CAS 1312716-27-0
:Scutebarbatine Y
Description:
Scutebarbatine Y is a chemical compound that belongs to a class of natural products known as alkaloids, which are often characterized by their complex structures and diverse biological activities. This particular compound is derived from certain plant species and exhibits a range of pharmacological properties, including potential anti-inflammatory and anti-cancer effects. Its molecular structure typically features multiple rings and functional groups that contribute to its reactivity and interaction with biological targets. Scutebarbatine Y may also demonstrate specific solubility characteristics, influencing its bioavailability and efficacy in therapeutic applications. Research into its mechanisms of action and potential uses in medicine is ongoing, as scientists explore its role in traditional medicine and its potential for drug development. As with many alkaloids, safety and toxicity profiles are important considerations in its application, necessitating thorough investigation in preclinical and clinical studies.
Formula:C33H35NO7
InChI:InChI=1S/C33H35NO7/c1-21-10-8-14-25-31(2,16-15-22-18-26(35)39-20-22)33(4,38)28(41-30(37)24-13-9-17-34-19-24)27(32(21,25)3)40-29(36)23-11-6-5-7-12-23/h5-7,9-13,15-19,25,27-28,38H,8,14,20H2,1-4H3/b16-15+/t25-,27+,28+,31-,32+,33+/m1/s1
InChI key:InChIKey=PFWQIGHLLAXZMX-IWSWVWQKSA-N
SMILES:C[C@@]12[C@@H](OC(=O)C3=CC=CC=C3)[C@H](OC(=O)C=4C=CC=NC4)[C@](C)(O)[C@@](/C=C/C=5COC(=O)C5)(C)[C@]1(CCC=C2C)[H]
Synonyms:- Scutebarbatine Y
- 3-Pyridinecarboxylic acid, (1R,2S,3R,4R,4aS,8aR)-1-(benzoyloxy)-4-[(1E)-2-(2,5-dihydro-5-oxo-3-furanyl)ethenyl]-1,2,3,4,4a,5,6,8a-octahydro-3-hydroxy-3,4,8,8a-tetramethyl-2-naphthalenyl ester
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Found 2 products.
Scutebarbatine Y
CAS:<p>Scutebarbatine Y is a natural product from Scutellaria barbata.</p>Formula:C33H35NO7Purity:98%Color and Shape:SolidMolecular weight:557.643Scutebarbatine Y
CAS:<p>Scutebarbatine Y is an alkaloid compound, which is derived from the traditional medicinal plant species, Scutellaria barbata. This compound is isolated through advanced extraction techniques aimed at preserving its bioactive properties. The mode of action for Scutebarbatine Y involves modulation of various biochemical pathways, particularly those involved in inflammation and cell proliferation. It has been observed to exhibit inhibitory effects on certain cellular enzymes and receptors that play critical roles in disease progression.</p>Formula:C33H35NO7Purity:Min. 95%Molecular weight:557.6 g/mol

