Mitoguazone
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Also known as MitoguazonamethylglyoxalbisguanylhydrazoneMethylglyoxalbis(guanylhydrazone)Methylglyoxal bis(guanylhydrazone)
Summary
Mitoguazone (CHEMBL216913) is a phase-3 clinical-stage small-molecule antineoplastic agent (ATC L01XX16); indicated across 2 conditions including neoplasm and lymphoma.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- ATC class: L01XX16
- Indications: 2 conditions
- Clinical trials: 2
- Chemistry: 184.2 Da · C5H12N8
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL216913 |
| Name | Mitoguazone |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 5351154 |
| ChEBI | CHEBI:43996 |
| ATC | L01XX16 |
| Molecular formula | C5H12N8 |
| Molecular weight | 184.2 |
| InChIKey | MXWHMTNPTTVWDM-NXOFHUPFSA-N |
SMILES: C/C(=N\N=C(N)N)/C=N/N=C(N)N
IUPAC name: 2-[(E)-[(1E)-1-(diaminomethylidenehydrazinylidene)propan-2-ylidene]amino]guanidine
ChEBI definition: A hydrazone obtained by formal condensation of the two carbonyl groups of methylglyoxal with the primary amino groups of two molecules of aminoguanidine.
Pharmacological roles (ChEBI): antineoplastic agent, apoptosis inducer, EC 4.1.1.50 (adenosylmethionine decarboxylase) inhibitor.
Also known as: Mitoguazona, Mitoguazone, methylglyoxalbisguanylhydrazone, Methylglyoxalbis(guanylhydrazone), MITOGUAZONE, Methylglyoxal bis(guanylhydrazone)
Parent form; salt/anhydrous children: CHEMBL1995011
Patent coverage: 8,895 distinct patent families (38,307 SureChEMBL compound mentions), from 3 matched compound structure(s). One matched structure accounts for 37,986 (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: S-adenosylmethionine decarboxylase proenzyme, Diamine oxidase [copper-containing].
Bioactivity
ChEMBL activities: 2 potent at pChembl ≥ 5 of 2 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| P17708 | 6 | IC50 | 1000 | nM | CHEMBL_ACT_179239 |
| P36633 | 5.82 | IC50 | 1500 | nM | CHEMBL_ACT_179240 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
2 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).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| neoplasm | 3 | MONDO:0005070 | EFO:0000616 |
| lymphoma | 3 | MONDO:0005062 | EFO:0000574 |
Clinical trials
Total trials: 2.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 1 |
| PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00920153 | PHASE3 | TERMINATED | Three Different Therapy Regimens in Treating Patients With Previously Untreated Hodgkin Lymphoma |
| NCT00002348 | PHASE2 | COMPLETED | A Study of Mitoguazone Dihydrochloride in Patients With AIDS-Related Non-Hodgkin’s Lymphoma |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).