Lambertianin D
Names | |
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Systematic IUPAC name (10aR,11S,12aR,25aR,25bS)-2,3,4,5,6,7,17,18,19,20,21,22-Dodecahydroxy-9,15,24,27-tetraoxo-9,10a,11,12a,13,15,24,25a,25b,27-decahydrodibenzo[g,i]dibenzo[6′,7′:8′,9′][1,4]dioxecino[2′,3′:4,5]pyrano[3,2-b][1,5]dioxacycloundecin-11-yl (310aR,311S,312aR,325aR,325bS,810aR,811S,812aR,825aR,825bS,1310aR,1311R,1312aR,1325aR,1325bS)-15,16,32,33,34,35,36,37,317,318,319,320,321,322,64,65,82,83,84,85,86,87,817,818,819,820,821,822,114,115,132,133,134,135,136,137,1317,1318,1319,1320,1321,1322,163,164,165-pentatetracontahydroxy-39,315,324,327,5,89,815,824,827,10,139,1315,1324,1327,15-pentadecaoxo-39,310a,311,312a,313,315,324,325a,325b,327,89,810a,811,812a,813,815,824,825a,825b,827,139,1310a,1311,1312a,1313,1315,1324,1325a,1325b,1327-triacontahydro-2,4,7,9,12,14-hexaoxa-3,8,13(22,11)-tris(dibenzo[g,i]dibenzo[6′,7′:8′,9′][1,4]dioxecino[2′,3′:4,5]pyrano[3,2-b][1,5]dioxacycloundecina)-1,16(1),6,11(1,3)-tetrabenzenahexadecaphane-13-carboxylate | |
Other names Rubusuaviin E | |
Identifiers | |
CAS Number |
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Properties | |
Chemical formula | C164H106O104 |
Molar mass | 3740.415 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
Lambertianin D is an ellagitannin found in Rubus lambertianus.[2]
It is tetramer of casuarictin linked by sanguisorbic acid ester groups between glucopyranose moieties.[2]
References
- ^ Yannai, Shmuel (2012). Dictionary of Food Compounds with CD-ROM. CRC Press. p. 1160. ISBN 9781420083521.
- ^ a b Tanaka T, Tachibana H, Nonaka G, et al. (July 1993). "Tannins and related compounds. CXXII. New dimeric, trimeric and tetrameric ellagitannins, lambertianins A-D, from Rubus lambertianus Seringe". Chemical & Pharmaceutical Bulletin. 41 (7): 1214–20. doi:10.1248/cpb.41.1214. PMID 8374992.
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Types of ellagitannins
- Diphenolic acid : Hexahydroxydiphenic acid (HHDP)
- Triphenolic acids : Nonahydroxytriphenic acid
- Sanguisorbic acid
- Valoneic acid
- Tetraphenolic acids : Isoterchebulic acid
- Terchebulinic acid
- Ellagic acid
- Gallagic acid
- Gallagic acid dilactone
- Luteic acid
- Sanguisorbic acid dilactone
- Valoneic acid dilactone
- Acetonyl geraniin
- Alnusiin
- Bicornin
- Carlesiin
- Casuarictin
- Emblicanin A and B
- Euscaphinin
- Galloyl pedunculagin
- Grandinin
- Helioscopinin B
- Jolkinin
- Lagerstannin A, B and C
- Macranganin
- Myrobalanitannin
- Nupharin A, B, C, D, E and F
- Pedunculagin
- Punicalagin
- Punigluconin
- Phyllanemblinin A, B, C, D, E and F
- Punicalin
- Roburin E
- Rugosin E
- Sanguiin H-5
- Stenophyllanin A, B and C
- Strictinin
- Tellimagrandin I and II
- Teracatain
- Terchebulin
- Terflavin A and B
- Tergallic acid
- Tergallic acid dilactone
C-glycosidic ellagitannins |
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Dehydroellagitannins (molecules with dehydrohexahydroxydiphenic acid (DHHDP) |
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Transformed ellagitannins |
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- Dimers
- Agrimoniin
- Cornusiin E (dimer of tellimagrandin II)
- Lambertianin A and B
- Nobotanin B
- Roburin A, B, C and D
- Sanguiin H-6
- Trimers
- Lambertianin C
- Raspberry ellagitannin
- Tetramers
- Lambertianin D
- Nobotanin S
- Pentamer
- Melastoflorin A
- Flavono-ellagitannins (hybrid type)
- Urolithins (metabolites)
- Pomegranate ellagitannins
This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |
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