Skip to main content
Free research Free research Free compound review with research home and workspace preview
Quick search ChEMBL 36
Compound Detail

CHEMBL245019

MIZORIBINE
🧪 Phase III
Enter ChEMBL ID:
Free Research Context This compound will appear in recent viewed items on the research home for this browser.
Research home View demo workspace
🧪 Phase III
NC(=O)c1ncn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c1O

Basic Information

ChEMBL ID CHEMBL245019
Name MIZORIBINE
Phase Phase III
Structure Type MOL
InChI Key HZQDCMWJEBCWBR-UUOKFMHZSA-N
Active Moiety CHEMBL1794685

Known Names

Bredinin Mizoribina Mizoribine NSC-289637
2
Targets
2
Activities
2
Assay Types
0
PK Parameters
20
Publications
4
Known Names
3
Indications
2
Mechanisms

Molecular Properties

259.2
MW (Da)
-2.70
ALogP
8
HBA
5
HBD
151.1
PSA (Ų)
0.40
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Chirality Single Enantiomer

Flags

Natural Product Prodrug
USAN Stem -ribine

Extended Properties

Molecular Formula C9H13N3O6
MW 259.22
Aromatic Rings 1
Heavy Atoms 18
NP-Likeness 0.95

Mechanism of Action

Mechanism Action Type Target Direct Efficacy
Inosine-5'-monophosphate dehydrogenase (IMPDH) inhibitor INHIBITOR Inosine-5'-monophosphate dehydrogenase (IMPDH)
GMP synthase [glutamine-hydrolyzing] inhibitor INHIBITOR GMP synthase [glutamine-hydrolyzing]

Indications

Arthritis, Rheumatoid Lupus Nephritis Nephrotic Syndrome

Activity Summary

IC50 1 meas. best 4.87
Ki 1 meas. best 4.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
SARS-CoV
CHEMBL4303836
IC50 4.87 4.87 13500.0 1
Unchecked
CHEMBL612545
Ki 4.0 4.0 100000.0 1

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
- 10.6019/CHEMBL4495565 SARS-CoV-2 4
33691794 10.1186/s13148-021-01037-1 A549 4
37468498 10.1038/s41467-023-40064-9 Nuclear receptor subfamily 1 group I member 2 3
37770001 10.1016/j.bmcl.2023.129490 Mus musculus 3
- 10.6019/CHEMBL4495564 Replicase polyprotein 1ab 2
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 2A 2
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 2B 2
- 10.6019/CHEMBL4808148 Histone deacetylase 6 2
37468498 10.1038/s41467-023-40064-9 Alpha-1A adrenergic receptor 2
37468498 10.1038/s41467-023-40064-9 Progesterone receptor 2
37468498 10.1038/s41467-023-40064-9 Peroxisome proliferator-activated receptor gamma 2
37468498 10.1038/s41467-023-40064-9 Androgen receptor 2
37468498 10.1038/s41467-023-40064-9 Gamma-aminobutyric acid receptor subunit alpha-1/alpha-2/beta-2/gamma-2 2
37468498 10.1038/s41467-023-40064-9 5-hydroxytryptamine receptor 1A 2
37468498 10.1038/s41467-023-40064-9 Alpha-2A adrenergic receptor 2
37468498 10.1038/s41467-023-40064-9 Cannabinoid receptor 1 2
17336519 10.1016/j.bmcl.2007.02.026 Unchecked 1
17417631 10.1038/nchembio873 Unchecked 1
1995901 10.1021/jm00106a045 SW480 1
1995901 10.1021/jm00106a045 KB 1

Data from ChEMBL 36 via Core Engine