(Q6948223)

5,7-dihydroxy-3-{[(3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}-2-(3,4,5-trihydroxyphenyl)chromen-4-one

inferred from SMILES

1 reference

1 reference

464.09547608 dalton

1 reference

5,7-dihydroxy-3-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one

inferred from SMILES

stereoisomer of

2 references

5,7-dihydroxy-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one

2 references

5,7-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one

2 references

5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one

2 references

5,7-dihydroxy-3-[(2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one

1 reference

5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one

1 reference

chemical formula

C₂₁H₂₀O₁₂

2 references

O=C1C(OC2OC(C)C(O)C(O)C2O)=C(OC=3C=C(O)C=C(O)C13)C=4C=C(O)C(O)=C(O)C4

0 references

isomeric SMILES

C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)Oc2c(=O)c3c(cc(cc3oc2c4cc(c(c(c4)O)O)O)O)O)O)O)O

0 references

found in taxon

Eugenia uniflora

3 references

Preliminary pharmacological studies on Eugenia uniflora leaves: Xanthine oxidase inhibitory activity

Two macrocyclic hydrolysable tannin dimers from Eugenia uniflora

Two macrocyclic hydrolysable tannin dimers from Eugenia uniflora

Oenothera howardii

1 reference

The Flavonoids of Oenothera Sect. Megapterium (Onagraceae)

Eugenia myrcianthes

1 reference

Xanthine Oxidase Inhibitory Activity of Flavonoids and Tannins fromHexachlamys edulis (Myrtaceae)

Limonium axillare

1 reference

A new flavonoid from Limonium axillare

Chrysophyllum marginatum

1 reference

Chemical study of leaves of Chrysophyllum marginatum (Hook. & Arn.) Radlk (Sapotaceae)

Euxylophora paraensis

1 reference

Fitoquímica e quimiossistemática de Euxylophora paraensis (Rutaceae)

Diplusodon astictus

1 reference

Flavonoids of Diplusodon (Lythraceae)

Diplusodon speciosus

1 reference

Flavonoids of Diplusodon (Lythraceae)

Polygonum senticosum

1 reference

Isolation and identification of some flavonoids from Polygonum species.

Persicaria senticosa

1 reference

Isolation and identification of some flavonoids from Polygonum species.

Myrtus communis L.

2 references

Identification and quantitation of polyphenols in leaves ofMyrtus communis L.

Polyphenolic Compounds from Pericarps of Myrtus communis

Pistacia lentiscus

1 reference

Identification and quantification of galloyl derivatives, flavonoid glycosides and anthocyanins in leaves of Pistacia lentiscus L.

Chondropetalum

1 reference

Variations in flavonoid patterns within the genus Chondropetalum (restionaceae)

Epilobium roseum

1 reference

Isolation and determination of flavonol glycosides from epilobium species

Epilobium montanum

1 reference

Isolation and determination of flavonol glycosides from epilobium species

Epilobium hirsutum

3 references

Isolation and determination of flavonol glycosides from epilobium species

Polyphenolic metabolites of Epilobium hirsutum

Polyphenolic metabolites of Epilobium hirsutum

Epilobium hybridum

1 reference

Isolation and determination of flavonol glycosides from epilobium species

Epilobium dodonaei

1 reference

Isolation and determination of flavonol glycosides from epilobium species

Epilobium tetragonum

1 reference

Isolation and determination of flavonol glycosides from epilobium species

Epilobium alpinum

1 reference

Isolation and determination of flavonol glycosides from epilobium species

Epilobium parviflorum

1 reference

Isolation and determination of flavonol glycosides from epilobium species

Cistus laurifolius

1 reference

UV Radiation Dependent Flavonoid Accumulation of Cistus laurifolius L

Flemingia stricta

1 reference

Flavonol 3-glycosides from the leaves of Flemingia stricta

Desmanthus illinoensis

1 reference

Flavonoids of Desmanthus illinoensis

Libocedrus plumosa

1 reference

Flavonoid profiles of new zealand Libocedrus and related genera

Polygonum aviculare

2 references

Melanopsichium on Polygonum aviculare

A Chemotaxonomic Study of Flavonoids from Japanese Polygonum Species

Leea thorelii

1 reference

Leeaoside, a new megastigmane diglycoside from the leaves of Leea thorelii Gagnep

