NCBI Taxonomy: 38386

Hymenophyllum (ncbi_taxid: 38386)

found 201 associated metabolites at genus taxonomy rank level.

Ancestor: Hymenophylloideae

Child Taxonomies: [Mecodium] wangii, Hymenophyllum fucoides, Hymenophyllum reniforme, Hymenophyllum rufum, Hymenophyllum rarum, Hymenophyllum fuscum, Hymenophyllum kuhnii, Hymenophyllum moorei, Hymenophyllum parvum, Hymenophyllum poolii, Hymenophyllum ooides, Hymenophyllum heimii, Hymenophyllum tunbrigense, Hymenophyllum exiguum, Hymenophyllum crispum, Hymenophyllum fragile, Hymenophyllum rugosum, Hymenophyllum bivalve, Hymenophyllum minimum, Hymenophyllum pumilum, Hymenophyllum flexile, Hymenophyllum obtusum, Hymenophyllum scabrum, Hymenophyllum howense, Hymenophyllum blandum, Hymenophyllum devolii, Hymenophyllum hayatae, Hymenophyllum lineare, Hymenophyllum pumilio, Hymenophyllum lyallii, Hymenophyllum leratii, Hymenophyllum sieberi, Hymenophyllum elegans, Hymenophyllum plumosum, Hymenophyllum barbatum, Hymenophyllum venustum, Hymenophyllum vestitum, Hymenophyllum wrightii, Hymenophyllum hirsutum, Hymenophyllum secundum, Hymenophyllum wilsonii, Hymenophyllum dentatum, Hymenophyllum exsertum, Hymenophyllum malingii, Hymenophyllum peltatum, Hymenophyllum perrieri, Hymenophyllum plicatum, Hymenophyllum mnioides, Hymenophyllum bryoides, Hymenophyllum coreanum, Hymenophyllum paniense, Hymenophyllum recurvum, Hymenophyllum australe, Hymenophyllum caudatum, Hymenophyllum villosum, Hymenophyllum cuneatum, Hymenophyllum pallidum, Hymenophyllum demissum, Hymenophyllum cruentum, Hymenophyllum tenellum, Hymenophyllum digitatum, Hymenophyllum angulosum, [Mecodium] szechuanense, Hymenophyllum cocosense, Hymenophyllum feejeense, Hymenophyllum taeniatum, Hymenophyllum revolutum, Hymenophyllum tortuosum, Hymenophyllum balfourii, Hymenophyllum capillare, Hymenophyllum rufescens, Hymenophyllum flexuosum, Hymenophyllum undulatum, Hymenophyllum decurrens, Hymenophyllum humbertii, Hymenophyllum latifrons, Hymenophyllum nitidulum, Hymenophyllum fuciforme, Hymenophyllum javanicum, Hymenophyllum mikawanum, Hymenophyllum asperulum, Hymenophyllum dilatatum, Hymenophyllum inaequale, Hymenophyllum pulchellum, Hymenophyllum deplanchei, Hymenophyllum dimidiatum, Hymenophyllum oligosorum, Hymenophyllum apiculatum, Hymenophyllum polyanthos, Hymenophyllum caespitosa, Hymenophyllum multifidum, Hymenophyllum atrovirens, Hymenophyllum imbricatum, Hymenophyllum serrulatum, Hymenophyllum riukiuense, Hymenophyllum pluviatile, Hymenophyllum subobtusum, Hymenophyllum ivohibense, Hymenophyllum splendidum, Hymenophyllum marginatum, Hymenophyllum corrugatum, Hymenophyllum holochilum, Hymenophyllum cordobense, Hymenophyllum ectocarpon, Hymenophyllum saenzianum, Hymenophyllum pectinatum, Hymenophyllum simonsianum, Hymenophyllum longissimum, Hymenophyllum punctisorum, Hymenophyllum fujisanense, Hymenophyllum delicatulum, Hymenophyllum acanthoides, Hymenophyllum ferrugineum, Hymenophyllum lanceolatum, Hymenophyllum triangulare, Hymenophyllum myriocarpum, Hymenophyllum flabellatum, Hymenophyllum microcarpum, Hymenophyllum soriemersum, Hymenophyllum frankliniae, Hymenophyllum armstrongii, Hymenophyllum semiglabrum, unclassified Hymenophyllum, Hymenophyllum trapezoidale, Hymenophyllum pilosissimum, Hymenophyllum falklandicum, Hymenophyllum denticulatum, Hymenophyllum praetervisum, Hymenophyllum asplenioides, Hymenophyllum gracilescens, Hymenophyllum palmatifidum, Hymenophyllum magellanicum, Hymenophyllum braithwaitei, Hymenophyllum caudiculatum, Hymenophyllum pulcherrimum, Hymenophyllum pachydermicum, Hymenophyllum trichophyllum, Hymenophyllum subdimidiatum, Hymenophyllum nephrophyllum, Hymenophyllum cupressiforme, Hymenophyllum macgillivrayi, Hymenophyllum novoguineense, Hymenophyllum tomaniiviense, Hymenophyllum consanguineum, Hymenophyllum hygrometricum, Hymenophyllum dicranotrichum, Hymenophyllum trichomanoides, Hymenophyllum paniculiflorum, Hymenophyllum neocaledonicum, Hymenophyllum sanguinolentum, Hymenophyllum sibthorpioides, Hymenophyllum parallelocarpum, Hymenophyllum chamaecyparicola, Hymenophyllum crassipetiolatum, Hymenophyllum rolandi-principis, Hymenophyllum cf. acutum Johns 9731, Hymenophyllum aff. dependens KYD-2022

Isovitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

C21H20O10 (432.105642)


Isovitexin is a C-glycosyl compound that consists of apigenin substituted by a 1,5-anhydro-D-glucitol moiety at position 6. It has a role as an EC 3.2.1.20 (alpha-glucosidase) inhibitor and a metabolite. It is a C-glycosyl compound and a trihydroxyflavone. It is functionally related to an apigenin. It is a conjugate acid of an isovitexin-7-olate. Isovitexin is a natural product found in Carex fraseriana, Rauhiella, and other organisms with data available. See also: Fenugreek seed (part of); Acai (part of); Crataegus monogyna flowering top (part of). [Raw Data] CBA25_Isovitexin_neg_20eV_1-7_01_1425.txt [Raw Data] CBA25_Isovitexin_neg_10eV_1-7_01_1369.txt [Raw Data] CBA25_Isovitexin_pos_30eV_1-7_01_1399.txt [Raw Data] CBA25_Isovitexin_neg_40eV_1-7_01_1427.txt [Raw Data] CBA25_Isovitexin_neg_30eV_1-7_01_1426.txt [Raw Data] CBA25_Isovitexin_neg_50eV_1-7_01_1428.txt [Raw Data] CBA25_Isovitexin_pos_20eV_1-7_01_1398.txt [Raw Data] CBA25_Isovitexin_pos_10eV_1-7_01_1358.txt [Raw Data] CBA25_Isovitexin_pos_40eV_1-7_01_1400.txt [Raw Data] CBA25_Isovitexin_pos_50eV_1-7_01_1401.txt Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB.

   

Isoorientin 7-O-(6'-O-(E)-feruloyl)glucoside

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C21H20O11 (448.100557)


Isoorientin 7-o-(6-o-(e)-feruloyl)glucoside, also known as homoorientin or luteolin-6-C-beta-D-glucoside, is a member of the class of compounds known as flavonoid c-glycosides. Flavonoid c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. Isoorientin 7-o-(6-o-(e)-feruloyl)glucoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Isoorientin 7-o-(6-o-(e)-feruloyl)glucoside can be synthesized from luteolin. Isoorientin 7-o-(6-o-(e)-feruloyl)glucoside is also a parent compound for other transformation products, including but not limited to, isoorientin 7-O-glucoside, 7-O-[alpha-L-rhamnosyl-(1->2)-beta-D-glucosyl]isoorientin, and 7-O-(6-sinapoylglucosyl)isoorientin. Isoorientin 7-o-(6-o-(e)-feruloyl)glucoside can be found in barley, which makes isoorientin 7-o-(6-o-(e)-feruloyl)glucoside a potential biomarker for the consumption of this food product. Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CBA21_Isoorientin_neg_20eV_1-3_01_1409.txt [Raw Data] CBA21_Isoorientin_pos_20eV_1-3_01_1382.txt [Raw Data] CBA21_Isoorientin_pos_50eV_1-3_01_1385.txt [Raw Data] CBA21_Isoorientin_neg_40eV_1-3_01_1411.txt [Raw Data] CBA21_Isoorientin_neg_10eV_1-3_01_1365.txt [Raw Data] CBA21_Isoorientin_neg_50eV_1-3_01_1412.txt [Raw Data] CBA21_Isoorientin_pos_10eV_1-3_01_1354.txt [Raw Data] CBA21_Isoorientin_pos_40eV_1-3_01_1384.txt [Raw Data] CBA21_Isoorientin_pos_30eV_1-3_01_1383.txt [Raw Data] CBA21_Isoorientin_neg_30eV_1-3_01_1410.txt Isoorientin is a potent inhibitor of COX-2 with an IC50 value of 39 μM. Isoorientin is a potent inhibitor of COX-2 with an IC50 value of 39 μM.

