80666-65-5

Basic information

• Product Name: clemontanoside C
• Synonyms: clemontanoside C
• CAS NO: 80666-65-5
• Molecular Formula: C₄₆H₇₄O₁₆
• Molecular Weight: 883.07016
• Mol File: 80666-65-5.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 975.1±65.0 °C(Predicted)
• Appearance: /
• Density: 1.38±0.1 g/cm3(Predicted)
• PKA: 4.63±0.70(Predicted)
• CAS DataBase Reference: clemontanoside C(CAS DataBase Reference)
• NIST Chemistry Reference: clemontanoside C(80666-65-5)
• EPA Substance Registry System: clemontanoside C(80666-65-5)

Safety Data

• Hazardous Substances Data: 80666-65-5(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 87733-76-4 mukurozisaponin Y₁ 
• 29781-27-9 hederagenin 3-O-β-D-glucopyranosyl-(1-4)-β-D-xylopyranosyl-(1-3)-α-L-rhamnopyranosyl-(1-2)-α-L-arabinopyranoside 
• 76729-67-4 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 
• 87733-78-6 hederagenin 3-O-(4-O-acetyl-β-D-xylopyranosyl)-(1->3)-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside 
• 87733-76-4 mukurozi-saponin Y₁ 
• 119742-55-1 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 
• 87733-79-7 hederagenin 3-O-(3,4-O-di-acetyl-α-L-arabinopyranoside)-(1->3)-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside 
• 87781-65-5 mukurozi-saponin Y₂ 
• 29781-27-9 C₅₂H₈₄O₂₁ 
• 76729-67-4 hederagenin 3-O-β-D-glucopyranosyl-(1->4)-β-D-glucopyranosyl-(1->4)-β-D-ribopyranosyl-(1->3)-α-L-rhamnopyranosyl-(1->2)-α-L-arabinopyranoside 
• 87733-79-7 C₅₀H₇₈O₁₈ 
• 104494-27-1 hishoushi-saponin A 
• 1157918-38-1 hederagenin 3-O-(3,4-di-O-acetyl-α-L-arabinopyranosyl)-(1->3)-α-L-rhamnopyranosyl-(1->2)-4-O-acetyl-α-L-arabinopyranoside 

Downstream Products

• 87-72-9 D-Xylose 
• 73-34-7 L-rhamnose 
• 87-72-9 L-(+)-arabinose 
• 465-99-6 hederagenin 
• 27013-91-8 hederagenin 3-O-α-L-rhamnopyranosyl-(1-2)-α-L-arabinopyranoside 
• 17184-21-3 hederogenin 3-O-α-L-arabinopyranoside 
• 27013-91-8 alpha-Hederin 

Relevant articles and documents

Antimicrobially active hederagenin glycosides from Cephalaria elmaliensis

A phytochemical investigation of the aerial parts of Cephalaria elmaliensis resulted in the isolation of ten hederagenin-type triterpene saponins (1-10) including three new ones, elmalienoside A (1), elmalienoside B (2), elmalienoside C (3), and two known flavonoid glycosides (11-12). Their structures were identified by extensive spectroscopic techniques (1D and 2D NMR, HR ESIMS) and chemical evidence. The antimicrobial activity of the extracts and the pure compounds was evaluated by the MIC method. According to the results, all pure compounds including the new ones were found to be very active against both gram-positive and gram-negative bacteria. Georg Thieme Verlag KG Stuttgart · New York.

Triterpene glycosides from Kalopanax septemlobum. 1. Glycosides A, B, C, F, G1, G2, I2, H, and J from leaves of Kalopanax septemlobum var. maximowichii introduced to Crimea

Eight known glycosides of hederagenin and the new triterpene glycoside 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-6-O-acetyl-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl ester of hederagenin were isolated by chromatographic methods from leaves of Kalopanax septemlobum var. maximowichii introduced to Crimea. The known 3-O-α-L-arabinopyranosyl-28-O-α-L-rhamnopyranosyl-(1→4) -O-6-O-acetyl-β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl ester of hederagenin was observed for the first time in Kalopanax septemlobum. 2005 Springer Science + Business Media, Inc.

Metabolism of kalopanaxsaponin K by human intestinal bacteria and antirheumatoid arthritis activity of their metabolites.

When kalopanaxsaponin K (KPK) from Kalopanax pictus was incubated for 24 h at 37 degrees C with human intestinal microflora, KPK was mainly metabolized to kalopanaxsaponin I (KPI) via kalopanaxsaponin H (KPH) rather than via kalopanaxsaponin J (KPJ), and then transformed to kalopanaxsaponin A (KPA) and hederagenin. Bacteroides sp., and Bifidobacterium sp. and Fusobacterium sp. transformed KPK to KPI and KPA and hederagenin via KPH or KPJ. However, Lactobacillus sp. and Streptococcus sp. transformed KPK to KPI, KPA, and hederagenin only via KPJ. The metabolite KPA of KPK showed potent antirheumatoid arthritis activity.