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Compound Detail

CHEMBL503798

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O=c1[nH]c(=S)ccn1[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](n3ccc(=S)[nH]c3=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@H]1O

Basic Information

ChEMBL ID CHEMBL503798
Phase Preclinical
Structure Type MOL
InChI Key HIKNCKKYLUUROS-NCOIDOBVSA-N
3
Targets
3
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

822.4
MW (Da)
-1.45
ALogP
21
HBA
10
HBD
370.3
PSA (Ų)
0.08
QED
3
Ro5 Violations
14
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C18H26N4O21P4S2
MW 822.44
Aromatic Rings 2
Heavy Atoms 49
NP-Likeness 0.69

Activity Summary

EC50 3 meas. best 7.52

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
P2Y purinoceptor 2
CHEMBL4398
EC50 7.52 7.52 30.0 1
P2Y purinoceptor 4
CHEMBL2123
EC50 7.1 7.1 80.0 1
P2Y purinoceptor 6
CHEMBL4714
EC50 5.69 5.69 2030.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
18514530 10.1016/j.bmc.2008.05.013 P2Y purinoceptor 2 1
18514530 10.1016/j.bmc.2008.05.013 P2Y purinoceptor 4 1
18514530 10.1016/j.bmc.2008.05.013 P2Y purinoceptor 6 1

Data from ChEMBL 36 via Core Engine