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SAGITTATOSIDE A, a natural compound derived from the roots of plants such as Sagittaria sagittifolia, belongs to the class of triterpenoid saponins. These compounds are recognized for their wide range of pharmacological activities, including anti-inflammatory, antioxidant, and anti-cancer properties. SAGITTATOSIDE A has demonstrated its potential in neuroprotection and may contribute to the treatment of neurodegenerative diseases, making it a promising candidate for further research and development in the medical field.

118525-35-2

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118525-35-2 Usage

Uses

Used in Pharmaceutical Industry:
SAGITTATOSIDE A is used as a therapeutic agent for its anti-inflammatory properties, helping to reduce inflammation in various conditions.
SAGITTATOSIDE A is used as an antioxidant, protecting cells from oxidative stress and potentially delaying the aging process and the onset of age-related diseases.
SAGITTATOSIDE A is used as an anti-cancer agent, exhibiting potential to combat cancer cells and inhibit tumor growth, as demonstrated in in-vitro and in-vivo studies.
Used in Neuroprotection:
SAGITTATOSIDE A is used as a neuroprotective agent for its potential to protect neurons and mitigate damage in neurodegenerative diseases, offering a new avenue for treatment and management of such conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 118525-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,2 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118525-35:
(8*1)+(7*1)+(6*8)+(5*5)+(4*2)+(3*5)+(2*3)+(1*5)=122
122 % 10 = 2
So 118525-35-2 is a valid CAS Registry Number.

118525-35-2SDS

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 sagittatoside A

1.2 Other means of identification

Product number -
Other names SagittatosideA

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:118525-35-2 SDS

118525-35-2Relevant academic research and scientific papers

Efficient preparation of rare Sagittatoside A from epimedin A, by recyclable aqueous organic two-phase enzymatic hydrolysis

Shen, Yuping,Lu, Yi,Gao, Jing,Zhu, Yeting,Wang, Man,Jing, Shunli,Xu, Lili,Yang, Huan,Jia, Xiaobin

, p. 3095 - 3102 (2019)

The rare secondary flavonol glycoside Sagittatoside A has much better in vivo bioactivities than epimedin A in Epimedii Folium. However, its current preparation methods are of low efficiency, with byproducts generated. The aim of this study was to establi

EPIMEDINS A, B AND C, FLAVONOID GLYCOSIDES OF EPIMEDIUM KOREANUM HERBS

Oshima, Yoshiteru,Okamoto, Maki,Hikino, Hiroshi

, p. 935 - 938 (2007/10/02)

Three new flavonoid glycosides, epimedins A, B and C, have been isolated from Epimedium koreanum herbs, the structures of which have been elucidated on the basis of chemical and spectroscopic data as shown in formulas I, II and III, respectively.

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