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Compound Detail

CHEMBL5280223

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C=C(C)[C@@H]1CC[C@]2(NCCC3(O)CCN(C(C)=O)CC3)CC[C@]3(C)[C@H](CC[C@@H]4[C@@]5(C)CC=C(C6=CC[C@](CF)(C(=O)O)CC6)C(C)(C)[C@@H]5CC[C@]43C)[C@@H]12

Basic Information

ChEMBL ID CHEMBL5280223
Phase Preclinical
Structure Type MOL
InChI Key SNSFRYFTKCGZBB-CTHDWTAISA-N
2
Targets
5
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

735.1
MW (Da)
9.44
ALogP
4
HBA
3
HBD
89.9
PSA (Ų)
0.22
QED
2
Ro5 Violations
8
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C46H71FN2O4
MW 735.08
Aromatic Rings 0
Heavy Atoms 53
NP-Likeness 1.54

Activity Summary

EC50 5 meas. best 8.77

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Human immunodeficiency virus 1
CHEMBL378
EC50 8.77 8.1867 1.7 3
Unchecked
CHEMBL612545
EC50 8.76 7.79 1.7 2

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
36441509 10.1021/acs.jmedchem.2c01618 Human immunodeficiency virus 1 3
36441509 10.1021/acs.jmedchem.2c01618 Unchecked 1
36441509 10.1021/acs.jmedchem.2c01618 MT2 1

Data from ChEMBL 36 via Core Engine