Insulin Human, Isophane
drugOn this page
Also known as InsulatardInsulin humanisophaneProtaphane
Summary
Insulin Human, Isophane (CHEMBL2108973) is an approved protein targeting INSR; indicated across 1 condition including diabetes mellitus.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Protein
- Targets: 1 (INSR)
- Indications: 1 condition
- Clinical trials: 5
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL2108973 |
| Name | Insulin Human, Isophane |
| Type | Protein |
| Max phase | 4 |
Also known as: Insulatard, Insulin human, isophane, Protaphane, INSULIN HUMAN, ISOPHANE
Targets
Targets
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| INSR | Insulin receptor | Agonist | 0.8% | P06213 |
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
Aggregated over 1 target gene(s): INSR.
Top Reactome pathways
11 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| PIP3 activates AKT signaling | 1 | INSR |
| Signal Transduction | 1 | INSR |
| Negative regulation of the PI3K/AKT network | 1 | INSR |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 1 | INSR |
| IRS activation | 1 | INSR |
| Signal attenuation | 1 | INSR |
| Insulin receptor signalling cascade | 1 | INSR |
| Signaling by Insulin receptor | 1 | INSR |
| Insulin receptor recycling | 1 | INSR |
| Intracellular signaling by second messengers | 1 | INSR |
| Signaling by Receptor Tyrosine Kinases | 1 | INSR |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| positive regulation of receptor internalization | 1 |
| heart morphogenesis | 1 |
| regulation of DNA-templated transcription | 1 |
| receptor-mediated endocytosis | 1 |
| G protein-coupled receptor signaling pathway | 1 |
| learning | 1 |
| memory | 1 |
| positive regulation of cell population proliferation | 1 |
| insulin receptor signaling pathway | 1 |
| epidermis development | 1 |
| male gonad development | 1 |
| male sex determination | 1 |
| adrenal gland development | 1 |
| positive regulation of cell migration | 1 |
| exocrine pancreas development | 1 |
Indications & clinical
Indications
1 indication (1 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 |
|---|---|---|---|
| diabetes mellitus | 4 | MONDO:0005015 | EFO:0000400 |
Clinical trials
Total trials: 5.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 5 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00329615 | PHASE4 | COMPLETED | Insulin Treatment in Cancer Cachexia |
| NCT00566124 | PHASE4 | COMPLETED | Basal Insulins - Pharmacodynamics |
| NCT00788840 | PHASE4 | COMPLETED | Detemir Energy Expenditure Study |
| NCT01269996 | PHASE4 | COMPLETED | JanUmet Before Insulin Lantus In Eastern Population Evaluation Program (JUBILEE) In Type 2 Diabetic Patients |
| NCT01649466 | PHASE4 | COMPLETED | Safety and Efficacy of Vildagliptin Versus NPH Insulin add-on to Glimepiride in Type 2 Diabetes Mellitus Patients. |
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
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
37 molecules share ≥1 primary target. Top 37 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| CRIZOTINIB | ChEMBL + PubChem | Phase 4 (approved) | INSR |
| BRIGATINIB | ChEMBL | Phase 4 (approved) | INSR |
| CERITINIB | ChEMBL | Phase 4 (approved) | INSR |
| ENTRECTINIB | ChEMBL | Phase 4 (approved) | INSR |
| FEDRATINIB | ChEMBL | Phase 4 (approved) | INSR |
| INFIGRATINIB | ChEMBL | Phase 4 (approved) | INSR |
| LAPATINIB | ChEMBL | Phase 4 (approved) | INSR |
| NERATINIB | ChEMBL | Phase 4 (approved) | INSR |
| NINTEDANIB | ChEMBL | Phase 4 (approved) | INSR |
| OSIMERTINIB | ChEMBL | Phase 4 (approved) | INSR |
| SORAFENIB | ChEMBL | Phase 4 (approved) | INSR |
| SUNITINIB | ChEMBL | Phase 4 (approved) | INSR |
| DOVITINIB | ChEMBL | Phase 3 | INSR |
| LESTAURTINIB | ChEMBL | Phase 3 | INSR |
| LINIFANIB | ChEMBL | Phase 3 | INSR |
| LINSITINIB | ChEMBL | Phase 3 | INSR |
| BMS-754807 | ChEMBL | Phase 2 | INSR |
| CENISERTIB | ChEMBL | Phase 2 | INSR |
| ELLAGIC ACID | ChEMBL | Phase 2 | INSR |
| FORETINIB | ChEMBL | Phase 2 | INSR |
| ILORASERTIB | ChEMBL | Phase 2 | INSR |
| OSI-632 | ChEMBL | Phase 2 | INSR |
| R-406 | ChEMBL | Phase 2 | INSR |
| SU-014813 | ChEMBL | Phase 2 | INSR |
| TOZASERTIB | ChEMBL | Phase 2 | INSR |
| Afatinib | PubChem | Approved | INSR |
| belumosudil | PubChem | Approved | INSR |
| Belzutifan | PubChem | Approved | INSR |
| Binimetinib | PubChem | Approved | INSR |
| dacomitinib | PubChem | Approved | INSR |
| Fostamatinib | PubChem | Approved | INSR |
| Gefitinib | PubChem | Approved | INSR |
| Idelalisib | PubChem | Approved | INSR |
| Pazopanib | PubChem | Approved | INSR |
| regorafenib | PubChem | Approved | INSR |
| Selumetinib | PubChem | Approved | INSR |
| Trametinib | PubChem | Approved | INSR |
Related Atlas pages
- Genes: INSR
- Diseases: diabetes mellitus
- Drugs: Crizotinib, Brigatinib, Ceritinib, Entrectinib, Fedratinib, Infigratinib, Lapatinib, Neratinib, Nintedanib, Osimertinib, Sorafenib, Sunitinib, Dovitinib, Lestaurtinib, Linifanib, Linsitinib, Afatinib, belumosudil, Belzutifan, Binimetinib, dacomitinib, Fostamatinib, Gefitinib, Idelalisib, Pazopanib, regorafenib, Selumetinib, Trametinib