114906-74-0

Basic information

• Product Name: Ciwujianoside C3
• Synonyms: Ciwujianoside C3
• CAS NO: 114906-74-0
• Molecular Formula: C₅₃H₈₆O₂₁
• Molecular Weight: 1059.24
• Mol File: 114906-74-0.mol

Chemical Properties

• Appearance: /
• Density: 1.43±0.1 g/cm3(Predicted)
• PKA: 12.50±0.70(Predicted)
• CAS DataBase Reference: Ciwujianoside C3(CAS DataBase Reference)
• NIST Chemistry Reference: Ciwujianoside C3(114906-74-0)
• EPA Substance Registry System: Ciwujianoside C3(114906-74-0)

Safety Data

• Hazardous Substances Data: 114906-74-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Ciwujianoside C3 is used as an anti-inflammatory agent for its ability to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Ciwujianoside C3 is used as an anti-viral agent for its potential to inhibit viral replication and protect against viral infections.
Ciwujianoside C3 is used as an anti-tumor agent for its capacity to inhibit the growth of various cancer cell lines and stimulate the immune system to combat cancer.
Used in Immunotherapy:
Ciwujianoside C3 is used as an immunostimulant to enhance the immune system's response to infections and diseases.
Used in Autoimmune Disease Treatment:
Ciwujianoside C3 is used as a therapeutic agent for autoimmune diseases, potentially modulating the immune system to reduce the severity of these conditions.
Used in Cardiovascular Disease Treatment:
Ciwujianoside C3 is used as a protective agent for cardiovascular health, potentially reducing the risk of cardiovascular disorders through its anti-inflammatory and other beneficial properties.
Used in Liver Disease Treatment:
Ciwujianoside C3 is used as a hepatoprotective agent for liver diseases, offering potential therapeutic benefits due to its protective effects on liver function and health.

Upstream product

• 114912-35-5 ciwujianoside D₁ 

Downstream Products

• 5328-37-0 L-arabinose 
• 3615-41-6 L-Rhamnose 
• 50-99-7 D-glucose 
• 508-02-1 Oleanolic acid 

Relevant articles and documents

Synthesis, biological evaluation and structure-activity relationship studies of hederacolchiside E and its derivatives as potential anti-Alzheimer agents

Inspired by the previously reported neuroprotective activity of hederacolchiside E (1), we synthesized hederacolchiside E for the first time along with eleven of its derivatives. The neuroprotective effects of these compounds were further evaluated agains

Saponins from Leaves of Acanthopanax senticosus HARMS., Ciwujia; Structures of Ciwujianosides B, C1, C2, C3, C4, D1, D2 and E

Eleven triterpenoid saponins were isolated from the leaves of a Chinese folk medicine, Acanthopanax senticosus (RUPR. et MAXIM) HARMS.Of these compounds, three were identified as known saponins.The structures of eight new saponins named ciwujianosides B (1), C1, (2), C2 (3), C3 (4), C4 (5), D1 (6), D2 (7), and E (8) were elucidated to be as follows: (1), 3-O-α-rhamnopyranosyl-(1->2)-β-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (2), 3-O-α-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (3), 3-O-α-rhamnopyranosyl-(1->2)-α-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (4), 3-O-α-arabinopyranosyl oleanolic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl(1->6)-β-glucopyranosyl ester; (5), 3-O-α-rhamnopyranosyl-(1->2)-α-arabinopyranosyl oleanolic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (6), 3-O-α-arabinopyranosyl oleanolic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl(1->6)-β-glucopyranosyl ester; (7), 3-O-α-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-b-glucopyranosyl-30-norolean-12,20(29)-dien-28-oic acid 28-O-α-rhamnopyranosyl-(1->4)-6-O-acetyl-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (8), 3-O-α-rhamnopyranosyl-(1->2)-α-arabinopyranosyl-30-norolean-12,20(29)-dien-28-oic acid.Keywords - Acanthopanax senticosus; Araliaceae; saponin; Chinese folk medicine; ciwujianoside; oleanolic acid glycoside; noroleanolic acid glycoside; 30-norolean-12,20(29)-dien-28-oic acid; ciwujia