Inosine

drug
On this page

Also known as Hypoxanthine ribosideHypoxanthosineINO-1001InosinaInotinNSC-20262SID8139984inosinSID144205075SID170465655

Summary

Inosine (CHEMBL1556) is a phase-3 clinical-stage small molecule (ATC D06BB05); indicated across 14 conditions including viral infectious disease and obstructive jaundice.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • ATC class: D06BB05 (+2 more)
  • Indications: 14 conditions
  • Clinical trials: 16
  • Chemistry: 268.23 Da · C10H12N4O5

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1556
NameInosine
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID135398641
ChEBICHEBI:17596
ATCD06BB05, G01AX02, S01XA10
Molecular formulaC10H12N4O5
Molecular weight268.23
InChIKeyUGQMRVRMYYASKQ-KQYNXXCUSA-N

SMILES: C1=NC2=C(C(=O)N1)N=CN2[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O

IUPAC name: 9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-purin-6-one

ChEBI definition: A purine nucleoside in which hypoxanthine is attached to ribofuranose via a β-N9-glycosidic bond.

Other ChEBI roles (chemical / environmental): human metabolite, Saccharomyces cerevisiae metabolite, Escherichia coli metabolite, mouse metabolite.

Also known as: Hypoxanthine riboside, Hypoxanthosine, INO-1001, Inosina, Inosine, Inotin, NSC-20262, inosine, SID8139984, inosin, INOSINE, SID144205075

Parent form; salt/anhydrous children: CHEMBL1213651, CHEMBL3833327

Patent coverage: 45,953 distinct patent families (151,796 SureChEMBL compound mentions), from 4 matched compound structure(s). One matched structure accounts for 150,944 (99%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 2 (assay-derived). Sample: Survival motor neuron protein, Ferritin light chain.

Bioactivity

ChEMBL activities: 2 potent at pChembl ≥ 5 of 2 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
P027916.05Potency891.3nMCHEMBL_ACT_4501044
SMN15.9Potency1259nMCHEMBL_ACT_3882367

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

14 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
viral infectious disease3MONDO:0005108EFO:0000763
obstructive jaundice3MONDO:0006874EFO:1001068
eye disorder3MONDO:0005328EFO:0003966
diabetic neuropathy3MONDO:0006626EFO:1000783
Parkinson disease3MONDO:0005180MONDO:0005180
stroke disorder3MONDO:0005098EFO:0000712
relapsing-remitting multiple sclerosis2MONDO:0005314EFO:0003929
multiple system atrophy2MONDO:0007803EFO:1001050
acute myocardial infarction2MONDO:0004781EFO:0008583
amyotrophic lateral sclerosis2MONDO:0004976MONDO:0004976
neoplasm2MONDO:0005070EFO:0000616
triple-negative breast carcinoma2MONDO:0005494EFO:0005537
melanoma1MONDO:0005105EFO:0000756
HIV infectious disease1MONDO:0005109EFO:0000764

Clinical trials

Total trials: 16.

Phase distribution

PhaseTrials
PHASE26
PHASE14
Not specified3
PHASE32
PHASE2/PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02642393PHASE3COMPLETEDStudy of Urate Elevation in Parkinson’s Disease, Phase 3
NCT03418935PHASE3COMPLETEDRemaxol® in Mechanical Jaundice of Non-malignant Origin
NCT05809336PHASE2/PHASE3COMPLETEDGut Microbial Metabolites Inosine Combined With PD-1/PD-L1 Inhibitor for Patients With Malignant Advanced Solid Tumors
NCT00067327PHASE2COMPLETEDTreatment of Multiple Sclerosis Using Over the Counter Inosine
NCT00271167PHASE2TERMINATEDA Trial of INO-1001 in Patients Undergoing Heart Surgery That Involves Heart-lung Bypass
NCT00271765PHASE2COMPLETEDA Study of INO-1001, an Intravenous PARP (Poly [ADP Ribose] Polymerase) Inhibitor in Acute Heart Attack Patients Undergoing Primary Percutaneous Coronary Intervention
NCT00833690PHASE2COMPLETEDSafety of Urate Elevation in Parkinson’s Disease
NCT03168711PHASE2COMPLETEDSafety of Urate Elevation in Amyotrophic Lateral Sclerosis (ALS)
NCT06355024PHASE2COMPLETEDInosine Reverse Chemo Resistance in Triple Negative Breast Cancer
NCT07170475PHASE1RECRUITINGA Phase Ib Trial of Combined Febuxostat and Inosine Therapy in Patients With Parkinson’s Disease
NCT00272415PHASE1TERMINATEDA Study of Intravenous INO-1001 Plus Oral Temozolomide to Evaluate Tolerability, Safety, and Pharmacokinetics in Patients With Melanoma
NCT02288091PHASE1COMPLETEDA Pilot Study of Inosine in Amyotrophic Lateral Sclerosis (ALS)
NCT02614469PHASE1COMPLETEDA Food-Drug Interaction Study of Serum Urate After Oral Inosine
NCT04890808Not specifiedNOT_YET_RECRUITINGTherapeutic Antioxidant Supplementation
NCT04476238Not specifiedCOMPLETEDInosine Energy Expenditure Study
NCT05297851Not specifiedCOMPLETEDCytoflavin in Combination With Reperfusion in Stroke Patients

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).