Phenoxodiol (Haginin E) - 10mM in DMSO , CAS No.81267-65-4

CAS: 81267-65-4 Cat. No.: P426105 Molecular Weight: 240.25 EC Number: 663-523-9 PubChem CID: 219100
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GRADE & PURITY 10mM in DMSO
Synonyms
7,4'-Dihydroxyisoflav-3-ene | Dehydroequol | SMR004701684 | 3-(4-hydroxy-phenyl)-2H-chromen-7-ol | 3-(4-Hydroxyphenyl)-2H-chromen-7-ol | BDBM50419932 | NCGC00346822-02 | SCHEMBL149612 | 4',7-dihydroxyisoflav-3-ene | XD161580 | FT-0602222 | IDRONOXIL COMPO
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
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Qty
1ml
P426105-1ml
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Information

Phenoxodiol (Haginin E, Idronoxil, Dehydroequol, NV 06, PXD) is an isoflavone analog with antineoplastic activity that activates thecaspasesystem, inhibitsXIAP (X-linked inhibitor of apoptosis), and disruptsFLICE inhibitory protein (FLIP)expression, resulting in tumor cellapoptosis. Phenoxodiol also inhibitsDNA topoisomerase II.

Targets

Caspase ; XIAP ; FLIP ; Topo II

In vitro

Primary ovarian cancer cells, isolated from ascitic fluids of ovarian cancer patients, resistant to conventional chemotherapy, undergo apoptosis following phenoxodiol treatment. This effect is dependent upon the activation of the caspase system, inhibiting XIAP, an inhibitor of apoptosis, and disrupting FLICE inhibitory protein (FLIP) expression through the Akt signal transduction pathway. Phenoxodiol is an efficient inducer of cell death in ovarian cancer cells and sensitizes the cancer cells to Fas-mediated apoptosis.

In vivo

In an in vivo colon cancer model, Balb/C mice administered low-dose Phenoxodiol (PXD), exhibits significantly reduced tumour growth rates and prolonged survival (in 40% of the animals).

Cell Research(from reference)

Cell lines:primary ovarian cancer cells 

Concentrations:0.1 μg/ml, 1 μg/ml, 10 μg/ml 

Incubation Time:24 h 

Specifications

Synonyms
7, 4'-Dihydroxyisoflav-3-ene | Dehydroequol | SMR004701684 | 3-(4-hydroxy-phenyl)-2H-chromen-7-ol | 3-(4-Hydroxyphenyl)-2H-chromen-7-ol | BDBM50419932 | NCGC00346822-02 | SCHEMBL149612 | 4', 7-dihydroxyisoflav-3-ene | XD161580 | FT-0602222 | IDRONOXIL COMPO
Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
Phenoxodiol (Haginin E, Idronoxil, Dehydroequol, NV 06, PXD) is an isoflavone analog with antineoplastic activity that activates the caspase system, inhibits XIAP (X-linked inhibitor of apoptosis), and disrupts FLICE inhibitory protein (FLIP) expression,
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers
Canonical SmilesC1C(=CC2=C(O1)C=C(C=C2)O)C3=CC=C(C=C3)O
IUPAC Name3-(4-hydroxyphenyl)-2H-chromen-7-ol
InChIKeyZZUBHVMHNVYXRR-UHFFFAOYSA-N
INCHI1S/C15H12O3/c16-13-4-1-10(2-5-13)12-7-11-3-6-14(17)8-15(11)18-9-12/h1-8,16-17H,9H2
Isomeric SMILES C1C(=CC2=C(O1)C=C(C=C2)O)C3=CC=C(C=C3)O
WGK Germany 3
PubChem CID 219100
Molecular Weight 240.25

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

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✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassPhenylpropanoids and polyketides
ClassIsoflavonoids
SubclassHydroxyisoflavonoids
Intermediate Tree Nodes Not available
Direct ParentHydroxyisoflavonoids
Alternative Parents Isoflav-3-enes  1-benzopyrans  Alkyl aryl ethers  1-hydroxy-2-unsubstituted benzenoids  Benzene and substituted derivatives  Oxacyclic compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Hydroxyisoflavonoid - Isoflav-3-ene skeleton - Benzopyran - 1-benzopyran - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Monocyclic benzene moiety - Benzenoid - Oxacycle - Ether - Organoheterocyclic compound - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as hydroxyisoflavonoids. These are organic compounds containing an isoflavonoid skeleton carrying one or more hydroxyl groups.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MRC5 (9203 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-231 (73002 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
Molecular Weight240.250 g/mol
XLogP32.700
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass240.079 Da
Monoisotopic Mass240.079 Da
Topological Polar Surface Area49.700 Ų
Heavy Atom Count18
Formal Charge0
Complexity318.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Solution Calculators
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