Thenalidine
drugOn this page
Also known as TenalidinaThenaldineThenophenopiperidineSID144206868AS-716
Summary
Thenalidine (CHEMBL2105458) is an approved small molecule (ATC R06AX53); indicated across 2 conditions including allergic disease.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: R06AX53 (+2 more)
- Indications: 2 conditions
- Chemistry: 286.4 Da · C17H22N2S
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL2105458 |
| Name | Thenalidine |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 27901 |
| ATC | R06AX53, D04AA03, R06AX03 |
| Molecular formula | C17H22N2S |
| Molecular weight | 286.4 |
| InChIKey | KLOHYVOVXOUKQI-UHFFFAOYSA-N |
SMILES: CN1CCC(CC1)N(CC2=CC=CS2)C3=CC=CC=C3
IUPAC name: 1-methyl-N-phenyl-N-(thiophen-2-ylmethyl)piperidin-4-amine
Also known as: Tenalidina, Thenaldine, Thenalidine, Thenophenopiperidine, SID144206868, THENALIDINE, AS-716, thenalidine
Patent coverage: 341 distinct patent families (1,236 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: 12 (assay-derived). Sample: Alpha-2A adrenergic receptor, D(1A) dopamine receptor, Muscarinic acetylcholine receptor M2, 5-hydroxytryptamine receptor 1A, Muscarinic acetylcholine receptor M1, Sodium-dependent noradrenaline transporter, Sodium-dependent serotonin transporter, Alpha-1A adrenergic receptor, Mu-type opioid receptor, D(3) dopamine receptor.
Bioactivity
ChEMBL activities: 9 potent at pChembl ≥ 5 of 12 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| SLC6A2 | 6.4 | AC50 | 398.7 | nM | CHEMBL_ACT_25145855 |
| CHRM2 | 6.16 | AC50 | 699.2 | nM | CHEMBL_ACT_25195591 |
| CHRM1 | 6.12 | AC50 | 761.6 | nM | CHEMBL_ACT_25210088 |
| SLC6A3 | 5.79 | AC50 | 1608 | nM | CHEMBL_ACT_25124814 |
| KCNH2 | 5.54 | AC50 | 2900 | nM | CHEMBL_ACT_25117378 |
| DRD3 | 5.35 | AC50 | 4458 | nM | CHEMBL_ACT_25194381 |
| OPRM1 | 5.13 | AC50 | 7422 | nM | CHEMBL_ACT_25158030 |
| ADRA2A | 5.07 | AC50 | 8451 | nM | CHEMBL_ACT_25156284 |
| HTR1A | 5.06 | AC50 | 8652 | nM | CHEMBL_ACT_25164879 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
2 indications (2 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 |
|---|---|---|---|
| allergic disease | 4 | MONDO:0005271 | MONDO:0005271 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 0.
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
- Diseases: allergic disease