Baeckea frutescens

2 references

A new flavonol glycoside from Millettia speciosa

Chemical constituents of Baeckea frutescens leaves inhibit copper-induced low-density lipoprotein oxidation

Petiveria alliacea

1 reference

6-C-formyl and 6-C-hydroxymethyl flavanones from Petiveria alliacea

Loropetalum chinense

1 reference

Hydrolysable tannins from Loropetalum chinense

Sedum sediforme

1 reference

Two phloroglucinol glucosides, flavan gallates and flavonol glycosides from Sedum sediforme flowers

Plinia pennata

1 reference

5,7,2′,5′-Tetrahydroxydihydroflavonol 3-rhamnoside from Plinia pinnata

Rhododendron ellipticum

1 reference

Quercetin 5,4′-dimethyl ether from Rhododendron ellipticum

Myrsine africana

1 reference

A flavonol glycoside from Myrsine africana leaves

Myrsine seguinii

2 references

Three flavonol glycosides from leaves of Myrsine seguinii

Myrseguinosides A-E, five new glycosides from the fruits of Myrsine seguinii

Rhoiptelea chiliantha

1 reference

Structures and Biogenesis of Rhoipteleanins, Ellagitannins Formed by Stereospecific Intermolecular C-C Oxidative Coupling, Isolated from Rhoiptelea chiliantha

Myrcia multiflora

1 reference

Antidiabetic principles of natural medicines. II. Aldose reductase and alpha-glucosidase inhibitors from Brazilian natural medicine, the leaves of Myrcia multiflora DC. (Myrtaceae): structures of myrciacitrins I and II and myrciaphenones A and B.

Phyllanthus tenellus

1 reference

Two Tannins fromPhyllanthus tenellus

Lysimachia congestiflora

1 reference

Flavonol glycosides from Lysimachia congestiflora

Phedimus aizoon

1 reference

Polyphenolic Compounds from Rubus saxatilis

Phyllanthus virgatus

1 reference

Tannins, flavonol sulfonates, and a norlignan from phyllanthus virgatus

Betula schmidtii

1 reference

Chemical Evaluation of Betula Species in Japan. VI. Constituents of Betula schmidtii.

Juglans mandshurica

4 references

Inhibition of human immunodeficiency virus type 1 reverse transcriptase and ribonuclease H activities by constituents of Juglans mandshurica

Anti-human immunodeficiency virus-type 1 activity of constituents from Juglans mandshurica

Anti-complement activity of constituents from the stem-bark of Juglans mandshurica

Anti-complement activity of constituents from the stem-bark of Juglans mandshurica

Cuphea hyssopifolia

1 reference

Macrocyclic ellagitannin dimers, cuphiins D1 and D2, and accompanying tannins from Cuphea hyssopifolia

Searsia thyrsiflora

1 reference

Cardanols from leaves of Rhus thyrsiflora.

Syzygium cumini

2 references

A new flavonol from leaves of Eugenia jambolana

Acylated flavonol glycosides from Eugenia jambolana leaves

Maesa lanceolata

1 reference

Flavonol glycosides of Warburgia ugandensis leaves

Phyllanthus emblica

1 reference

Two new acylated flavanone glycosides from the leaves and branches of Phyllanthus emblica

Manilkara zapota

1 reference

Bioactive novel polyphenols from the fruit of Manilkara zapota (Sapodilla).

Warburgia stuhlmannii

1 reference

Flavonol and drimane-type sesquiterpene glycosides of Warburgia stuhlmannii leaves

Nymphaea lotus

1 reference

Two very unusual macrocyclic flavonoids from the water lily Nymphaea lotus

Diospyros glaucifolia

1 reference

Flavonol Glycosides in Two Diospyros Plants and Their Radical Scavenging Activity

Clausena dunniana

1 reference

Dinorditerpene, Diterpenes, Alkaloids, and Coumarins fromClausena dunniana

Limonium caspium

1 reference

Flavonoids of the roots ofLimonium caspium

Juniperus phoenicea

1 reference

Biflavones of some Cupressaceae plants

Phedimus kamtschaticus

2 references

Flavonoids of some species ofSedum

Flavonoids of some species of Sedum

Phedimus selskianus

1 reference

Gallomyricitrin — A new acylated flavonoid from Sedum selskianum

Sedum montanum

1 reference

Myricetin 3-O-arabinofuranoside from Sedum montanum ssp. orientale

Dianthus caryophyllus

1 reference

3-Hydroxyacetophenone in carnations is a phytoanticipin active against Fusarium oxysporum f. sp. dianthi

Lysimachia christinae

1 reference

Flavonoid Glycosides from Lysimachiae Herba and Lysimachia christianae var. typica1

Oenothera deserticola

1 reference

FLAVONOID SURVEY OF OENOTHERA (ONAGRACEAE): SECTS. GAUROPSIS, HARTMANNIA, KNEIFFIA, PARADOXUS, AND XYLOPLEURUM

Oenothera kunthiana

1 reference

FLAVONOID SURVEY OF OENOTHERA (ONAGRACEAE): SECTS. GAUROPSIS, HARTMANNIA, KNEIFFIA, PARADOXUS, AND XYLOPLEURUM

Oenothera multicaulis

1 reference

FLAVONOID SURVEY OF OENOTHERA (ONAGRACEAE): SECTS. GAUROPSIS, HARTMANNIA, KNEIFFIA, PARADOXUS, AND XYLOPLEURUM

Oenothera tetraptera

1 reference

FLAVONOID SURVEY OF OENOTHERA (ONAGRACEAE): SECTS. GAUROPSIS, HARTMANNIA, KNEIFFIA, PARADOXUS, AND XYLOPLEURUM

Oenothera speciosa

2 references

FLAVONOID SURVEY OF OENOTHERA (ONAGRACEAE): SECTS. GAUROPSIS, HARTMANNIA, KNEIFFIA, PARADOXUS, AND XYLOPLEURUM

Polyphenolic profile and bioactivity study of Oenothera speciosa Nutt. aerial parts.

Licania heteromorpha

1 reference

Flavonoids and triterpenoids from Licania heteromorpha (Chrysobalanaceae)

Syzygium corynocarpum

1 reference

Flavan-3-ols isolated from some medicinal plants inhibiting COX-1 and COX-2 catalysed prostaglandin biosynthesis

Syzygium malaccense

1 reference

Flavan-3-ols isolated from some medicinal plants inhibiting COX-1 and COX-2 catalysed prostaglandin biosynthesis

Norantea guianensis

1 reference

Flavonol glycosides of Norantea guianensis flowers

Sideroxylon spinosum

1 reference

Polyphenol investigation ofArgania spinosa (Sapotaceae)endemic tree from Morocco

Myrcia neoglabra

1 reference

Flavonoids and other phenolics from leaves of two Marlierea species (Myrtaceae)

Alchornea glandulosa

1 reference

Biological activity of phenolic compounds from Alchornea glandulosa

Oenothera glaucifolia

1 reference

The flavonoids of Stenosiphon (Onagraceae)

Bridelia ferruginea

1 reference

Terpenoids and flavonoids of Bridelia ferruginea

Platycladus orientalis

1 reference

Phenolic constituents of Lyonia ovalifolia

Diploknema butyracea

2 references

Butyracic Acid, A New Sapogenin fromMadhuca butyracea

Flavonoids from the flowers of Nymphaea alba L.

Catha edulis

1 reference

Myricetin, Dihydromyricetin, and Quercetin Glycosides from Catha edulis

Saxifraga cernua

1 reference

Further studies of flavonoids in Saxifraga

Corylus avellana

1 reference

Flavonoids of the bark ofCorylus avellana

Parinari capensis

1 reference

Chemosystematic Studies in the Chrysobalanaceae. I. Flavonoids in Parinari

Parinari congolana

1 reference

Chemosystematic Studies in the Chrysobalanaceae. I. Flavonoids in Parinari

Hypericum aucheri

1 reference

Biflavone, flavonol, and xanthone glycosides from Hypericum aucheri

Lysimachia nummularia

1 reference

Two flavonol glycosides from Lysimachia nummularia

Flemingia faginea

1 reference

Flavonol Glycosides from Moghania faginea

Eriogonum umbellatum

1 reference

Metabolites of Eriogonum umbellatum

Berchemia racemosa

1 reference

Constituents of Berchemia racemosa Sieb. et Zucc

Euphorbia hirta

2 references

Two novel butanol rhamnosides from an Indian traditional herb, Euphorbia hirta.

