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Compound Detail

CHEMBL116696

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N#C/C(=C\c1ccc([N+](=O)[O-])o1)c1n[nH]c(Cc2ccccc2)n1

Basic Information

ChEMBL ID CHEMBL116696
Phase Preclinical
Structure Type MOL
InChI Key NTIDGBCKTXTYPD-FMIVXFBMSA-N
12
Targets
12
Activities
1
Assay Types
0
PK Parameters
13
Publications
0
Known Names

Molecular Properties

321.3
MW (Da)
2.96
ALogP
6
HBA
1
HBD
121.6
PSA (Ų)
0.44
QED
0
Ro5 Violations
5
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C16H11N5O3
MW 321.30
Aromatic Rings 3
Heavy Atoms 24
NP-Likeness -1.63

Activity Summary

IC50 12 meas. best 6.54

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
LCLC-103H cell line
CHEMBL614066
IC50 6.54 6.54 290.0 1
SISO
CHEMBL613527
IC50 6.43 6.43 370.0 1
5637
CHEMBL612565
IC50 6.4 6.4 400.0 1
KYSE-70 cell line
CHEMBL614012
IC50 6.4 6.4 400.0 1
TERT-RPE1
CHEMBL615013
IC50 6.38 6.38 420.0 1
YAPC
CHEMBL612815
IC50 6.35 6.35 450.0 1
DAN-G
CHEMBL614033
IC50 6.31 6.31 490.0 1
MCF7
CHEMBL387
IC50 6.21 6.21 610.0 1
KYSE-150 cell line
CHEMBL613998
IC50 6.21 6.21 620.0 1
KYSE-520 cell line
CHEMBL612701
IC50 6.12 6.12 750.0 1
RT-112
CHEMBL614145
IC50 6.12 6.12 750.0 1
RT-4
CHEMBL614884
IC50 5.86 5.86 1370.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
15189040 10.1021/jm0311036 SISO 2
15189040 10.1021/jm0311036 LCLC-103H cell line 2
15189040 10.1021/jm0311036 KYSE-510 1
15189040 10.1021/jm0311036 RT-4 1
15189040 10.1021/jm0311036 RT-112 1
15189040 10.1021/jm0311036 5637 1
15189040 10.1021/jm0311036 KYSE-70 cell line 1
15189040 10.1021/jm0311036 KYSE-150 cell line 1
15189040 10.1021/jm0311036 KYSE-520 cell line 1
15189040 10.1021/jm0311036 YAPC 1
15189040 10.1021/jm0311036 MCF7 1
15189040 10.1021/jm0311036 DAN-G 1
15189040 10.1021/jm0311036 TERT-RPE1 1

Data from ChEMBL 36 via Core Engine