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Serratagenic acid is a naturally occurring chemical compound found in the plant species Satureja douglasii, commonly known as yerba buena. It belongs to the class of monoterpenoid acids and exhibits various biological activities, such as anti-inflammatory, antimicrobial, and antioxidant properties. Serratagenic acid is structurally similar to other monoterpenoid acids like rosmarinic acid and carnosic acid, and it is known for its potential therapeutic applications in treating various health conditions, including inflammation, infections, and oxidative stress-related disorders. The compound's unique chemical structure and diverse pharmacological effects make it an interesting subject for further research and development in the field of natural products and medicinal chemistry.

6488-64-8

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6488-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6488-64-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,8 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6488-64:
(6*6)+(5*4)+(4*8)+(3*8)+(2*6)+(1*4)=128
128 % 10 = 8
So 6488-64-8 is a valid CAS Registry Number.
InChI:InChI=1/C30H46O5/c1-25(2)20-9-12-29(6)21(27(20,4)11-10-22(25)31)8-7-18-19-17-26(3,23(32)33)13-15-30(19,24(34)35)16-14-28(18,29)5/h7,19-22,31H,8-17H2,1-6H3,(H,32,33)(H,34,35)/t19-,20?,21-,22+,26?,27+,28-,29-,30+/m1/s1

6488-64-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β-hydroxy-olean-12-ene-28,29-dioic acid

1.2 Other means of identification

Product number -
Other names serratagenic acid

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:6488-64-8 SDS

6488-64-8Downstream Products

6488-64-8Relevant academic research and scientific papers

Chemical components from Metapanax delavayi leaves and their anti-BHP activities in vitro

Sun, Chongzhi,Wu, Yang,Jiang, Bei,Peng, Ying,Wang, Mengyue,Li, Jiaxun,Li, Xiaobo

, p. 56 - 60 (2019/02/15)

Two previously undescribed oleanane-type triterpene saponins named liangwanosides III–IV, and one undescribed eudesmane glycoside named liangwanoside A were obtained from the leaves of Metapanax delavayi, a Chinese folk medicine especially for tea used in Yunnan, together with four known compounds. The structures of the undescribed compounds were determined by detailed spectroscopic (1D/2D NMR), HR-ESI-MS data analysis and chemical evidence. The activity against human benign prostate hyperplasia was evaluated with BPH-1 cell line. Most of the isolated compounds showed moderate inhibitory activity against BPH-1 cells at 100 and 50 μM in vitro.

New approaches to the structural modification of olean-type pentacylic triterpenes via microbial oxidation and glycosylation

Zhu, Yu-Yao,Qian, Li-Wu,Zhang, Jian,Liu, Ji-Hua,Yu, Bo-Yang

experimental part, p. 4206 - 4211 (2011/07/08)

Microbial transformation of 4 olean-type pentacyclic triterpenes (OPTs), 3-oxo oleanolic acid (1), 3-acetyl oleanolic acid (2), oleanolic acid (3), and esculentoside A (4) was studied. After the screening of 12 strains of microbes, preparative biotransformation by two strains of Streptomyces griseus ATCC 13273 and Aspergillus ochraceus CICC 40330 resulted in the isolation of 10 metabolites. The microbial catalyzed high efficient regio-selective methyl oxidation and glycosylation were discovered, which could be provided as an alternative method to expand the structural diversity of OPTs. All the structures of the metabolites were elucidated unambiguously by ESI-MS, 1H NMR, 13C NMR, and 2D-NMR spectroscopy.

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