   

Vitexin 6'-O-malonyl 2'-O-xyloside

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C21H20O10 (432.105642)


Vitexin 6-o-malonyl 2-o-xyloside, also known as apigenin 8-C-glucoside or 8-glycosyl-apigenin, is a member of the class of compounds known as flavonoid 8-c-glycosides. Flavonoid 8-c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Vitexin 6-o-malonyl 2-o-xyloside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Vitexin 6-o-malonyl 2-o-xyloside can be synthesized from apigenin. Vitexin 6-o-malonyl 2-o-xyloside is also a parent compound for other transformation products, including but not limited to, vitexin 2-O-beta-L-rhamnoside, 7-O-methylvitexin 2-O-beta-L-rhamnoside, and vitexin 2-O-beta-D-glucoside. Vitexin 6-o-malonyl 2-o-xyloside can be found in common beet, which makes vitexin 6-o-malonyl 2-o-xyloside a potential biomarker for the consumption of this food product. Vitexin, also known as apigenin 8-C-glucoside or 8-glycosylapigenin, belongs to the class of organic compounds known as flavonoid 8-C-glycosides. Flavonoid 8-C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Vitexin is also described as an apigenin flavone glucoside. Vitexin has been found in passion flower, chasteberry, bamboo leaves, millet and Hawthorn. Vitexin has shown a wide range of pharmacological effects, such as antioxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects (PMID: 27693342). Vitexin has also been shown to directly inhibit thyroid peroxidase and potentially contributes to goiter (PMID: 1696490). It is sometimes called a goitrogen. Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CBA68_Vitexin_neg_10eV.txt [Raw Data] CBA68_Vitexin_neg_30eV.txt [Raw Data] CBA68_Vitexin_pos_20eV.txt [Raw Data] CBA68_Vitexin_neg_50eV.txt [Raw Data] CBA68_Vitexin_neg_40eV.txt [Raw Data] CBA68_Vitexin_pos_40eV.txt [Raw Data] CBA68_Vitexin_pos_30eV.txt [Raw Data] CBA68_Vitexin_pos_10eV.txt [Raw Data] CBA68_Vitexin_neg_20eV.txt Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].

   

Orientin

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

C21H20O11 (448.100557)


Orientin is a C-glycosyl compound that is luteolin substituted by a beta-D-glucopyranosyl moiety at position 8. It has a role as an antioxidant and a metabolite. It is a C-glycosyl compound, a tetrahydroxyflavone and a 3-hydroxyflavonoid. It is functionally related to a luteolin. Orientin is a natural product found in Itea chinensis, Vellozia epidendroides, and other organisms with data available. See also: Cannabis sativa subsp. indica top (part of); Fenugreek seed (part of); Acai fruit pulp (part of). Orientin is found in barley. Orientin is isolated from Hordeum vulgare (barley) and Passiflora incarnata (maypops).Orientin is a flavone, a chemical flavonoid-like compound found in the passion flower, the palm and Anadenanthera peregrina. Orientin is also reported in millets and in the Phyllostachys nigra bamboo leaves Isolated from Hordeum vulgare (barley) and Passiflora incarnata (maypops) [Raw Data] CBA20_Orientin_pos_40eV_1-2_01_1380.txt [Raw Data] CBA20_Orientin_neg_20eV_1-2_01_1405.txt [Raw Data] CBA20_Orientin_neg_50eV_1-2_01_1408.txt [Raw Data] CBA20_Orientin_neg_40eV_1-2_01_1407.txt [Raw Data] CBA20_Orientin_pos_50eV_1-2_01_1381.txt [Raw Data] CBA20_Orientin_neg_30eV_1-2_01_1406.txt [Raw Data] CBA20_Orientin_pos_20eV_1-2_01_1378.txt [Raw Data] CBA20_Orientin_pos_30eV_1-2_01_1379.txt [Raw Data] CBA20_Orientin_pos_10eV_1-2_01_1353.txt [Raw Data] CBA20_Orientin_neg_10eV_1-2_01_1364.txt Orientin is a naturally occurring bioactive flavonoid that possesses diverse biological properties, including anti-inflammation, anti-oxidative, anti-tumor, and cardio protection. Orientin is a promising neuroprotective agent suitable for therapy for neuropathic pain[1][2]. Orientin is a naturally occurring bioactive flavonoid that possesses diverse biological properties, including anti-inflammation, anti-oxidative, anti-tumor, and cardio protection. Orientin is a promising neuroprotective agent suitable for therapy for neuropathic pain[1][2].

   

Mangiferol

1,3,6,7-tetrahydroxy-2-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-9H-xanthen-9-one

C19H18O11 (422.0849078)


Mangiferol, also known as alpizarin or chinomin, is a member of the class of compounds known as xanthones. Xanthones are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. Mangiferol is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Mangiferol can be found in mango, which makes mangiferol a potential biomarker for the consumption of this food product. Mangiferin is a Nrf2 activator. Mangiferin suppresses nuclear translocation of the NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, antidiabetic, antihyperuricemic, antiviral, anticancer and antiinflammatory activities[1][2][3]. Mangiferin is a Nrf2 activator. Mangiferin suppresses nuclear translocation of the NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, antidiabetic, antihyperuricemic, antiviral, anticancer and antiinflammatory activities[1][2][3].

   

Isoorientin

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

C21H20O11 (448.100557)


Isoorientin is a flavone C-glycoside consisting of luteolin having a beta-D-glucosyl residue at the 6-position. It has a role as a radical scavenger and an antineoplastic agent. It is a tetrahydroxyflavone and a flavone C-glycoside. It is functionally related to a luteolin. It is a conjugate acid of an isoorientin(1-). Isoorientin is a natural product found in Carex fraseriana, Itea chinensis, and other organisms with data available. See also: Acai fruit pulp (part of). A C-glycosyl compound consisting of luteolin having a beta-D-glucosyl residue at the 6-position. Isoorientin is a potent inhibitor of COX-2 with an IC50 value of 39 μM. Isoorientin is a potent inhibitor of COX-2 with an IC50 value of 39 μM.

   

Vitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

C21H20O10 (432.105642)


Vitexin is an apigenin flavone glycoside, which is found in the passion flower, bamboo leaves and pearl millet It has a role as a platelet aggregation inhibitor, an EC 3.2.1.20 (alpha-glucosidase) inhibitor, an antineoplastic agent and a plant metabolite. It is a C-glycosyl compound and a trihydroxyflavone. It is functionally related to an apigenin. It is a conjugate acid of a vitexin-7-olate. Vitexin is a natural product found in Itea chinensis, Salacia chinensis, and other organisms with data available. See also: Cannabis sativa subsp. indica top (part of); Cytisus scoparius flowering top (part of); Fenugreek seed (part of) ... View More ... An apigenin flavone glycoside, which is found in the passion flower, bamboo leaves and pearl millet Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].

   

Vitexin

8-beta-D-Glucopyranosyl-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

C21H20O10 (432.105642)


Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].

   

Isoorientin

Luteolin 6-C-glucoside

C21H20O11 (448.100557)


Isoorientin is a potent inhibitor of COX-2 with an IC50 value of 39 μM. Isoorientin is a potent inhibitor of COX-2 with an IC50 value of 39 μM.

   

Mangiferin

1,3,6,7-tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-9H-xanthen-9-one

C19H18O11 (422.0849078)


Mangiferin is found in fruits. Mangiferin is a constituent of Mangifera indica (mango) Constituent of Mangifera indica (mango). Mangiferin is found in mango and fruits. Mangiferin is a Nrf2 activator. Mangiferin suppresses nuclear translocation of the NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, antidiabetic, antihyperuricemic, antiviral, anticancer and antiinflammatory activities[1][2][3]. Mangiferin is a Nrf2 activator. Mangiferin suppresses nuclear translocation of the NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, antidiabetic, antihyperuricemic, antiviral, anticancer and antiinflammatory activities[1][2][3].

   

Isoorientin

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C21H20O11 (448.100557)


   

Isovitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C21H20O10 (432.105642)


   

Vitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4H-chromen-4-one

C21H20O10 (432.105642)


Vitexin is a member of the class of compounds known as flavonoid 8-c-glycosides. Flavonoid 8-c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to 8-position of a 2-phenylchromen-4-one flavonoid backbone. Vitexin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Vitexin can be found in a number of food items such as flaxseed, prairie turnip, mung bean, and tree fern, which makes vitexin a potential biomarker for the consumption of these food products. Vitexin is an apigenin flavone glucoside, a chemical compound found in the passion flower, Vitex agnus-castus (chaste tree or chasteberry), in the Phyllostachys nigra bamboo leaves, in the pearl millet (Pennisetum millet), and in Hawthorn . Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].

   

Mangiferin

1,3,6,7-Tetrahydroxy-2-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-9H-xanthen-9-one

C19H18O11 (422.0849078)


Mangiferin is a C-glycosyl compound consisting of 1,3,6,7-tetrahydroxyxanthen-9-one having a beta-D-glucosyl residue at the 6-position. It has a role as a hypoglycemic agent, an antioxidant, an anti-inflammatory agent and a plant metabolite. It is a C-glycosyl compound and a member of xanthones. It is functionally related to a xanthone. It is a conjugate acid of a mangiferin(1-). Mangiferin is a natural product found in Salacia chinensis, Smilax bracteata, and other organisms with data available. See also: Mangifera indica bark (part of). A C-glycosyl compound consisting of 1,3,6,7-tetrahydroxyxanthen-9-one having a beta-D-glucosyl residue at the 6-position. Origin: Plant Mangiferin is a Nrf2 activator. Mangiferin suppresses nuclear translocation of the NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, antidiabetic, antihyperuricemic, antiviral, anticancer and antiinflammatory activities[1][2][3]. Mangiferin is a Nrf2 activator. Mangiferin suppresses nuclear translocation of the NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, antidiabetic, antihyperuricemic, antiviral, anticancer and antiinflammatory activities[1][2][3].

   

Vitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]chromen-4-one

C21H20O10 (432.105642)


Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2]. Vitexin is a c-glycosylated flavone, and is found in various medicinal plants species such as Trigonella foenum-graecum Linn. Vitexin has a wide range of pharmacological effects, including anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects[1][2].

