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Compound Detail

CHEMBL102324

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CCC(CC)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(=O)N1CCCC1)C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)O

Basic Information

ChEMBL ID CHEMBL102324
Phase Preclinical
Structure Type MOL
InChI Key VRSTZDVILMURLO-LEAZDLGRSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

583.7
MW (Da)
0.00
ALogP
7
HBA
6
HBD
211.3
PSA (Ų)
0.14
QED
2
Ro5 Violations
17
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C27H45N5O9
MW 583.68
Aromatic Rings 0
Heavy Atoms 41
NP-Likeness -0.14

Activity Summary

IC50 1 meas. best 4.96

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
IC50 4.96 4.96 11000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 11000.0 nM 4.96 Inhibition of Herpes simplex virus type 1 ribonucleotide reductase 8411018

Literature References

PubMed DOI Target Context # Activities
8411018 10.1021/jm00072a021 Unchecked 1

Data from ChEMBL 36 via Core Engine