Details
Stereochemistry | MIXED |
Molecular Formula | C14H19N3O.2C12H19NO3 |
Molecular Weight | 695.8885 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 0 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(CC)C(=O)C1CC=CCC1C(O)=O.CCN(CC)C(=O)C2CC=CCC2C(O)=O.COC3=CC4=C(C=C3)N=CC=C4NCCN(C)C
InChI
InChIKey=IYQFWDZTTDVVBP-UHFFFAOYSA-N
InChI=1S/C14H19N3O.2C12H19NO3/c1-17(2)9-8-16-14-6-7-15-13-5-4-11(18-3)10-12(13)14;2*1-3-13(4-2)11(14)9-7-5-6-8-10(9)12(15)16/h4-7,10H,8-9H2,1-3H3,(H,15,16);2*5-6,9-10H,3-4,7-8H2,1-2H3,(H,15,16)
Molecular Formula | C14H19N3O |
Molecular Weight | 245.3202 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C12H19NO3 |
Molecular Weight | 225.2842 |
Charge | 0 |
Count |
|
Stereochemistry | MIXED |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Quinetolate is a quinolone derivative patented by The Geschickter Fund for Medical Research, Inc. for the treatment of bronchial asthma. In preclinical studies, Quinetolate antagonized the effect of histamine on the lung in rabbits and blocked arrhythmias induced by chloroform in mice. Quinetholate shows potent antiarrhythmic activities on ouabain-induced tachycardia. Quinetholate caused the longest lasting reversions of ouabain-induced tachycardia, i.e. usually lasting at least 30 min after infusion was stopped.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:45:08 GMT 2023
by
admin
on
Fri Dec 15 18:45:08 GMT 2023
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Record UNII |
56UTZ1RCNO
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29712
Created by
admin on Fri Dec 15 18:45:08 GMT 2023 , Edited by admin on Fri Dec 15 18:45:08 GMT 2023
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56UTZ1RCNO
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227-207-0
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C017700
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C152123
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2112
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DTXSID30972605
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21947
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5714-76-1
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SUB10212MIG
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100000080296
Created by
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