Rhododendron simsii

1 reference

Flavonoid biosynthesis in petals of Rhododendron simsii

Xylonagra arborea

1 reference

The flavonoids of Xylonagra (onagraceae)

Astilbe thunbergii

1 reference

Flavonoids of Astilbe and Rodgersia compared to Aruncus

Myrica cerifera

1 reference

The diarylheptanoid (+)-aR,11S-myricanol and two flavones from bayberry (Myrica cerifera) destabilize the microtubule-associated protein tau.

Lens culinaris

2 references

Changes in the content of bioactive polyphenolic compounds of lentils by the action of exogenous enzymes. Effect on their antioxidant activity

Phenolic composition of the cotyledon and the seed coat of lentils ( Lens culinaris L.)

Rubus

1 reference

Flavonoid glycosides and antioxidant capacity of various blackberry, blueberry and red grape genotypes determined by high-performance liquid chromatography/mass spectrometry

Vaccinium corymbosum

1 reference

Flavonoid glycosides and antioxidant capacity of various blackberry, blueberry and red grape genotypes determined by high-performance liquid chromatography/mass spectrometry

Vitis aestivalis

1 reference

Flavonoid glycosides and antioxidant capacity of various blackberry, blueberry and red grape genotypes determined by high-performance liquid chromatography/mass spectrometry

Vitis vinifera

1 reference

Flavonoid glycosides and antioxidant capacity of various blackberry, blueberry and red grape genotypes determined by high-performance liquid chromatography/mass spectrometry

Camellia crassicolumna

1 reference

Phenolic antioxidants from green tea produced from Camellia crassicolumna Var. multiplex

Camellia crassicolumna var. multiplex

1 reference

Phenolic antioxidants from green tea produced from Camellia crassicolumna Var. multiplex

Castanopsis fissa

1 reference

Triterpene hexahydroxydiphenoyl esters and a quinic acid purpurogallin carbonyl ester from the leaves of Castanopsis fissa

Chrysophyllum cainito

1 reference

Polyphenolic antioxidants from the fruits of Chrysophyllum cainito L. (Star Apple).

Dichrostachys cinerea

1 reference

Meroterpenes from Dichrostachys cinerea inhibit protein farnesyl transferase activity

Fagopyrum megacarpum

1 reference

Studies on nepalese crude drugs. XXVIII. Chemical constituents of Bhote Khair, the underground parts of Eskemukerjea megacarpum HARA.

Eugenia selloi

1 reference

Polyoxygenated flavonoids from Eugenia edulis.

Euphorbia petiolata

1 reference

Free radical scavengers from the aerial parts of Euphorbia petiolata

Limonium aureum

1 reference

Flavonoids of Limonium aureum

Limonium gmelini

1 reference

Biologically active compounds from Limonium Gmelinii and L. Popovii I

Limonium popovii

1 reference

Biologically active compounds from Limonium Gmelinii and L. Popovii I

Limonium sinense

2 references

Flavonoids and phenolics from Limonium sinense.

Anti-herpes simplex virus type-1 flavonoids and a new flavanone from the root of Limonium sinense

Melaleuca quinquenervia

1 reference

ChemInform Abstract: Flavonoids of Melaleuca quinquenervia.

Miconia cabucu

1 reference

An unusual C6–C6″ linked flavonoid from Miconia cabucu (Melastomataceae)

Plinia cauliflora

1 reference

Bioactive Depsides and Anthocyanins from Jaboticaba (Myrciariacauliflora)

Morella esculenta

1 reference

A new monoterpenoid glycoside from Myrica esculenta and the inhibition of angiotensin I-converting enzyme

Morella nana

1 reference

A new diarylheptanoid from the bark of Myrica nana

Platycarya strobilacea

1 reference

ent-Eudesmane sesquiterpenoids, galloyl esters of the oak lactone precursor, and a 3-O-methylellagic acid glycoside from the wood of Platycarya strobilacea

Rhododendron dahuricum

1 reference

Flavonols ofRhododendron luteum andRh. dahuricum

Rhododendron luteum

1 reference

Phenolic compounds ofRhododendron luteum

Ribes alpinum

1 reference

Three new flavonol malonylrhamnosides from Ribes alpinum

Rodgersia podophylla

1 reference

Hepatoprotective flavonol glycosides from the aerial parts of Rodgersia podophylla

Sageretia thea

1 reference

Polar Constituents fromSageretia TheaLeaf Characterized by HPLC-SPE-NMR Assisted Approaches

Sclerocarya birrea

1 reference

Chemical composition and antioxidant activity of phenolic compounds from wild and cultivated Sclerocarya birrea(Anacardiaceae) leaves.

