Details
Stereochemistry | ACHIRAL |
Molecular Formula | C28H24N6 |
Molecular Weight | 444.5304 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 2 |
SHOW SMILES / InChI
SMILES
CC1=C(N(\N=N\N2C3=[N+](C=CC=C3)C(C)=C2C4=CC=CC=C4)C5=[N+]1C=CC=C5)C6=CC=CC=C6
InChI
InChIKey=NJAGGYXZTILBMJ-QVIHXGFCSA-N
InChI=1S/C28H24N6/c1-21-27(23-13-5-3-6-14-23)33(25-17-9-11-19-31(21)25)29-30-34-26-18-10-12-20-32(26)22(2)28(34)24-15-7-4-8-16-24/h3-20H,1-2H3/q+2/b30-29+
Molecular Formula | C28H24N6 |
Molecular Weight | 444.5304 |
Charge | 2 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/6113885
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6113885
Fazadinium (used as a bromide salt) is a muscle relaxant, which was applied in anesthesia under the name Fazadon. The current marketing status is unknown and the drug is supposed to be discontinued.
Originator
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6113885
The recommended dose is 1.5 mg/kg.
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6108148
The guinea-pig isolated hypogastric nerve-vas deferens preparation and isolated phrenic nerve-diaphragm preparation were incubated with fazadinium at a concentration from 10(-5) to 3.2*10(-4) M. EC50 for neuromuscular blockade was 2.8*10(-5) M and EC50 for ganglion blockade was 6.4*10(-5) M.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:06:51 UTC 2023
by
admin
on
Fri Dec 15 16:06:51 UTC 2023
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Record UNII |
0R97XIX3OA
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C29696
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WHO-ATC |
M03AC08
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NCI_THESAURUS |
C66886
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SUB02104MIG
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C80979
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100000087500
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C084773
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Fazadinium
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0R97XIX3OA
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4535
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DTXSID801021594
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36653-54-0
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5487713
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |