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Yangonin - ≥98%, high purity , CAS No.500-62-9

    Grade & Purity:
  • ≥98%
In stock
Item Number
Y276449
Grouped product items
SKU Size
Availability
Price Qty
Y276449-5mg
5mg
3
$165.90
Y276449-10mg
10mg
2
$260.90
Y276449-25mg
25mg
2
$587.90
Y276449-50mg
50mg
2
$1,057.90

Potent NF-κβ inhibitor. Selective CB 1 agonist. Antioxidant.

Basic Description

Synonyms CCG-208617 | YANGONIN [MI] | 4-Methoxy-6-[(E)-2-(4-methoxyphenyl)ethenyl]-2H-pyran-2-one | 4-methoxy-6-[2-(4-methoxyphenyl)ethenyl]pyran-2-one | NCGC00260096-01 | SR-05000002174-2 | 2H-Pyran-2-one, 4-methoxy-6-(2-(4-methoxyphenyl)ethenyl)-, (E)- | 4-Metho
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms Potent NF-κβ inhibitor. Selective CB 1 agonist. (K i values are 0.7 and 10 μM for CB 1 and CB 2 respectively). Shows potent antioxidant effects. Active in vivo.
Storage Temp Store at -20°C,Desiccated
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Note Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Phenylpropanoids and polyketides
Class Kavalactones
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Kavalactones
Alternative Parents Styrenes  Phenoxy compounds  Methoxybenzenes  Anisoles  Pyranones and derivatives  Alkyl aryl ethers  Vinylogous esters  Heteroaromatic compounds  Lactones  Oxacyclic compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents Kavalactone - Anisole - Phenoxy compound - Phenol ether - Styrene - Methoxybenzene - Pyranone - Alkyl aryl ether - Benzenoid - Monocyclic benzene moiety - Pyran - Vinylogous ester - Heteroaromatic compound - Lactone - Ether - Organoheterocyclic compound - Oxacycle - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as kavalactones. These are lactones, which is structurally characterized by a benzene ring and a pyranone moiety, linked to each other to form a 4-methoxy-6-(2-phenylethyl)-2H-pyran-2-one skeleton.
External Descriptors alpha-Pyrones

Associated Targets(Human)

NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
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ACHE Tclin Acetylcholinesterase (18204 Activities)
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PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CXCL8 Tchem Interleukin-8 (642 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AHR Tclin Aryl hydrocarbon receptor (1071 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
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NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
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CASP1 Tchem Caspase-1 (6235 Activities)
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CASP7 Tchem Caspase-7 (3146 Activities)
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TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
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ACHN (49357 Activities)
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CAKI-1 (44928 Activities)
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CCRF-CEM (65223 Activities)
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COLO 205 (50209 Activities)
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DU-145 (51482 Activities)
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HL-60 (67320 Activities)
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HT-29 (80576 Activities)
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K562 (73714 Activities)
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KM12 (47707 Activities)
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M14 (47487 Activities)
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MCF7 (126967 Activities)
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MOLT-4 (49676 Activities)
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OVCAR-3 (48710 Activities)
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OVCAR-4 (44535 Activities)
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OVCAR-5 (45555 Activities)
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OVCAR-8 (47708 Activities)
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PC-3 (62116 Activities)
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RPMI-8226 (44974 Activities)
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RXF 393 (41971 Activities)
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SF-295 (48000 Activities)
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SK-MEL-2 (46422 Activities)
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SK-MEL-28 (48833 Activities)
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SK-MEL-5 (47095 Activities)
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SK-OV-3 (52876 Activities)
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SN12C (47755 Activities)
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SNB-19 (46794 Activities)
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TK-10 (45540 Activities)
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U-251 (51189 Activities)
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UACC-257 (46019 Activities)
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UACC-62 (47335 Activities)
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UO-31 (46270 Activities)
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786-0 (47912 Activities)
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A549 (127892 Activities)
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NCI/ADR-RES (33767 Activities)
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T47D (39041 Activities)
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EKVX (44102 Activities)
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HCC 2998 (41480 Activities)
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HCT-116 (91556 Activities)
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HOP-92 (41141 Activities)
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Associated Targets(non-human)

Echinochloa crus-galli (3685 Activities)
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Fusarium solani (1274 Activities)
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Fusarium oxysporum (3998 Activities)
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Trichoderma viride (1263 Activities)
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PC-12 (7051 Activities)
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Lactuca sativa (1092 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
BCHE Cholinesterase (8742 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Colletotrichum gloeosporioides (560 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mapt Microtubule-associated protein tau (6 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PA Polymerase acidic protein (806 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)
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Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504763360
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504763360
IUPAC Name 4-methoxy-6-[(E)-2-(4-methoxyphenyl)ethenyl]pyran-2-one
INCHI InChI=1S/C15H14O4/c1-17-12-6-3-11(4-7-12)5-8-13-9-14(18-2)10-15(16)19-13/h3-10H,1-2H3/b8-5+
InChIKey XLHIYUYCSMZCCC-VMPITWQZSA-N
Smiles COC1=CC=C(C=C1)C=CC2=CC(=CC(=O)O2)OC
Isomeric SMILES COC1=CC=C(C=C1)/C=C/C2=CC(=CC(=O)O2)OC
PubChem CID 5281575
Molecular Weight 258.27

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot Number Certificate Type Date Item
G2214487 Certificate of Analysis Apr 18, 2023 Y276449
G2214493 Certificate of Analysis Apr 18, 2023 Y276449
G2214261 Certificate of Analysis Apr 18, 2023 Y276449
G2214240 Certificate of Analysis Apr 18, 2023 Y276449

Chemical and Physical Properties

Solubility Soluble in ethanol (with heating)
Sensitivity Light sensitive
Molecular Weight 258.269 g/mol
XLogP3 2.700
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 4
Exact Mass 258.089 Da
Monoisotopic Mass 258.089 Da
Topological Polar Surface Area 44.800 Ų
Heavy Atom Count 19
Formal Charge 0
Complexity 412.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 1
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 1
Covalently-Bonded Unit Count 1

Solution Calculators

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