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Autophagy
Isorhapontigenin - >96.0%(HPLC), high purity , CAS No.32507-66-7

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Isorhapontigenin - >96.0%(HPLC), high purity , CAS No.32507-66-7

2 Citations

COA

Grade & Purity:

≥96%(HPLC)

Cas Number: 32507-66-7
Molecular Weight: 258.27
MDL number: MFCD12407151
PubChem CID: 5318650
PubChem SID: 488195336

In stock

Item Number

I157676

Grouped product items
SKU	Size	Availability	Price
I157676-10mg	10mg	5	$89.90
I157676-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$212.90
I157676-50mg	50mg	4	$339.90

View related series

Autophagy (1917) Chemical preventive agent (37) Phenylpropanoids (153)

Basic Description

Synonyms	I0804 \| MFCD12407151 \| AC-7023 \| ACon1_000713 \| 1,3-Benzenediol, 5-[2-(4-hydroxy-3-methoxyphenyl)ethenyl]- \| ANNNBEZJTNCXHY-NSCUHMNNSA-N \| HY-N2593 \| MEGxp0_001015 \| AMY40659 \| (E)-5-(4-hydroxy-3-methoxystyryl)benzene-1,3-diol \| ?isorhapontigenin \| NCGC00
Specifications & Purity	≥96%(HPLC)
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Phenylpropanoids and polyketides
  - Class Stilbenes

Kingdom	Organic compounds
Superclass	Phenylpropanoids and polyketides
Class	Stilbenes
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Stilbenes
Alternative Parents	Methoxyphenols Styrenes Resorcinols Phenoxy compounds Methoxybenzenes Anisoles Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Stilbene - Methoxyphenol - Anisole - Phenoxy compound - Phenol ether - Resorcinol - Styrene - Methoxybenzene - 1-hydroxy-4-unsubstituted benzenoid - Phenol - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Monocyclic benzene moiety - Benzenoid - Ether - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Mus musculus (284745 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Influenza A virus (11224 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

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	488195336
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488195336
IUPAC Name	5-[(E)-2-(4-hydroxy-3-methoxyphenyl)ethenyl]benzene-1,3-diol
INCHI	InChI=1S/C15H14O4/c1-19-15-8-10(4-5-14(15)18)2-3-11-6-12(16)9-13(17)7-11/h2-9,16-18H,1H3/b3-2+
InChIKey	ANNNBEZJTNCXHY-NSCUHMNNSA-N
Smiles	COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O
Isomeric SMILES	COC1=C(C=CC(=C1)/C=C/C2=CC(=CC(=C2)O)O)O
WGK Germany	3
Molecular Weight	258.27
Reaxy-Rn	2285028
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2285028&ln=

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.

5 results found

Lot Number	Certificate Type	Date	Item
G2113175	Certificate of Analysis	Apr 03, 2025	I157676
G2113176	Certificate of Analysis	Apr 03, 2025	I157676
C23111069	Certificate of Analysis	Feb 10, 2023	I157676
C23111067	Certificate of Analysis	Feb 10, 2023	I157676
C23111112	Certificate of Analysis	Feb 10, 2023	I157676

Chemical and Physical Properties

Sensitivity	air & heat & light sensitive
Melt Point(°C)	182 °C
Molecular Weight	258.269 g/mol
XLogP3	3.200
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	3
Exact Mass	258.089 Da
Monoisotopic Mass	258.089 Da
Topological Polar Surface Area	69.900 Å²
Heavy Atom Count	19
Formal Charge	0
Complexity	295.000
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

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Qiang Zheng, Yuan Zhang, Xiaofeng Wang, Fudong Wang, Hongyu Zhao. (2022) Isorhapontigenin Modulates SOX9/TOLLIP Expression to Attenuate Cell Apoptosis and Oxidative Stress in Paraquat-Induced Acute Kidney Injury. Oxidative Medicine and Cellular Longevity, 2022 (3328623).
2. Huiyan Zha, Shuying Lv, Yuming Hu, Yaochen Xie, Lingkun Wang, Chen Yang, Guilin Li, Shuchen Gong, Li Ping, Difeng Zhu, Jiajia Wang, Qinjie Weng, Qiaojun He, Jincheng Wang. (2025) Isorhapontigenin alleviates acetaminophen-induced liver injury by promoting fatty acid oxidation. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1871 (167575).

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