Pulchinenoside E4 CAS 1415553-83-1

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Pulchinenoside E4 CAS 1415553-83-1

CAS: 1415553-83-1
Molecular Formula: C59H96O25
Molecular Weight: 1205.39
EINECS: /

Synonyms: Oleanolicacid-3-O-α-L-rhamnosyl(1→6)β-D-Galactosyl(1→3)-β-D-glucosyl(1→3)-α-L-rhamnosyl(1→2)-α-L-arabinoside; (3β)-3-[(O-6-Deoxy-α-L-mannopyranosyl-(1→6)-O-β-D-glucopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→3)-O-6-deoxy-α-L-mannopyranosyl-(1→2)-α-L-arabinopyranosyl)oxy]olean-12-en-28-oicacid;Oleanolicacid-3-O-α-L-rhamnosyl(1→6)β-D-Galactosyl(1→3)-β-D-glucosyl(1→3)-α-L-rhamnosyl(1→2)-α; 3)-β-D-glucosyl(1→6)β-D-Galactosyl(1→Oleanolicacid-3-O-α-L-rhamnosyl(1→Olean-12-en-28-oicacid,3-[(O-6-deoxy-α-L-mannopyranosyl-(1→6)-O-β-D-glucopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→3)-O-6-deoxy-α-L-mannopyranosyl-(1→2)-α-L-arabinopyranosyl)oxy]-,(3β)-; PulchinenosideE4

What is Pulchinenoside E4 CAS 1415553-83-1?

Pulchinenoside E4 CAS 1415553-83-1 is a naturally occurring triterpenoid glycoside classified as an oleanane-type saponin, most commonly isolated from the medicinal plant Pulsatilla chinensis (Ranunculaceae), historically recognized for its array of bioactive constituents; it is distinct from small molecule drugs and instead is supplied commercially as a high-purity (>95 %) analytical/reference standard for use in biological research, particularly in studies probing cytotoxic mechanisms and the roles of saponins in cellular models.

Specification

Item Value
Density 1.46±0.1 g/cm3(Predicted)
Color white to off-white
Form Powder

Feature

  • Plant Origin: Derived primarily from the roots of Pulsatilla chinensis (often referred to in traditional Chinese medicine), placing it among saponins associated with this botanical source.
  • Saponin Class: An oleanane-type triterpenoidal saponin, indicating a pentacyclic terpenoid backbone glycosylated with multiple sugar residues typical of plant secondary metabolites.
  • Natural Product Standard: Supplied commercially with high purity (~95–99 %) and analytical documentation (HPLC, MS, NMR), making it suitable for quality control and reference use in laboratory settings.
  • Cytotoxic Activity: Reported in vitro studies indicate cytotoxic effects in cell-based assays, making it of interest in preliminary antitumor or cell viability research contexts.
  • Research Model Use: Employed as a model compound in investigations of triterpenoid saponin interactions with biological membranes, cellular uptake mechanisms, and efflux transporter modulation.
  • Chemical Reference: Utilized in analytical chemistry and phytochemical profiling as a benchmark compound to identify and quantify saponin constituents in complex botanical extracts.
  • Non-clinical Grade: Intended exclusively for research purposes and not approved for therapeutic, dietary, or clinical diagnostic use.

Application

  • Preclinical Research: Incorporated in cell culture and experimental designs to assess cytotoxic responses and membrane-associated phenomena in pharmacological studies.
  • Analytical Chemistry: Used as a standard in chromatographic and spectroscopic assays for identification and quantification of saponins in botanical and natural product extracts.
  • Compound Libraries: Included in natural product libraries for screening in high-throughput assays to identify biological activities or mechanistic insights.
  • Mechanistic Biology: Applied in biochemical investigations of transporter function, such as P-glycoprotein modulation, in research contexts evaluating drug–plant extract interactions.

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