BIOMAT Database Logo BIOMAT Database Logo

[Thin layer chromatographic detection of s-triazolo[1,5-a]pyrimidines and2-amino-1,2,4-triazole derivatives]. 1976

I Bornschein, and E Tenor

UI MeSH Term Description Entries
D011743 Pyrimidines A family of 6-membered heterocyclic compounds occurring in nature in a wide variety of forms. They include several nucleic acid constituents (CYTOSINE; THYMINE; and URACIL) and form the basic structure of the barbiturates.
D002855 Chromatography, Thin Layer Chromatography on thin layers of adsorbents rather than in columns. The adsorbent can be alumina, silica gel, silicates, charcoals, or cellulose. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) Chromatography, Thin-Layer,Thin Layer Chromatography,Chromatographies, Thin Layer,Chromatographies, Thin-Layer,Thin Layer Chromatographies,Thin-Layer Chromatographies,Thin-Layer Chromatography
D000640 Amitrole A non-selective post-emergence, translocated herbicide. According to the Seventh Annual Report on Carcinogens (PB95-109781, 1994) this substance may reasonably be anticipated to be a carcinogen. (From Merck Index, 12th ed) It is an irreversible inhibitor of CATALASE, and thus impairs activity of peroxisomes. Aminotriazole,3-Amino-1,2,4-triazole
D014230 Triazoles Heterocyclic compounds containing a five-membered ring with two carbon atoms and three nitrogen atoms with the molecular formula C2H3N3. Triazole

Related Publications

I Bornschein, and E Tenor
Discovery of [1,2,4]triazolo[1,5-a]pyrimidines derivatives as potential anticancer agents.
February 2021, European journal of medicinal chemistry,
I Bornschein, and E Tenor
1,2,4-Triazolo[1,5-a]pyrimidines in drug design.
March 2019, European journal of medicinal chemistry,
I Bornschein, and E Tenor
[Synthesis of new s-triazolo (1,5-a)pyrimidines].
January 1978, Die Pharmazie,
I Bornschein, and E Tenor
[Condensation with hydrazine-N,N'-dicarboxylic acid diamidine. 4. Parent compounds and ethyl derivatives of 3-amino-s-triazolo(4,3-a)pyrimidines and 2-amino-s-- triazolo(1,5-a)pyrimidines].
August 1970, Die Pharmazie,
I Bornschein, and E Tenor
[Trisubstituted s-triazolo(1,5-a)pyrimidines (author's transl)].
February 1976, Archiv der Pharmazie,
I Bornschein, and E Tenor
Synthesis and fungicidal activities of new 1,2,4-triazolo[1,5-a]pyrimidines.
August 2009, Chemistry & biodiversity,
I Bornschein, and E Tenor
Design, synthesis and evaluation of photoactivatable derivatives of microtubule (MT)-active [1,2,4]triazolo[1,5-a]pyrimidines.
July 2018, Bioorganic & medicinal chemistry letters,
I Bornschein, and E Tenor
A novel synthesis of 1,2,4-triazolo[1,5-a]isoindolinetrione, 1,2,4-triazolo[1,5-a]pyrimidine and 1,2,4-triazolo[2,3-a]quinazolinedione derivatives and their antibacterial activity.
January 1997, Die Pharmazie,
I Bornschein, and E Tenor
Synthesis and anti-tumor activities of novel [1,2,4]triazolo[1,5-a]pyrimidines.
May 2007, Molecules (Basel, Switzerland),
I Bornschein, and E Tenor
Synthesis of monomeric and dimeric steroids containing [1,2,4]triazolo[1,5-a]pyrimidines.
December 2016, Steroids,
Copied contents to your clipboard!