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Details

Stereochemistry ACHIRAL
Molecular Formula C16H12O5
Molecular Weight 284.2635
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHYSCIONE

SMILES

COC1=CC(O)=C2C(=O)C3=C(C=C(C)C=C3O)C(=O)C2=C1

InChI

InChIKey=FFWOKTFYGVYKIR-UHFFFAOYSA-N
InChI=1S/C16H12O5/c1-7-3-9-13(11(17)4-7)16(20)14-10(15(9)19)5-8(21-2)6-12(14)18/h3-6,17-18H,1-2H3

HIDE SMILES / InChI

Molecular Formula C16H12O5
Molecular Weight 284.2635
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P20719
Gene ID: 3202.0
Gene Symbol: HOXA5
Target Organism: Homo sapiens (Human)
PubMed

PubMed

TitleDatePubMed
Pharmacokinetics of anthraquinones in Xiexin decoction and in different combinations of its constituent herbs.
2009-03
Structural elucidation of in vitro metabolites of emodin by liquid chromatography-tandem mass spectrometry.
2008-11
Anthraquinone pharmacokinetics in Xiexin decoction and the different combinations of its constituent herbs.
2008-09-10
Anthraquinone-benzisochromanquinone dimers from the roots of Berchemia floribunda.
2008-09
Development and validation of a UPLC method for quality control of rhubarb-based medicine: fast simultaneous determination of five anthraquinone derivatives.
2008-08-05
Phenols from the roots of Rheum palmatum attenuate chemotaxis in rat hepatic stellate cells.
2008-08
Simultaneous determination of anthraquinones in radix Polygoni multiflori by capillary gas chromatography coupled with flame ionization and mass spectrometric detection.
2008-07-18
Anti-proliferative effects of estrogen receptor-modulating compounds isolated from Rheum palmatum.
2008-06
Study of interactions of anthraquinones with DNA using ethidium bromide as a fluorescence probe.
2008-06
Tolerance of the lichen Xanthoria parietina (L.) Th. Fr. to metal stress.
2008-06
[Studies on chemical constituents and volatile oil of Xiaochengqi decoction].
2008-05
Lipoxygenase inhibitory constituents from rhubarb.
2008-05
Simultaneous determination of eight major bioactive compounds in Dachengqi Tang (DT) by high-performance liquid chromatography.
2008-04-29
A new spiroketal from Aspergillus terreus, an endophytic fungus in Opuntia ficusindica Mill.
2008-04
Anthraquinones from Polygonum cuspidatum as tyrosinase inhibitors for dermal use.
2008-04
[Theoretical and experimental studies on solubility parameters of multiple components for traditional Chinese materia medica with HPLC].
2008-03
[A new qualitative and quantitative analytical method of chromatographic fingerprints: total quantum statistical moment].
2008-02
Purification of hydroxyanthraquinones and cinnamic acid from the roots of Rheum officinale Baill.
2008-02
Simultaneous identification and quantification of anthraquinones, polydatin, and resveratrol in Polygonum multiflorum, various Polygonum species, and dietary supplements by liquid chromatography and microscopic study of Polygonum species.
2008-01-16
Determination of pharmacologically active compounds in root extracts of Cassia alata L. by use of high performance liquid chromatography.
2008-01-15
Optimization and validation of a chromatographic method for the simultaneous quantification of six bioactive compounds in Rhizoma et Radix Polygoni Cuspidati.
2008-01
Penicidones A-C, three cytotoxic alkaloidal metabolites of an endophytic Penicillium sp.
2008-01
Prenylated anthraquinones and other constituents from the seeds of Vismia laurentii.
2007-11
Anthraquinones from the seeds of Cassia tora with inhibitory activity on protein glycation and aldose reductase.
2007-11
Lichen secondary metabolites from the cultured lichen mycobionts of Teloschistes chrysophthalmus and Ramalina celastri and their antiviral activities.
2007-10-05
[Study on correlation of soil nutrients and content of active constituents in root of Rumex gmelini].
2007-10
A new isocoumarin from Hypericum annulatum.
2007-10
In situ synthesis of molecularly imprinted polymers on glass microspheres in a column.
2007-10
[Application of macroporous resin in purification for effective part from Polygonum cuspidatum].
2007-06
Anthraquinones, Cdc25B phosphatase inhibitors, isolated from the roots of Polygonum multiflorum Thunb.
2007-05-20
Synergistic interaction of physcion and chrysophanol on plant powdery mildew.
2007-05
Simultaneous quantification of five anthraquinones in rat plasma by high-performance liquid chromatography with fluorescence detection.
2007-05
Simultaneous analysis of eight bioactive compounds in Danning tablet by HPLC-ESI-MS and HPLC-UV.
2007-02-19
Antimicrobial activity of the methanolic extracts and compounds from Vismia laurentii De Wild (Guttiferae).
2007-02-12
Alterations in secondary metabolism of aposymbiotically grown mycobionts of Xanthoria elegans and cultured resynthesis stages.
2007-02
Rapid separation and determination of structurally related anthraquinones in Rhubarb by pressurized capillary electrochromatography.
2007-01-04
Preparative isolation and purification of hydroxyanthraquinones from Rheum tanguticum Maxim. on normal phase silica gel: using a Flash Master Personal system.
2007
Anti-HIV-1 constituents from leaves and twigs of Cratoxylum arborescens.
2006-12
Chaetopyranin, a benzaldehyde derivative, and other related metabolites from Chaetomium globosum, an endophytic fungus derived from the marine red alga Polysiphonia urceolata.
2006-11
[Effect of preparation on the major chemical constituents of Polygonum multiflorum].
2006-10
[Isolation of the chemical constituents from Shuanghuanglian injection and their structural identification].
2006-10
[Induction of hairy roots and anthraquinone production in Rheum palmatum].
2006-09
Supercritical CO2 extraction of emodin and physcion from Polygonum cuspidatum and subsequent isolation by semipreparative chromatography.
2006-09
A new anthraquinone from Galium verum L.
2006-09
Neoplaether, a new cytotoxic and antifungal endophyte metabolite from Neoplaconema napellum IFB-E016.
2006-08
New flavonol glycosides and new xanthone from Polygala japonica.
2006-07-26
Laurentixanthones A and B, antimicrobial xanthones from Vismia laurentii.
2006-07
[HPLC fingerprint of Rhizoma Polygoni Cuspidati].
2006-06
[Studies on the chemical constituents in stem rind of Wikstroemia indica].
2006-05
[Studies on chemical constituents of hairy root of Cassia obtusifolia].
2006-02
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:30:26 GMT 2025
Edited
by admin
on Mon Mar 31 19:30:26 GMT 2025
Record UNII
H6PT94IV61
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHYSCIONE
Common Name English
EMODIN 3-METHYL ETHER
MI  
Preferred Name English
PHYSCION
Common Name English
ANTHRAQUINONE, 1,8-DIHYDROXY-3-METHOXY-6-METHYL-
Systematic Name English
RHEOCHRYSIDIN
Common Name English
1,8-DIHYDROXY-3-METHOXY-6-METHYLANTHRAQUINONE
Systematic Name English
NSC-251670
Code English
CHRYSOPHANIC ACID, 6-METHOXY-
Common Name English
PARIETIN
Common Name English
EMODIN 3-METHYL ETHER [MI]
Common Name English
6-O-METHYLEMODIN
Common Name English
PHYSCIONE-
Common Name English
Code System Code Type Description
EVMPD
SUB33881
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY
CAS
521-61-9
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID20200101
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY
MESH
C008905
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY
PUBCHEM
10639
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY
FDA UNII
H6PT94IV61
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY
CHEBI
38167
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY
MERCK INDEX
m4888
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY Merck Index
NSC
251670
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-315-7
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY
SMS_ID
100000127769
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY
WIKIPEDIA
PARIETIN
Created by admin on Mon Mar 31 19:30:26 GMT 2025 , Edited by admin on Mon Mar 31 19:30:26 GMT 2025
PRIMARY
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