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Compound Detail

CHEMBL3634340

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C[C@]1(c2cc(NC(=O)c3ccc(Cl)cn3)ccc2F)N=C(N)CO[C@@H]1F

Basic Information

ChEMBL ID CHEMBL3634340
Phase Preclinical
Structure Type MOL
InChI Key HBJCZLYQYZGGRO-DLBZAZTESA-N
1
Targets
2
Activities
1
Assay Types
4
PK Parameters
13
Publications
0
Known Names

Molecular Properties

380.8
MW (Da)
3.02
ALogP
5
HBA
2
HBD
89.6
PSA (Ų)
0.86
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C17H15ClF2N4O2
MW 380.78
Aromatic Rings 2
Heavy Atoms 26
NP-Likeness -1.41

Activity Summary

IC50 2 meas. best 8.28

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Beta-secretase 1
CHEMBL4822
IC50 8.28 8.205 5.2 2

Pharmacokinetic Data

Parameter Value Units Species
Fu 0.019 - Rattus norvegicus
Fu 0.18 - Homo sapiens
Fu 0.14 - Mus musculus
Fu - - Canis lupus familiaris

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
26378740 10.1021/acs.jmedchem.5b01101 ADMET 4
26378740 10.1021/acs.jmedchem.5b01101 Plasma 3
26378740 10.1021/acs.jmedchem.5b01101 Beta-secretase 1 2
26378740 10.1021/acs.jmedchem.5b01101 Liver microsome 2
26378740 10.1021/acs.jmedchem.5b01101 Cytochrome P450 2D6 2
26378740 10.1021/acs.jmedchem.5b01101 No relevant target 1
26378740 10.1021/acs.jmedchem.5b01101 Brain 1
26378740 10.1021/acs.jmedchem.5b01101 Cytochrome P450 1A2 1
26378740 10.1021/acs.jmedchem.5b01101 Cytochrome P450 2C9 1
26378740 10.1021/acs.jmedchem.5b01101 Cytochrome P450 2C19 1
26378740 10.1021/acs.jmedchem.5b01101 Cytochrome P450 3A4 1
26378740 10.1021/acs.jmedchem.5b01101 Voltage-gated inwardly rectifying potassium channel KCNH2 1
29809004 10.1021/acs.jmedchem.8b00304 Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine