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Compound Detail

CHEMBL2368145

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Cc1cccc2c1OP(=O)(OC[C@H]1O[C@@H](n3cc(/C=C/Br)c(=O)[nH]c3=O)C[C@@H]1OC(=O)[C@H](C)N)OC2.O=C(O)C(F)(F)F

Basic Information

ChEMBL ID CHEMBL2368145
Phase Preclinical
Structure Type MOL
InChI Key JWXLOIHXNYXJKH-VVCOBREGSA-N
Parent Compound CHEMBL2368811
Active Moiety CHEMBL2368811
1
Targets
1
Activities
1
Assay Types
2
PK Parameters
5
Publications
0
Known Names

Molecular Properties

586.3
MW (Da)
2.49
ALogP
11
HBA
2
HBD
161.2
PSA (Ų)
0.36
QED
2
Ro5 Violations
7
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C24H26BrF3N3O11P
MW 700.35
Aromatic Rings 2
Heavy Atoms 36
NP-Likeness 0.44

Activity Summary

EC50 1 meas. best 4.6

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Nucleic Acid
CHEMBL345
EC50 4.6 4.6 25300.0 1

Pharmacokinetic Data

Parameter Value Units Species
T1/2 1.26 - -
T1/2 1.43 - -

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Nucleic Acid EC50 = 25300.0 nM 4.6 Effective concentration for the inhibition of Epstein-Barr virus EBV-DNA synthes... 12408726

Literature References

PubMed DOI Target Context # Activities
12408726 10.1021/jm0209275 ADMET 2
12408726 10.1021/jm0209275 No relevant target 1
12408726 10.1021/jm0209275 Nucleic Acid 1
12408726 10.1021/jm0209275 P3HR-1 1
12408726 10.1021/jm0209275 Unchecked 1

Data from ChEMBL 36 via Core Engine