(Q23055215)

inferred from SMILES

mass

578.164±0 dalton

1 reference

Isorhoifolin (English)

Apigenin 7-(6''-O-alpha-rhamnosyl-beta-glucoside)

13 October 2016

stereoisomer of

1 reference

inferred from InChIKey

apigenin 7-rutinoside

2 references

inferred from InChIKey

7-((6-O-(6-deoxy-α-L-mannopyranosyl)-α-D-glucopyranosyl)oxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one

inferred from InChI

1 reference

5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one

inferred from InChI

1 reference

inferred from InChI

chemical formula

C₂₇H₃₀O₁₄

1 reference

Isorhoifolin (English)

13 October 2016

canonical SMILES

CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O

1 reference

Isorhoifolin (English)

13 October 2016

isomeric SMILES

C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O

1 reference

Identification of the Flavonoids in Papilionaceae Flowers Using Paper Chromatography

Isorhoifolin (English)

13 October 2016

1 reference

Desmodium gangeticum

1 reference

Identification of the Flavonoids in Papilionaceae Flowers Using Paper Chromatography

Osmanthus × fortunei

1 reference

Studies on the Constituents of Osmanthus Species. IV. On the Components of the Leaves of Osmanthus fortunei CARR.

Tecoma stans

1 reference

Phytochemical and biological studies on the leaves of Tecoma mollis Humb. And Bonpl cultivated in Egypt

Achillea collina

1 reference

Flavonoids in Achillea collina

Achillea pannonica

1 reference

Flavon- and flavonolglycosides from Achillea pannonica Scheele.

Astragalus onobrychis

1 reference

Flavonoids from Astragalus onobrychis

Wild Carrot

1 reference

Flavone glucosides and other constituents of the Egyptian variety of Daucus carota var. boissieri grown in Egypt

Euchresta formosana

1 reference

Phylogenetic analysis in genus Euchresta based on secondary metabolites

Ligustrum vulgare

2 references

An ethnopharmacological study on common privet (Ligustrum vulgare) and phillyrea (Phillyrea latifolia)

Studies on anti-complementary activity of extracts and isolated flavones from Ligustrum vulgare and Phillyrea latifolia leaves (Oleaceae)

Phillyrea latifolia

1 reference

Studies on anti-complementary activity of extracts and isolated flavones from Ligustrum vulgare and Phillyrea latifolia leaves (Oleaceae)

Pratia nummularia

1 reference

Secondary Metabolites in Cyanobacteria

Buddleja officinalis

1 reference

A new iridoid and effect on the rat aortic vascular smooth muscle cell proliferation of isolated compounds from Buddleja officinalis

Abies nephrolepis

1 reference

Phenolic compounds of Abies nephrolepis and their NO production inhibitory activities.

Baptisia sphaerocarpa

1 reference

Sphaerobiosid, ein Isoflavonglykosid aus Baptisia sphaerocarpa

Barleria strigosa

1 reference

Phenylethanoid and iridoid glycosides from the Thai medicinal plant, Barleria strigosa

Biebersteinia orphanidis

1 reference

A distinctive flavonoid chemistry for the anomalous genus Biebersteinia

Campanula persicifolia

1 reference

Flavonoids and other natural compounds from Campanula persicifolia. IV

Cremanthodium ellisii

1 reference

Nor-lignan and sesquiterpenes from Cremanthodium ellisii

Lycianthes synanthera

1 reference

Three new furostanol saponins from the leaves of Lycianthes synanthera ("Chomte"), an edible Mesoamerican plant.

Meehania urticifolia

1 reference

New phenolic compounds from Meehania urticifolia

Mentha piperita

1 reference

Antiallergic effect of flavonoid glycosides obtained from Mentha piperita L.

