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Compound Detail

CHEMBL4454160

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CC(C)[C@@H]1NC(=O)[C@H](Cc2ccc(F)cc2)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)CCCSC[C@@H](C(=O)N2CCC[C@H]2C(=O)NCCCCNC(=N)N)NC(=O)[C@H](CC(N)=O)NC1=O

Basic Information

ChEMBL ID CHEMBL4454160
Phase Preclinical
Structure Type MOL
InChI Key HHXSLPKOTCDMNX-VGNPQVDOSA-N
2
Targets
4
Activities
1
Assay Types
2
PK Parameters
6
Publications
0
Known Names

Molecular Properties

940.1
MW (Da)
-0.83
ALogP
11
HBA
11
HBD
320.1
PSA (Ų)
0.06
QED
3
Ro5 Violations
14
Rot. Bonds

Drug Information

Molecule Type Unknown
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C44H62FN11O9S
MW 940.11
Aromatic Rings 2
Heavy Atoms 66
NP-Likeness 0.21

Activity Summary

EC50 4 meas. best 7.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Vasopressin V2 receptor
CHEMBL1790
EC50 7.0 7.0 100.0 1
Vasopressin V1b receptor
CHEMBL1921
EC50 6.75 6.75 180.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 8.7 mL.min-1.kg-1 Rattus norvegicus
CL 45.0 % Rattus norvegicus

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
31022340 10.1021/acs.jmedchem.9b00132 ADMET 3
31022340 10.1021/acs.jmedchem.9b00132 Vasopressin V2 receptor 1
31022340 10.1021/acs.jmedchem.9b00132 Vasopressin V1b receptor 1
31022340 10.1021/acs.jmedchem.9b00132 Unchecked 1
31022340 10.1021/acs.jmedchem.9b00132 Vasopressin V1a receptor 1
31022340 10.1021/acs.jmedchem.9b00132 Oxytocin receptor 1

Data from ChEMBL 36 via Core Engine