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5F-PB-22
AM-2201
BB-22
JWH-018
NM-2201
NNE1
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5F-CUMYL-PINACA
5F-SDB-006
APINACA
CUMYL-PICA
CUMYL-PINACA
CUMYL-THPINACA
SDB-001
SDB-005
STS-135
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The release of nociceptive neurotransmitters such as substance P, GABA, dopamine, acetylcholine, and noradrenaline is then inhibited [A39637]. Opioids close N-type voltage-operated calcium channels (OP2-receptor agonist), also preventing neurotransmitter release [A39637]. Sufentanil and other opioids open calcium-dependent inwardly rectifying potassium channels, resulting in hyperpolarization and reduced neuronal excitability [A39636], [A39637].
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Opioids close N-type voltage-operated calcium channels (OP2-receptor agonist), also preventing neurotransmitter release [A39637]. Sufentanil and other opioids open calcium-dependent inwardly rectifying potassium channels, resulting in hyperpolarization and reduced neuronal excitability [A39636], [A39637].Thenylfentanyl Powder
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Chemical and physical data
Formula: C22H28N2O4SMolar mass: 416.54 g·mol?1
See also
Sufentanil
List of fentanyl analogues
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Chemical and physical data
Formula C23H21FN2O
Molar mass 360.42 g/mol g·mol?1
3D model (JSmol) InteractiveSee also
AM-694
AM-1235
AM-2232
AM-2233
FUBIMINA
JWH-018
List of AM cannabinoids
List of JWH cannabinoids
NM-2201
THJ-018
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Trefentanyl POWDER is most similar to short-acting fentanyl analogues such as alfentanil. In comparative studies, trefentanil was slightly more potent and shorter acting than alfentanil as an analgesic, but induced significantly more severe respiratory depression. For this reason trefentanil has not been adopted for clinical use, although it is still used in research.
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Timeline
Inhalation (tentative due to a lack of information)
Total: 1 2 hours
Onset: Under 10 minutes
See also
AB-001
AM-1221
4–HTMPIPO
FAB-144
JTE 7-31
JWH-018
N-(S)-Fenchyl-1-(2-morpholinoethyl)-7-methoxyindole-3-carboxamide
XLR-11
Tetramethylcyclopropylfentanyl
UR-144 Powder
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Valerylfentanyl POWDER Valerylfentanyl is an opioid analgesic that is an analog of fentanyl and has been sold online as a designer drug. It has been seldom reported on illicit markets and there is little information about it, though it is believed to be less potent than butyrfentanyl but more potent than benzylfentanyl.
