VALACYCLOVIR

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C13H20N6O4
Molecular Weight	324.3357
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of VALACYCLOVIR

Structure Search

SMILES

CC(C)[C@H](N)C(=O)OCCOCN1C=NC2=C1N=C(N)NC2=O

InChI

InChIKey=HDOVUKNUBWVHOX-QMMMGPOBSA-N

InChI=1S/C13H20N6O4/c1-7(2)8(14)12(21)23-4-3-22-6-19-5-16-9-10(19)17-13(15)18-11(9)20/h5,7-8H,3-4,6,14H2,1-2H3,(H3,15,17,18,20)/t8-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C13H20N6O4
Molecular Weight	324.3357
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 16:44:02 UTC 2023` Edited by `admin` on `Sat Dec 16 16:44:02 UTC 2023`
Record UNII	MZ1IW7Q79D
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

VALACYCLOVIR

Common Name

English

Valaciclovir [WHO-DD]

Common Name

English

L-VALINE 2-((2-AMINO-1,6-DIHYDRO-6-OXO-9H-PURIN-9-YL)METHOXY)ETHYL ESTER

Systematic Name

English

VALACICLOVIR

Official Name

English

VALACYCLOVIR [MI]

Common Name

English

VALACV

Common Name

English

valaciclovir [INN]

Common Name

English

L-VALINE, 2-((2-AMINO-1,6-DIHYDRO-6-OXO-9H-PURIN-9-YL)METHOXY)ETHYL ESTER

Common Name

English

L-VALINE, ESTER WITH 9-((2-HYDROXYETHOXY)METHYL)GUANINE

Common Name

English

VALACYCLOVIR [VANDF]

Common Name

English

L-VALINE ESTER WITH 9-((2-HYDROXYETHOXY)METHYL)GUANINE

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C281

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

NDF-RT

N0000175459

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

NDF-RT

N0000180187

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

WHO-ATC

J05AB11

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

NCI_THESAURUS

C29575

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

NCI_THESAURUS

C1556

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

NDF-RT

N0000175459

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

LIVERTOX

NBK548655

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

WHO-VATC

QJ05AB11

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

NDF-RT

N0000020060

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

NDF-RT

N0000175459

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

NDF-RT

N0000175468

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

NDF-RT

N0000180188

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

Code System Code Type Description

EVMPD

SUB00003MIG

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

RXCUI

73645

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

RxNorm

ChEMBL

CHEMBL1349

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

MESH

C084555

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

CAS

124832-26-4

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

HSDB

8084

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

INN

7106

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

EPA CompTox

DTXSID1023732

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

CHEBI

35854

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

WIKIPEDIA

VALACICLOVIR

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

PUBCHEM

135398742

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

MERCK INDEX

m11355

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

Merck Index

DRUG CENTRAL

2798

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

DAILYMED

MZ1IW7Q79D

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

SMS_ID

100000092738

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

DRUG BANK

DB00577

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

FDA UNII

MZ1IW7Q79D

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

LACTMED

Valacyclovir

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

NCI_THESAURUS

C28235

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

IUPHAR

4824

Created by admin on Sat Dec 16 16:44:03 UTC 2023 , Edited by admin on Sat Dec 16 16:44:03 UTC 2023

PRIMARY

Related Record Type Details


					91L39G324W

PEPT-2

TRANSPORTER -> SUBSTRATE


					JF64RVR4E3

VALACYCLOVIR HYDROCHLORIDE MONOHYDRATE

SALT/SOLVATE -> PARENT

Amount:


					G447S0T1VC

VALACYCLOVIR HYDROCHLORIDE

SALT/SOLVATE -> PARENT

Amount:


					XYD5147M6H

PEPT-1

TRANSPORTER -> INHIBITOR


					6D53G0FD0Z

PLASMA PROTEIN FRACTION (HUMAN)

BINDER->LIGAND

Interaction Type:

BINDING

Amount:


					A7JO128919

VALACYCLOVIR HYDROCHLORIDE DIHYDRATE

SALT/SOLVATE -> PARENT

Amount:


					XYD5147M6H

PEPT-1

TRANSPORTER -> SUBSTRATE

Related Record Type Details


					X4HES1O11F

ACYCLOVIR

METABOLITE ACTIVE -> PRODRUG

Amount:

Related Record Type Details


					X4HES1O11F

ACYCLOVIR

ACTIVE MOIETY

Amount:

Name	Property Type	Amount	Referenced Substance	Defining	Parameters	References
Biological Half-life	PHARMACOKINETIC