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Compound Detail

CHEMBL1092765

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C[C@H](c1cccnc1F)c1c(CCN(C)C)sc2ccccc12

Basic Information

ChEMBL ID CHEMBL1092765
Phase Preclinical
Structure Type MOL
InChI Key KLFVGKSTNOVPOR-CYBMUJFWSA-N
3
Targets
3
Activities
2
Assay Types
4
PK Parameters
11
Publications
0
Known Names

Molecular Properties

328.5
MW (Da)
4.69
ALogP
3
HBA
0
HBD
16.1
PSA (Ų)
0.63
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C19H21FN2S
MW 328.46
Aromatic Rings 3
Heavy Atoms 23
NP-Likeness -1.07

Activity Summary

IC50 2 meas. best 5.64
Ki 1 meas. best 8.77

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Histamine H1 receptor
CHEMBL231
Ki 8.77 8.77 1.7 1
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.64 5.64 2300.0 1
Cytochrome P450 2D6
CHEMBL289
IC50 5.12 5.12 7500.0 1

Pharmacokinetic Data

Parameter Value Units Species
AUC 0.64 ng.hr.mL-1 Homo sapiens
CL 12.1 mL.min-1.kg-1 Homo sapiens
F 23.0 % Homo sapiens
T1/2 13.0 hr Homo sapiens

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
20188547 10.1016/j.bmcl.2010.01.134 Rattus norvegicus 13
20188547 10.1016/j.bmcl.2010.01.134 Unchecked 5
20188547 10.1016/j.bmcl.2010.01.134 Homo sapiens 5
20188547 10.1016/j.bmcl.2010.01.134 Voltage-gated inwardly rectifying potassium channel KCNH2 2
20188547 10.1016/j.bmcl.2010.01.134 Caco-2 2
20188547 10.1016/j.bmcl.2010.01.134 Histamine H1 receptor 1
20188547 10.1016/j.bmcl.2010.01.134 Muscarinic acetylcholine receptor M1 1
20188547 10.1016/j.bmcl.2010.01.134 Cytochrome P450 2D6 1
20188547 10.1016/j.bmcl.2010.01.134 Cytochrome P450 3A4 1
20188547 10.1016/j.bmcl.2010.01.134 Brain 1
20188547 10.1016/j.bmcl.2010.01.134 ADMET 1

Data from ChEMBL 36 via Core Engine