Betadex
drug drugOn this page
Also known as .beta.-cyclodextrinBeta cyclodextrinBeta-cyclodextrinBeta-schardinger dextrinBetacdCavamax w7Cyclodextrin bCyclodextrinbeta-CycloheptaamyloseCycloheptaglucanCyclomaltoheptaoseE-459E459INS NO.459INS-459KleptoseNSC-269471NSC-314334
Summary
Betadex (CHEMBL415690) is a phase-3 clinical-stage oligosaccharide.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Oligosaccharide
- Clinical trials: 1
- Chemistry: 1135 Da · C42H70O35
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL415690 |
| Name | Betadex |
| Type | Oligosaccharide |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 444041 |
| ChEBI | CHEBI:495055 |
| Molecular formula | C42H70O35 |
| Molecular weight | 1135 |
| InChIKey | WHGYBXFWUBPSRW-FOUAGVGXSA-N |
SMILES: C([C@@H]1[C@@H]2[C@@H]([C@H]([C@H](O1)O[C@@H]3[C@H](O[C@@H]([C@@H]([C@H]3O)O)O[C@@H]4[C@H](O[C@@H]([C@@H]([C@H]4O)O)O[C@@H]5[C@H](O[C@@H]([C@@H]([C@H]5O)O)O[C@@H]6[C@H](O[C@@H]([C@@H]([C@H]6O)O)O[C@@H]7[C@H](O[C@@H]([C@@H]([C@H]7O)O)O[C@@H]8[C@H](O[C@H](O2)[C@@H]([C@H]8O)O)CO)CO)CO)CO)CO)CO)O)O)O
IUPAC name: (1S,3R,5R,6S,8R,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36R,37R,38R,39R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R)-5,10,15,20,25,30,35-heptakis(hydroxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29,32,34-tetradecaoxaoctacyclo[31.2.2.23,6.28,11.213,16.218,21.223,26.228,31]nonatetracontane-36,37,38,39,40,41,42,43,44,45,46,47,48,49-tetradecol
ChEBI definition: A cyclodextrin composed of seven α-(1→4) linked D-glucopyranose units.
Also known as: .beta.-cyclodextrin, Beta cyclodextrin, Beta-cyclodextrin, Beta-schardinger dextrin, Betacd, Betadex, Cavamax w7, Cyclodextrin b, Cyclodextrin, beta-, Cycloheptaamylose, Cycloheptaglucan
Patent coverage: 38,934 distinct patent families (83,677 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: 3 (assay-derived). Sample: 4’-phosphopantetheinyl transferase ffp, Thyrotropin receptor, Aldehyde dehydrogenase 1A1.
Bioactivity
ChEMBL activities: 2 potent at pChembl ≥ 5 of 4 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| TSHR | 7.8 | Potency | 15.8 | nM | CHEMBL_ACT_3915456 |
| TSHR | 7.8 | Potency | 15.8 | nM | CHEMBL_ACT_4719129 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
0 indication records carry no mapped disease name (EFO/MeSH-only); none shown.
Clinical trials
Total trials: 1.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01960621 | PHASE4 | WITHDRAWN | Effect of Cyclodextrin on Sensory Nerve Activity: A Novel Anti-tussive Therapy |
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.