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Compound Detail

CHEMBL5189040

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CC(C)(C)c1ccc(-n2cc(-c3ccc(CN4CC(C(=O)[O-])C4)cc3)nn2)cc1.[Na+]

Basic Information

ChEMBL ID CHEMBL5189040
Phase Preclinical
Structure Type MOL
InChI Key BNPMLGWISKFZPR-UHFFFAOYSA-M
Parent Compound CHEMBL5222050
Active Moiety CHEMBL5222050
1
Targets
2
Activities
1
Assay Types
8
PK Parameters
8
Publications
0
Known Names

Molecular Properties

390.5
MW (Da)
3.75
ALogP
5
HBA
1
HBD
71.2
PSA (Ų)
0.72
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H25N4NaO2
MW 412.47
Aromatic Rings 3
Heavy Atoms 29
NP-Likeness -1.61

Activity Summary

EC50 2 meas. best 7.19

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Sphingosine 1-phosphate receptor 1
CHEMBL4333
EC50 7.19 7.08 64.9 2

Pharmacokinetic Data

Parameter Value Units Species
AUC 370.8 ng.hr.mL-1 Rattus norvegicus
AUC 93.4 ng.hr.mL-1 Rattus norvegicus
CL 44.7 mL.min-1.kg-1 Rattus norvegicus
Cmax 61.21 nM Rattus norvegicus
F 2.5 % Rattus norvegicus
T1/2 1.2 hr Rattus norvegicus
T1/2 1.4 hr Rattus norvegicus
Tmax 1.4 hr Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
35077170 10.1021/acs.jmedchem.1c01979 ADMET 12
35077170 10.1021/acs.jmedchem.1c01979 Sphingosine 1-phosphate receptor 1 2
35077170 10.1021/acs.jmedchem.1c01979 Sphingosine 1-phosphate receptor 3 1
35077170 10.1021/acs.jmedchem.1c01979 Cytochrome P450 1A2 1
35077170 10.1021/acs.jmedchem.1c01979 Cytochrome P450 2C19 1
35077170 10.1021/acs.jmedchem.1c01979 Cytochrome P450 2D6 1
35077170 10.1021/acs.jmedchem.1c01979 Cytochrome P450 2C9 1
35077170 10.1021/acs.jmedchem.1c01979 Cytochrome P450 3A4 1

Data from ChEMBL 36 via Core Engine