Welcome to LookChem.com Sign In|Join Free
  • or
Olean-18-en-28-oic acid,3-hydroxy,(3b)is a naturally occurring triterpenoid compound found in plants such as olive oil, basil, and rosemary. It is known for its anti-inflammatory and antioxidant properties and has been studied for its potential therapeutic applications in treating conditions such as cancer, diabetes, and cardiovascular disease.
Used in Pharmaceutical Industry:
Olean-18-en-28-oic acid,3-hydroxy,(3b)is used as a therapeutic agent for its potential in treating conditions such as cancer, diabetes, and cardiovascular disease due to its anti-inflammatory and antioxidant properties.
Used in Dietary Supplements:
Olean-18-en-28-oic acid,3-hydroxy,(3b)is used as a dietary supplement for its beneficial effects on human health, including its anti-inflammatory and antioxidant properties.
Used in Traditional Medicine:
Olean-18-en-28-oic acid,3-hydroxy,(3b)has been used in traditional medicine for its healing properties, particularly for its potential therapeutic applications in treating various conditions.

559-68-2

Post Buying Request

559-68-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

559-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 559-68-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,5 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 559-68:
(5*5)+(4*5)+(3*9)+(2*6)+(1*8)=92
92 % 10 = 2
So 559-68-2 is a valid CAS Registry Number.

559-68-2SDS

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 Morolsaeure

1.2 Other means of identification

Product number -
Other names OLEAN-18-EN-28-OIC ACID,3-HYDROXY-,(3B)-

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:559-68-2 SDS

559-68-2Upstream product

559-68-2Relevant academic research and scientific papers

Anti-AIDS agents. 48. Anti-HIV activity of moronic acid derivatives and the new melliferone-related triterpenoid isolated from Brazilian propolis

Ito,Chang,Wang,Park,Ikegaki,Kilgore,Lee

, p. 1278 - 1281 (2001)

A new triterpenoid named melliferone (1), three known triterpenoid, moronic acid (2), anwuweizonic acid (3), and betulonic acid (4), and four known aromatic compounds (5-8) were isolated from Brazilian propolis and tested for anti-HIV activity in H9 lymphocytes. Moronic acid (2) showed significant anti-HIV activity (EC50 186) and was modified to develop more potent anti-AIDS agents.

Antimicrobial activity of Schinus lentiscifolius (Anacardiaceae)

Gehrke, Ilaine T.S.,Neto, Alexandre T.,Pedroso, Marcelo,Mostardeiro, Clarice P.,Da Cruz, Ivana B.M.,Silva, Ubiratan F.,Ilha, Vinicius,Dalcol, Ionara I.,Morel, Ademir F.

, p. 486 - 491 (2013/07/26)

Ethnopharmacological relevance Schinus lentiscifolius Marchand (syn. Schinus weinmannifolius Engl) is a plant native to Rio Grande do Sul (Southern Brazil) and has been used in Brazilian traditional medicine as antiseptic and antimicrobial for the treatment of many different health problems as well as to treat leucorrhea and to assist in ulcer and wound healing. Although it is a plant widely used by the population, there are no studies proving this popular use. Material and methods The crude aqueous extract, the crude neutral methanol extract, fractions prepared from this extract (n-hexane, ethyl acetate, and n-butanol), pure compounds isolated from these fractions, and derivatives were investigated in vitro for antimicrobial activities against five Gram positive bacteria: Bacillus subtilis, Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus saprophyticus, Streptococcus pyogenes, three Gram negative bacteria: Escherichia coli, Pseudomonas aeruginosa, and Shigella sonnei, and four yeasts: Candida albicans, Candida tropicalis, Cryptococcus neoformans, and Saccharomyces cerevisiae. The isolated compound moronic acid, which is the most active, was tested against a range of other bacteria such as two Gram positive bacteria, namely, Bacillus cereus, Enterococcus spp, and six Gram negative bacteria, namely, Burkholderia cepacia, Providencia stuartii, Morganella morganii, Enterobacter cloacae, Enterobacter aerogenes, and Proteus mirabilis. Results The leaf aqueous extract (decoction) of Schinus lentiscifolius showed a broad spectrum of antibacterial activity, ranging from 125 to 250 μg/ml (MIC) against the tested bacteria and fungi. The n-hexane extract, despite being very little active against bacteria, showed an excellent antifungal activity, especially against Candida albicans (MIC=25 μg/ml), Candida tropicalis (MIC=15.5 μg/ml), and Cryptococcus neoformans, (MIC=15.5 μg/ml). From the acetate fraction (the most active against bacteria), compounds 1-6 were isolated: nonadecanol (1), moronic acid (2), gallic acid methyl ester (3), gallic acid (4), quercetin (5) and quercitrin (6). The minimal inhibitory concentration (MIC) of moronic acid between 1.5 and 3 μg/ml against most of the tested bacteria shows that it is one of the metabolites responsible for the antibacterial activity of Schinus lentiscifolius. Conclusion The antimicrobial activity and some constituents of Schinus lentiscifolius are reported for the first time. The results of the present study provide scientific basis for the popular use of Schinus lentiscifolius for a number of different health problems.

Anti-AIDS agents 81. design, synthesis, and structure-activity relationship study of betulinic acid and moronic acid derivatives as potent HIV maturation inhibitors

Qian, Keduo,Kuo, Reen-Yun,Chen, Chin-Ho,Huang, Li,Morris-Natschke, Susan L.,Lee, Kuo-Hsiung

experimental part, p. 3133 - 3141 (2010/09/18)

In our continuing study of triterpene derivatives as potent anti-HIV agents, different C-3 conformationally restricted betulinic acid (BA, 1) derivatives were designed and synthesized in order to explore the conformational space of the C-3 pharmacophore. 3-O-Monomethylsuccinyl-betulinic acid (MSB) analogues were also designed to better understand the contribution of the C-3′ dimethyl group of bevirimat (2), the first-in-class HIV maturation inhibitor, which is currently in phase IIb clinical trials. In addition, another triterpene skeleton, moronic acid (MA, 3), was also employed to study the influence of the backbone and the C-3 modification toward the anti-HIV activity of this compound class. This study enabled us to better understand the structure-activity relationships (SAR) of triterpene-derived anti-HIV agents and led to the design and synthesis of compound 12 (EC50: 0.0006 μM), which displayed slightly better activity than 2 as a HIV-1 maturation inhibitor.

Efficient synthesis of morolic acid and related triterpenes starting from betulin

Zhang, Pu,Hao, Jia,Liu, Jun,Zhang, Luyong,Sun, Hongbin

experimental part, p. 4304 - 4309 (2009/10/09)

Morolic acid (1) is a naturally occurring pentacyclic triterpene whose derivatives exhibit promising anti-HIV and other biological activities. An efficient synthesis of 1 has been accomplished in 11 steps with a total yield of 24% starting from betulin. S

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 559-68-2