)". Chemical & Pharmaceutical Bulletin. 43 (5): 868–871. doi:10.1248/cpb.43.868. INIST 3610745 External links Foeniculoside I at the Human Metabolome Database vteOligostilbenoids and their glycosides Diptoindonesin C Diptoindonesin F Gnetin H Hemsleyanol D Isohopeaphenol Laetevirenol A, B, C, D and E Suffruticosol A and B Viniferal E-ω-viniferin Z-ω-viniferin Dimers Diptoindonesin G Jezonodione B Scirpusin A Tibeticanol (piceatannol dimer) Trimers Amurensin B Gnetin E Gneyulin A Johorenol A Ampelopsin E Vaticanol G Tetramers: Dibalanocarpol Gnetin J (3"-hydroxygnetin E) Gnetin K (3"-methoxygnetin E) Gnetuhainin R (isorhapontigenin tetramer) Laetevirenol F and G Higher polymers(five units or more) Vaticanol D, H, I and J Oligomeric formsof resveratrolDimers Amurensin A and H Ampelopsin A B D and F Balanocarpol Cyphostemmin A and B δ-viniferin ε-viniferin Gnetin A and C Leachinol F Malibatol A Pallidol Parthenocissin A Quadrangularin A Restrytisol A, B and C Vitisinol D Trimers α-viniferin Ampelopsin C Amurensin C, D and G Hopeanolin Malaysianol A Miyabenol C Resviniferin A and B trans-diptoindonesin B Tetramers Ampelopsin H Amurensin K Caraphenol B Carasinol B Flexuosol A Hopeaphenol Kobophenol A Miyabenol A Vaticanol B and C Vaticaphenol A Vitisin A B and C β-viniferin (cyclic resveratrol tetramer) Pentamers Amurensin E and F Hexamers Chunganenol Higher polymers γ-viniferin Valeriaphenol A Glycosides or conjugates Diptoindonesin A (C-glucoside of ε-viniferin) Foeniculoside I (glucoside of miyabenol C), II, III and IV Laevifonol (an ε-viniferin-ascorbic acid hybrid compound) Laevifoside (O-glucoside of ampelopsin A) This article about an aromatic compound is a stub. You can help Wikipedia by adding missing information.vte
