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Tinosporide, a diterpenoid lactone, is a natural chemical compound derived from the Tinospora cordifolia plant, commonly known as Guduchi or Giloy. It possesses a range of potential medicinal properties, such as anti-inflammatory, immune-modulating, and antioxidant effects, making it a promising candidate for various therapeutic applications.

17226-41-4

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17226-41-4 Usage

Uses

Used in Pharmaceutical Applications:
Tinosporide is used as a therapeutic agent for its potential in treating various ailments, including diabetes, arthritis, and cancer. Its anti-inflammatory properties make it a promising candidate for the treatment of inflammatory diseases.
Used in Immune System Support:
Tinosporide is used as an immune-modulating agent, supporting the immune system and potentially enhancing its ability to fight off infections and diseases.
Used in Antioxidant Applications:
Tinosporide is used as an antioxidant, protecting against oxidative stress and potentially reducing the risk of various diseases associated with oxidative damage.
Used in Modern Medicine Research:
Tinosporide is used as a subject of research in modern medicine, with ongoing studies exploring its therapeutic potential and possible applications in the development of new treatments for various health conditions. Further research is needed to fully understand the extent of its benefits and how it can be best utilized in medical practice.

Check Digit Verification of cas no

The CAS Registry Mumber 17226-41-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,2 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17226-41:
(7*1)+(6*7)+(5*2)+(4*2)+(3*6)+(2*4)+(1*1)=94
94 % 10 = 4
So 17226-41-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H22O7/c1-18-7-11(9-4-6-24-8-9)25-16(21)10(18)3-5-19(2)14(18)12-13-15(26-13)20(19,23)17(22)27-12/h4,6,8,10-15,23H,3,5,7H2,1-2H3/t10-,11-,12+,13+,14+,15+,18-,19-,20+/m1/s1

17226-41-4SDS

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 palmarin

1.2 Other means of identification

Product number -
Other names Palmarin

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:17226-41-4 SDS

17226-41-4Downstream Products

17226-41-4Relevant academic research and scientific papers

Studies on the Constituents of Jateorhiza palmata Miers (Colombo Root), II. - Separation and Structure of Six New Furanoid Diterpene Glucosides: Palmatoside B, C, D, E, F, and G

Yonemitsu, Michiko,Fukuda, Naomichi,Kimura, Takeatsu,Komori, Tetsuya

, p. 193 - 197 (2007/10/02)

Six new furanoid diterpene glucosides, named palmatoside B(1), C(2), D(3), E(4), F(5), and G(6) were isolated from the dried roots of Jateorhiza palmata Miers (Colombo root).The structures were elucidated by chemical and spectroscopic evidence to be 4-O-(β-D-glucopyranosyl)chasmanthin, 4-O-(β-D-glucopyranosyl)columbin, 4-O-(β-D-glucopyranosyl)isocolumbin, 4-O-(β-D-glucopyranosyl)isojateorin, 4-O-(β-D-glucopyranosyl)jateorin, and -2-(3-furanyl)-6a-(β-D-glucopyranosyloxymethyl)1,2,4a,5,6,6a,7,10,10a,10b-decahydro-10b-methyl-4H-naphthopyran-4,7-dione, respectively

Studies on the Constituents of Jateorhiza palmata Miers (Colombo Root), I.- Separation and Structure of a New Furanoid Diterpene Glucoside (Palmatoside A)

Yonemitsu, Michiko,Fukuda, Naomichi,Kimura, Takeatsu,Komori, Tetsuya

, p. 1327 - 1333 (2007/10/02)

In addition to five already known diterpenoids, columbin (2), isocolumbin (3), chasmanthin (4), palmarin (5), and isojateorin (6), a new furanoid diterpene glucoside named palmatoside A (1) was isolated from the dried roots of Jateorhiza palmata Miers (Colombo root).The structure of 1 was elucidated by chemical and spectroscopic evidence to be 4-O-(β-D-glucopyranosyl)palmarin.

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