azole - definição. O que é azole. Significado, conceito
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O que (quem) é azole - definição

ANY HETEROCYCLIC COMPOUND HAVING A FIVE-MEMBERED AROMATIC RING WITH AT LEAST ONE NITROGEN HETEROATOM
Azoles; Dioxoles; Azole antifungals; Azole drugs; -azole; Azole fungicide; Azole fungicide resistance

Azole         
  • [[Imidazole]]
  • [[Pyrazole]]
  • [[1,2,3-Triazole]]
  • [[1,2,4-Triazole]]
  • [[Tetrazole]]
  • [[Pentazole]]
  • [[Oxazole]]
  • [[Isoxazole]]
  • 1,2,3-oxadiazole (unstable)
  • [[Oxadiazole]](1,2,4-Oxadiazole)
  • [[Furazan]](1,2,5-oxadiazole)
  • 1,3,4-oxadiazole
  • [[Thiazole]]
  • [[Isothiazole]]
  • [[Thiadiazole]](1,2,3-Thiadiazole)
  • 1,2,4-thiadiazole
  • 1,2,5-thiadiazole
  • 1,3,4-thiadiazole
·add. ·noun Any of a large class of compounds characterized by a five-membered ring which contains an atom of nitrogen and at least one other noncarbon atom (nitrogen, oxygen, sulphur). The prefixes furo-, thio, and pyrro- are used to distinguish three subclasses of azoles, which may be regarded as derived respectively from furfuran, thiophene, and pyrrol by replacement of the CH group by nitrogen; as, furo-monazole. Names exactly analogous to those for the azines are also used; as, oxazole, diazole, ·etc.
Azole         
  • [[Imidazole]]
  • [[Pyrazole]]
  • [[1,2,3-Triazole]]
  • [[1,2,4-Triazole]]
  • [[Tetrazole]]
  • [[Pentazole]]
  • [[Oxazole]]
  • [[Isoxazole]]
  • 1,2,3-oxadiazole (unstable)
  • [[Oxadiazole]](1,2,4-Oxadiazole)
  • [[Furazan]](1,2,5-oxadiazole)
  • 1,3,4-oxadiazole
  • [[Thiazole]]
  • [[Isothiazole]]
  • [[Thiadiazole]](1,2,3-Thiadiazole)
  • 1,2,4-thiadiazole
  • 1,2,5-thiadiazole
  • 1,3,4-thiadiazole
Azoles are a class of five-membered heterocyclic compounds containing a nitrogen atom and at least one other non-carbon atom (i.e.
pyrrole         
  • [[Zwitterion]]ic structure of both proline enantiomers: (''S'')-proline (left) and (''R'')-proline
  • Ciamician–Dennstedt rearrangement
  • Synthesis of pyrroles via Diels–Alder cyclization
  • Heme b
  • The Paal–Knorr pyrrole synthesis
  • Mechanism of biosynthesis of porphobilinogen
  • Figure 1: Structure of Prodigiosin 1 highlighting the A, B, and C pyrrole rings
  • Figure 2: biosynthesis of pyrrole ring A
  • Biosynthesis of pyrrole ring B
  • Vilsmeier–Haack formylation of pyrrole
  • Pyrrole ''C''-metalation
  • Pyrrole DA
  • Pyrrole electrophilic substitution
  • Synthesis of pyrrole via silver click chemistry
  • Synthesis of pyrrole from ammonium mucate
  • Mechanism of the Van Leusen reaction to form pyrroles
HETEROCYCLIC AROMATIC ORGANIC COMPOUND CONTAINING A NITROGEN ATOM
Pyrole; Pyrrhole; Pyrrol; Pyrroles; Piloty–Robinson pyrrole synthesis; True Pyrrole; Piloty-Robinson pyrrole synthesis; Pyrrole ring; Pyrhole
['p?r??l]
¦ noun Chemistry a sweet-smelling heterocyclic liquid compound present in bone oil and coal tar.
Origin
C19: from Gk purrhos 'reddish' + L. oleum 'oil'.

Wikipédia

Azole

Azoles are a class of five-membered heterocyclic compounds containing a nitrogen atom and at least one other non-carbon atom (i.e. nitrogen, sulfur, or oxygen) as part of the ring. Their names originate from the Hantzsch–Widman nomenclature. The parent compounds are aromatic and have two double bonds; there are successively reduced analogs (azolines and azolidines) with fewer. One, and only one, lone pair of electrons from each heteroatom in the ring is part of the aromatic bonding in an azole. Names of azoles maintain the prefix upon reduction (e.g., pyrazoline, pyrazolidine). The numbering of ring atoms in azoles starts with the heteroatom that is not part of a double bond, and then proceeds towards the other heteroatom.

Imidazole and other five-membered aromatic heterocyclic systems with two nitrogens are extremely common in nature and form the core of many biomolecules, such as histidine.