BIOMAT Database Logo BIOMAT Database Logo

[Synthesis of thiocarbanilide derivatives with biological action]. 1986

M Ungureanu, and E Stefănescu, and N Stavri, and C Radu, and A Hriscu, and M Pavelescu

UI MeSH Term Description Entries
D002224 Carbanilides Compounds consisting of two phenyl groups joined by a urea. Derivatives may be used as ANTIPARASITIC AGENTS. Diphenylurea Compounds,Compounds, Diphenylurea
D004285 Dogs The domestic dog, Canis familiaris, comprising about 400 breeds, of the carnivore family CANIDAE. They are worldwide in distribution and live in association with people. (Walker's Mammals of the World, 5th ed, p1065) Canis familiaris,Dog
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D000959 Antihypertensive Agents Drugs used in the treatment of acute or chronic vascular HYPERTENSION regardless of pharmacological mechanism. Among the antihypertensive agents are DIURETICS; (especially DIURETICS, THIAZIDE); ADRENERGIC BETA-ANTAGONISTS; ADRENERGIC ALPHA-ANTAGONISTS; ANGIOTENSIN-CONVERTING ENZYME INHIBITORS; CALCIUM CHANNEL BLOCKERS; GANGLIONIC BLOCKERS; and VASODILATOR AGENTS. Anti-Hypertensive,Anti-Hypertensive Agent,Anti-Hypertensive Drug,Antihypertensive,Antihypertensive Agent,Antihypertensive Drug,Anti-Hypertensive Agents,Anti-Hypertensive Drugs,Anti-Hypertensives,Antihypertensive Drugs,Antihypertensives,Agent, Anti-Hypertensive,Agent, Antihypertensive,Agents, Anti-Hypertensive,Agents, Antihypertensive,Anti Hypertensive,Anti Hypertensive Agent,Anti Hypertensive Agents,Anti Hypertensive Drug,Anti Hypertensive Drugs,Anti Hypertensives,Drug, Anti-Hypertensive,Drug, Antihypertensive,Drugs, Anti-Hypertensive,Drugs, Antihypertensive
D001419 Bacteria One of the three domains of life (the others being Eukarya and ARCHAEA), also called Eubacteria. They are unicellular prokaryotic microorganisms which generally possess rigid cell walls, multiply by cell division, and exhibit three principal forms: round or coccal, rodlike or bacillary, and spiral or spirochetal. Bacteria can be classified by their response to OXYGEN: aerobic, anaerobic, or facultatively anaerobic; by the mode by which they obtain their energy: chemotrophy (via chemical reaction) or PHOTOTROPHY (via light reaction); for chemotrophs by their source of chemical energy: CHEMOLITHOTROPHY (from inorganic compounds) or chemoorganotrophy (from organic compounds); and by their source for CARBON; NITROGEN; etc.; HETEROTROPHY (from organic sources) or AUTOTROPHY (from CARBON DIOXIDE). They can also be classified by whether or not they stain (based on the structure of their CELL WALLS) with CRYSTAL VIOLET dye: gram-negative or gram-positive. Eubacteria
D013329 Structure-Activity Relationship The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups. Relationship, Structure-Activity,Relationships, Structure-Activity,Structure Activity Relationship,Structure-Activity Relationships

Related Publications

M Ungureanu, and E Stefănescu, and N Stavri, and C Radu, and A Hriscu, and M Pavelescu
Synthesis and biological action of 5-oxo-1,2,4-triazine derivatives.
July 1999, Die Pharmazie,
M Ungureanu, and E Stefănescu, and N Stavri, and C Radu, and A Hriscu, and M Pavelescu
Synthesis, mode of action, and biological activities of rebeccamycin bromo derivatives.
May 1999, Journal of medicinal chemistry,
M Ungureanu, and E Stefănescu, and N Stavri, and C Radu, and A Hriscu, and M Pavelescu
New Thiosemicarbazide Derivatives with Multidirectional Biological Action.
March 2024, Molecules (Basel, Switzerland),
M Ungureanu, and E Stefănescu, and N Stavri, and C Radu, and A Hriscu, and M Pavelescu
Diarylamine-Guided Carboxamide Derivatives: Synthesis, Biological Evaluation, and Potential Mechanism of Action.
January 2022, Frontiers in chemistry,
M Ungureanu, and E Stefănescu, and N Stavri, and C Radu, and A Hriscu, and M Pavelescu
Synthesis of isothiazole derivatives with potential biological activity.
July 1992, Die Pharmazie,
M Ungureanu, and E Stefănescu, and N Stavri, and C Radu, and A Hriscu, and M Pavelescu
[Synthesis of new pyridazine derivatives with biological activity].
January 1987, Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi,
M Ungureanu, and E Stefănescu, and N Stavri, and C Radu, and A Hriscu, and M Pavelescu
Synthesis, Biological Activity and Action Mechanism Study of Novel Chalcone Derivatives Containing Malonate.
April 2020, Chemistry & biodiversity,
M Ungureanu, and E Stefănescu, and N Stavri, and C Radu, and A Hriscu, and M Pavelescu
Design, Synthesis, Biological Activity Evaluation and Action Mechanism of Myricetin Derivatives Containing Thiazolebisamide.
March 2023, Chemistry & biodiversity,
M Ungureanu, and E Stefănescu, and N Stavri, and C Radu, and A Hriscu, and M Pavelescu
[Synthesis of sulfanylalkylpyrimidine derivatives with potential immunomodulating action].
October 2003, Die Pharmazie,
M Ungureanu, and E Stefănescu, and N Stavri, and C Radu, and A Hriscu, and M Pavelescu
[Synthesis of pyridine derivatives with potential circulatory action].
August 1961, Archiv der Pharmazie und Berichte der Deutschen Pharmazeutischen Gesellschaft,
Copied contents to your clipboard!