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Songorine

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    Songorine
  • Songorine
Cat No: 34601
Biochemicals - Ion Channel Modulation
Cayman

Songorine is a diterpene alkaloid that has been found in Aconitum and has diverse biological activities.{62354,62355,46695,62356} It is an antagonist of the GABAA receptor (IC50 = 7.06 µM in rat brain membranes).{62354} Songorine (20-80 µM) reduces th...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • (3R,6S,6aR,6bR,9R,11R,11aR,12R,12aR,14R)-1-ethyldodecahydro-6,11-dihydroxy-3-methyl-10-methylene-12,3,6a-ethanylylidene-9,11a-methanoazuleno[2,1-b]azocin-8(9H)-one
Correlated keywords:
  • 1354-90-1 1362-38-5 1368-38-3 Bullatine G Napellonin Napellonine Zongorine SK-OV-3 SKOV-3
Product Overview:
Songorine is a diterpene alkaloid that has been found in Aconitum and has diverse biological activities.{62354,62355,46695,62356} It is an antagonist of the GABAA receptor (IC50 = 7.06 µM in rat brain membranes).{62354} Songorine (20-80 µM) reduces the viability and migration of, and induces apoptosis in, SKOV3 and A2780 epithelial ovarian cancer cells.{62355} It also decreases the levels of β-catenin and phosphorylated GSK3β in the same cells and reduces tumor growth in a SKOV3 mouse xenograft model when administered at doses of 0.25 and 2.5 mg/kg. Songorine (0.025 mg/kg) prevents and inhibits paw edema in a mouse model of carrageenan-induced inflammation.{46695} It also has antinociceptive activity in the early phase of the formalin test in mice when administered at a dose of 46.4 mg/kg.{62356}
Size 1 mg
Shipping dry ice
CAS Number 509-24-0
Molecular Formula C22H31NO3
SMILES O[C@@H]1[C@@]23[C@@]4([H])[C@]5(C[C@H](C([C@H]5O)=C)C(C4)=O)[C@@H]6[C@@]2([H])N(C[C@@]([C@H]3C6)(CC1)C)CC
Molecular Weight 357,5
Formulation A solid
Purity ≥98%
Custom Code 2914.40
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.

Accreditations
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.

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