Tenacissoside I

>=98%(HPLC)

Reagent Code: #241163
fingerprint
CAS Number 191729-44-9

science Other reagents with same CAS 191729-44-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 814.965 g/mol
Formula C₄₄H₆₂O₁₄
inventory_2 Storage & Handling
Storage 2-8ºC

description Product Description

Tenacissoside I is a C-21 steroidal glycoside isolated from the stems of Marsdenia tenacissima. Used in research for its potential anti-cancer properties, particularly in studies involving apoptosis induction in tumor cells. Shows activity in inhibiting cell proliferation in certain types of liver and lung cancer cell lines. Also investigated for its role in modulating signaling pathways related to inflammation and oxidative stress. Due to its natural origin and structural complexity, it serves as a lead compound in the development of novel chemotherapeutic agents. Limited to laboratory and preclinical studies; not used in clinical medicine.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 20 mg
10-20 days ฿12,070.00
Tenacissoside I
No image available

Tenacissoside I is a C-21 steroidal glycoside isolated from the stems of Marsdenia tenacissima. Used in research for its potential anti-cancer properties, particularly in studies involving apoptosis induction in tumor cells. Shows activity in inhibiting cell proliferation in certain types of liver and lung cancer cell lines. Also investigated for its role in modulating signaling pathways related to inflammation and oxidative stress. Due to its natural origin and structural complexity, it serves as

Tenacissoside I is a C-21 steroidal glycoside isolated from the stems of Marsdenia tenacissima. Used in research for its potential anti-cancer properties, particularly in studies involving apoptosis induction in tumor cells. Shows activity in inhibiting cell proliferation in certain types of liver and lung cancer cell lines. Also investigated for its role in modulating signaling pathways related to inflammation and oxidative stress. Due to its natural origin and structural complexity, it serves as a lead compound in the development of novel chemotherapeutic agents. Limited to laboratory and preclinical studies; not used in clinical medicine.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...