Stachys cinerea

1 reference

Meroterpenes from Dichrostachys cinerea inhibit protein farnesyl transferase activity

Syzygium levinei

1 reference

Alkyl phloroglucinol derivatives from Syzygium levinei and their differentiation-inducing activity

Syzygium samarangense

1 reference

Flavonoids and coumarins from Leaves of Phellodendron chinense.

Bauhinia glauca

1 reference

Potential therapeutic agents for circulatory diseases from Bauhinia glauca Benth.subsp. pernervosa. (Da Ye Guan Men).

Hypericum scabrum

1 reference

Prenylated benzophenones and xanthones from Hypericum scabrum.

Stachys germanica

1 reference

Meroterpenes from Dichrostachys cinerea inhibit protein farnesyl transferase activity

Schnella microstachya

1 reference

Phytochemical and Pharmacological Analysis of Bauhinia microstachya (Raddi) Macbr. (Leguminosae)

Cheniella glauca

1 reference

Potential therapeutic agents for circulatory diseases from Bauhinia glauca Benth.subsp. pernervosa. (Da Ye Guan Men).

Aeschynomene brasiliana

1 reference

Flavonoid constituents from larix needles

Nymphaea nouchali var. caerulea

2 references

Antioxidant constituents of Nymphaea caerulea flowers

Flavonoids from blue flowers of Nymphaèa caerulea

Myrica rubra

5 references

Inhibitory effect of Myrica bark on lipase activity in mouse plasma and gastrointestinal tract

Bioactive constituents of Chinese natural medicines. VII. Inhibitors of degranulation in RBL-2H3 cells and absolute stereostructures of three new diarylheptanoid glycosides from the bark of Myrica rubra

Studies of cuticle drugs from natural sources. III. Inhibitory effect of Myrica rubra on melanin biosynthesis

Anti-androgenic activity of Myricae Cortex--isolation of active constituents from bark of Myrica rubra

Anti-allergic effect of the flavonoid myricitrin from Myrica rubra leaf extracts in vitro and in vivo

Betula pendula

1 reference

High-performance liquid chromatographic determination of flavonoids in Betula pendula and Betula pubescens leaves

Cupressus sempervirens

2 references

High-performance quantitative thin-layer chromatography of flavonoid glycosides and biflavonoids ofCupressus sempervirens in relation to cypress canker

Biflavones of some Cupressaceae plants

Potentilla anserina

1 reference

Flavan-3-ols and flavonoids from Potentilla anserina

Euphorbia lunulata

1 reference

Inhibitory effects of constituents from Euphorbia lunulata on differentiation of 3T3-L1 cells and nitric oxide production in RAW264.7 cells.

Lotus herbaceus

1 reference

Flavonoids of Dorycnium intermedium

Betula oycoviensis

1 reference

Flavonoids in the leaves of Polish species of the genus Betula L. V. The taxonomic position on the basis of flavonoid composition

Kalanchoe pinnata

1 reference

Two new flavonol glycosides and a metabolite profile of Bryophyllum pinnatum, a phytotherapeutic used in obstetrics and gynaecology.

Myrcia splendens

1 reference

Screening of Panamanian Plant Extracts for Pesticidal Properties and HPLC-Based Identification of Active Compounds.

Schotia brachypetala

1 reference

Potential of South African medicinal plants targeting the reduction of Aβ42 protein as a treatment of Alzheimer's disease

Pistacia weinmannifolia

1 reference

Gallotannins and related polyphenols from Pistacia weinmannifolia

Berchemia floribunda

1 reference

Constituents of Berchemia racemosa Sieb. et Zucc

Morella rubra

5 references

Bioactive constituents of Chinese natural medicines. VII. Inhibitors of degranulation in RBL-2H3 cells and absolute stereostructures of three new diarylheptanoid glycosides from the bark of Myrica rubra

Inhibitory effect of Myrica bark on lipase activity in mouse plasma and gastrointestinal tract

