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Saikogenin D is a natural compound derived from the plant genus Bupleurum, which is known for its medicinal properties. It is a triterpenoid saponin with a unique chemical structure that exhibits various biological activities. Saikogenin D has gained attention for its potential applications in agriculture and pharmaceutical industries due to its non-toxic nature and ability to promote plant growth without the need for chemical pesticides.
Source:
Saikogenin D is typically extracted from the roots of Bupleurum plants, which are widely distributed across various regions, including Asia, Europe, and North America.
Production Methods:
The production of Saikogenin D involves the extraction and purification of the compound from Bupleurum plant roots. Various extraction techniques, such as solvent extraction, ultrasound-assisted extraction, and supercritical fluid extraction, can be employed to obtain Saikogenin D with high purity and yield.

5573-16-0

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5573-16-0 Usage

Uses

Used in Agriculture:
Saikogenin D is used as a natural growth promoter in cultivation methods, offering an eco-friendly alternative to chemical pesticides. It enhances plant growth and development by stimulating root elongation, increasing chlorophyll content, and improving nutrient uptake.
Used in Pharmaceutical Industry:
Saikogenin D is used as a research compound for studying its potential therapeutic effects. SAIKOGENIN D and its metabolites can be analyzed using ultra-fast liquid chromatography-tandem mass spectrometry (UFLC-MS/MS) method, which allows for the identification and quantification of Saikogenin D in biological samples.

Check Digit Verification of cas no

The CAS Registry Mumber 5573-16-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5573-16:
(6*5)+(5*5)+(4*7)+(3*3)+(2*1)+(1*6)=100
100 % 10 = 0
So 5573-16-0 is a valid CAS Registry Number.

5573-16-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β,16α,23,28-Tetrahydroxyoleana-11(12),13(18)-diene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5573-16-0 SDS

5573-16-0Upstream product

5573-16-0Downstream Products

5573-16-0Relevant academic research and scientific papers

Monodesmosidic oleanene-type saponins from kidney vetch (Anthyllis vulneraria L.) with hemolytic activity

Bunse, Marek,Kammerer, Dietmar R.,Klaiber, Iris,Lorenz, Peter,Pfeiffer, Tanja,Stintzing, Florian C.,Conrad, Jürgen

, p. 21 - 28 (2021/09/28)

Two undescribed monodesmosidic oleanene-type saponins, namely 3β-O-{[β-D-glucopyranosyl-(1→4)]-α-L-arabinopyranosyl}-saikogenin G (1) and 3β-O-{[β-D-glucopyranosyl-(1→4)]-α-L-arabinopyranosyl}-16-deoxysaikogenin F (2), named anthylloside A and B, have been isolated from an acetone-water extract from aerial parts of kidney vetch (A. vulneraria L.). Isolation of 1 and 2 was achieved by solvent partition with EtOAc and subsequent repeated chromatographic purification. The structures of the isolated compounds were elucidated by spectrometric (HR-MS) and spectroscopic methods (1H- and 13C-NMR, UV, IR and CD), as well as GC–MS analysis of samples after 1 N HCl hydrolysis and subsequent derivatization. The configuration and conformation of both 1 and 2 were assigned by means of comprehensive 2D-NMR analyses including 1H-1H?COSY, ROESY, decoupled gHSQC, gHMBC and selective 1D-TOCSY experiments. Moreover, 1 and 2 possess significant hemolytic activity, which was assessed in a blood agar assay and compared to that of three reference saponins.

Triterpenoid Glycosides of Corchorus acutangulus Lam.

Mahato, Shashi B.,Pal, Bikas C.

, p. 629 - 634 (2007/10/02)

Four new triterpenoid glycosides, corchorusins A,B,C, and D, isolated from the aerial part of Corchorus acutangulus Lam. were respectively defined as longispinogenin 3-O-β-D-galactopyranoside (1), saikogenin F 3-O-β-D-galactopyranoside (12), 23-hydroxylongispinogenin 3-O-β-D-galactopyranoside (6), and saikogenin E 3-O-β-D-glucopyranosyl(12)-β-D-galactopyranoside (15) based on their spectral properties and some chemical transformations.

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