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Compound Detail

CHEMBL3250430

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CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)CNC)C(C)C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](COC)C(=O)O

Basic Information

ChEMBL ID CHEMBL3250430
Phase Preclinical
Structure Type BOTH
InChI Key JBJSMFKQGARKLI-BVJBXUKBSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
2
Publications
0
Known Names

Molecular Properties

956.1
MW (Da)
-2.28
ALogP
13
HBA
13
HBD
364.3
PSA (Ų)
0.02
QED
3
Ro5 Violations
28
Rot. Bonds

Drug Information

Molecule Type Protein
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C44H69N13O11
MW 956.12
Aromatic Rings 2
Heavy Atoms 68
NP-Likeness -0.03

Activity Summary

Kd 1 meas. best 9.66

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
Kd 9.66 9.66 0.2 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked Kd = 0.2188 nM 9.66 Antagonist activity at angiotensin 2 receptor in rabbit aortic strip assessed as... 836496

Literature References

PubMed DOI Target Context # Activities
836496 10.1021/jm00212a013 Rattus norvegicus 6
836496 10.1021/jm00212a013 Unchecked 2

Data from ChEMBL 36 via Core Engine