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C10465, also known as Iridin, is a glycosyloxyisoflavone derived from the iris species. It is characterized by the presence of a beta-D-glucopyranosyl residue at position 7, which is connected to the irigenin molecule through a glycosidic linkage. Iridin exhibits a range of biological activities, including antioxidant, antidiabetic, and alpha-amylase inhibitory properties, making it a versatile compound with potential applications in various industries.

491-74-7

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491-74-7 Usage

Uses

Used in Pharmaceutical Industry:
C10465 is used as a dual Src/Abl tyrosine kinase inhibitor for its potent antiproliferative activity. This makes it a promising candidate for the development of novel therapeutics targeting various diseases, including cancer.
Used in Antioxidant Applications:
C10465 is used as an antioxidant agent due to its ability to neutralize free radicals and protect cells from oxidative stress. This property can be harnessed in the development of supplements and nutraceuticals aimed at promoting overall health and well-being.
Used in Antidiabetic Applications:
C10465 is used as an antidiabetic agent, as it exhibits inhibitory effects on alpha-amylase, an enzyme involved in the breakdown of carbohydrates. This can help in managing blood sugar levels and may be useful in the development of treatments for diabetes.
Used in Lactate Dehydrogenase Inhibition:
C10465 is used as a lactate dehydrogenase inhibitor, which can be beneficial in various medical applications, such as the treatment of certain metabolic disorders and the enhancement of athletic performance.

Check Digit Verification of cas no

The CAS Registry Mumber 491-74-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 491-74:
(5*4)+(4*9)+(3*1)+(2*7)+(1*4)=77
77 % 10 = 7
So 491-74-7 is a valid CAS Registry Number.
InChI:InChI=1/C24H26O13/c1-32-13-5-9(4-11(26)22(13)33-2)10-8-35-12-6-14(23(34-3)19(29)16(12)17(10)27)36-24-21(31)20(30)18(28)15(7-25)37-24/h4-6,8,15,18,20-21,24-26,28-31H,7H2,1-3H3/t15-,18-,20+,21-,24-/m1/s1

491-74-7SDS

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 iridin

1.2 Other means of identification

Product number -
Other names 5-hydroxy-3-(3-hydroxy-4,5-dimethoxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one

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:491-74-7 SDS

491-74-7Upstream product

491-74-7Relevant academic research and scientific papers

Long-chain fatty acid acylated derivatives of isoflavone glycosides from the rhizomes of Iris domestica

Li, Jiayuan,Liu, Yanfei,Ni, Gang,Wang, Renzhong,Yu, Dequan

, (2021/11/01)

Six undescribed long-chain fatty acid esters of isoflavone glycosides were obtained from the rhizomes of Iris domestica (L.). Their structures were elucidated by comprehensive spectroscopic data, alkaline hydrolysis, and acid hydrolysis. This is the first report of the long-chain (C14–C18) fatty acid derivatives of isoflavone glycosides from natural products. Belamcandnoate B and D exhibited moderate cytotoxic activities against HCT-116, HepG2, and BGC823 cell lines with IC50 values of 1.69–6.86 μM. Belamcandnoate B and E exhibited 72.27 and 58.98% inhibitory activities, respectively, against Fe2+/cysteine-induced liver microsomal lipid peroxidation at a concentration of 10 μM.

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