24827-37-0

Usage

Uses

Used in Pharmaceutical Industry:
1-(4-CHLOROBENZYL)-2-THIOUREA is used as a precursor in the synthesis of antitumor and antiviral drugs due to its unique chemical structure and potential biological activity, which can be leveraged to develop new therapeutic agents.
Used in Organic Synthesis:
1-(4-CHLOROBENZYL)-2-THIOUREA is used as a building block in the synthesis of other organic compounds, contributing to the creation of novel molecules with potential applications in various fields.
Used in Chemical Reactions:
1-(4-CHLOROBENZYL)-2-THIOUREA is used as a reagent in chemical reactions, facilitating specific transformations and providing a means to access complex molecular structures.
Used in Research and Development:
1-(4-CHLOROBENZYL)-2-THIOUREA is used in biological research to explore its potential biological activity, with the aim of discovering new therapeutic targets and applications in medicine.

InChI:InChI=1/C8H9ClN2S/c9-7-3-1-6(2-4-7)5-11-8(10)12/h1-4H,5H2,(H3,10,11,12)

Upstream product

• 3694-45-9 4-chlorobenzylisothiocyanate 
• 333-20-0 potassium thioacyanate 
• 104-86-9 4-chlorobenzylamine 
• 106-47-8 4-chloro-aniline 
• 1147550-11-5 ammonium thiocyanate 
• 145383-00-2 N-((4-chlorobenzyl)carbamothioyl)benzamide 

Downstream Products

• 93187-19-0 2-(4-chloro-benzylamino)-5-propyl-thiazol-4-one 
• 93568-82-2 5-butyl-2-(4-chloro-benzylamino)-thiazol-4-one 
• 92854-18-7 2-(4-chloro-benzylamino)-5-(4-chloro-phenyl)-thiazol-4-one 
• 92854-17-6 2-(4-chloro-benzylamino)-5-(2-chloro-phenyl)-thiazol-4-one 
• 91066-29-4 2-(4-chloro-benzylamino)-5-methyl-thiazol-4-one 
• 1239691-18-9 1-(4-chlorobenzyl)-3-(methoxycarbonylmethyl)-6-(methylthio)-1,3,5-triazine-2,4(1H,3H)-dion 
• 1239685-51-8 1-(4-chlorobenzyl)-4-(dodecylthio)-6-(3-fluoro-4-isopropoxyphenylamino)-1,3,5-triazine-2(1H)-one 
• 1239685-50-7 4-benzylamino-1-(4-chlorobenzyl)-6-(3-fluoro-4-isopropoxyphenylamino)-1,3,5-triazine-2(1H)-one 
• 1239691-19-0 1-(4-chlorobenzyl)-6-(3-fluoro-4-isopropoxyphenylamino)-4-(2-(tetrahydro-2H-pyrane-2-yloxy)ethoxy)-1,3,5-triazine-2(1H)-one 
• 1239685-49-4 1-(4-chlorobenzyl)-6-(3-fluoro-4-isopropoxyphenylamino)-4-(2-hydroxyethoxy)-1,3,5-triazine-2(1H)-one 
• 1239685-48-3 4-chloro-1-(4-chlorobenzyl)-6-(3-fluoro-4-isopropoxyphenylamino)-1,3,5-triazine-2(1H)-one 
• 1239685-47-2 1-(4-chlorobenzyl)-6-(3-fluoro-4-isopropoxyphenylamino)-3-(methylcarbamoylmethyl)-1,3,5-triazine-2,4(1H,3H)-dion 
• 1239685-45-0 1-(4-chlorobenzyl)-6-(3-fluoro-4-isopropoxyphenylamino)-3-(methoxycarbonylmethyl)-1,3,5-triazine-2,4(1H,3H)-dion 
• 1239685-46-1 1-(4-chlorobenzyl)-6-(3-fluoro-4-isopropoxyphenylamino)-3-(hydroxycarbonylmethyl)-1,3,5-triazine-2,4(1H,3H)-dion 

Relevant academic research and scientific papers

Synthesis, biological evaluation, and metabolic stability of chlorogenic acid derivatives possessing thiazole as potent inhibitors of α-MSH-stimulated melanogenesis

A series of catechol and dioxolane analogs containing thiazole CGA derivatives have been synthesized and evaluated for their inhibitory activity against α-MSH. The inhibitory activity was improved by replacing an α,β-unsaturated carbonyl of previously reported caffeamides with thiazole motif. Surprisingly, compound 7d, one of the derivatives of dioxolane analogs, displayed the most potent inhibitory activity with an IC50 of 0.90 μM. Further studies on metabolic stability and bioactivation potential were also accomplished.

Novel Chlorogenic Acid Derivatives and Anti-Inflammatory and Skin Whitening Composition Comprising the Same

The present invention relates to a novel chlorogenic acid derivative compound having an anti-inflammatory activity and a skin whitening activity, a use of the compound, and a manufacturing method of the compound. The compound of the present invention inhibits an NF- κB activation path, and inhibits an activity of α-melanocyte-stimulating hormone (α-MSH), thereby having the anti-inflammatory activity and the skin whitening activity. The compound of the present invention can be developed as a treating agent of inflammatory diseases and a skin whitening agent.

COMPOSITIONS AND METHODS FOR THE TREATMENT OF MALARIA

The present invention provides aminohydantoin anti-malarial agents. In some embodiments, these agents have the property of functions of targeting malarial aspartic proteases while at the same time having low activity against human BACE. Methods of employing such agents are also provided.

Clobenpropit analogs as dual activity ligands for the histamine H3 and H4 receptors: Synthesis, pharmacological evaluation, and cross-target QSAR studies

Previous studies have demonstrated that clobenpropit (N-(4-chlorobenzyl)-S-[3-(4(5)-imidazolyl)propyl]isothiourea) binds to both the human histamine H3 receptor (H3R) and H4 receptor (H4R). In this paper, we describe the synthesis and pharmacological characterization of a series of clobenpropit analogs, which vary in the functional group adjacent to the isothiourea moiety in order to study structural requirements for H3R and H4R ligands. The compounds show moderate to high affinity for both the human H3R and H4R. Furthermore, the changes in the functional group attached to the isothiourea moiety modulate the intrinsic activity of the ligands at the H4R, ranging from neutral antagonism to full agonism. QSAR models have been generated in order to explain the H3R and H4R affinities.

Isothiourea analogues of histamine as potent agonists or antagonists of the histamine H3-receptor

The synthesis and H3-activity of a series of isothiourea analogues of histamine have been described. It has been shown that S-[2-(4(5)-imidazolyl)ethylisothiourea (VUF 8325) is a potent H3-agonist measured as the electrically evoked contraction of the guinea-pig ileum. Upon methylation of the imidazole system or the isothiourea moiety a decrease in affinity was observed leading to either weak agonists or weak antagonists. Introduction of N-(phenylalkyl) substituents at the isothiourea part gives rise to highly potent H3-antagonists. Particularly the 4-chlorobenzyl group appeared to be favourable in the series described resulting in a histamine H3-antagonist with a pA2-value of 9.9.