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Compound Detail

CHEMBL430890

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Cc1n[nH]c(/C(C#N)=C/c2ccc([N+](=O)[O-])s2)n1

Basic Information

ChEMBL ID CHEMBL430890
Phase Preclinical
Structure Type MOL
InChI Key MNGLNFZJMXZYMX-QPJJXVBHSA-N
12
Targets
12
Activities
1
Assay Types
0
PK Parameters
13
Publications
0
Known Names

Molecular Properties

261.3
MW (Da)
2.15
ALogP
6
HBA
1
HBD
108.5
PSA (Ų)
0.52
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C10H7N5O2S
MW 261.27
Aromatic Rings 2
Heavy Atoms 18
NP-Likeness -2.51

Activity Summary

IC50 12 meas. best 6.66

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
5637
CHEMBL612565
IC50 6.66 6.66 220.0 1
LCLC-103H cell line
CHEMBL614066
IC50 6.48 6.48 330.0 1
MCF7
CHEMBL387
IC50 6.42 6.42 380.0 1
YAPC
CHEMBL612815
IC50 6.39 6.39 410.0 1
KYSE-70 cell line
CHEMBL614012
IC50 6.36 6.36 440.0 1
SISO
CHEMBL613527
IC50 6.29 6.29 510.0 1
KYSE-150 cell line
CHEMBL613998
IC50 6.25 6.25 560.0 1
DAN-G
CHEMBL614033
IC50 6.24 6.24 570.0 1
KYSE-520 cell line
CHEMBL612701
IC50 6.22 6.22 600.0 1
RT-112
CHEMBL614145
IC50 6.17 6.17 670.0 1
TERT-RPE1
CHEMBL615013
IC50 6.16 6.16 690.0 1
RT-4
CHEMBL614884
IC50 6.05 6.05 900.0 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