Pentetic Acid
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Also known as Acide pentetiqueAcido penteticoDTP-ADTPANanodtpaNSC-7340Diethylenetriaminepentaacetic acidSID11111089SID11111090SID26753562SID50106210SID85231007SID90341568SID104171146Diethylene-triamine pentaacetic acidSID144203682SID170465150Diethylene triamine pentaacetic acidGADOPENTETIC-ACID
Summary
Pentetic Acid (CHEMBL780) is an approved small-molecule copper chelator; indicated across 2 conditions including lymphoma and brain neoplasm.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- Indications: 2 conditions
- Clinical trials: 11
- Chemistry: 393.35 Da · C14H23N3O10
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL780 |
| Name | Pentetic Acid |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 3053 |
| ChEBI | CHEBI:35739 |
| Molecular formula | C14H23N3O10 |
| Molecular weight | 393.35 |
| InChIKey | QPCDCPDFJACHGM-UHFFFAOYSA-N |
SMILES: C(CN(CC(=O)O)CC(=O)O)N(CCN(CC(=O)O)CC(=O)O)CC(=O)O
IUPAC name: 2-[bis[2-[bis(carboxymethyl)amino]ethyl]amino]acetic acid
Pharmacological roles (ChEBI): copper chelator.
Also known as: Acide pentetique, Acido pentetico, DTP-A, DTPA, Nanodtpa, NSC-7340, Pentetic acid, Diethylenetriaminepentaacetic acid, SID11111089, SID11111090, SID26753562, SID50106210
Parent form; salt/anhydrous children: CHEMBL1200424, CHEMBL1200945
Patent coverage: 24,935 distinct patent families (71,355 SureChEMBL compound mentions), from 1 matched compound structure(s). 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: 19 (assay-derived). Sample: Tyrosyl-DNA phosphodiesterase 1, Lysine-specific demethylase 4E, Fructose-bisphosphate aldolase, Prelamin-A/C, RecQ-like DNA helicase BLM, Endonuclease 4, Peripheral myelin protein 22, Alpha-2A adrenergic receptor, Thyrotropin receptor, D(1A) dopamine receptor, Muscarinic acetylcholine receptor M2, Sodium-dependent noradrenaline transporter, Sodium-dependent serotonin transporter, Alpha-1A adrenergic receptor, D(3) dopamine receptor, Sodium-dependent dopamine transporter, Histamine H3 receptor, Polyunsaturated fatty acid lipoxygenase ALOX15, Cytochrome P450 2C19.
Bioactivity
ChEMBL activities: 21 potent at pChembl ≥ 5 of 30 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| CYP2C19 | 8.6 | Potency | 2.5 | nM | CHEMBL_ACT_4014261 |
| CYP2C19 | 8.6 | AC50 | 2.51 | nM | CHEMBL_ACT_6004214 |
| SLC6A4 | 7.37 | AC50 | 42.9 | nM | CHEMBL_ACT_25151125 |
| LMNA | 6.9 | Potency | 125.9 | nM | CHEMBL_ACT_3663352 |
| TDP1 | 6.7 | Potency | 199.5 | nM | CHEMBL_ACT_3932929 |
| TDP1 | 6.65 | Potency | 223.9 | nM | CHEMBL_ACT_3937724 |
| BLM | 6.35 | Potency | 446.7 | nM | CHEMBL_ACT_4750007 |
| BLM | 6.35 | Potency | 446.7 | nM | CHEMBL_ACT_4937916 |
| P0A6C1 | 6.15 | Potency | 707.9 | nM | CHEMBL_ACT_4069585 |
| ALOX15 | 6.1 | Potency | 794.3 | nM | CHEMBL_ACT_4454723 |
| ADRA1A | 5.89 | AC50 | 1282 | nM | CHEMBL_ACT_25218680 |
| ADRA2A | 5.88 | AC50 | 1319 | nM | CHEMBL_ACT_25156227 |
| DRD3 | 5.64 | AC50 | 2265 | nM | CHEMBL_ACT_25194325 |
| TDP1 | 5.5 | Potency | 3162 | nM | CHEMBL_ACT_3935817 |
| CHRM2 | 5.41 | AC50 | 3914 | nM | CHEMBL_ACT_25195534 |
| A8B2U2 | 5.4 | Potency | 3972 | nM | CHEMBL_ACT_4586268 |
| KDM4E | 5.2 | Potency | 6310 | nM | CHEMBL_ACT_3740956 |
| ALOX15 | 5.2 | Potency | 6310 | nM | CHEMBL_ACT_4463601 |
| SLC6A3 | 5.19 | AC50 | 6511 | nM | CHEMBL_ACT_25124757 |
| A8B2U2 | 5.1 | Potency | 7924 | nM | CHEMBL_ACT_4609814 |
| DRD1 | 5.06 | AC50 | 8707 | nM | CHEMBL_ACT_25115008 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
2 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.
| Disease (in trials) | Phase | MONDO | EFO |
|---|---|---|---|
| lymphoma | 1 | MONDO:0005062 | EFO:0000574 |
| brain neoplasm | 1 | MONDO:0021211 | EFO:0003833 |
Clinical trials
Total trials: 11.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 5 |
| PHASE1/PHASE2 | 2 |
| PHASE2 | 2 |
| EARLY_PHASE1 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT07596173 | PHASE3 | NOT_YET_RECRUITING | A Study on the Immune Response and Safety of a Combined Vaccine Against Diphtheria, Tetanus and Acellular Pertussis (dTpa) in Healthy Japanese Adolescents Aged 11 Years to <13 Years |
| NCT07596199 | PHASE3 | NOT_YET_RECRUITING | A Study on the Immune Response and Safety of a Combined Vaccine Against Diphtheria, Tetanus and Acellular Pertussis (dTpa) in Japanese Healthy Pregnant Women |
| NCT00290342 | PHASE3 | COMPLETED | Evaluation of the Immunogenicity, Safety and Reactogenicity of the Combined DTPa-IPV Vaccine in Healthy Infants |
| NCT01027845 | PHASE3 | COMPLETED | Primary and Booster Vaccination Study With Pneumococcal Vaccine GSK1024850A in Healthy Japanese Children |
| NCT05169905 | PHASE3 | COMPLETED | A Study to Evaluate the Safety and Immune Response to an Unadjuvanted RSV Maternal Vaccine in Healthy Non-pregnant Females From 9 to 49 Years of Age |
| NCT00019227 | PHASE1/PHASE2 | COMPLETED | Monoclonal Antibody Therapy in Treating Patients With Leukemia |
| NCT00126984 | PHASE2 | COMPLETED | Study in Children to Evaluate the Immunogenicity and Safety of 4 Formulations of GSK Bio MenACWY-TT Conjugate Vaccine |
| NCT02946190 | PHASE2 | COMPLETED | The PertADO Geneva Trial |
| NCT02947022 | PHASE1/PHASE2 | TERMINATED | Effects of IV-Administered Ca-DTPA and Zn-DTPA To Treat Patients With Gadolinium Deposition Disease |
| NCT01034514 | EARLY_PHASE1 | TERMINATED | 4D-CT-based Ventilation Imaging for Adaptive Functional Guidance in Radiotherapy |
| NCT02278510 | EARLY_PHASE1 | COMPLETED | Topotecan Using Convection-Enhanced Delivery (CED) in High Grade Glioma |
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).
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.