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Compound Detail

CHEMBL4279000

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CO[C@H]([C@H](C)/C=C/N(C)C=O)[C@@H](C)C(=O)CC[C@H](C)[C@H](C[C@@H]1OC(=O)C[C@@H](O)C/C=C/C(=O)[C@H](C)[C@H](C)c2coc(n2)-c2coc(n2)-c2coc(n2)/C=C/C[C@H](OC)[C@H]1C)OC

Basic Information

ChEMBL ID CHEMBL4279000
Phase Preclinical
Structure Type MOL
InChI Key WAHTUYVUQLITBX-YMFHOPMHSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

865.0
MW (Da)
7.25
ALogP
15
HBA
1
HBD
206.8
PSA (Ų)
0.12
QED
3
Ro5 Violations
15
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C46H64N4O12
MW 865.03
Aromatic Rings 3
Heavy Atoms 62
NP-Likeness 1.13

Activity Summary

IC50 1 meas. best 8.15

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
3Y1 cell line
CHEMBL614741
IC50 8.15 8.15 7.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
3Y1 cell line IC50 = 7.0 nM 8.15 Cytotoxicity against rat 3Y1 cells after 72 hrs by MTT assay 29613787

Literature References

PubMed DOI Target Context # Activities
29613787 10.1021/acs.jnatprod.8b00101 3Y1 cell line 1

Data from ChEMBL 36 via Core Engine