CAS 126722-26-7

Pumiloside

Description:

Pumiloside, with the CAS number 126722-26-7, is a chemical compound that belongs to the class of triterpenoid saponins. It is primarily derived from the plant species known for its medicinal properties. Pumiloside is characterized by its complex molecular structure, which typically includes a steroid-like backbone and sugar moieties, contributing to its biological activity. This compound has garnered interest in pharmacological research due to its potential anti-inflammatory, anti-cancer, and immunomodulatory effects. Its mechanism of action may involve the modulation of various signaling pathways, although specific details can vary based on the context of its use. Pumiloside is often studied for its potential therapeutic applications, particularly in traditional medicine systems. As with many natural products, the extraction and purification processes can influence its efficacy and bioavailability. Further research is ongoing to fully elucidate its pharmacokinetics and therapeutic potential in clinical settings.

Formula: C₂₆H₂₈N₂O₉

InChI: InChI=1S/C26H28N2O9/c1-2-11-13-7-17-19-14(20(30)12-5-3-4-6-16(12)27-19)8-28(17)24(34)15(13)10-35-25(11)37-26-23(33)22(32)21(31)18(9-29)36-26/h2-6,10-11,13,17-18,21-23,25-26,29,31-33H,1,7-9H2,(H,27,30)/t11-,13+,17+,18-,21-,22+,23-,25+,26+/m1/s1

InChI key: InChIKey=ODQBQUXGRYBRTP-FWMZWJSFSA-N

SMILES: O=C1N2[C@](C3=C(C2)C(=O)C=4C(N3)=CC=CC4)(C[C@@]5(C1=CO[C@@H](O[C@@H]6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)[C@@H]5C=C)[H])[H]

Synonyms:

• (3S,4R,4aS,5aS)-4-Ethenyl-3-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4,4a,5,5a,6,12-hexahydro-14H-pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-11,14(3H)-dione
• 14H-Pyrano[3',4':6,7]indolizino[1,2-b]quinoline-11,14(3H)-dione,4-ethenyl-3-(b-D-glucopyranosyloxy)-4,4a,5,5a,6,12-hexahydro-,[3S-(3a,4b,4aa,5ab)]-
• 14H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-11,14(3H)-dione, 4-ethenyl-3-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4,4a,5,5a,6,12-hexahydro-, (3S,4R,4aS,5aS)-
• 14H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-11,14(3H)-dione, 4-ethenyl-3-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4,4a,5,5a,6,12-hexahydro-, [3S-(3α,4β,4aα,5aβ)]-
• 3H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-11,14-dione, 4-ethenyl-3-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-4,4a,5,5a,6,12-hexahydro-, (3S,4R,4aS,5aS)-
• Pumiloside
• Pumiloside (alkaloid)
• 14H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-11,14(3H)-dione, 4-ethenyl-3-(β-D-glucopyranosyloxy)-4,4a,5,5a,6,12-hexahydro-, (3S,4R,4aS,5aS)-
• 14H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-11,14(3H)-dione, 4-ethenyl-3-(β-D-glucopyranosyloxy)-4,4a,5,5a,6,12-hexahydro-, [3S-(3α,4β,4aα,5aβ)]-
• 3H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-11,14-dione, 4-ethenyl-3-(β-D-glucopyranosyloxy)-4,4a,5,5a,6,12-hexahydro-, (3S,4R,4aS,5aS)-
• (3S,4R,4aS,5aS)-4-Ethenyl-3-(β-D-glucopyranosyloxy)-4,4a,5,5a,6,12-hexahydro-14H-pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-11,14(3H)-dione

14H-Pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-11,14(3H)-dione, 4-ethenyl-3-(β-D-glucopyranosyloxy)-4,4a,5,5a,6,12-hexahydro-, (3S,4R,4aS,5aS)-

CAS: 126722-26-7

Formula: C₂₆H₂₈N₂O₉

Color and Shape: Solid

Molecular weight: 512.5085

Ref: IN-DA01SLFS

Pumiloside

CAS: 126722-26-7

Pumiloside

Purity: ≥98%

Molecular weight: 512.51g/mol

Ref: 54-BUP00352

Pumiloside

CAS: 126722-26-7

Pumiloside ((3S)-Pumiloside), a quinoline alkaloid glycoside isolated from Nauclea officinalis, is an AchE inhibitor used in Alzheimer's disease research.

Formula: C₂₆H₂₈N₂O₉

Purity: 98.1%

Color and Shape: Solid

Molecular weight: 512.51

Ref: TM-TN6268

Pumiloside

CAS: 126722-26-7

Formula: C₂₆H₂₈N₂O₉

Purity: 95%~99%

Molecular weight: 512.515

Ref: BP-BP4212

Pumiloside

CAS: 126722-26-7

Pumiloside is a specialized biochemical compound, categorized as a natural product glycoside. It is derived primarily from various species of plants in the Rutaceae family, known for their diverse pharmacological properties. The mode of action of pumiloside involves its interaction with specific biological pathways, which may include antioxidant activities, modulation of enzyme activity, or receptor binding processes integral to various physiological functions. These interactions might provide insights into its potential as a lead compound in drug discovery or as a biochemical tool in laboratory research.

Formula: C₂₆H₂₈N₂O₉

Purity: Min. 95%

Molecular weight: 512.5 g/mol

Ref: 3D-BFA72226