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Compound Detail

CHEMBL186312

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CC(C)[C@@H]1CC[C@]2(CO)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC[C@H](OC(=O)CC(C)(C)CC(=O)O)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12

Basic Information

ChEMBL ID CHEMBL186312
Phase Preclinical
Structure Type MOL
InChI Key YVORLYFGKZWWMI-XONOOPINSA-N
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

586.9
MW (Da)
8.52
ALogP
4
HBA
2
HBD
83.8
PSA (Ų)
0.29
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 C37H62O5
MW 586.90
Aromatic Rings 0
Heavy Atoms 42
NP-Likeness 2.55

Activity Summary

EC50 1 meas. best 8.89
IC50 1 meas. best 4.59

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus 1
CHEMBL378
EC50 8.89 8.89 1.3 1
H9
CHEMBL614806
IC50 4.59 4.59 25690.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
15501054 10.1016/j.bmcl.2004.09.033 H9 1
15501054 10.1016/j.bmcl.2004.09.033 Human immunodeficiency virus 1 1
15501054 10.1016/j.bmcl.2004.09.033 ADMET 1

Data from ChEMBL 36 via Core Engine