Hesperetin-13C-d3

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Hesperetin-¹³C-d₃

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Cat No: 28806

Biochemicals - Isotopically Labeled Standards

Hesperetin-13C-d3 is intended for use as an internal standard for the quantification of hesperetin (Item No. 10006084) by GC- or LC-MS. Hesperetin is a flavonoid that has been found in citrus fruits and has diverse biological activities.{10842,12523,5...

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Territorial Availability: Available through Bertin Technologies only in France

Synonyms:

5,7-dihydroxy-2-(3-hydroxy-4-(methoxy-13C-d3)phenyl)chroman-4-one

Correlated keywords:

GCMS LCMS deuterated deuterium Hep-G2 ACAT-2 Apo-B RBL2H3 anti histamine interleukin IL6 IL1? BV2 nos RBL2H3

Product Overview:
Hesperetin-13C-d3 is intended for use as an internal standard for the quantification of hesperetin (Item No. 10006084) by GC- or LC-MS. Hesperetin is a flavonoid that has been found in citrus fruits and has diverse biological activities.{10842,12523,53902,53903,53904} It reduces ApoB protein levels, ACAT2 expression, and LDL degradation in HepG2 cells when used at a concentrations ranging from 10 to 200 µM.{10842} Hesperetin inhibits IgG-induced β-hexosaminidase release from RBL-2H3 cells (IC50 = 0.099 mg/ml).{12523} It inhibits LPS-induced nitric oxide (NO) production and reduces levels of inducible nitric oxide synthase (iNOS), IL-6, and IL-1β in BV-2 microglial cells.{53902} Hesperetin (5 mg/kg) inhibits passive cutaneous anaphylaxis in mice.{12523} It reduces body weight loss, colon shortening, and ulcer severity in a mouse model of TNBS-induced ulcerative colitis.{53903} Hesperetin reduces cortical and hippocampal neuronal apoptosis and increases time spent in the target quadrant in the Morris water maze in a mouse model of LPS-induced neuronal inflammation.{53904}

Size	500 µg
Shipping	dry ice
Molecular Formula	C₁₅[¹³C]H₁₁D₃O₆
SMILES	OC1=C(O[13C]([2H])([2H])[2H])C=CC(C2CC(C3=C(O)C=C(O)C=C3O2)=O)=C1
Molecular Weight	306,3
Formulation	A solid
Purity	≥99% deuterated forms (d1-d3).
Custom Code	3822.19
UNSPSC code	12352100

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Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

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ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.