- Antagonists. N,n -diethyl-1-methyl-3-aryl-1, 2, 5, 6-tetrahydropyridine-5-
carboxamides (Ph.D. thesis).
University of Michigan. doi:10.7302/11268.
Archived from...
- 3-component
reaction to
produce α-acyloxy
carboxamides and the Ugi 4-component reaction,
which yields the α-amino
carboxamides.
Examples of
three component reactions:...
- A. Zajac; A. G.
Myers (2006). "Efficient
Transamidation of
Primary Carboxamides by in situ
Activation with N,N-Dialkylformamide
Dimethyl Acetals". J...
-
Legal status Legal status US: OTC
Identifiers IUPAC name pyridine-3-
carboxamide CAS
Number 98-92-0 Y
PubChem CID 936
DrugBank DB02701
ChemSpider 911...
- life-threatening side effects.
Cenobamate (2019). The
following are
carboxamides:
Carbamazepine (1963). A po****r
anticonvulsant that is
available in...
-
group –OH
replaced by an
amine group –NR2. Some
important subclasses are
carboxamides, or
organic amides,
where E = carbon, with the
general formula RC(=O)NR2...
- "Design, synthesis, and structure–activity
relationships of indole-3-
carboxamides as
novel water soluble cannabinoid CB1
receptor agonists". MedChemComm...
- naphthoylpyrroles, naphthylmethylindenes, indole-3-
carboxamides, indole-3-carboxylates, indazole-3-
carboxamides and
sometimes others, each with
specific substitutions...
- 5-Aminoimidazole-4-
carboxamide ribonucleotide (AICAR) is an
intermediate in the
generation of
inosine monophosphate.
AICAR is an
analog of
adenosine monophosphate...
- In enzymology, a
phosphoribosylaminoimidazolecarboxamide formyltransferase (EC 2.1.2.3), also
known by the
shorter name
AICAR transformylase, is an enzyme...
