(Q15427839)

Tamarixetin (English)

5 October 2016

chemical formula

C₁₆H₁₂O₇

1 reference

Tamarixetin (English)

5 October 2016

canonical SMILES

COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O

1 reference

Troupin, A 4-methylcoumarin from Tamarix troupii

Tamarixetin (English)

5 October 2016

1 reference

Costus spicatus

1 reference

Flavonol glycosides from Costus spicatus

Vellozia streptophylla

1 reference

Differences in flavonoid patterns between genera within the velloziaceae

Achyrocline flaccida

2 references

Phenolic constituents of four Achyrocline species

Flavonoids from Achyrocline flaccida

Alhagi graecorum

1 reference

Flavonoids of Alhagi kirgisorum

Alnus glutinosa

1 reference

Variation in the flavonoid aglycone mixture excreted on the leaves of black alder (Alnus glutinosa), from 12 different geographical origins

Artemisia afra

1 reference

In vitro antiplasmodial evaluation of medicinal plants from Zimbabwe

Artemisia annua

1 reference

Methoxylated flavones and coumarins from Artemisia annua

Balsamorhiza deltoidea

2 references

Flavonoids of Balsamorhiza deltoidea and Wyethia mollis

Flavonoids of Balsamorhiza and Wyethia

Balsamorhiza macrophylla

2 references

Methylated flavonols from Wyethia bolanderi and Balsamorhiza macrophylla

Flavonoids of Balsamorhiza and Wyethia

Croton steenkampianus

1 reference

Bioactive diterpenes and other constituents of Croton steenkampianus

Ginkgo biloba

3 references

Biologically active secondary metabolites from myxobacteria

Biologically active secondary metabolites from Ginkgo biloba

Inhibition of human cytochromes P450 by components of Ginkgo biloba

Tamarix aphylla

2 references

Tannins and polyphenolics of the galls of Tamarix aphylla. I.

Tannins and polyphenolics of the galls of Tamarix aphylla. II

Tamarix nilotica

2 references

A new ferulic acid ester and other constituents from Tamarix nilotica leaves.

Chemical and biological studies on Tamarix nilotica growing in Egypt

Cyperus teneriffae

1 reference

Benzodihydrofurans from Cyperus teneriffae

Aegiceras corniculatum

1 reference

Oleanane triterpenes from Aegiceras corniculatum

Allium cepa

1 reference

Antibacterial and antioxidant activities of quercetin oxidation products from yellow onion (Allium cepa) skin

Anthemis altissima

1 reference

Sesquiterpene lactones from Anthemis altissima and their anti-Helicobacter pylori activity

Blumea balsamifera

1 reference

Sesquiterpenes from Blumea balsamifera

Piptocoma rufescens

1 reference

Cytotoxic and NF-κB inhibitory sesquiterpene lactones from Piptocoma rufescens.

Syzygium nervosum

1 reference

Flavonoids from Cleistocalyx operculatus Buds and their Cytotoxic Activity

Tamarix

1 reference

Survey of anthoxanthins. Part VI. Colouring matter of tamarix troupii. Constitution of the aglycone and its synthesis

Bupleurum spinosum

1 reference

Polyacetylenes, terpenoids and flavonoids from Bupleurum spinosum

Ageratina altissima

1 reference

Flavonoids from Eupatorium odoratum with Death Receptor 5 Promoter Enhancing Activity

Reaumuria vermiculata

1 reference

Cytotoxic ellagitannins from Reaumuria vermiculata.

Piptocoma antillana

1 reference

Cytotoxic and NF-κB inhibitory sesquiterpene lactones from Piptocoma rufescens.

Tamarix senegalensis

2 references

Chemical and biological studies on Tamarix nilotica growing in Egypt

A new ferulic acid ester and other constituents from Tamarix nilotica leaves.

Chromolaena odorata

3 references

Phenolic compounds of Chromolaena odorata protect cultured skin cells from oxidative damage: implication for cutaneous wound healing

Exudate flavonoids in a tropical weed, Chromolaena odorata (L.) R. M. King et H. Robinson

Platelet-activating factor (PAF) receptor binding antagonist activity of the methanol extracts and isolated flavonoids from Chromolaena odorata (L.) King and Robinson

Cota altissima

1 reference

Sesquiterpene lactones from Anthemis altissima and their anti-Helicobacter pylori activity

Identifiers

InChI

InChI=1S/C16H12O7/c1-22-11-3-2-7(4-9(11)18)16-15(21)14(20)13-10(19)5-8(17)6-12(13)23-16/h2-6,17-19,21H,1H3

1 reference

Tamarixetin (English)

5 October 2016

2 references

Tamarixetin (English)

5 October 2016

ChEBI release 2020-09-01

2 references

https://commonchemistry.cas.org/detail?cas_rn=603-61-2

tamarixetin (English)

5 October 2016

6 April 2021

1 reference

TAMARIXETIN (English)

5 October 2016

2 references

Tamarixetin (English)

5 October 2016

Reaxys registry number

324993

1 reference

tamarixetin (English)

5 October 2016

ChEBI ID

67492

mapping relation type

2 references

tamarixetin (English)

5 October 2016

International Chemical Identifier

InChI

InChI=1S/C16H12O7/c1-22-11-3-2-7(4-9(11)18)16-15(21)14(20)13-10(19)5-8(17)6-12(13)23-16/h2-6,17-19,21H,1H3

1 reference

TAMARIXETIN (English)

5 October 2016

2 references

inferred from InChIKey

splash10-0udi-0159000000-8cbfa8b1a365861c08b1

1 reference

0 references

DSSTox substance ID

DTXSID00209056

2 references

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

DSSTOX compound identifier

DTXCID20131547

0 references

EC number

210-050-7

1 reference

Global Substance Registration System

UNII

73WRA8Z8M8

TAMARIXETIN (English)

ECHA Substance Infocard ID

5 October 2016

100.009.137

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.009.137

27 December 2018

3,5,7-trihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-benzopyrone (English)

quotation

CAS no.: 603-61-2 (English)

3 references

tamarixetin (English)

5 October 2016

based on heuristic

inferred from InChIKey

UNII

73WRA8Z8M8

2 references

Global Substance Registration System

UNII

73WRA8Z8M8

TAMARIXETIN (English)

5 October 2016

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

0 references

0 references

1 reference