clematoside S

Base Information

• Chemical Name: clematoside S
• CAS No.: 72629-76-6
• Molecular Formula: C46H74 O16
• Molecular Weight: 883.084
• Mol file: 72629-76-6.mol

Synonyms:ClematosideS; Prosapogenin CP6; Saponin CP6

Chemical Property of clematoside S

Chemical Property:

• Boiling Point: 975.1±65.0 °C(Predicted)
• PKA: 4.63±0.70(Predicted)
• Flash Point: 280.8oC
• PSA: 254.52000
• Density: 1.38±0.1 g/cm3 (20 ºC 760 Torr)
• LogP: 1.98440

Purity/Quality:

95%-98% ^*data from raw suppliers

Prosapogenin CP6 ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of clematoside S

There total 26 articles about clematoside S which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 71.0%

hederagenin 3-O-(3,4-di-O-acetyl-α-L-arabinopyranosyl)-(1->3)-α-L-rhamnopyranosyl-(1->2)-4-O-acetyl-α-L-arabinopyranoside (1157918-38-1) → hederagenin?3?O?[β?D?xylopyranosyl?(1→3)]?[α?L?rhamnopyranosyl?(1→2)]?α?L?arabinopyranoside (29321-28-6,30994-75-3,72629-76-6,80666-65-5)

Guidance literature:

With methanol; sodium methylate; at 20 ℃; for 3h;

DOI:10.1248/cpb.57.198

Reference yield:

hederagenin-3-O-β-D-xylopyranosyl-(1->3)-O-α-L-rhamnopyranosyl-(1->2)-O-α-L-arabinopyranosyl-28-O-α-L-rhamnopyranosyl-(1->4)-O-β-D-glucopyranosyl-(1->6)-O-β-D-glucopyranosyl ester (119742-55-1) → hedaragenin (465-99-6) + prosapogenin (17184-21-3) + sapindoside B (29321-28-6,72629-76-6,80666-65-5,30994-75-3) + alpha-Hederin (27013-91-8)

Guidance literature:

With Bacteroides JY-6; Bifidobacterium K-111; In various solvent(s); at 37 ℃; for 36h;

DOI:10.1248/bpb.21.360

Reference yield:

3-O-β-D-xylopyranosyl(1->3)-α-L-rhamnopyranosyl(1->2)-α-L-arabinopyranosyl hederagenin 28-O-β-D-xylopyranosyl(1->4)-β-D-glycopyranosyl(1->6)-β-D-glycopyranoside → hedaragenin (465-99-6) + sapindoside B (29321-28-6,72629-76-6,80666-65-5,30994-75-3)

Guidance literature:

With hydrogenchloride; In ethanol; for 0.666667h; Heating;

upstream raw materials:

methanol

mukurozisaponin Y₁

hederagenin 3-O-β-D-glucopyranosyl-(1-4)-β-D-xylopyranosyl-(1-3)-α-L-rhamnopyranosyl-(1-2)-α-L-arabinopyranoside

hederagenin 3-O-β-D-glucopyranosyl-(1-4)-β-D-glucopyranosyl-(1-4)-β-D-xylopyranosyl-(1-3)-α-L-rhamnopyranosyl-(1-2)-α-L-arabinopyranoside

Downstream raw materials:

D-Xylose

L-rhamnose

L-(+)-arabinose

hederagenin

Refernces

• 1、 Asao, Yasunobu,Morikawa, Toshio,Yuanyuan,Okamoto, Masaki,Hamao, Makoto,Matsuda, Hisashi,Muraoka, Osamu,Yuan, Dan,Yoshikawa, Masayuki. "Structures of acetylated oleanane-type triterpene saponins, rarasaponins IV, V, and VI, and anti-Hyperlipidemic constituents from the pericarps of sapindus rarak". experimental part. p. 198 - 203. Retrieved 2009/09/25.
• 2、 Panov,Grishkovets,Kachala,Shashkov. "Triterpene glycosides from Kalopanax septemlobum. II. Glycosides E, K, and L from leaves of Kalopanax septemlobum var. maximowiczii introduced to Crimea". . p. 322 - 325. Retrieved 2008/02/01.