Anti-androgenic activity of Myricae Cortex--isolation of active constituents from bark of Myrica rubra

Studies of cuticle drugs from natural sources. III. Inhibitory effect of Myrica rubra on melanin biosynthesis

Anti-allergic effect of the flavonoid myricitrin from Myrica rubra leaf extracts in vitro and in vivo

Diospyros japonica

1 reference

Flavonol Glycosides in Two Diospyros Plants and Their Radical Scavenging Activity

Rhododendron latoucheae

1 reference

Quercetin 5,4′-dimethyl ether from Rhododendron ellipticum

Clausena anisata

1 reference

Dinorditerpene, Diterpenes, Alkaloids, and Coumarins fromClausena dunniana

Persicaria pubescens

2 references

Isolation and identification of some flavonoids from Polygonum species.

A Chemotaxonomic Study of Flavonoids from Japanese Polygonum Species

Elegia deusta

1 reference

Variations in flavonoid patterns within the genus Chondropetalum (restionaceae)

Moquilea pyrifolia

1 reference

Phytochemical investigations of Licania genus. Flavonoids from Licania pyrifolia

Lotus dorycnium

1 reference

Flavonoids of Dorycnium intermedium

Rhus chinensis

1 reference

Studies on the constituents of the leaves of Rhus and of some species of related genera in Japan

Choerospondias axillaris

1 reference

Studies on the constituents of the leaves of Rhus and of some species of related genera in Japan

Oenothera rosea

1 reference

FLAVONOID SURVEY OF OENOTHERA (ONAGRACEAE): SECTS. GAUROPSIS, HARTMANNIA, KNEIFFIA, PARADOXUS, AND XYLOPLEURUM

Parinari curatellifolia

1 reference

Chemosystematic Studies in the Chrysobalanaceae. I. Flavonoids in Parinari

Sedum crassularia

1 reference

Two phloroglucinol glucosides, flavan gallates and flavonol glycosides from Sedum sediforme flowers

Phedimus selskanianus

3 references

Gallomyricitrin — A new acylated flavonoid from Sedum selskianum

Flavonoids of some species ofSedum

Flavonoids of some species of Sedum

Syzygium aqueum

1 reference

Syzygium aqueum leaf extract and its bioactive compounds enhances pre-adipocyte differentiation and 2-NBDG uptake in 3T3-L1 cells

Guiera senegalensis

1 reference

Flavonoids as Nutraceuticals

Euphorbiaceae

1 reference

Crotogossamide, a cyclic nonapeptide from the latex of Croton gossypifolius

Identifiers

InChI

InChI=1S/C21H20O12/c1-6-14(26)17(29)18(30)21(31-6)33-20-16(28)13-9(23)4-8(22)5-12(13)32-19(20)7-2-10(24)15(27)11(25)3-7/h2-6,14,17-18,21-27,29-30H,1H3/t6-,14-,17+,18+,21-/m0/s1

