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Compound Detail

CHEMBL504768

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CC[C@@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CCCNC(=N)N)N=[N+]=[N-])C(=O)N[C@@H](CC(C)C)C(=O)O

Basic Information

ChEMBL ID CHEMBL504768
Phase Preclinical
Structure Type BOTH
InChI Key HLSORHLOWZGVQE-CSJNAZMVSA-N
1
Targets
3
Activities
3
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

843.0
MW (Da)
0.25
ALogP
10
HBA
12
HBD
366.8
PSA (Ų)
0.02
QED
2
Ro5 Violations
25
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C38H62N14O8
MW 843.00
Aromatic Rings 1
Heavy Atoms 60
NP-Likeness 0.13

Activity Summary

EC50 1 meas. best 9.11
IC50 1 meas. best 9.01
Ki 1 meas. best 9.14

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Neurotensin receptor type 1
CHEMBL4123
Ki 9.14 9.14 0.7 1
Neurotensin receptor type 1
CHEMBL4123
EC50 9.11 9.11 0.8 1
Neurotensin receptor type 1
CHEMBL4123
IC50 9.01 9.01 1.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
19290594 10.1021/jm801072v Serum 4
19290594 10.1021/jm801072v Neurotensin receptor type 1 4
19290594 10.1021/jm801072v Rattus norvegicus 2

Data from ChEMBL 36 via Core Engine