   

Isoorientin

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]-4-chromenone

C21H20O11 (448.100557)


Isolated from wheat leaves (Triticum species). Isoorientin 6-diglucoside is found in wheat and cereals and cereal products. Isoorientin is a member of the class of compounds known as flavonoid c-glycosides. Flavonoid c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. Isoorientin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Isoorientin can be found in a number of food items such as oat, prairie turnip, common buckwheat, and common salsify, which makes isoorientin a potential biomarker for the consumption of these food products. Isoorientin (or homoorientin) is a flavone, a chemical flavonoid-like compound. It is the luteolin-6-C-glucoside. Bioassay-directed fractionation techniques led to isolation of isoorientin as the main hypoglycaemic component in Gentiana olivieri . Isoorientin is a potent inhibitor of COX-2 with an IC50 value of 39 μM. Isoorientin is a potent inhibitor of COX-2 with an IC50 value of 39 μM.

   
   

Orientin

2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

C21H20O11 (448.100557)


Orientin is a C-glycosyl compound that is luteolin substituted by a beta-D-glucopyranosyl moiety at position 8. It has a role as an antioxidant and a metabolite. It is a C-glycosyl compound, a tetrahydroxyflavone and a 3-hydroxyflavonoid. It is functionally related to a luteolin. Orientin is a natural product found in Itea chinensis, Vellozia epidendroides, and other organisms with data available. See also: Cannabis sativa subsp. indica top (part of); Fenugreek seed (part of); Acai fruit pulp (part of). A C-glycosyl compound that is luteolin substituted by a beta-D-glucopyranosyl moiety at position 8. Orientin is a naturally occurring bioactive flavonoid that possesses diverse biological properties, including anti-inflammation, anti-oxidative, anti-tumor, and cardio protection. Orientin is a promising neuroprotective agent suitable for therapy for neuropathic pain[1][2]. Orientin is a naturally occurring bioactive flavonoid that possesses diverse biological properties, including anti-inflammation, anti-oxidative, anti-tumor, and cardio protection. Orientin is a promising neuroprotective agent suitable for therapy for neuropathic pain[1][2].

   

Isovitexin

5,7-dihydroxy-2-(4-hydroxyphenyl)-6-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)-4H-chromen-4-one

C21H20O10 (432.105642)


Isovitexin is a C-glycosyl compound that consists of apigenin substituted by a 1,5-anhydro-D-glucitol moiety at position 6. It has a role as an EC 3.2.1.20 (alpha-glucosidase) inhibitor and a metabolite. It is a C-glycosyl compound and a trihydroxyflavone. It is functionally related to an apigenin. It is a conjugate acid of an isovitexin-7-olate. Isovitexin is a natural product found in Carex fraseriana, Rauhiella, and other organisms with data available. See also: Fenugreek seed (part of); Acai (part of); Crataegus monogyna flowering top (part of). A C-glycosyl compound that consists of apigenin substituted by a 1,5-anhydro-D-glucitol moiety at position 6. Isovitexin is a member of the class of compounds known as flavonoid c-glycosides. Flavonoid c-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. Isovitexin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Isovitexin can be found in a number of food items such as common salsify, winged bean, flaxseed, and common buckwheat, which makes isovitexin a potential biomarker for the consumption of these food products. Isovitexin (or homovitexin, saponaretin) is a flavone. the apigenin-6-C-glucoside. It can be found in the passion flower, Cannabis, and the açaí palm . Constituent of Cucumis sativus (cucumber). Isovitexin 2-(6-p-coumaroylglucoside) 4-glucoside is found in cucumber and fruits. Constituent of young green barley leaves (Hordeum vulgare variety nudum). Isovitexin 7-(6-sinapoylglucoside) is found in barley and cereals and cereal products. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB. Isovitexin is a flavonoid isolated from passion flower, Cannabis and, and the palm, possesses anti-inflammatory and anti-oxidant activities; Isovitexin acts like a JNK1/2 inhibitor and inhibits the activation of NF-κB.

   

Chinoinin

1,3,6,7-tetrahydroxy-2-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-tetrahydropyranyl]-9-xanthenone

C19H18O11 (422.0849078)


Mangiferin is a Nrf2 activator. Mangiferin suppresses nuclear translocation of the NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, antidiabetic, antihyperuricemic, antiviral, anticancer and antiinflammatory activities[1][2][3]. Mangiferin is a Nrf2 activator. Mangiferin suppresses nuclear translocation of the NF-κB subunits p65 and p50. Mangiferin exhibits antioxidant, antidiabetic, antihyperuricemic, antiviral, anticancer and antiinflammatory activities[1][2][3].

   

(2r,3r,4s,5r,6r)-2-[(3s)-3,4-dihydroxy-2-methylidenebutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

(2r,3r,4s,5r,6r)-2-[(3s)-3,4-dihydroxy-2-methylidenebutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

C11H20O8 (280.115812)


   

(2r,3s,4s,5r,6r)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(2r,3s,4s,5r,6r)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C23H26O11 (478.14750460000005)


   

(2r,3r,4s,5r,6r)-3-hydroxy-2-(hydroxymethyl)-5-{[2-(4-hydroxyphenyl)acetyl]oxy}-6-{[(2r,4r)-2-methyl-6-oxooxan-4-yl]oxy}oxan-4-yl 2-(4-hydroxyphenyl)acetate

(2r,3r,4s,5r,6r)-3-hydroxy-2-(hydroxymethyl)-5-{[2-(4-hydroxyphenyl)acetyl]oxy}-6-{[(2r,4r)-2-methyl-6-oxooxan-4-yl]oxy}oxan-4-yl 2-(4-hydroxyphenyl)acetate

C28H32O12 (560.1893672)


   

[3,4,5-trihydroxy-6-(1,3,6,7-tetrahydroxy-9-oxoxanthen-2-yl)oxan-2-yl]methyl acetate

[3,4,5-trihydroxy-6-(1,3,6,7-tetrahydroxy-9-oxoxanthen-2-yl)oxan-2-yl]methyl acetate

C21H20O12 (464.09547200000003)


   

(2r,3r,4s,5s,6r)-4,5-dihydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-3-yl 2-(3,4-dihydroxyphenyl)acetate

(2r,3r,4s,5s,6r)-4,5-dihydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-3-yl 2-(3,4-dihydroxyphenyl)acetate

C19H26O10 (414.1525896)


   

(2r,3r,4s,5r,6r)-3-hydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-2-(hydroxymethyl)-5-{[2-(4-hydroxyphenyl)acetyl]oxy}oxan-4-yl 2-(4-hydroxyphenyl)acetate

(2r,3r,4s,5r,6r)-3-hydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-2-(hydroxymethyl)-5-{[2-(4-hydroxyphenyl)acetyl]oxy}oxan-4-yl 2-(4-hydroxyphenyl)acetate

C27H32O11 (532.1944522)


   

[(2s,3s,4r,5r,6s)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

[(2s,3s,4r,5r,6s)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

C19H26O11 (430.1475046)


   

(2r,3r,4s,5s,6r)-2-(3,4-dihydroxy-2-methylidenebutoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

(2r,3r,4s,5s,6r)-2-(3,4-dihydroxy-2-methylidenebutoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

C11H20O8 (280.115812)


   

(2s,3r,4s,5r,6r)-2-{[(2s,3r,4r,5r,6r)-6-{[(1s,3r,4s,4ar,8ar)-3,4,8,8a-tetramethyl-4-[(3s)-3-methyl-3-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}pent-4-en-1-yl]-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy}-4-hydroxy-2-methyl-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

(2s,3r,4s,5r,6r)-2-{[(2s,3r,4r,5r,6r)-6-{[(1s,3r,4s,4ar,8ar)-3,4,8,8a-tetramethyl-4-[(3s)-3-methyl-3-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}pent-4-en-1-yl]-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy}-4-hydroxy-2-methyl-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

C44H74O18 (890.4874904000001)


   

[(2r,3r,4s,5r,6r)-3,4-bis({[2-(3,4-dihydroxyphenyl)acetyl]oxy})-5-hydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

[(2r,3r,4s,5r,6r)-3,4-bis({[2-(3,4-dihydroxyphenyl)acetyl]oxy})-5-hydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

C35H38O17 (730.2108898)


   

(2r,3s,4s,5r,6r)-4,5-dihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(2r,3s,4s,5r,6r)-4,5-dihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C20H26O11 (442.14750460000005)


   

[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

C19H26O10 (414.1525896)


   

(2r,3r,4s,5r,6r)-3-hydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-2-(hydroxymethyl)-5-{[2-(4-hydroxyphenyl)acetyl]oxy}oxan-4-yl 2-(3,4-dihydroxyphenyl)acetate

(2r,3r,4s,5r,6r)-3-hydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-2-(hydroxymethyl)-5-{[2-(4-hydroxyphenyl)acetyl]oxy}oxan-4-yl 2-(3,4-dihydroxyphenyl)acetate

C27H32O12 (548.1893672)


   

[(2r,3r,4s,5r,6r)-5-{[2-(3,4-dihydroxyphenyl)acetyl]oxy}-3-hydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-4-{[2-(4-hydroxyphenyl)acetyl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

[(2r,3r,4s,5r,6r)-5-{[2-(3,4-dihydroxyphenyl)acetyl]oxy}-3-hydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-4-{[2-(4-hydroxyphenyl)acetyl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

C35H38O15 (698.2210598)


   

(2r,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[(2r,4r)-2-methyl-6-oxooxan-4-yl]oxy}oxan-3-yl 2-(3,4-dihydroxyphenyl)acetate

(2r,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[(2r,4r)-2-methyl-6-oxooxan-4-yl]oxy}oxan-3-yl 2-(3,4-dihydroxyphenyl)acetate

C20H26O11 (442.14750460000005)


   

(2s,3r,4s,5r,6r)-2-{[(2s,3r,4r,5r,6r)-6-{[(1s,3r,4s,4ar,8ar)-3,4,8,8a-tetramethyl-4-[(3s)-3-methyl-3-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}pent-4-en-1-yl]-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy}-4-hydroxy-2-methyl-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

