calycosin (Q5024637)

Calycosin (English)

5 October 2016

C₁₆H₁₂O₅

1 reference

Calycosin (English)

5 October 2016

COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O

1 reference

Calycosin (English)

5 October 2016

Astragalus membranaceus

8 references

Constituents of Astragalus membranaceus

Micellar electrokinetic chromatography for the quantitative analysis of flavonoids in the radix of Astragalus membranaceus var. mongholicus

Antioxidative components isolated from the roots ofAstragalus membranaceusBunge (Astragali Radix)

Inhibitory effects of isoflavones in roots ofAstragalus membranaceus BUNGE (Astragali Radix) on lipid peroxidation by reactive oxygen species

Kumatakenin from Astragalus membranaceus

Liquid chromatography-electrospray ionization mass spectrometry study of the flavonoids of the roots of Astragalus mongholicus and A. membranaceus

Accumulation of calycosin and its 7-O-beta-D-glucoside and related gene expression in seedlings of Astragalus membranaceus Bge. var. mongholicus (Bge.) Hsiao induced by low temperature stress

Solvent effect in 1H NMR spectra of 3'-hydroxy-4'-methoxy isoflavonoids from Astragalus membranaceus var. mongholicus

Astragalus mongholicus

8 references

Constituents of Astragalus membranaceus

Micellar electrokinetic chromatography for the quantitative analysis of flavonoids in the radix of Astragalus membranaceus var. mongholicus

Liquid chromatography-electrospray ionization mass spectrometry study of the flavonoids of the roots of Astragalus mongholicus and A. membranaceus

Solvent effect in 1H NMR spectra of 3'-hydroxy-4'-methoxy isoflavonoids from Astragalus membranaceus var. mongholicus

Inhibitory effects of isoflavones in roots ofAstragalus membranaceus BUNGE (Astragali Radix) on lipid peroxidation by reactive oxygen species

Antioxidative components isolated from the roots ofAstragalus membranaceusBunge (Astragali Radix)

Kumatakenin from Astragalus membranaceus

Accumulation of calycosin and its 7-O-beta-D-glucoside and related gene expression in seedlings of Astragalus membranaceus Bge. var. mongholicus (Bge.) Hsiao induced by low temperature stress

Trifolium pratense

3 references

Identification of isoflavone conjugates in red clover (Trifolium pratense) by liquid chromatography–mass spectrometry after two-dimensional solid-phase extraction

Analysis of flavonoids from red clover by liquid chromatography—electrospray mass spectrometry

Identification of isoflavones calycosin and pseudobaptigenin in Trifolium pratense

Wisteria brachybotrys

1 reference

Isoflavones from the gall and wood of Wisteria brachybotrys

Dalbergia parviflora

1 reference

Flavonoids from the heartwood of the Thai medicinal plant Dalbergia parviflora and their effects on estrogenic-responsive human breast cancer cells

Sophora fraseri

1 reference

Isoflavonoids in roots of sophora fraseri

Astragalus trimestris

8 references

Antioxidative components isolated from the roots ofAstragalus membranaceusBunge (Astragali Radix)

Inhibitory effects of isoflavones in roots ofAstragalus membranaceus BUNGE (Astragali Radix) on lipid peroxidation by reactive oxygen species

Kumatakenin from Astragalus membranaceus

Liquid chromatography-electrospray ionization mass spectrometry study of the flavonoids of the roots of Astragalus mongholicus and A. membranaceus

Constituents of Astragalus membranaceus

Micellar electrokinetic chromatography for the quantitative analysis of flavonoids in the radix of Astragalus membranaceus var. mongholicus

Accumulation of calycosin and its 7-O-beta-D-glucoside and related gene expression in seedlings of Astragalus membranaceus Bge. var. mongholicus (Bge.) Hsiao induced by low temperature stress

Solvent effect in 1H NMR spectra of 3'-hydroxy-4'-methoxy isoflavonoids from Astragalus membranaceus var. mongholicus

Glycyrrhiza pallidiflora

5 references

Flavonoids from Glycyrrhiza pallidiflora hairy root cultures

Flavonoids from Glycyrrhiza pallidiflora hairy root cultures

Structures of Prenylated Dihydrochalcone, Gancaonin J and Homoisoflavonone, Gancaonin K from Glycyrrhiza pallidiflora

Structures of Prenylated Dihydrochalcone, Gancaonin J and Homoisoflavonone, Gancaonin K from Glycyrrhiza pallidiflora

Flavonoids from Glycyrrhiza pallidiflora hairy root cultures

Millettia laurentii

3 references

An isoflavan-quinone and a flavonol from Millettia laurentii1Part 10 in the series “The Millettia of Cameroon”.1

