Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H15N5O3 |
Molecular Weight | 253.2578 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC2=C(N=CN2CCC(CO)CO)C(=O)N1
InChI
InChIKey=JNTOCHDNEULJHD-UHFFFAOYSA-N
InChI=1S/C10H15N5O3/c11-10-13-8-7(9(18)14-10)12-5-15(8)2-1-6(3-16)4-17/h5-6,16-17H,1-4H2,(H3,11,13,14,18)
Molecular Formula | C10H15N5O3 |
Molecular Weight | 253.2578 |
Charge | 0 |
Count |
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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 15:44:24 UTC 2023
by
admin
on
Fri Dec 15 15:44:24 UTC 2023
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Record UNII |
359HUE8FJC
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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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WHO-ATC |
J05AB13
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admin on Fri Dec 15 15:44:24 UTC 2023 , Edited by admin on Fri Dec 15 15:44:24 UTC 2023
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NDF-RT |
N0000175468
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NDF-RT |
N0000175459
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WHO-VATC |
QD06BB06
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NDF-RT |
N0000020060
Created by
admin on Fri Dec 15 15:44:24 UTC 2023 , Edited by admin on Fri Dec 15 15:44:24 UTC 2023
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NCI_THESAURUS |
C29575
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NDF-RT |
N0000175459
Created by
admin on Fri Dec 15 15:44:24 UTC 2023 , Edited by admin on Fri Dec 15 15:44:24 UTC 2023
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WHO-VATC |
QJ05AB13
Created by
admin on Fri Dec 15 15:44:24 UTC 2023 , Edited by admin on Fri Dec 15 15:44:24 UTC 2023
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WHO-ATC |
D06BB06
Created by
admin on Fri Dec 15 15:44:24 UTC 2023 , Edited by admin on Fri Dec 15 15:44:24 UTC 2023
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NCI_THESAURUS |
C281
Created by
admin on Fri Dec 15 15:44:24 UTC 2023 , Edited by admin on Fri Dec 15 15:44:24 UTC 2023
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NDF-RT |
N0000175459
Created by
admin on Fri Dec 15 15:44:24 UTC 2023 , Edited by admin on Fri Dec 15 15:44:24 UTC 2023
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NCI_THESAURUS |
C1556
Created by
admin on Fri Dec 15 15:44:24 UTC 2023 , Edited by admin on Fri Dec 15 15:44:24 UTC 2023
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Code System | Code | Type | Description | ||
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2079
Created by
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PRIMARY | |||
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PENCICLOVIR
Created by
admin on Fri Dec 15 15:44:24 UTC 2023 , Edited by admin on Fri Dec 15 15:44:24 UTC 2023
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PRIMARY | |||
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SUB09661MIG
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PRIMARY | |||
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DB00299
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PRIMARY | |||
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C66337
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PRIMARY | |||
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59839
Created by
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PRIMARY | RxNorm | ||
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759624
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PRIMARY | |||
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6437
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PRIMARY | |||
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7956
Created by
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PRIMARY | |||
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100000091073
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CHEMBL1540
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PRIMARY | |||
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8123
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PRIMARY | |||
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EE-83
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PRIMARY | |||
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m8462
Created by
admin on Fri Dec 15 15:44:24 UTC 2023 , Edited by admin on Fri Dec 15 15:44:24 UTC 2023
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PRIMARY | Merck Index | ||
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359HUE8FJC
Created by
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PRIMARY | |||
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Penciclovir
Created by
admin on Fri Dec 15 15:44:24 UTC 2023 , Edited by admin on Fri Dec 15 15:44:24 UTC 2023
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PRIMARY | |||
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39809-25-1
Created by
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PRIMARY | |||
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359HUE8FJC
Created by
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PRIMARY | |||
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DTXSID9046491
Created by
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PRIMARY | |||
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C053539
Created by
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PRIMARY | |||
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135398748
Created by
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PRIMARY |
Related Record | Type | Details | ||
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TARGET ORGANISM->INHIBITOR |
The in vitro activities of penciclovir against HSV-1, HSV-2 and VZV are similar to those of aciclovir, with median IC50 values of 0.4, 1.5 and 4.0 µg/mL, respectively, in MRC-5 cells.
IC50
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TARGET ORGANISM->INHIBITOR |
The in vitro activities of penciclovir against HSV-1, HSV-2 and VZV are similar to those of aciclovir, with median IC50 values of 0.4, 1.5 and 4.0 µg/mL, respectively, in MRC-5 cells.
IC50
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TARGET ORGANISM->INHIBITOR |
The in vitro activities of penciclovir against HSV-1, HSV-2 and VZV are similar to those of aciclovir, with median IC50 values of 0.4, 1.5 and 4.0 µg/mL, respectively, in MRC-5 cells.
IC50
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SALT/SOLVATE -> PARENT |
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TRANSPORTER -> SUBSTRATE |
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Related Record | Type | Details | ||
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PRODRUG -> METABOLITE ACTIVE |
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METABOLITE INACTIVE -> PARENT |
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Related Record | Type | Details | ||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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