1 reference

DCYOADKBABEMIQ-OWMUPTOHSA-N

PubChem

InChIKey

2 references

PubChem

ChEBI release 2020-09-01

CAS Registry Number

17912-87-7

2 references

DCYOADKBABEMIQ-OWMUPTOHSA-N

InChIKey

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=17912-87-7

ChemSpider ID

4444992

1 reference

PubChem CID

5281673

1 reference

ChEBI ID

70082

mapping relation type

exact match

1 reference

ChEMBL ID

CHEMBL454576

1 reference

MSBNK-Univ_Toyama-TY000151

1 reference

MassBank accession ID

MSBNK-Fiocruz-FIO00195

0 references

MSBNK-Fiocruz-FIO00196

0 references

MSBNK-Fiocruz-FIO00197

0 references

MSBNK-Fiocruz-FIO00198

0 references

MSBNK-Fiocruz-FIO00199

0 references

MSBNK-Fiocruz-FIO00200

0 references

MSBNK-Fiocruz-FIO00201

0 references

MSBNK-Fiocruz-FIO00202

0 references

MSBNK-Fiocruz-FIO00203

0 references

MSBNK-Fiocruz-FIO00204

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

0 references

SPLASH

splash10-014i-0109000000-47802379c3d771bd3b38

0 references

splash10-014i-0009000000-5d5e3c212e800610fb03

0 references

splash10-014i-0009000000-ce179f0c2bbddfa6d01b

0 references

splash10-014i-0219000000-35e5219a7017a2acee30

0 references

splash10-03di-0000900000-08c451e234a7f538aab2

0 references

splash10-03di-0001900000-5badfd6ca0a3c7108087

0 references

splash10-014i-0009200000-0ac02050a9f2ba2566cd

0 references

splash10-014i-0019000000-a5151ba54ece5590a461

0 references

splash10-01b9-0195000000-0a4501fef811344909b6

0 references

splash10-014i-0009100000-1a3364496e36694dea0e

0 references

splash10-02t9-0179800000-5cbee419595a10fbae63

0 references

splash10-03di-0003900002-339b58d6a0ea8a5a3b4a

0 references

splash10-014i-0059000000-a7f210805630398804a2

0 references

splash10-03di-0000900000-37862f98814d88b32c00

0 references

splash10-014i-2019000000-166993f5f127f48a6c4f

0 references

splash10-014i-1109000000-190e4799bf4134c3c43f

0 references

splash10-000i-0002900003-3457896b749822436c35

0 references

splash10-014i-3219000000-a7fb88f89a1143a4c804

0 references

splash10-02t9-0189500000-7698cce10f4e9c393351

0 references

splash10-02t9-0189600000-d188fa9c829aebcd6edd

0 references

splash10-014i-3109000000-7697decd21290c29abbf

0 references

splash10-03di-0000900001-f32d4630aedaf6242f45

0 references

splash10-014i-0009000000-cceb83d64da4466bf4f2

0 references

splash10-014i-0009000000-969b54e5c5dec80be5e4

0 references

splash10-014i-0009200000-4c7cd295aad404663a90

0 references

splash10-014i-0009300000-32e66ab4bbe548a32eff

0 references

splash10-0006-0009200000-7c97b8b4992a6ac8f1b4

0 references

splash10-0006-0009200000-85c6e012894b49c8e088

0 references

splash10-0537-0003900000-06292ec04cb664342f68

0 references

splash10-000y-0003900000-f08f5b6df986fb77bc4c

0 references

splash10-014i-0009600000-f77cf8348e684190a4db

0 references

splash10-014i-1309000000-76eaadadad4c06d2989e

0 references

splash10-014i-5109000000-720f79651ac4dabec1cc

0 references

splash10-01bi-9006000000-495dc0766f7a836d83bb

0 references

splash10-01bi-9006000000-329eac502e3ea32a9b6d

0 references

splash10-03di-0000900000-2d3b8a06cc3b6b17b820

0 references

splash10-03di-0000900000-c91aaf6dcdc0a4cc11ff

0 references

splash10-02t9-0009700000-76a74171c9751ffa6685

0 references

splash10-014i-0009100000-e5cd1edea0df66b5eda0

0 references

splash10-014i-0009000000-886818f52193a15ad844

0 references

splash10-014i-0049000000-9656a5ba7493a3e8c0fa

0 references

splash10-014i-0007900000-f80227e799e66f151e86

0 references

splash10-014i-1209000000-c376a42aa20f0fe8efa4

0 references

splash10-014i-7109000000-b7d3598062125b73d9fd

0 references

splash10-01b9-9008000000-7b245f284b1502e2cca6

0 references

splash10-03di-0000900000-29c58ce8d8c606b1666f

0 references

splash10-03di-0000900000-cb5b051369919962194f

0 references

splash10-02t9-0009800000-ee07c5b5ff324ef35093

0 references

splash10-014i-0009100000-f4069eb2258657bd6d2d

0 references

splash10-014i-0009000000-ec7e3ed20021a3e32e99

0 references

splash10-014i-0049000000-d40ae58f9bb177d47f9e

0 references

splash10-02t9-0019500000-8a172735850735aaec6b

0 references

splash10-014i-0119000000-c85bca2dff39e7c9a7b0

0 references

DSSTox substance ID

DTXSID40170771

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

0 references

0 references

241-856-7

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.038.036

retrieved

27 December 2018

title

3-[(6-deoxy-α-L-mannopyranosyl)oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-benzopyran-4-one (English)

quotation

CAS no.: 17912-87-7 (English)

ECHA Substance Infocard ID

100.038.036

1 reference