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Tubeimoside I

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    Tubeimoside I
  • Tubeimoside I
Cat No: 22276
Biochemicals - Natural Products
Cayman

Tubeimoside I is a natural triterpenoid saponin isolated from the medicinal herb B. paniculatum which possesses broad anticancer activity.{39096,39097,39098,39099} Tubeimoside I exhibits antiproliferative activity against hepatoma HepG2 cells (IC50 = ...

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Territorial Availability: Available through Bertin Technologies only in France
Synonyms:
  • (2?,3?,4?)-olean-12-en-28-oic acid, 3-[[2-O-[4-O-[(3S)-4-carboxy-3-hydroxy-3-methyl-1-oxobutyl]-?-L-arabinopyranosyl]-?-D-glucopyranosyl]oxy]-2,23-dihydroxy-28-(O-?-D-xylopyranosyl-(1?3)-O-6-deoxy-?-L-mannopyranosyl-(1?2)-?-L-arabinopyranosyl) ester, intramol. 4''(3)?4''(28)-ester
Correlated keywords:
  • 123714-94-3 anti-proliferative Hep-G2 NCIH460 1
Product Overview:
Tubeimoside I is a natural triterpenoid saponin isolated from the medicinal herb B. paniculatum which possesses broad anticancer activity.{39096,39097,39098,39099} Tubeimoside I exhibits antiproliferative activity against hepatoma HepG2 cells (IC50 = 15.5 μM) and induces nuclear condensation and fragmentation, cell cycle arrest, mitochondrial membrane disruption, and activation of caspase-3 and caspase-9.{39096} Treatment of HeLa cells with tubeimoside I (IC50 = 25 μM) similarly initiates mitochondrial dysfunction, endoplasmic reticulum stress, and cytoskeletal rearrangement.{39097} In vivo, tubeimoside I (5 mg/kg) administration to nude mice with flank xenografts of human large-cell lung carcinoma cells decreases tumor volume and microvessel density.{39098} It also decreases metastasis of breast cancer cell line MDA-MB-231 in vivo by decreasing expression of C-X-C chemokine receptor type 4 (CXCR4).{39099}
Size 5 mg
Shipping dry ice
CAS Number 102040-03-9
Molecular Formula C63H98O29
SMILES CC1(C)CC[C@]23CC[C@@]4(C)[C@]5(C)CC[C@@]6([H])[C@@](CO)(C)[C@](O[C@@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O[C@]8([H])OC[C@H](OC(C[C@@](O)(C)CC(O[C@@H]9[C@@H](O[C@@]%10([H])[C@H](O)[C@@H](O)[C@H](O)CO%10)[C@@H](O)[C@H](O[C@@]%11([H])[C@H](OC3=O)OC[C@H](O)[C@
Molecular Weight 1319,4
Formulation A crystalline solid
Purity ≥98%
Custom Code 2914.50
UNSPSC code 12352100

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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.

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