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Compound Detail

CHEMBL216252

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CCC(C)N(CC1CC1)[C@H]1C[C@@H](C)OC(O[C@@H]2[C@@H](C)[C@H](OC3C[C@@](C)(OC)[C@@H](O)[C@H](C)O3)[C@@H](C)C(=O)O[C@H](CC)[C@@]3(C)OC(=O)N(CCc4ccc(Cl)cc4)[C@@H]3[C@@H](C)C(=O)[C@H](C)C[C@]2(C)OC)[C@@H]1O

Basic Information

ChEMBL ID CHEMBL216252
Phase Preclinical
Structure Type MOL
InChI Key QJFIHIWKNRXYSU-KNPUDJCRSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

993.7
MW (Da)
7.75
ALogP
14
HBA
2
HBD
172.0
PSA (Ų)
0.16
QED
3
Ro5 Violations
15
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C53H85ClN2O13
MW 993.72
Aromatic Rings 1
Heavy Atoms 69
NP-Likeness 0.92

Activity Summary

Ki 1 meas. best 7.56

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Gonadotropin-releasing hormone receptor
CHEMBL1855
Ki 7.56 7.56 27.5 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
15006412 10.1016/j.bmcl.2003.12.059 Gonadotropin-releasing hormone receptor 1
15006412 10.1016/j.bmcl.2003.12.059 Staphylococcus aureus 1
15006412 10.1016/j.bmcl.2003.12.059 Staphylococcus epidermidis 1
15006412 10.1016/j.bmcl.2003.12.059 Micrococcus luteus 1
15006412 10.1016/j.bmcl.2003.12.059 Enterococcus faecium 1
15006412 10.1016/j.bmcl.2003.12.059 Streptococcus equinus 1
15006412 10.1016/j.bmcl.2003.12.059 Streptococcus agalactiae 1
15006412 10.1016/j.bmcl.2003.12.059 Streptococcus pyogenes 1

Data from ChEMBL 36 via Core Engine