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Compound Detail

CHEMBL2419835

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CC[C@H](C)[C@H]1C(=O)N2CCC[C@H]2C(=O)O[C@H](C(C)(C)C)C[C@@H](C)C[C@H](O)[C@H](C)C2=N[C@@H](/C=C(\C)C(=O)N[C@@H](Cc3ccc(OC)cc3)C(=O)N(C)[C@@H](C)C(=O)N1C)C[S+]2[O-]

Basic Information

ChEMBL ID CHEMBL2419835
Phase Preclinical
Structure Type MOL
InChI Key XQTNLJKLCLNKBG-BJAMGVOOSA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

856.1
MW (Da)
4.29
ALogP
10
HBA
2
HBD
181.2
PSA (Ų)
0.32
QED
1
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

Natural Product First in Class Prodrug

Extended Properties

Molecular Formula C45H69N5O9S
MW 856.14
Aromatic Rings 1
Heavy Atoms 60
NP-Likeness 1.16

Activity Summary

IC50 1 meas. best 7.05

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
NCI-H460
CHEMBL396
IC50 7.05 7.05 89.9 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
NCI-H460 IC50 = 89.9 nM 7.05 Cytotoxicity against human NCI-H460 cells after 48 hrs by MTT assay 24016099

Literature References

PubMed DOI Target Context # Activities
24016099 10.1021/np4004992 NCI-H460 1

Data from ChEMBL 36 via Core Engine