(2s,3r,4s,5r,6r)-2-{[(2s,3r,4r,5r,6r)-6-{[(1s,3r,4s,4ar,8ar)-3,4,8,8a-tetramethyl-4-[(3s)-3-methyl-3-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}pent-4-en-1-yl]-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy}-4-hydroxy-2-methyl-5-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

C43H72O18 (876.4718412)


   

3-{4-[2-(2,3-dihydroxyphenyl)ethyl]phenoxy}-5-[2-(3-hydroxyphenyl)ethyl]benzene-1,2-diol

3-{4-[2-(2,3-dihydroxyphenyl)ethyl]phenoxy}-5-[2-(3-hydroxyphenyl)ethyl]benzene-1,2-diol

C28H26O6 (458.17292960000003)


   

(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(2r,3s,4r,5r,6r)-4,5-dihydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C20H26O10 (426.15258960000006)


   

[(2r,3s,4s,5r,6r)-5-{[2-(3,4-dihydroxyphenyl)acetyl]oxy}-3,4-dihydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

[(2r,3s,4s,5r,6r)-5-{[2-(3,4-dihydroxyphenyl)acetyl]oxy}-3,4-dihydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

C27H32O13 (564.1842822)


   

(2r,3r,4r,5r,6r)-2-[(3s)-3,4-dihydroxy-2-methylidenebutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

(2r,3r,4r,5r,6r)-2-[(3s)-3,4-dihydroxy-2-methylidenebutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol

C11H20O8 (280.115812)


   

(2s,3r,4s,5r,6r)-2-{[(2s,3r,4r,5r,6r)-6-{[(1s,3r,4s,4ar,8ar)-3,4,8,8a-tetramethyl-4-[(3s)-3-methyl-3-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}pent-4-en-1-yl]-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy}-4-hydroxy-2-methyl-5-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

(2s,3r,4s,5r,6r)-2-{[(2s,3r,4r,5r,6r)-6-{[(1s,3r,4s,4ar,8ar)-3,4,8,8a-tetramethyl-4-[(3s)-3-methyl-3-{[(2s,3r,4s,5s)-3,4,5-trihydroxyoxan-2-yl]oxy}pent-4-en-1-yl]-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy}-4-hydroxy-2-methyl-5-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

C43H72O18 (876.4718412)


   

(2r,3r,4s,5r,6r)-3-{[2-(3,4-dihydroxyphenyl)acetyl]oxy}-5-hydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-4-yl 2-phenylacetate

(2r,3r,4s,5r,6r)-3-{[2-(3,4-dihydroxyphenyl)acetyl]oxy}-5-hydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-4-yl 2-phenylacetate

C27H32O11 (532.1944522)


   

[(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

[(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C20H26O11 (442.14750460000005)


   

[(2r,3r,4r,5r,6r)-4,5-bis({[2-(3,4-dihydroxyphenyl)acetyl]oxy})-3-hydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

[(2r,3r,4r,5r,6r)-4,5-bis({[2-(3,4-dihydroxyphenyl)acetyl]oxy})-3-hydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

C35H38O17 (730.2108898)


   

(2s,3r,4s,5r,6r)-2-{[(2s,3r,4r,5r,6r)-6-{[(1s,3r,4s,4ar,8ar)-3,4,8,8a-tetramethyl-4-[(3s)-3-methyl-3-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}pent-4-en-1-yl]-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy}-4-hydroxy-2-methyl-5-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

(2s,3r,4s,5r,6r)-2-{[(2s,3r,4r,5r,6r)-6-{[(1s,3r,4s,4ar,8ar)-3,4,8,8a-tetramethyl-4-[(3s)-3-methyl-3-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}pent-4-en-1-yl]-1,2,3,4a,5,6-hexahydronaphthalen-1-yl]oxy}-4-hydroxy-2-methyl-5-{[(2s,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl]oxy}-6-methyloxane-3,4,5-triol

C44H74O18 (890.4874904000001)


   

[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(1,3,6,7-tetrahydroxy-9-oxoxanthen-2-yl)oxan-2-yl]methyl acetate

[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-(1,3,6,7-tetrahydroxy-9-oxoxanthen-2-yl)oxan-2-yl]methyl acetate

C21H20O12 (464.09547200000003)


   

(2r,3r,4r,5s,6r)-2-(3,4-dihydroxy-2-methylidenebutoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

(2r,3r,4r,5s,6r)-2-(3,4-dihydroxy-2-methylidenebutoxy)-6-(hydroxymethyl)oxane-3,4,5-triol

C11H20O8 (280.115812)


   

(2r,3r,4s,5r,6r)-3-{[2-(3,4-dihydroxyphenyl)acetyl]oxy}-5-hydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-4-yl 2-(3,4-dihydroxyphenyl)acetate

(2r,3r,4s,5r,6r)-3-{[2-(3,4-dihydroxyphenyl)acetyl]oxy}-5-hydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-4-yl 2-(3,4-dihydroxyphenyl)acetate

C27H32O13 (564.1842822)


   

