(5S)-5-methylimidazolidine-2,4-dione

AlkaPlorer ID: AK078296

Synonym: None

IUPAC Name: (5S)-5-methylimidazolidine-2,4-dione

Structure

SMILES: C[C@@H]1N=C(O)N=C1O

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InChI: InChI=1S/C4H6N2O2/c1-2-3(7)6-4(8)5-2/h2H,1H3,(H2,5,6,7,8)/t2-/m0/s1

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InChIKey: VMAQYKGITHDWKL-REOHCLBHSA-N

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Reference

PubChem CID: 6419931

CAS: 40856-73-3

SuperNatural Ⅲ: SN0393922-01

NPASS: NPC249154

Source

Species Genus Family Order Class Phylum Kingdom Domain
Pueraria montana Pueraria Fabaceae Fabales Magnoliopsida Streptophyta Viridiplantae Eukaryota

Properties Information

Molecule Weight: 114.10399999999998

TPSA: 65.18

MolLogP: 0.259

Number of H-Donors: 2

Number of H-Acceptors: 2

RingCount: 1

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Homo sapiens Histone deacetylase 6 Inhibition -10.1 % 10.6019/CHEMBL4808148
Homo sapiens Histone deacetylase 6 Inhibition 10.35 % 10.6019/CHEMBL4808148
Severe acute respiratory syndrome coronavirus 2 Replicase polyprotein 1ab Inhibition 12.73 % 10.6019/CHEMBL4495564
Severe acute respiratory syndrome coronavirus 2 SARS-CoV-2 IC50 19952.62 nM 10.6019/CHEMBL4651402
Severe acute respiratory syndrome coronavirus 2 SARS-CoV-2 IC50 20000.0 nM 10.6019/CHEMBL4651402
Severe acute respiratory syndrome coronavirus 2 SARS-CoV-2 Inhibition 0.07 % 10.6019/CHEMBL4495565
Severe acute respiratory syndrome coronavirus 2 SARS-CoV-2 Inhibition 1.39 % 10.21203/rs.3.rs-23951/v1

Metabolism Information

AKRT ID Reaction Reaction Link ID
AKRT013005 C[C@@H]1NC(=O)NC1=O>>C[C@H](NC(N)=O)C(=O)O enzymemap_78478
AKRT013006 C[C@@H]1NC(=O)NC1=O>>C[C@H]1NC(=O)NC1=O None
AKRT014050 C[C@H]1NC(=O)NC1=O>>C[C@@H]1NC(=O)NC1=O None