Details
Stereochemistry | ACHIRAL |
Molecular Formula | C20H22N4O5 |
Molecular Weight | 398.4125 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CN(C)C(=O)COC(=O)CC1=CC=C(OC(=O)C2=CC=C(NC(N)=N)C=C2)C=C1
InChI
InChIKey=XASIMHXSUQUHLV-UHFFFAOYSA-N
InChI=1S/C20H22N4O5/c1-24(2)17(25)12-28-18(26)11-13-3-9-16(10-4-13)29-19(27)14-5-7-15(8-6-14)23-20(21)22/h3-10H,11-12H2,1-2H3,(H4,21,22,23)
Molecular Formula | C20H22N4O5 |
Molecular Weight | 398.4125 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:42:12 UTC 2023
by
admin
on
Fri Dec 15 15:42:12 UTC 2023
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Record UNII |
0FD207WKDU
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Record Status |
Validated (UNII)
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Record Version |
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-
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Name | Type | Language | ||
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Official Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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WHO-VATC |
QB02AB04
Created by
admin on Fri Dec 15 15:42:12 UTC 2023 , Edited by admin on Fri Dec 15 15:42:12 UTC 2023
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WHO-ATC |
B02AB04
Created by
admin on Fri Dec 15 15:42:12 UTC 2023 , Edited by admin on Fri Dec 15 15:42:12 UTC 2023
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NCI_THESAURUS |
C783
Created by
admin on Fri Dec 15 15:42:12 UTC 2023 , Edited by admin on Fri Dec 15 15:42:12 UTC 2023
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FDA ORPHAN DRUG |
338211
Created by
admin on Fri Dec 15 15:42:12 UTC 2023 , Edited by admin on Fri Dec 15 15:42:12 UTC 2023
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Code System | Code | Type | Description | ||
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C034532
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m3000
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admin on Fri Dec 15 15:42:12 UTC 2023 , Edited by admin on Fri Dec 15 15:42:12 UTC 2023
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PRIMARY | Merck Index | ||
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DTXSID6044010
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471
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PRIMARY | |||
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135632
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59721-28-7
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DB13729
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CHEMBL590799
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2536
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PRIMARY | |||
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C73213
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PRIMARY | |||
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0FD207WKDU
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PRIMARY | |||
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100000081618
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SUB06066MIG
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5068
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PRIMARY | |||
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CAMOSTAT
Created by
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PRIMARY | |||
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6432
Created by
admin on Fri Dec 15 15:42:12 UTC 2023 , Edited by admin on Fri Dec 15 15:42:12 UTC 2023
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PRIMARY |
Related Record | Type | Details | ||
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TARGET ORGANISM->INHIBITOR |
In vitro study showed that Camostat reduces significantly the infection of Calu-3 lung cells by SARS-CoV-2, the virus responsible for COVID-19.
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TARGET -> INHIBITOR |
IC50
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SALT/SOLVATE -> PARENT |
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Related Record | Type | Details | ||
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METABOLITE ACTIVE -> PARENT |
MAJOR
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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