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Olean-12-ene-3β,16β,21β,23,28-pentol is a naturally occurring pentacyclic triterpenoid alcohol that belongs to the oleanane group of triterpenes. It is found in certain plants and herbs and is known for its diverse biological activities, including potential anti-inflammatory, anti-cancer, and anti-diabetic properties. Olean-12-ene-3β,16β,21β,23,28-pentol has also demonstrated promise in supporting liver health, reducing cholesterol levels, and exhibiting hepatoprotective, antioxidant, and anti-aging effects in traditional medicine. Olean-12-ene-3β,16β,21β,23,28-pentol is an area of ongoing research for its potential therapeutic applications and may offer a range of health benefits.

19942-02-0

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19942-02-0 Usage

Uses

Used in Pharmaceutical Industry:
Olean-12-ene-3β,16β,21β,23,28-pentol is used as a therapeutic agent for its potential anti-inflammatory, anti-cancer, and anti-diabetic properties. Its diverse biological activities make it a promising candidate for the development of new drugs to treat various health conditions.
Used in Liver Health Supplements:
Olean-12-ene-3β,16β,21β,23,28-pentol is used as a hepatoprotective and antioxidant supplement to support liver health and reduce the risk of liver-related diseases. Its ability to protect the liver from damage and promote its overall function makes it a valuable ingredient in liver health supplements.
Used in Cholesterol-Lowering Products:
Olean-12-ene-3β,16β,21β,23,28-pentol is used as a cholesterol-lowering agent to help reduce high cholesterol levels and maintain cardiovascular health. Its potential to lower cholesterol levels makes it a beneficial component in dietary supplements and functional foods aimed at promoting heart health.
Used in Anti-Aging Products:
Olean-12-ene-3β,16β,21β,23,28-pentol is used as an anti-aging agent in skincare and cosmetic products due to its antioxidant properties. Its ability to protect the skin from oxidative stress and promote skin health makes it a valuable ingredient in anti-aging formulations.
Used in Traditional Medicine:
Olean-12-ene-3β,16β,21β,23,28-pentol has been used in traditional medicine for its hepatoprotective, antioxidant, and anti-aging effects. Its long history of use and potential health benefits make it a valuable component in various traditional medicine formulations and practices.

Check Digit Verification of cas no

The CAS Registry Mumber 19942-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,4 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19942-02:
(7*1)+(6*9)+(5*9)+(4*4)+(3*2)+(2*0)+(1*2)=130
130 % 10 = 0
So 19942-02-0 is a valid CAS Registry Number.

19942-02-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3β,16β,21β)-olean-12-ene-3,16,21,23,28-pentol

1.2 Other means of identification

Product number -
Other names Gymnestrogenin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19942-02-0 SDS

19942-02-0Downstream Products

19942-02-0Relevant articles and documents

Triterpene saponins from Pleurospermum kamtschaticum and their biological activity

Lee, Il Kyun,Choi, Sang Un,Lee, Kang Ro

, p. 1011 - 1018 (2012)

Eleven new triterpene saponins (1-11), together with fourteen known triterpene and triterpene saponins (12-25) were isolated from a MeOH extract of Pleurospermum kamtschaticum HOFFMANN (Umbelliferae). The chemical structures of the new compounds (1-11) were determined by means of MS, 1H-NMR, 13C-NMR, correlated spectroscopy (COSY), heteronuclear multiple bond correlation (HMBC), total correlated spectroscopy (TOCSY) and nuclear Overhauser effect spectroscopy (NOESY) to be pleurosaponin A (1)-K (11). The isolated compounds were tested for their cytotoxicity against four human tumor cell lines (A549, SK-OV-3, SK-MEL-2, HCT15) in vitro using the sulforhodamine B bioassay (SRB) assay. All compounds showed little cytotoxicity against tested cell lines (IC50 >30 μM).

Molecular decodification of gymnemic acids from Gymnema sylvestre. Discovery of a new class of liver X receptor antagonists

Renga, Barbara,Festa, Carmen,De Marino, Simona,Di Micco, Simone,D'Auria, Maria Valeria,Bifulco, Giuseppe,Fiorucci, Stefano,Zampella, Angela

, p. 121 - 131 (2015)

The individual chemical components of commercial extract of Gymnema sylvestre, a medicinal plant used in the traditional systems of the Indian medicine for its antidiabetic and hypolipidemic properties, were isolated and evaluated for their capability to act as modulators of nuclear and membrane receptors involved in glucose and lipid homeostasis. The study disclosed for the first time that individual gymnemic acids are potent and selective antagonists for the β isoform of LXR. Indeed the above activity was shared by the most abundant aglycone gymnemagenin (10) whereas gymnestrogenin (11) was endowed with a dual LXRα/β antagonistic profile. Deep pharmacological investigation demonstrated that gymnestrogenin, reducing the expression of SREBP1c and ABCA1 in vitro, is able to decrease lipid accumulation in HepG2 cells. The results of this study substantiate the use of G. sylvestre extract in LXR mediated dislypidemic diseases.

GLOCHIDIOSIDE, A TRITERPENE GLYCOSIDE FROM GLOCHIDION HEYNEANUM

Srivastava, Rashmi,Kulshreshtha, Dinesh K.

, p. 2672 - 2674 (2007/10/02)

Key Word Index - Glochidion heyneanum; Euphorbiaceae; triterpenoid glycoside; glochidioside.A new triterpenoid glycoside, glochidioside, has been isolated from Glochidion heyneanum.Its structure has been established as 3β 3)-O-α-L-arabinopyranosyl)oxy>-16β-benzoyloxy-olean-12-ene-21β,23,28-triol by chemical and spectroscopic mehtods.

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