Details
Stereochemistry | ACHIRAL |
Molecular Formula | C9H8N2S |
Molecular Weight | 176.238 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC(=CS1)C2=CC=CC=C2
InChI
InChIKey=PYSJLPAOBIGQPK-UHFFFAOYSA-N
InChI=1S/C9H8N2S/c10-9-11-8(6-12-9)7-4-2-1-3-5-7/h1-6H,(H2,10,11)
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/6970807
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6970807
Phenthiazamine was developed by Sekizawa et al. as a centrally acting anesthetic for fish. The time required to reduce the positive ganglionic potential in the sympathetic ganglion by phenthiazamine was prolonged in the presence of higher concentrations of Ca2+. The Ca2+-dependent action potential of guinea-pig ureter was reduced by this compound, whereas it did not affect the Na+-dependent action potential.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6970807
Curator's Comment: CNS active in fish and frog
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6970807
Curator's Comment: Phenthiazamine was developed by Sekizawa et al. as a centrally acting anesthetic for fish.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: GO:0005262 Sources: https://www.ncbi.nlm.nih.gov/pubmed/6970807 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6970807 |
Primary | Unknown Approved UseUnknown |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6970807
Increase in the amplitude of the slow P potential was found in all the specimens of Frog sympathetic ganglion with Phenthiazamine at 0.5 mM
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2010-06-2
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2528
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40302
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WF2822RIUS
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DTXSID4043804
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217-926-8
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SUBSTANCE RECORD