AntibioticMech

valacyclovir

CHEBI:35854 ·resolve ·ANTIVIRAL ·EXACT SEEDED

Classification

Strictly broader compounds or drug classes this molecule belongs to.

• CHEBI:35855 CHEBI:35855

Chemical structure

Computed structure properties

Molecular formula	C13H20N6O4
Charge	0
Average mass	324.341 Da
Monoisotopic mass	324.1546 Da
Source	ChEBI
InChIKey	HDOVUKNUBWVHOX-QMMMGPOBSA-N

SMILES

CC(C)[C@H](N)C(=O)OCCOCn1cnc2c(=O)nc(N)nc21

InChI

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

Also called

• 2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl L-valinate (EXACT_SYNONYM)— chebi
• L-Valine ester with 9-((2-hydroxyethoxy)methyl)guanine (EXACT_SYNONYM)— chebi
• L-Valine, 2-((2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy)ethyl ester (EXACT_SYNONYM)— chebi

Cross-references

Equivalent identifiers for this same structure in other resources.

• beilstein:8160931
• cas:124832-26-4
• drugcentral:2798
• lincs.smallmolecule:LSM-5571
• wikipedia.en:Valacyclovir

Activity roles

Every antimicrobial role a source asserts for this compound — the unreduced evidence behind its antimicrobial_class.

• CHEBI:36044 CHEBI:36044

Source concepts

Every upstream concept that resolved to this record. The merge is the product: this is what shows ChEBI and CARD are describing the same structure.

Upstream concepts merged into this record

Source	Native ID	Label	Minted CURIE	Version
CHEBI	CHEBI:35854	valacyclovir	antibioticmech:chebi-9a1c605b07	2026-08-30

Curation history

1. SEEDED_FROM_SOURCES 2026-08-30 · seed_from_sources

   Seeded from data/raw/ inventories (CHEBI)

2. RESEEDED_FROM_SOURCES 2026-08-30 · seed_from_sources

   Re-seeded from updated data/raw/ inventories

3. RESEEDED_FROM_SOURCES 2026-08-30 · seed_from_sources

   Re-seeded from updated data/raw/ inventories

Provenance

Seeded by scripts/seed_from_sources.py from the committed inventories in data/raw/. View the record.