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Compound Detail

CHEMBL5614312

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CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@H](Cc1ccccc1)C(=O)OC)OC)N(C)C(=O)[C@@H](NC(=O)c1ccc(N)cc1)C(C)C

Basic Information

ChEMBL ID CHEMBL5614312
Phase Preclinical
Structure Type MOL
InChI Key HNVUPWGVRNNFKX-AMGHRQRZSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

752.0
MW (Da)
3.84
ALogP
9
HBA
3
HBD
169.6
PSA (Ų)
0.14
QED
1
Ro5 Violations
19
Rot. Bonds

Drug Information

Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C41H61N5O8
MW 751.97
Aromatic Rings 2
Heavy Atoms 54
NP-Likeness 0.31

Activity Summary

IC50 1 meas. best 9.92

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
KARPAS-299
CHEMBL2366156
IC50 9.92 9.92 0.1 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
KARPAS-299 IC50 = 0.12 nM 9.92 Cytotoxicity against human KARPAS-299 cells incubated for 96 hrs by Alamar blue ... 39068862

Literature References

PubMed DOI Target Context # Activities
39068862 10.1016/j.ejmech.2024.116709 KARPAS-299 1

Data from ChEMBL 36 via Core Engine