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pseudophrynaminol
blocks nicotinic receptor channels; RN given for (3aR-(3aalpha(E),8aalpha))-isomer; structure in first source
Networked:
1
relevant articles (
0
outcomes,
0
trials/studies)
Bio-Agent Context: Research Results
Heterocyclic Compounds: 198
1-Ring Heterocyclic Compounds
Azoles: 2138
Pyrroles: 369
pseudophrynaminol: 1
Fused-Ring Heterocyclic Compounds
2-Ring Heterocyclic Compounds
Indoles: 200
pseudophrynaminol: 1
Related Diseases
1.
Pheochromocytoma
03/07/1997 - "
(+/-)-Pseudophrynaminol inhibited carbamylcholine-elicited sodium-22 influx with an IC50 value of about 0.3 microM in both rat pheochromocytoma PC12 cells (ganglionic-type nicotinic receptor) and human medulloblastoma TE671 cells (neuromuscular-type nicotinic receptor).
"
2.
Medulloblastoma
03/07/1997 - "
(+/-)-Pseudophrynaminol inhibited carbamylcholine-elicited sodium-22 influx with an IC50 value of about 0.3 microM in both rat pheochromocytoma PC12 cells (ganglionic-type nicotinic receptor) and human medulloblastoma TE671 cells (neuromuscular-type nicotinic receptor).
"
Related Drugs and Biologics
1.
Nicotinic Receptors (Nicotinic Acetylcholine Receptor)
2.
Carbachol (Carbastat)
3.
Sodium-22