Compounds of the general formula (1): Q1-Q2-C(=O)-N(R?1)-Q3-N(R2)-T1-Q4¿; and drugs which contain the compounds and are efficacious for thrombosis and embolism. Data sources include IBM Watson Micromedex (updated 6 Jan 2021), Cerner Multum™ (updated 4 Jan 2021), ASHP … ETHYLENEDIAMINE DERIVATIVES OF (ARYLOXY)PROPANOLAMINES HAVING ESTERS ON THE ARYL FUNCTION. PLEASE NOTE: Because prescription drug programs vary by group, the inclusion of a drug in this formulary does not imply coverage. Name Ethylenediamine Derivatives Accession Number DBCAT003721 Description Not Available Drugs. Authors I Noyszewska-Skibińska, A … Triethylenetetramine (TETA and trien), also called trientine (), is an organic compound with the formula [CH 2 NHCH 2 CH 2 NH 2] 2.This oily liquid is colorless but, like many amines, assumes a yellowish color due to impurities resulting from air-oxidation.It is soluble in polar solvents. Ethylenediamine is an organic compound that is used as a building block for the production of many other chemical products. 2019 Oct 15;222:115002. doi: 10.1016/j.carbpol.2019.115002. Chemischer Informationsdienst 1983, 14 (50) DOI: 10.1002/chin.198350126. 1999 Mar;73(3):145-9. doi: 10.1016/s0162-0134(99)00009-4. [Pharmacological study of new ethylenediamine derivatives with antiarrhythmic activity]. February 2012; Medicinal chemistry (Shāriqah (United Arab Emirates)) 8(2):252-65 Ethylenediamine (abbreviated as en when a ligand) is the organic compound with the formula C 2 H 4 (NH 2) 2.This colorless liquid with an ammonia-like odor is a strongly basic amine.It is a widely used building block in chemical synthesis, with approximately 500,000 tonnes produced in 1998. ethanolamine derivatives; ethylenediamine derivatives; first gen. antihist. Poly(amidoamine), or PAMAM, is a class of dendrimer which is made of repetitively branched subunits of amide and amine functionality.PAMAM dendrimers, sometimes referred to by the trade name Starburst, have been extensively studied since their synthesis in 1985, and represent the most well-characterized dendrimer family as well as the first to be commercialized. Identification Name Ethylenediamine Accession Number DB14189 Description. Other uses ethylenediamine derivatives heterocycle aromatic ring compounds general formula Prior art date 2000-04-05 Application number PCT/JP2001/002945 Other languages French (fr) Japanese (ja) Inventor Toshiharu Yoshino Tsutomu Nagata Noriyasu Haginoya Kenji Yoshikawa Hideyuki Kanno Masatoshi Nagamochi Original Assignee Daiichi Pharmaceutical Co., Ltd. These drugs are often referred to simply as "piperazine" which may cause confusion between the specific anthelmintic drugs, the entire class of piperazine-containing compounds, and the compound itself. Results and discussion 2.1. This means it is still under development and may contain inaccuracies. ChemInform Abstract: ULTRA-SHORT-ACTING β-ADRENERGIC RECEPTOR BLOCKING AGENTS. This material is provided for educational purposes only and is not intended for medical advice, diagnosis or treatment. It is also used as an excipient in many pharmacological preparations such as creams. Hydroxyethylethylenediamine is another commercially significant chelating agent. Ernest K. Mentioned compounds, studied on several species of animals, decrease blood pressure and the heart rate, modify catecholamine-induced effects, show properties characteristic for the beta-receptor blocking agents. It is a bacteriostatic antimycobacterial drug, effective against Mycobacterium tuberculosis and some other mycobacteria. The pharmacology of new ethylenediamine derivatives (ROM-126, ROM-131, MK-142) with antiarrhythmic action. It is scheduled to be annotated soon. These compounds … b) Ethylenediamine derivatives. substituted ethylenediamine ethylenediamine derivative derivative Prior art date 1983-12-01 Legal status (The legal status is an assumption and is not a legal conclusion. Drugs & Drug Targets. Ethambutol is an ethylenediamine derivative that is ethane-1,2-diamine in which one hydrogen attached to each of the nitrogens is sutstituted by a 1-hydroxybutan-2-yl group (S,S-configuration). Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.) DRUGS THAT BLOCK THE RELEASED HISTAMINE a) H1 ANTAGONISTS(FIRST GENERATION DRUGS): • These are classical antihistamines. Biochemical, morphochemical and pharmacodynamic evaluation of accumulation of ethylenediamine derivatives (ROM-203, MK-142) in some rat tissues. development of novel drug-carrier systems, although its sim-ple structure limits the types of hybrids that can be produced. c) Propyl amine derivatives. Usually, PEG is converted to a carboxyl derivative and conju-gated with a protein as a simple acyl moiety. This drug entry is a stub and has not been fully annotated. 2D Chemometrics Analyses of Tetrahydroquinoline and Ethylenediamine Derivatives with Antimalarial Activity. ethylenediamine derivatives ethylenediamine derivatives Prior art date 2000-04-05 Application number ARP010101613A Other languages Spanish (es) Original Assignee Daiichi Seiyaku Co Priority date (The priority date is an assumption and is not a legal conclusion. We designed an amino acid type PEG (aaPEG) for preparation of a multi- Allergy to ethylenediamine, Ethylenediamine allergy, Ethylenediamine dihydrochloride allergy, 1-2-Ethanediamine dihydrochloride allergy, 1-2-Diaminoethane dihydrochloride allergy, Chlorethamine allergy, C2H10Cl2N2 allergy. Precursor to chelation agents, drugs, and agrochemicals A most prominent derivative of ethylenediamine is the chelating agent EDTA, which is derived from ethylenediamine via a Strecker synthesis involving cyanide and formaldehyde. General pharmacological properties. (14)C-Labeled ethylenediamine (EDA) was accumulated by slices of adult rat cerebral cortex, although the tissue:medium ratios were much lower than those for gamma-aminobutyric acid.EDA uptake was temp-dependent and appeared to take place by both sodium dependent and sodium independent mechanisms. ; FIRST gen. antihist bacteriostatic antimycobacterial drug, effective against Mycobacterium tuberculosis and some other mycobacteria Accession Number DBCAT003721 not... Representation as to the accuracy of the status listed. treat some types of filariasis ( ROM-203, ). Hydrate market amounted to $ 350 million as an excipient in many Pharmacological preparations such as the ethylenediamine derivatives drugs drugs.. 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