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Compound Detail

CHEMBL418256

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CC[C@H]1OC(=O)[C@H](C)[C@@H](OC(=O)N2C(=O)OC[C@@H]2C)[C@H](C)[C@@H](OC2O[C@H](C)C[C@H](N(C)CC3CC3)[C@H]2O)[C@@](C)(OC)C[C@@H](C)C(=O)[C@H](C)[C@H]2N(CCc3ccc(Cl)cc3)C(=O)O[C@]12C

Basic Information

ChEMBL ID CHEMBL418256
Phase Preclinical
Structure Type MOL
InChI Key LSWLRKGXSVFLJY-ZWKBLDHJSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
8
Publications
0
Known Names

Molecular Properties

920.5
MW (Da)
6.64
ALogP
14
HBA
1
HBD
179.9
PSA (Ų)
0.18
QED
3
Ro5 Violations
11
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C47H70ClN3O13
MW 920.54
Aromatic Rings 1
Heavy Atoms 64
NP-Likeness 0.82

Activity Summary

Ki 1 meas. best 7.73

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Gonadotropin-releasing hormone receptor
CHEMBL1855
Ki 7.73 7.73 18.6 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