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929881-46-9

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929881-46-9 Usage

General Description

Cucumegastigmane I is a natural chemical compound isolated from the roots of Cucumis sativus L. It has been found to possess significant anti-inflammatory and anticancer activities. Cucumegastigmane I has been shown to inhibit the production of nitric oxide and prostaglandin E2, both of which are involved in inflammation. Additionally, it has demonstrated cytotoxic effects on cancer cells, making it a potential candidate for the development of new anticancer drugs. Further research on the pharmacological properties and therapeutic potential of cucumegastigmane I is warranted to fully elucidate its potential applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 929881-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,9,8,8 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 929881-46:
(8*9)+(7*2)+(6*9)+(5*8)+(4*8)+(3*1)+(2*4)+(1*6)=229
229 % 10 = 9
So 929881-46-9 is a valid CAS Registry Number.

929881-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4S)-4-[(1E,3S)-3,4-Dihydroxy-1-buten-1-yl]-4-hydroxy-3,5,5-trime thyl-2-cyclohexen-1-one

1.2 Other means of identification

Product number -
Other names -

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:929881-46-9 SDS

929881-46-9Downstream Products

929881-46-9Relevant articles and documents

Chodatiionosides A and B: two new megastigmane glycosides from Chorisia chodatii leaves

Samy, Mamdouh Nabil,Fahim, John Refaat,Sugimoto, Sachiko,Otsuka, Hideaki,Matsunami, Katsuyoshi,Kamel, Mohamed Salah

, p. 321 - 328 (2017)

Phytochemical investigation of Chorisia chodatii Hassl. leaves led to the isolation of an unusual rearranged megastigmane glycoside; chodatiionoside A (1) and another new megastigmane glycoside; chodatiionoside B (2), together with three known megastigmane glycosides (3–5) and one known flavonoid glycoside (6). Their structures were elucidated by spectroscopic methods including 1D and 2D NMR experiments (1H, 13C, DEPT, COSY, HSQC and HMBC) in combination with HR-ESI–MS, CD and modified Mosher’s method. As a result, chodatiionoside A has been elucidated as a first example of an unusual rearranged form of megastigmane.

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