-
Ziconotide, sold
under the
brand name Prialt, also
called intrathecal ziconotide (ITZ)
because of its
administration route, is an
atypical analgesic agent...
-
protein thombospondin,
independently from
their action at
calcium channels.
Ziconotide, a
peptide compound derived from the omega-conotoxin, is a
selective N-type...
-
usually does not develop. However,
tolerance may
develop in some cases.
Ziconotide, a
blocker of
potent N-type voltage-gated
calcium channels, is administered...
-
analogues (enalapril, lisinopril, perindopril, ramipril, etc.) were produced.
Ziconotide is a
synthetically made
version of the ω-conotoxin made by the cone snail...
-
selective Cav2.2
blocker ziconotide is an
active analgesic with
similar efficacy to
strong opioid drugs.
Unlike ziconotide, TROX-1 is not so selective...
-
animals produce several important drugs, e.g., ACE
inhibitors and
Prialt (
Ziconotide). To find new venoms,
scientists turn to
phylogenetics to
screen for closely...
-
version of ω-conotoxin M VII A has
found application as an
analgesic drug
ziconotide (Prialt).
Alpha conotoxins have two
types of
cysteine arrangements, and...
-
opioids include nausea and vomiting,
pruritus and
urinary retention.
Ziconotide.
Amphotericin B is
administered intrathecally to
treat fungal infections...
- neurotransmitters, and in pain pathways. N-type
calcium channels are the
target of
ziconotide, the drug
prescribed to
relieve intractable cancer pain.
There are many...
-
related P/Q-type voltage-gated
calcium channel (Cav2.1).
Relative to
ziconotide,
leconotide is
advantageous in that it is
significantly less toxic, and...
