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Compound Detail

CHEMBL350999

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Cc1c(C)c2ccc3c(c2oc1=O)[C@@H](OC(=O)C12CCC(C)(C(=O)O1)C2(C)C)[C@@H](OC(=O)C12CCC(C)(C(=O)O1)C2(C)C)C(C)(C)O3

Basic Information

ChEMBL ID CHEMBL350999
Phase Preclinical
Structure Type MOL
InChI Key XITCYMFLMPETLK-QYWJQYFGSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

650.7
MW (Da)
5.32
ALogP
11
HBA
0
HBD
144.6
PSA (Ų)
0.24
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 C36H42O11
MW 650.72
Aromatic Rings 2
Heavy Atoms 47
NP-Likeness 1.34

Activity Summary

EC50 1 meas. best 5.72

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
H9
CHEMBL614806
EC50 5.72 5.72 1920.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
H9 EC50 = 1920.0 nM 5.72 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