Welcome to LookChem.com Sign In|Join Free
  • or
methyl 3-methoxybenzenecarbimidothioate hydroiodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154142-59-3

Post Buying Request

154142-59-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

154142-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154142-59-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,1,4 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 154142-59:
(8*1)+(7*5)+(6*4)+(5*1)+(4*4)+(3*2)+(2*5)+(1*9)=113
113 % 10 = 3
So 154142-59-3 is a valid CAS Registry Number.

154142-59-3Relevant academic research and scientific papers

An evaluation of Minor Groove Binders as anti-lung cancer therapeutics

Scott, Fraser J.,Puig-Sellart, Mireia,Khalaf, Abedawn I.,Henderson, Catherine J.,Westrop, Gareth,Watson, David G.,Carter, Katharine,Grant, M. Helen,Suckling, Colin J.

supporting information, p. 3478 - 3486 (2016/07/22)

A series of 47 structurally diverse MGBs, derived from the natural product distamycin, was evaluated for anti-lung cancer activity by screening against the melanoma cancer cell line B16-F10. Five compounds have been found to possess significant activity, more so than a standard therapy, Gemcitabine. Moreover, one compound has been found to have an activity around 70-fold that of Gemcitabine and has a favourable selectivity index of greater than 125. Furthermore, initial studies have revealed this compound to be metabolically stable and thus it represents a lead for further optimisation towards a novel treatment for lung cancer.

Antimicrobial lexitropsins containing amide, amidine, and alkene linking groups

Anthony, Nahoum G.,Breen, David,Clarke, Joanna,Donoghue, Gavin,Drummond, Allan J.,Ellis, Elizabeth M.,Gemmell, Curtis G.,Helesbeux, Jean-Jacques,Hunter, Iain S.,Khalaf, Abedawn I.,Mackay, Simon P.,Parkinson, John A.,Suckling, Colin J.,Waigh, Roger D.

, p. 6116 - 6125 (2008/09/16)

The synthesis and properties of 80 short minor groove binders related to distamycin and the thiazotropsins are described. The design of the compounds was principally predicated upon increased affinity arising from hydrophobic interactions between minor groove binders and DNA. The introduction of hydrophobic aromatic head groups, including quinolyl and benzoyl derivatives, and of alkenes as linkers led to several strongly active antibacterial compounds with MIC for Staphylococcus aureus, both methicillin-sensitive and -resistant strains, in the range of 0.1-5 μg mL-1, which is comparable to many established antibacterial agents. Antifungal activity was also found in the range of 20-50 μg mL-1 MIC against Aspergillus niger and Candida albicans, again comparable with established antifungal drugs. A quinoline derivative was found to protect mice against S. aureus infection for a period of up to six days after a single intraperitoneal dose of 40 mg kg-1.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 154142-59-3