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1-(2-Morpholinoethyl)-2-thiourea is a chemical compound that is widely recognized for its potent inhibitory effect on the enzyme nitric oxide synthase, which is responsible for the synthesis of nitric oxide. 1-(2-MORPHOLINOETHYL)-2-THIOUREA is a morpholino derivative, a class of synthetic molecules that are designed to selectively bind RNA. It is utilized in the development of pharmaceutical products and is a subject of interest in various scientific studies that focus on the cardiovascular, immunological, and neurological systems due to its influence on nitric oxide levels. 1-(2-MORPHOLINOETHYL)-2-THIOUREA's physiological effects can be both beneficial and toxic, varying with concentration, the specific biological system, and other factors.

122641-10-5

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122641-10-5 Usage

Uses

Used in Pharmaceutical Industry:
1-(2-Morpholinoethyl)-2-thiourea is used as an active pharmaceutical ingredient for the development of different pharmaceutical products, leveraging its ability to inhibit nitric oxide synthase and potentially offering therapeutic benefits in various medical conditions.
Used in Scientific Research:
1-(2-Morpholinoethyl)-2-thiourea is used as a research tool in studies focused on cardiovascular, immunological, and neurological systems. Its impact on nitric oxide levels makes it a valuable compound for investigating the roles of nitric oxide in these systems and for exploring potential treatments for related disorders.
Used in Drug Delivery Systems:
In the context of drug delivery, 1-(2-Morpholinoethyl)-2-thiourea may be employed as a component in the design of drug delivery systems, potentially enhancing the efficacy and targeted delivery of therapeutic agents by modulating nitric oxide levels in the body.

Check Digit Verification of cas no

The CAS Registry Mumber 122641-10-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,6,4 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 122641-10:
(8*1)+(7*2)+(6*2)+(5*6)+(4*4)+(3*1)+(2*1)+(1*0)=85
85 % 10 = 5
So 122641-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H15N3OS/c8-7(12)9-1-2-10-3-5-11-6-4-10/h1-6H2,(H3,8,9,12)

122641-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-Morpholinoethyl)-2-thiourea

1.2 Other means of identification

Product number -
Other names 2-morpholin-4-ylethylthiourea

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:122641-10-5 SDS

122641-10-5Relevant academic research and scientific papers

ANTIVIRAL COMPOUNDS AND USE THEREOF

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Page/Page column 36; 39, (2019/10/04)

The present invention relates to compounds of formula (I), their use as medicaments, in particular as broad spectrum antiviral agents, their combination with a further antiviral agent and relative pharmaceutical compositions. In particular, the compounds of the invention are useful in the treatment of a disease caused by an enveloped virus.

Continuous-flow processing of gaseous ammonia using a Teflon AF-2400 tube-in-tube reactor: Synthesis of thioureas and in-line titrations

Browne, Duncanl.,O'Brien, Matthew,Koos, Peter,Cranwell, Philippa B.,Polyzos, Anastasios,Ley, Steven V.

scheme or table, p. 1402 - 1406 (2012/07/27)

A simple tube-in-tube reactor based on the gas-permeable membrane Teflon AF-2400 was used in the continuous flow reaction of gaseous ammonia with isothiocyanates and one isocyanate. A colourimetric in-line titration technique is also reported as a simple method to quantify the amount of ammonia taken up by the solvent in the system. Georg Thieme Verlag Stuttgart · New York.

Synthesis of thiophene-2-carboxamidines containing 2-aminothiazoles and their biological evaluation as urokinase inhibitors

Wilson, Kenneth J.,Illig, Carl R.,Subasinghe, Nalin,Hoffman, James B.,Jonathan Rudolph,Soll, Richard,Molloy, Christopher J.,Bone, Roger,Green, David,Randall, Troy,Zhang, Marie,Lewandowski, Frank A.,Zhou, Zhao,Sharp, Celia,Maguire, Diane,Grasberger, Bruce,DesJarlais, Renee L.,Spurlino, John

, p. 915 - 918 (2007/10/03)

The serine protease urokinase (uPa) has been implicated in the progression of both breast and prostate cancer. Utilizing structure based design, the synthesis of a series of substituted 4-[2-amino-1,3-thiazolyl]-thiophene-2-carboxamidines is described. Further optimization of this series by substitution of the terminal amine yielded urokinase inhibitors with excellent activities.

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