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Compound Detail

CHEMBL5201690

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CC(C)(C)c1ccc(C2CC(c3ccc(CN4CC(C(=O)[O-])C4)cc3)=NO2)cc1.[Na+]

Basic Information

ChEMBL ID CHEMBL5201690
Phase Preclinical
Structure Type MOL
InChI Key DGBGDTPWBADAKB-UHFFFAOYSA-M
Parent Compound CHEMBL5222521
Active Moiety CHEMBL5222521
1
Targets
2
Activities
1
Assay Types
8
PK Parameters
8
Publications
0
Known Names

Molecular Properties

392.5
MW (Da)
4.37
ALogP
4
HBA
1
HBD
62.1
PSA (Ų)
0.82
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C24H27N2NaO3
MW 414.48
Aromatic Rings 2
Heavy Atoms 29
NP-Likeness -0.93

Activity Summary

EC50 2 meas. best 7.46

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Sphingosine 1-phosphate receptor 1
CHEMBL4333
EC50 7.46 7.205 34.6 2

Pharmacokinetic Data

Parameter Value Units Species
AUC 1155.5 ng.hr.mL-1 Rattus norvegicus
AUC 5187.6 ng.hr.mL-1 Rattus norvegicus
CL 13.1 mL.min-1.kg-1 Rattus norvegicus
Cmax 2728.66 nM Rattus norvegicus
F 44.9 % Rattus norvegicus
T1/2 2.4 hr Rattus norvegicus
T1/2 3.1 hr Rattus norvegicus
Tmax 2.3 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