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Details

Stereochemistry ACHIRAL
Molecular Formula C18H16O8
Molecular Weight 360.3148
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CENTAUREIDIN

SMILES

COC1=CC=C(C=C1O)C2=C(OC)C(=O)C3=C(O2)C=C(O)C(OC)=C3O

InChI

InChIKey=BZXULYMZYPRZOG-UHFFFAOYSA-N
InChI=1S/C18H16O8/c1-23-11-5-4-8(6-9(11)19)16-18(25-3)15(22)13-12(26-16)7-10(20)17(24-2)14(13)21/h4-7,19-21H,1-3H3

HIDE SMILES / InChI

Molecular Formula C18H16O8
Molecular Weight 360.3148
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Quasi-drugs developed in Japan for the prevention or treatment of hyperpigmentary disorders.
2010-06-18
Protective effect on human lymphocytes of some flavonoids isolated from two Achillea species.
2010-05
Bioactivity-guided isolation of cytotoxic sesquiterpenes and flavonoids from Anthemis ruthenica.
2010-01
Aqueous extracts from dietary supplements influence the production of inflammatory cytokines in immortalized and primary T lymphocytes.
2009-12-14
Mechanisms regulating skin pigmentation: the rise and fall of complexion coloration.
2009-09-15
Antiproliferative effect of flavonoids and sesquiterpenoids from Achillea millefolium s.l. on cultured human tumour cell lines.
2009-05
Flavonoids, centaurein and centaureidin, from Bidens pilosa, stimulate IFN-gamma expression.
2007-06-13
Inhibition of inducible nitric oxide synthase and cyclooxygenase-2 expression by flavonoids isolated from Tanacetum microphyllum.
2006-11
Cytotoxic constituents of Achillea clavennae from Montenegro.
2006-05
Centaureidin promotes dendrite retraction of melanocytes by activating Rho.
2006-03
In vitro antimicrobial activity of extracts of four Achillea species: the composition of Achillea clavennae L. (Asteraceae) extract.
2005-10-03
Three new diterpenes and the biological activity of different extracts of Jasonia montana.
2005-04
Antioxidant and free radical scavenging activities of 5,7,3'-trihydroxy-3,6,4'-trimethoxyflavone from Brickellia veronicaefolia.
2004-05
Flavonoids and a sesquiterpene lactone from Tanacetum microphyllum inhibit anti-inflammatory mediators in LPS-stimulated mouse peritoneal macrophages.
2004-01
Bioactive flavonoids of Tanacetum parthenium revisited.
2003-09
Sesquiterpenes and flavonoid aglycones from a Hungarian taxon of the Achillea millefolium group.
2003-02-04
Antifungal highly oxygenated guaianolides and other constituents from Ajania fruticulosa.
2001-12
Phenolic compounds with anti-inflammatory activity from Eupatorium buniifolium.
2001-11
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:59:41 GMT 2025
Edited
by admin
on Mon Mar 31 19:59:41 GMT 2025
Record UNII
548R7290J9
Record Status Validated (UNII)
Record Version
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Name Type Language
NSC-106969
Preferred Name English
CENTAUREIDIN
Common Name English
Code System Code Type Description
WIKIPEDIA
CENTAUREIDIN
Created by admin on Mon Mar 31 19:59:41 GMT 2025 , Edited by admin on Mon Mar 31 19:59:41 GMT 2025
PRIMARY
EPA CompTox
DTXSID50169530
Created by admin on Mon Mar 31 19:59:41 GMT 2025 , Edited by admin on Mon Mar 31 19:59:41 GMT 2025
PRIMARY
CAS
17313-52-9
Created by admin on Mon Mar 31 19:59:41 GMT 2025 , Edited by admin on Mon Mar 31 19:59:41 GMT 2025
PRIMARY
NSC
106969
Created by admin on Mon Mar 31 19:59:41 GMT 2025 , Edited by admin on Mon Mar 31 19:59:41 GMT 2025
PRIMARY
PUBCHEM
5315773
Created by admin on Mon Mar 31 19:59:41 GMT 2025 , Edited by admin on Mon Mar 31 19:59:41 GMT 2025
PRIMARY
FDA UNII
548R7290J9
Created by admin on Mon Mar 31 19:59:41 GMT 2025 , Edited by admin on Mon Mar 31 19:59:41 GMT 2025
PRIMARY