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Compound Detail

CHEMBL1808911

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N=C(N)NCCC[C@H](NC(=O)Cc1ccccc1)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)NCc1ccc(C(=N)N)cc1

Basic Information

ChEMBL ID CHEMBL1808911
Phase Preclinical
Structure Type MOL
InChI Key KCKQLYSYMKXATG-QKDODKLFSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

716.9
MW (Da)
-1.22
ALogP
8
HBA
13
HBD
318.8
PSA (Ų)
0.04
QED
2
Ro5 Violations
21
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C34H48N14O4
MW 716.85
Aromatic Rings 3
Heavy Atoms 52
NP-Likeness -0.29

Activity Summary

Ki 1 meas. best 8.2

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Furin
CHEMBL2611
Ki 8.2 8.2 6.3 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Furin Ki = 6.3 nM 8.2 Inhibition of recombinant human furin expressed in CHO cells using pyroGlu- Arg-... 21757345

Literature References

PubMed DOI Target Context # Activities
21757345 10.1016/j.bmcl.2011.06.091 Furin 1

Data from ChEMBL 36 via Core Engine