Monarda punctata

1 reference

A lipase inhibitor monoterpene and monoterpene glycosides from Monarda punctata

Saussurea medusa

2 references

Biologically active phenols from Saussurea medusa

Bioactive constituents from Chinese natural medicines. XV. Inhibitory effect on aldose reductase and structures of Saussureosides A and B from Saussurea medusa

Scutellaria caucasica

1 reference

Investigation of the flavonoids ofScutellaria polyodon. II

Sicyos edulis

1 reference

Study of flavonoids of Sechium edule (Jacq) Swartz (Cucurbitaceae) different edible organs by liquid chromatography photodiode array mass spectrometry

Sechium edule

1 reference

Study of flavonoids of Sechium edule (Jacq) Swartz (Cucurbitaceae) different edible organs by liquid chromatography photodiode array mass spectrometry

Artemisia judaica

1 reference

Flavonoids of Artemisia judaica, A. Monosperma and A. herba-alba

Phlomis aurea

1 reference

Flavonoids of Phlomis aurea and P. floccosa

Phlomis floccosa

1 reference

Flavonoids of Phlomis aurea and P. floccosa

Adenocarpus anagyrifolius

1 reference

Flavonoids as chemosystematic markers for the genus Adenocarpus

Adenocarpus cincinnatus

1 reference

Flavonoids as chemosystematic markers for the genus Adenocarpus

Adenocarpus complicatus

1 reference

Flavonoids as chemosystematic markers for the genus Adenocarpus

Adenocarpus decorticans

1 reference

Flavonoids as chemosystematic markers for the genus Adenocarpus

Adenocarpus telonensis

1 reference

Flavonoids as chemosystematic markers for the genus Adenocarpus

Hoya australis

1 reference

Investigations on Hoya species. IV. Leaf Phenolics and Leaf-Wax Triterpenes of Hoya australis R. BR. ex TRAILL in Relation to Leaf Age

0 references

Identifiers

InChI

InChI=1S/C27H30O14/c1-10-20(31)22(33)24(35)26(38-10)37-9-18-21(32)23(34)25(36)27(41-18)39-13-6-14(29)19-15(30)8-16(40-17(19)7-13)11-2-4-12(28)5-3-11/h2-8,10,18,20-29,31-36H,9H2,1H3/t10-,18+,20-,21+,22+,23-,24+,25+,26+,27+/m0/s1

1 reference

Isorhoifolin (English)

FKIYLTVJPDLUDL-XPQRYFGPNA-N

13 October 2016

InChIKey

reason for deprecated rank

deprecated identifier value

1 reference

KNApSAcK ID

C00004156

FKIYLTVJPDLUDL-SLNHTJRHSA-N

1 reference

Global Substance Registration System

Isorhoifolin (English)

13 October 2016

2 references

UNII

0B66T65281

isorhoifolin (English)

FKIYLTVJPDLUDL-SLNHTJRHSA-N

13 October 2016

InChIKey

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=552-57-8

1 reference

5-Hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl 6-O-(6-deoxy-a-L-mannopyranosyl)-b-D-glucopyranoside (English)

13 October 2016

1 reference

Isorhoifolin (English)

13 October 2016

1 reference

splash10-0udi-0023009000-61c0a8fb06582071b0cc

ISORHOIFOLIN (English)

13 October 2016

1 reference

MassBank accession ID

0 references

0 references

0 references

0 references

0 references

0 references

0 references

splash10-014i-0090010000-8ea6338d537401f35ff6

0 references

splash10-001i-0000900000-0328806ce0f780a52190

0 references

splash10-014i-0090000000-f8491f7afa950ba678fe

0 references

DSSTox substance ID

DTXSID50970527

0 references

DSSTOX compound identifier

DTXCID201398058

0 references

EC number

209-015-9

2 references

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.008.197

27 December 2018

7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-5-hydroxy-2-(4-hydroxyphenyl)-4H-benzopyran-4-one (English)

quotation

CAS no.: 552-57-8 (English)

Global Substance Registration System

UNII

0B66T65281

isorhoifolin (English)

ECHA Substance Infocard ID

13 October 2016

100.008.197

2 references

reference URL

http://echa.europa.eu/de/information-on-chemicals/registered-substances

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.008.197

27 December 2018

Human Metabolome Database ID

7-[[6-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-5-hydroxy-2-(4-hydroxyphenyl)-4H-benzopyran-4-one (English)

quotation

CAS no.: 552-57-8 (English)

HMDB0037349

1 reference

Global Substance Registration System

inferred from InChIKey

0 references

1 reference

UNII

0B66T65281

isorhoifolin (English)