99365-19-2 Usage
Description
[(4R)-16β,23,28-Trihydroxy-9,11,12,13-tetradehydrooleanan-3β-yl]3-O-(β-D-glucopyranosyl)-6-deoxy-β-D-galactopyranoside is a complex glycoside chemical compound, consisting of a tetradehydrooleanane triterpenoid attached to a sugar molecule, which includes glucose and galactose. [(4R)-16β,23,28-Trihydroxy-9,11,12,13-tetradehydrooleanan-3β-yl]3-O-(β-D-glucopyranosyl)-6-deoxy-β-D-galactopyranoside is known for its diverse biological activities and potential pharmacological or medicinal properties, making it a subject of interest for further research and development.
Uses
Used in Pharmaceutical Applications:
[(4R)-16β,23,28-Trihydroxy-9,11,12,13-tetradehydrooleanan-3β-yl]3-O-(β-D-glucopyranosyl)-6-deoxy-β-D-galactopyranoside is used as a potential pharmaceutical compound for its diverse biological activities and potential medicinal properties. [(4R)-16β,23,28-Trihydroxy-9,11,12,13-tetradehydrooleanan-3β-yl]3-O-(β-D-glucopyranosyl)-6-deoxy-β-D-galactopyranoside's unique structure and the presence of both triterpenoid and sugar moieties may contribute to its therapeutic effects.
Used in Research and Development:
In the field of research and development, [(4R)-16β,23,28-Trihydroxy-9,11,12,13-tetradehydrooleanan-3β-yl]3-O-(β-D-glucopyranosyl)-6-deoxy-β-D-galactopyranoside is used as a subject of study to explore its potential pharmacological applications and to understand its biological activities. This may lead to the discovery of new treatments for various diseases and conditions.
Used in Drug Delivery Systems:
Similar to gallotannin, [(4R)-16β,23,28-Trihydroxy-9,11,12,13-tetradehydrooleanan-3β-yl]3-O-(β-D-glucopyranosyl)-6-deoxy-β-D-galactopyranoside may be employed in the development of novel drug delivery systems. These systems could potentially enhance the compound's delivery, bioavailability, and therapeutic outcomes, making it more effective for various applications.
Used in the Cosmetics Industry:
Given the compound's potential pharmacological properties, it may also find use in the cosmetics industry for the development of skincare products that could benefit from its biological activities, such as anti-aging or skin healing products.
Used in the Food Industry:
[(4R)-16β,23,28-Trihydroxy-9,11,12,13-tetradehydrooleanan-3β-yl]3-O-(β-D-glucopyranosyl)-6-deoxy-β-D-galactopyranoside's potential medicinal properties may also be harnessed in the food industry for the development of functional foods or dietary supplements that could provide health benefits to consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 99365-19-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,6 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 99365-19:
(7*9)+(6*9)+(5*3)+(4*6)+(3*5)+(2*1)+(1*9)=182
182 % 10 = 2
So 99365-19-2 is a valid CAS Registry Number.
99365-19-2Relevant articles and documents
Oleanene glycosides of the aerial parts and seeds of Bupleurum falcatum and the aerial parts of Bupleurum rotundifolium, and their evaluation as anti-hepatitis agents
Nakahara, Yuko,Okawa, Masafumi,Kinjo, Junei,Nohara, Toshihiro
, p. 1329 - 1339 (2011)
To facilitate effective resource utilization, we have investigated triterpene saponins such as saikosaponin from the aerial parts of Bupleurum (B.) falcatum L., which are commonly discarded. Seven oleanene saponins were isolated from this plant; they were classified as the 13,28-epoxy type, 12-ene type, 9(11),12-diene type, and 28-acid type on the basis of their structural characteristics. For comparison, we also examined the oleanene saponins of the seeds of B. falcatum and the aerial parts of B. rotundifolium L. to obtain seven saponins and one sapogenol from the former and thirteen oleanene saponins from the latter. Several compounds obtained from them were investigated for their hepatoprotective activity and hepatotoxicity. The 13,28-epoxy type saponins had hepatoprotectivity. Ursane type showed hepatotoxicity from middle concentration. The 11,13(18)-diene type saponins did not express hepatoprotective activity. The 28-acid type saponin which has a glucosyl carboxy group showed hepatoprotective action.
New derivatives of saikosaponins
Shimizu,Amagaya,Ogihara
, p. 3349 - 3355 (2007/10/02)
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