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1,4-Benzenedicarboxamide,N1,N4-bis[4-(4,5-dihydro-1H-imidazol-2-yl)phenyl]-2-fluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21696-09-3

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21696-09-3 Usage

Chemical class

Benzenedicarboxamide derivative

Functional groups

Fluoro-substituted phenyl rings, imidazolyl group

Pharmaceutical industry use

Potential antitumor and antineoplastic properties

Chemical structure

Unique structure with two fluoro-substituted phenyl rings and an imidazolyl group

Interaction with biological targets

Ability to interact with specific biological targets, potentially leading to therapeutic effects

Mechanisms of action

Not fully understood, but may involve interaction with cellular targets to inhibit tumor growth

Therapeutic potential

Shows promise as a potential drug candidate for the treatment of various types of cancer

Further research needed

Additional studies are required to fully understand its mechanisms of action and therapeutic potential
Please note that this list is based on the provided material and may not be exhaustive. Further research and information may reveal additional properties and specific content related to this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 21696-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,9 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21696-09:
(7*2)+(6*1)+(5*6)+(4*9)+(3*6)+(2*0)+(1*9)=113
113 % 10 = 3
So 21696-09-3 is a valid CAS Registry Number.

21696-09-3SDS

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 1-N,4-N-bis[4-(4,5-dihydro-1H-imidazol-2-yl)phenyl]-2-fluorobenzene-1,4-dicarboxamide

1.2 Other means of identification

Product number -
Other names ',4''-di-2-imidazolin-2-yl

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:21696-09-3 SDS

21696-09-3Downstream Products

21696-09-3Relevant academic research and scientific papers

Identification and Structure-Activity Relationships of Novel Compounds that Potentiate the Activities of Antibiotics in Escherichia coli

Haynes, Keith M.,Abdali, Narges,Jhawar, Varsha,Zgurskaya, Helen I.,Parks, Jerry M.,Green, Adam T.,Baudry, Jerome,Rybenkov, Valentin V.,Smith, Jeremy C.,Walker, John K.

, p. 6205 - 6219 (2017/08/02)

In Gram-negative bacteria, efflux pumps are able to prevent effective cellular concentrations from being achieved for a number of antibiotics. Small molecule adjuvants that act as efflux pump inhibitors (EPIs) have the potential to reinvigorate existing antibiotics that are currently ineffective due to efflux mechanisms. Through a combination of rigorous experimental screening and in silico virtual screening, we recently identified novel classes of EPIs that interact with the membrane fusion protein AcrA, a critical component of the AcrAB-TolC efflux pump in Escherichia coli. Herein, we present initial optimization efforts and structure-activity relationships around one of those previously described hits, NSC 60339 (1). From these efforts we identified two compounds, SLUPP-225 (17h) and SLUPP-417 (17o), which demonstrate favorable properties as potential EPIs in E. coli cells including the ability to penetrate the outer membrane, improved inhibition of efflux relative to 1, and potentiation of the activity of novobiocin and erythromycin.

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