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Compound Detail

CHEMBL439290

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Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)O)[C@H](O)[C@H]1OP(=O)(O)OC[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](OP(=O)(O)OC[C@H]2O[C@@H](n3cnc4c(N)ncnc43)[C@H](OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](OP(=O)(O)O)[C@@H]3O)[C@@H]2O)[C@@H]1O

Basic Information

ChEMBL ID CHEMBL439290
Phase Preclinical
Structure Type MOL
InChI Key ARWCLLJIZYWWEN-ALXODACISA-N
1
Targets
1
Activities
1
Assay Types
0
PK Parameters
1
Publications
0
Known Names

Molecular Properties

1414.8
MW (Da)

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C40H51N20O28P5
MW 1414.83

Activity Summary

EC50 1 meas. best 6.4

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
2-5A-dependent ribonuclease
CHEMBL2687
EC50 6.4 6.4 396.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
2-5A-dependent ribonuclease EC50 = 396.0 nM 6.4 Activation of mouse RNase L assessed as ability to cleave 5'-[32P]r(C11U2C7) 16789752

Literature References

PubMed DOI Target Context # Activities
16789752 10.1021/jm050401v 2-5A-dependent ribonuclease 2

Data from ChEMBL 36 via Core Engine