An isoflavan-quinone and a flavonol from Millettia laurentii1Part 10 in the series “The Millettia of Cameroon”.1

An isoflavan-quinone and a flavonol from Millettia laurentii1Part 10 in the series “The Millettia of Cameroon”.1

Myroxylon balsamum

2 references

Isoflavonoids from Myroxylon balsamum☆

Isoflavonoids from Myroxylon balsamum☆

Psorothamnus arborescens

3 references

Isoflavonoids and other compounds from Psorothamnus arborescens with antiprotozoal activities

Isoflavonoids and other compounds from Psorothamnus arborescens with antiprotozoal activities

Isoflavonoids and other compounds from Psorothamnus arborescens with antiprotozoal activities

Dermatophyllum secundiflorum

4 references

Isoflavonoids in roots of Sophora secundiflora

Isoflavonoids in roots of Sophora secundiflora

Isoflavanones in roots of Sophora secundiflora

Unanisoflavan, a new isoflavan from DC

Amorpha fruticosa

2 references

A prenylated flavanone from roots of Amorpha fruticosa

A prenylated flavanone from roots of Amorpha fruticosa

Andira inermis

4 references

Andinermals A-C, antiplasmodial constituents from Andira inermis

Antiplasmodial activity of isoflavones from Andira inermis

Antiplasmodial activity of isoflavones from Andira inermis

Andinermals A-C, antiplasmodial constituents from Andira inermis

Calycotome villosa

1 reference

Flavonoids from Calicotome villosa

Centrolobium paraense

2 references

Diarylheptanoids and isoflavonoids from Centrolobium species

Diarylheptanoids and isoflavonoids from Centrolobium species

Centrolobium sclerophyllum

3 references

Diarylheptanoids and isoflavonoids from Centrolobium species

Diarylheptanoids and isoflavonoids from Centrolobium species

Antileishmanial activity of compounds extracted and characterized from Centrolobium sclerophyllum

Cicer arietinum

2 references

Cytochrome P450-dependent methylenedioxy bridge formation in Cicer arietinum

Accumulation of Phenolic Compounds and Phytoalexins in Sliced and Elicitor-Treated Cotyledons of Cicer arietinum L.

Cyclopia intermedia

1 reference

Phenolic Compounds from Cyclopia intermedia (Honeybush Tea). 1

Glycyrrhiza uralensis

2 references

Phenolic Constituents of Liquorice. VII. A New Chalcone with a Potent Radical Scavenging Activity and Accompanying Phenolics from Liquorice.

Formation of chalcones and isoflavones by callus culture of Glycyrrhiza uralensis with different production patterns.

Hedysarum polybotrys

2 references

Studies on the constituents of Hedysarum polybotrys Hand.-Mazz.

Studies on the constituents of Hedysarum polybotrys Hand.-Mazz.

Machaerium aristulatum

2 references

Antigiardial isoflavones from Machaerium aristulatum

Antigiardial isoflavones from Machaerium aristulatum

Virgilia oroboides

1 reference

Flavonoids and isoflavonoids from the heartwood ofVirgilia oroboides

Bowdichia virgilioides

1 reference

Two new isoflavonoids from Bowdichia virgilioides

Cyclolobium claussenii

1 reference

Isoflavonoids from Cyclolobium species

Machaerium mucronulatum

1 reference

Mucronulatol, mucroquinone and mucronucarpan, isoflavonoids from Machaerium mucronulatum and M. villosum

Myroxylon peruiferum

1 reference

Isoflavonoids from Myroxylon peruiferum

Spatholobus suberectus

2 references

Ultrasonic/microwave assisted extraction and diagnostic ion filtering strategy by liquid chromatography-quadrupole time-of-flight mass spectrometry for rapid characterization of flavonoids in Spatholobus suberectus

Bioactive constituents of Spatholobus suberectus in regulating tyrosinase-related proteins and mRNA in HEMn cells

Ammopiptanthus mongolicus

3 references

( )-3α-Hydroxylupanine, a new alkaloid from Ammopiptanthus mongolicus (MAXIM.) CHENG F.

Three New Isoflavonoids from the Aerial Parts ofAmmopiptanthus mongolicus

Chemical study of plants of the mongolian flora isoflavones of Ammopiptanthus mongolicus

Andira surinamensis

1 reference

NMR spectral assignments of a new [C--O--C] isoflavone dimer from Andira surinamensis

Astragalus microcephalus

1 reference

Flavonoids from Astragalus microcephalus

Bolusanthus speciosus

1 reference

Antimicrobial and antioxidant flavonoids from the root wood of Bolusanthus speciosus

Maackia amurensis

2 references

Isoflavonoid composition of a callus culture of the relict tree Maackia amurensis Rupr. et Maxim

Minor polyphenols from Maackia amurensis wood

Melilotus messanensis

1 reference

1 reference

Chemical Constituents from Mucuna membranacea

Oxytropis falcata

1 reference

Flavonoids in the Poisonous Plant Oxytropis falcata

Megaselia flavescens

1 reference

Efficient production and capture of 8-prenylnaringenin and leachianone G-biosynthetic intermediates of sophoraflavanone G--by the addition of cork tissue to cell suspension cultures of Sophora flavescens

Pycnanthus angolensis

1 reference

Antimicrobial activities of the CH2Cl2-CH3OH (1:1) extracts and compounds from the roots and fruits of Pycnanthus angolensis (Myristicaceae).

Sophora flavescens

1 reference

Efficient production and capture of 8-prenylnaringenin and leachianone G-biosynthetic intermediates of sophoraflavanone G--by the addition of cork tissue to cell suspension cultures of Sophora flavescens

Styphnolobium japonicum

1 reference

A new isoflavone glycoside from the stem bark of Sophora japonica

Sophora moorcroftiana

1 reference

Studies on the constituents of Sophora species. XXII. Constituents of the root of Sophora moorcroftiana BENTH. ex BAKER.(1).

Trigonella foenum-graecum

1 reference

New flavonoids with 2BS cell proliferation promoting effect from the seeds of Trigonella foenum-graecum L.

Cyclolobium brasiliense

1 reference

Isoflavonoids from Cyclolobium species

Butea superba

1 reference

Isolation of New Isoflavonolignans, Butesuperins A and B, from a Thai Miracle Herb, Butea superba

Psorothamnus arborescens var. minutifolius

1 reference

Isoflavonoids and other compounds from Psorothamnus arborescens with antiprotozoal activities

Thermopsis fabacea

1 reference

Isoflavonoids in the roots of Thermopsis fabacea D.C. (Leguminosae).

Phyllolobium chinense

1 reference

The Constituents of Semen.

Bowdichia nitida

1 reference

Natürlich vorkommende Chinone, XXIV1) Über die Inhaltsstoffe vonBowdichia nitida Benth.: Erstmalige Isolierung eines Isoflavonchinons

Melilotus siculus

1 reference

Q104991982

Thermopsis lanceolata

1 reference

Isoflavonoids in the roots of Thermopsis fabacea D.C. (Leguminosae).

Propolis

2 references

Constituents of Brazilian red propolis and their preferential cytotoxic activity against human pancreatic PANC-1 cancer cell line in nutrient-deprived condition.

Cytotoxic constituents from Brazilian red propolis and their structure-activity relationship.

Commons category

Calycosin

0 references

Identifiers

InChI

InChI=1S/C16H12O5/c1-20-14-5-2-9(6-13(14)18)12-8-21-15-7-10(17)3-4-11(15)16(12)19/h2-8,17-18H,1H3

1 reference

Calycosin (English)

5 October 2016

2 references

Calycosin (English)

5 October 2016

ChEBI release 2020-09-01

CAS Registry Number

20575-57-9

2 references

Global Substance Registration System

UNII

09N3E8P7TA

CALYCOSIN (English)

5 October 2016

https://commonchemistry.cas.org/detail?cas_rn=20575-57-9

9 April 2021

1 reference

Calycosin (English)

5 October 2016

2 references

English

Calycosin (English)

5 October 2016

Reaxys registry number

1292488

1 reference

calycosin (English)

5 October 2016

mapping relation type

2 references

English

calycosin (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C16H12O5/c1-20-14-5-2-9(6-13(14)18)12-8-21-15-7-10(17)3-4-11(15)16(12)19/h2-8,17-18H,1H3

1 reference

CALYCOSIN (English)

5 October 2016

2 references

inferred from InChIKey

splash10-0fmi-0095000000-6ec29a29afa09372aaed

1 reference

0 references

HSDB ID

8109

1 reference

Hazardous Substances Data Bank

28 October 2019

Calycosin (English)

10 May 2021

2 references

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

DSSTOX compound identifier

0 references

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.222.904

27 December 2018

ECHA Substance Infocard ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 20575-57-9 (English)

100.222.904

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.222.904

27 December 2018

Human Metabolome Database ID

[No public or meaningful name is available] (English)

quotation

CAS no.: 20575-57-9 (English)

HMDB0249566

2 references

based on heuristic

inferred from InChIKey

3 references

calycosin (English)

5 October 2016

inferred from InChIKey

UNII

09N3E8P7TA

2 references

Global Substance Registration System

UNII

09N3E8P7TA

English

CALYCOSIN (English)

5 October 2016