(2r,3s,4s,5r,6r)-4,5-dihydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(2r,3s,4s,5r,6r)-4,5-dihydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-2-(hydroxymethyl)oxan-3-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C20H26O10 (426.15258960000006)


   

(2r,3r,4s,5s,6r)-4,5-dihydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-3-yl 2-(4-hydroxyphenyl)acetate

(2r,3r,4s,5s,6r)-4,5-dihydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-3-yl 2-(4-hydroxyphenyl)acetate

C19H26O9 (398.1576746)


   

[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}oxan-2-yl]methyl 4-hydroxybenzoate

[(2r,3s,4s,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}oxan-2-yl]methyl 4-hydroxybenzoate

C18H24O9 (384.14202539999997)


   

(2r,3r,4s,5r,6r)-3-{[2-(3,4-dihydroxyphenyl)acetyl]oxy}-5-hydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-4-yl 2-(4-hydroxyphenyl)acetate

(2r,3r,4s,5r,6r)-3-{[2-(3,4-dihydroxyphenyl)acetyl]oxy}-5-hydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-4-yl 2-(4-hydroxyphenyl)acetate

C27H32O12 (548.1893672)


   

(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[(2r,4r)-2-methyl-6-oxooxan-4-yl]oxy}oxan-3-yl 2-(3,4-dihydroxyphenyl)acetate

(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-{[(2r,4r)-2-methyl-6-oxooxan-4-yl]oxy}oxan-3-yl 2-(3,4-dihydroxyphenyl)acetate

C20H26O11 (442.14750460000005)


   

[(2r,3s,4r,5r,6r)-3,5-bis({[2-(3,4-dihydroxyphenyl)acetyl]oxy})-4-hydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

[(2r,3s,4r,5r,6r)-3,5-bis({[2-(3,4-dihydroxyphenyl)acetyl]oxy})-4-hydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

C35H38O17 (730.2108898)


   

(2r,3r,4r,5r,6r)-3,5-dihydroxy-2-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-4-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

(2r,3r,4r,5r,6r)-3,5-dihydroxy-2-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-4-yl (2e)-3-(3,4-dihydroxyphenyl)prop-2-enoate

C20H26O11 (442.14750460000005)


   

2-({6-[(3,4,8,8a-tetramethyl-4-{3-methyl-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]pent-4-en-1-yl}-1,2,3,4a,5,6-hexahydronaphthalen-1-yl)oxy]-4-hydroxy-2-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol

2-({6-[(3,4,8,8a-tetramethyl-4-{3-methyl-3-[(3,4,5-trihydroxyoxan-2-yl)oxy]pent-4-en-1-yl}-1,2,3,4a,5,6-hexahydronaphthalen-1-yl)oxy]-4-hydroxy-2-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol

C43H72O18 (876.4718412)


   

2-({6-[(3,4,8,8a-tetramethyl-4-{3-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]pent-4-en-1-yl}-1,2,3,4a,5,6-hexahydronaphthalen-1-yl)oxy]-4-hydroxy-2-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol

2-({6-[(3,4,8,8a-tetramethyl-4-{3-methyl-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]pent-4-en-1-yl}-1,2,3,4a,5,6-hexahydronaphthalen-1-yl)oxy]-4-hydroxy-2-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-3-yl}oxy)-6-methyloxane-3,4,5-triol

C44H74O18 (890.4874904000001)


   

6-[2-(3,4-dihydroxyphenyl)ethoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate

6-[2-(3,4-dihydroxyphenyl)ethoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl 3-(3,4-dihydroxyphenyl)prop-2-enoate

C23H26O11 (478.14750460000005)


   

[(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

[(2r,3s,4r,5r,6r)-3,4,5-trihydroxy-6-{[(2e)-4-hydroxy-2-(hydroxymethyl)but-2-en-1-yl]oxy}oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)acetate

C19H26O11 (430.1475046)


   

(2r,3r,4s,5r,6s)-3-hydroxy-2-(hydroxymethyl)-5-{[2-(4-hydroxyphenyl)acetyl]oxy}-6-{[(2r,4r)-2-methyl-6-oxooxan-4-yl]oxy}oxan-4-yl 2-(4-hydroxyphenyl)acetate

(2r,3r,4s,5r,6s)-3-hydroxy-2-(hydroxymethyl)-5-{[2-(4-hydroxyphenyl)acetyl]oxy}-6-{[(2r,4r)-2-methyl-6-oxooxan-4-yl]oxy}oxan-4-yl 2-(4-hydroxyphenyl)acetate

C28H32O12 (560.1893672)


   

(2r,3r,4s,5r,6r)-3,5-dihydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-4-yl 2-(3,4-dihydroxyphenyl)acetate

(2r,3r,4s,5r,6r)-3,5-dihydroxy-2-{[(2e)-4-hydroxy-2-methylbut-2-en-1-yl]oxy}-6-(hydroxymethyl)oxan-4-yl 2-(3,4-dihydroxyphenyl)acetate

C19H26O10 (414.1525896)