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Compound Detail

CHEMBL423428

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CC1(C)Oc2ccc3c4c(c(=O)oc3c2[C@@H](OC(=O)C23CCC(C)(C(=O)O2)C3(C)C)[C@H]1OC(=O)C12CCC(C)(C(=O)O1)C2(C)C)CCCC4

Basic Information

ChEMBL ID CHEMBL423428
Phase Preclinical
Structure Type MOL
InChI Key UJNLTLUNIGHSRZ-QYPIKLKCSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

676.8
MW (Da)
5.58
ALogP
11
HBA
0
HBD
144.6
PSA (Ų)
0.23
QED
3
Ro5 Violations
4
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C38H44O11
MW 676.76
Aromatic Rings 2
Heavy Atoms 49
NP-Likeness 1.28

Activity Summary

EC50 1 meas. best 5.67

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
H9
CHEMBL614806
EC50 5.67 5.67 2120.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
H9 EC50 = 2120.0 nM 5.67 Inhibitory activity against HIV-1 replication in H9 lymphocytes 11262077

Literature References

PubMed DOI Target Context # Activities
11262077 10.1021/jm000070g H9 2
11262077 10.1021/jm000070g ADMET 1

Data from ChEMBL 36 via Core Engine