Details
Stereochemistry | ACHIRAL |
Molecular Formula | 2C7H8N4O2.C2H8N2 |
Molecular Weight | 420.4264 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NCCN.CN1C2=C(N=CN2)C(=O)N(C)C1=O.CN3C4=C(N=CN4)C(=O)N(C)C3=O
InChI
InChIKey=FQPFAHBPWDRTLU-UHFFFAOYSA-N
InChI=1S/2C7H8N4O2.C2H8N2/c2*1-10-5-4(8-3-9-5)6(12)11(2)7(10)13;3-1-2-4/h2*3H,1-2H3,(H,8,9);1-4H2
Approval Year
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Classification Tree | Code System | Code | ||
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WHO-VATC |
QR03DB05
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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WHO-ATC |
R03DB05
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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WHO-VATC |
QR03DA05
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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WHO-ATC |
R03DA55
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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NCI_THESAURUS |
C744
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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WHO-VATC |
QR03DA55
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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LIVERTOX |
41
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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WHO-ATC |
R03DA05
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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NCI_THESAURUS |
C319
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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Code System | Code | Type | Description | ||
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DB01223
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m1731
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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PRIMARY | Merck Index | ||
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100000092236
Created by
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2659
Created by
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C47393
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317-34-0
Created by
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221
Created by
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9433
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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PRIMARY | |||
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Aminophylline
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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376
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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689
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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7919
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SUB05444MIG
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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CHEMBL190
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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27Y3KJK423
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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D000628
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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206-264-5
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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27Y3KJK423
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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AMINOPHYLLINE
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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AMINOPHYLLINE
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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PRIMARY | Description: White or slightly yellowish granules or powder; odour, slightly ammoniacal. Solubility: Freely soluble in water (the solution may become cloudy in the presence of carbon dioxide); slightly soluble in ethanol (~750 g/l) TS; practically insoluble in ether R. Category: Antispasmodic; diuretic; coronary vasodilator.Storage. Aminophylline should be kept in a tightly closed container, protected from light. Additional information: Aminophylline contains a variable quantity of water of hydration. Upon exposure to air Aminophylline gradually loses ethylenediamine and absorbs carbon dioxide with the liberation of free theophylline. Even in the absence of light, Aminophylline is gradually degraded on exposure to a humid atmosphere, the decomposition being faster at higher temperatures. Definition: Aminophylline contains not less than 78.0% and not more than 86.0% of theophylline (C7H8N4O2), and not less than 12.8% and not more than 15.0% of ethylenediamine (C2H8N2), both calculated with reference to the anhydrous substance. | ||
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DTXSID40883359
Created by
admin on Fri Dec 15 15:10:39 UTC 2023 , Edited by admin on Fri Dec 15 15:10:39 UTC 2023
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD