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101234-68-8

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101234-68-8 Usage

General Description

1-(diphenylmethoxycarbonylmethyl)-4-thiopyridone, also known as DT-13, is a chemical compound with potential anti-tumor and anti-inflammatory properties. It has been studied for its potential use in cancer therapy due to its ability to inhibit the growth of cancer cells and induce apoptosis. DT-13 has also shown anti-inflammatory effects by inhibiting the production of pro-inflammatory cytokines. Furthermore, it has been demonstrated to have antioxidant activity, making it a promising candidate for the development of new therapeutic agents for cancer and inflammatory diseases. Additionally, DT-13 has been found to have low toxicity, making it a potentially safe and effective treatment option. Further research and clinical trials are needed to fully understand the potential of DT-13 in medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 101234-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,2,3 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 101234-68:
(8*1)+(7*0)+(6*1)+(5*2)+(4*3)+(3*4)+(2*6)+(1*8)=68
68 % 10 = 8
So 101234-68-8 is a valid CAS Registry Number.

101234-68-8Downstream Products

101234-68-8Relevant articles and documents

Synthesis and biological activity of 3-(N-substituted pyridinium-4-thiomethyl)-7α-formamido cephalosporins

Guest,Adams,Basker,Brain,Branch,Harrington,Neale,Pearson,Zomaya

, p. 1279 - 1288 (2007/10/02)

The synthesis and antibacterial activity of a series of 3-(1-substituted pyridinium-4-thiomethyl)-7α-formamido cephalosporins is described. All the derivatives showed good potency and stability to bacterial β-lactamases. The antibacterial efficacy seen with the N-alkyl pyridinium substituents was enhanced by the introduction of a catecholic side chain at C-7 and by preparation of N-(substituted amino)pyridinium derivatives.

Cephalosporin derivatives

-

, (2008/06/13)

This is a class of antibacterial compounds of the formula: STR1 wherein Y is straight or branched alkyl or alkenyl chain, cycloalkanomethyl of 3-6 carbon atoms, each group being optionally substituted by halogen, or a group STR2 wherein n is 0 or an integer of 1-3, A is a group --COR3 wherein R3 is hydroxy, a group STR3 wherein R4 and R5, which may be the same or different, are hydrogen or alkyl of 1-5 carbon atoms, a group STR4 or a 5- or 6-membered heterocyclic group containing nitrogen and/or sulfur, and R1 and R2, which may be the same or different, are hydrogen, alkyl of 1-5 carbon atoms, or R1 and R2 may be combined together to form cycloalkylidene of 3-5 carbon atoms, and Z is a group of the formula: STR5 wherein m is 0 or an integer of 3-5, R6 is hydrogen or alkyl of 1-3 carbon atoms, and R7, when m is an integer of 3-5, is alkyl of 1-5 carbon atoms, alkenyl, cyclopropyl, a group --(CH2)p B wherein p is 0 or an integer of 1-3 and B is amino, alkyl-substituted amino, hydroxy, carboxy, carbamoyl, trifluoromethyl, sulfonic acid, sulfonic acid amide, alkylthio or cyano or, when m is 0, is alkyl of 1-5 carbon atoms, which may optionally be substituted by halogen, alkenyl, a group STR6 wherein R8 is hydrogen, alkyl of 1-4 carbon atoms or phenyl, or cyclopropyl, and a salt thereof.

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