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35110-20-4

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35110-20-4 Usage

Uses

A metabolite of Diosmetin (D485000)

Check Digit Verification of cas no

The CAS Registry Mumber 35110-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,1 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35110-20:
(7*3)+(6*5)+(5*1)+(4*1)+(3*0)+(2*2)+(1*0)=64
64 % 10 = 4
So 35110-20-4 is a valid CAS Registry Number.

35110-20-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name diosmentin-7-O-β-D-glucuronopyranoside

1.2 Other means of identification

Product number -
Other names DIOSMETIN-7-O-GLUCURONIDE

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:35110-20-4 SDS

35110-20-4Downstream Products

35110-20-4Relevant articles and documents

Enzymatic Synthesis of Bioactive O-Glucuronides Using Plant Glucuronosyltransferases

Yue, Tian,Chen, Ridao,Chen, Dawei,Liu, Jimei,Xie, Kebo,Dai, Jungui

, p. 6275 - 6284 (2019/06/13)

Many O-glucuronides exhibiting various pharmacological activities have been found in nature and in drug metabolism. The glucuronidation of bioactive natural products or drugs to generate glucuronides with better activity and druggability is important in drug discovery and research. In this study, by using two uridine diphosphate (UDP)-dependent glucuronosyltransferases (GATs, UGT88D4 and UGT88D7) from plants, we developed two glucuronidation approaches, pure enzyme catalysis in vitro and recombinant whole-cell catalysis in vivo, to efficiently synthesize bioactive O-glucuronides by the glucuronidation of natural products. In total, 14 O-glucuronides with different structures, including flavonoids, anthraquinones, coumarins, and lignans, were obtained, 7 of which were new compounds. Furthermore, one of the biosynthesized O-glucuronides, kaempferol-7-O-β-d-glucuronide (3a), potently inhibited protein tyrosine phosphatase (PTP) 1B with an IC50 value of 8.02 × 10-6 M. Some of the biosynthesized O-glucuronides also exhibited significant antioxidant activities.

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