Arecatannin B1
Chemical structure of arecatannin B1
Names
IUPAC name
[(2R,3R,4R)-Flavan-3,3′,4′,5,7-pentol]-(4→8)-[(2R,3R,4S)-flavan-3,3′,4′,5,7-pentol]-(4→6)-[(2R,3S)-flavan-3,3′,4′,5,7-pentol]
Systematic IUPAC name
(12R,13R,14R,22R,23R,24S,32R,33S)-12,22,32-Tris(3,4-dihydroxyphenyl)-13,14,23,24,33,34-hexahydro-12H,22H,32H-[14,28:24,36-ter-1-benzopyran]-13,15,17,23,25,27,33,35,37-nonol
Other names
Epicatechin-(4β→8)-epicatechin-(4β→6)-catechin
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
KEGG
UNII
  • InChI=1S/C45H38O18/c46-18-10-26(53)33-32(11-18)62-43(16-2-5-21(48)24(51)8-16)40(59)37(33)35-27(54)13-28(55)36-38(41(60)44(63-45(35)36)17-3-6-22(49)25(52)9-17)34-29(56)14-31-19(39(34)58)12-30(57)42(61-31)15-1-4-20(47)23(50)7-15/h1-11,13-14,30,37-38,40-44,46-60H,12H2/t30-,37+,38-,40+,41+,42+,43+,44+/m0/s1 checkY
    Key: PBYRKMXDROOXMU-XKDUFCMJSA-N checkY
  • InChI=1/C45H38O18/c46-18-10-26(53)33-32(11-18)62-43(16-2-5-21(48)24(51)8-16)40(59)37(33)35-27(54)13-28(55)36-38(41(60)44(63-45(35)36)17-3-6-22(49)25(52)9-17)34-29(56)14-31-19(39(34)58)12-30(57)42(61-31)15-1-4-20(47)23(50)7-15/h1-11,13-14,30,37-38,40-44,46-60H,12H2/t30-,37+,38-,40+,41+,42+,43+,44+/m0/s1
    Key: PBYRKMXDROOXMU-XKDUFCMJBX
  • Oc1ccc(cc1O)[C@H]9Oc2cc(O)cc(O)c2[C@H](c8c(O)cc(O)c3c8O[C@@H]([C@H](O)[C@H]3c6c(O)cc5O[C@H](c4ccc(O)c(O)c4)[C@@H](O)Cc5c6O)c7ccc(O)c(O)c7)[C@H]9O
Properties
C45H38O18
Molar mass 866.77 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Infobox references

Arecatannin B1 is a B type proanthocyanidin found in the betel nut.[1] It is an arecatannin trimer with a 4β→6 bond.

References

  1. ↑ Screening of various plant extracts used in Ayurvedic medicine for inhibitory effects on human immunodeficiency virus type 1 (HIV-1) protease. Kusumoto I.T., Nakabayashi T., Kida H., Miyashiro H., Hattori M., Namba T. and Shimotohno K., PTR. Phytotherapy research, 1995, vol. 9, no3, pp. 180-184, INIST 3499215
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.