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4-methyl-2-oxo-2H-chromen-7-yl beta-D-ribopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66912-32-1

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66912-32-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66912-32-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,1 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66912-32:
(7*6)+(6*6)+(5*9)+(4*1)+(3*2)+(2*3)+(1*2)=141
141 % 10 = 1
So 66912-32-1 is a valid CAS Registry Number.

66912-32-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylumbellifer-7-yl β-D-ribopyranoside

1.2 Other means of identification

Product number -
Other names 4-Methyl-7-((2S,3R,4R,5R)-3,4,5-trihydroxy-tetrahydro-pyran-2-yloxy)-chromen-2-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:66912-32-1 SDS

66912-32-1Downstream Products

66912-32-1Relevant academic research and scientific papers

Glycosyl coumarin carbonic anhydrase IX and XII inhibitors strongly attenuate the growth of primary breast tumors

Touisni, Nadia,Maresca, Alfonso,McDonald, Paul C.,Lou, Yuanmei,Scozzafava, Andrea,Dedhar, Shoukat,Winum, Jean-Yves,Supuran, Claudiu T.

, p. 8271 - 8277 (2012/02/06)

A series of 7-substituted coumarins incorporating various glycosyl moieties were synthesized and investigated for the inhibition of the zinc enzyme carbonic anhydrase (CA, EC 4.2.1.1). These coumarins were very weak or ineffective as inhibitors of the housekeeping, offtarget isoforms CA I and II, but some of them inhibited tumor-associated CA IX and XII in the low nanomolar range. They also significantly inhibited the growth of primary tumors by the highly aggressive 4T1 syngeneic mouse mammary tumor cells at 30 mg/kg, constituting interesting candidates for the development of conceptually novel anticancer drugs. Because CA IX is overexpressed in hypoxic tumors and exhibits very limited expression in normal tissues, such compounds may be useful for treating cancers not responsive to classic chemo- and radiotherapy.

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