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Resveratrol (GMP)

CAT: 0804-HY-16561G-01Size: 10 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-16561G-01Size:10 mg
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Description
Resveratrol (GMP) is Resveratrol produced by using GMP guidelines. GMP small molecules work appropriately as an auxiliary reagent for cell therapy manufacture. Resveratrol (trans-Resveratrol; SRT501), a natural polyphenolic phytoalexin that possesses anti-oxidant, anti-inflammatory, cardioprotective, and anti-cancer properties. Resveratrol (SRT 501) has a wide spectrum of targets including mTOR, JAK, β-amyloid, Adenylyl cyclase, IKKβ, DNA polymerase. Resveratrol also is a specific SIRT1 activator[1][2][3][4]. Resveratrol is a potent pregnane X receptor (PXR) inhibitor[5]. Resveratrol is an Nrf2 activator, ameliorates aging-related progressive renal injury in mice model[6]. Resveratrol increases production of NO in endothelial cells[7].
CAS Number
501-36-0
Product Name Alternative
Trans-Resveratrol (GMP) ; SRT501 (GMP)
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H335
Target
Apoptosis; Autophagy; Bacterial; Fungal; IKK; Keap1-Nrf2; Mitophagy; Sirtuin
Type
GMP Small Molecules
Related Pathways
Anti-infection; Apoptosis; Autophagy; Cell Cycle/DNA Damage; Epigenetics; NF-κB
Field of Research
Cancer; Infection; Inflammation/Immunology
Assay Protocol
https://www.medchemexpress.com/resveratrol-gmp.html
Purity
99.8
Smiles
OC1=CC=C(/C=C/C2=CC(O)=CC(O)=C2)C=C1
Molecular Formula
C14H12O3
Molecular Weight
228.24
Precautions
H302, H315, H319, H335
References & Citations
[1]Pirola L, et al. Resveratrol: one molecule, many targets. IUBMB Life. 2008 May;60 (5) :323-32.|[2]Lu R, et al. Resveratrol, a natural product derived from grape, exhibits antiestrogenic activity and inhibits the growth of human breast cancer cells. J Cell Physiol. 1999 Jun;179 (3) :297-304.|[3]Lee MH, et al. Resveratrol suppresses growth of human ovarian cancer cells in culture and in a murine xenograft model: eukaryotic elongation factor 1A2 as a potential target. Cancer Res. 2009 Sep 15;69 (18) :7449-58.|[4]Du LL, et al. Activation of sirtuin 1 attenuates cerebral ventricular streptozotocin-induced tau hyperphosphorylation and cognitive injuries in rat hippocampi. Age (Dordr) . 2014 Apr;36 (2) :613-23.|[5]Smutny T, et al. Resveratrol as an inhibitor of pregnane X receptor (PXR) : another lesson in PXR antagonism. J Pharmacol Sci. 2014;126 (2) :177-8.|[6]Eun Nim Kim, et al. Resveratrol, an Nrf2 activator, ameliorates aging-related progressive renal injury. Aging (Albany NY) . 2018 Jan; 10 (1) : 83–99.|[7]Huige Li, et al. Resveratrol and Vascular Function. Int J Mol Sci. 2019 Apr 30;20 (9) :2155.
Shipping Conditions
Blue Ice
Storage Conditions
Keep sealed, protected from light and store at room temperature
Scientific Category
GMP Small Molecules
Clinical Information
No Development Reported
Isoform
IKK-β

Chemical Information

Resveratrol

Resveratrol is a stilbenol that is stilbene in which the phenyl groups are substituted at positions 3, 5, and 4' by hydroxy groups. It has a role as a glioma-associated oncogene inhibitor, a geroprotector, an antioxidant and a phytoalexin. It is a polyphenol, a member of resorcinols and a stilbenol.

CAS Number501-36-0
PubChem CID445154
IUPAC Name5-[(E)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol
Molecular FormulaC14H12O3
Molecular Weight228.24
XLogP3.1
Topological Polar Surface Area60.7
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Heavy Atom Count17
Formal Charge0
Complexity246
SMILES
C1=CC(=CC=C1/C=C/C2=CC(=CC(=C2)O)O)O
InChI
InChI=1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1+
InChIKey
LUKBXSAWLPMMSZ-OWOJBTEDSA-N
Chemical Structure
2D Structure
2D structure of Resveratrol
CAS: 501-36-0
CID: 445154
Formula: C14H12O3
MW: 228.24
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight228.24
XLogP33.1
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass228.078644241
Monoisotopic Mass228.078644241
Topological Polar Surface Area60.7 Ų
Heavy Atom Count17
Formal Charge0
Complexity246
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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