Sodium Lauryl Sulfate
drug drugOn this page
Also known as E487NSC-402488Sodium dodecyl sulfateSodium laurilsulfatesyntheticTexapon k 12 psodium dodecylsulphateSodiumdodecylsulfateSID17388729SID17388731SID26752879SID144204610sodium dodecylsulfateSID144210469SID144208812SID170465474sodium lauryl sulphate
Summary
Sodium Lauryl Sulfate (CHEMBL23393) is an approved small-molecule detergent; indicated across 7 conditions including allergic disease and skin disorder.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- Indications: 7 conditions
- Clinical trials: 9
- Chemistry: 288.38 Da · C12H25NaO4S
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL23393 |
| Name | Sodium Lauryl Sulfate |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | yes |
| PubChem CID | 3423265 |
| ChEBI | CHEBI:8984 |
| Molecular formula | C12H25NaO4S |
| Molecular weight | 288.38 |
| InChIKey | DBMJMQXJHONAFJ-UHFFFAOYSA-M |
SMILES: CCCCCCCCCCCCOS(=O)(=O)[O-].[Na+]
IUPAC name: sodium dodecyl sulfate
ChEBI definition: An organic sodium salt that is the sodium salt of dodecyl hydrogen sulfate.
Other ChEBI roles (chemical / environmental): detergent.
Also known as: E487, NSC-402488, Sodium dodecyl sulfate, Sodium laurilsulfate, Sodium lauryl sulfate, synthetic, Texapon k 12 p, sodium dodecyl sulfate, sodium dodecylsulphate, Sodiumdodecylsulfate, SID17388729, SID17388731
Patent coverage: 353,250 distinct patent families (864,340 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: 8 (assay-derived). Sample: ATP-dependent DNA helicase Q1, 15-hydroxyprostaglandin dehydrogenase [NAD(+)], Thyrotropin receptor, Bifunctional epoxide hydrolase 2, Alpha-galactosidase A, Cruzipain, Mitogen-activated protein kinase 1, Lethal factor.
Bioactivity
ChEMBL activities: 2 potent at pChembl ≥ 5 of 10 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| P15917 | 7 | Potency | 100 | nM | CHEMBL_ACT_4671073 |
| EPHX2 | 5.26 | IC50 | 5500 | nM | CHEMBL_ACT_19307232 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
5 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 |
|---|---|---|---|
| allergic disease | 3 | MONDO:0005271 | MONDO:0005271 |
| skin disorder | 1 | MONDO:0005093 | EFO:0000701 |
| tinea pedis | 1 | MONDO:0005984 | EFO:0007512 |
| disease of the tendon | 1 | MONDO:0100010 | EFO:1001434 |
| lice infestation | 1 | MONDO:0003472 | MONDO:0003472 |
2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 9.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE1 | 8 |
| Not specified | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00680095 | PHASE1 | COMPLETED | Cumulative Irritation Test |
| NCT00781664 | PHASE1 | COMPLETED | Cumulative Irritation Test |
| NCT01430312 | PHASE1 | COMPLETED | 21 Day Irritancy Test of Azelaic Acid Pre-foam Formulation |
| NCT02061813 | PHASE1 | COMPLETED | Dermal Safety Study to Evaluate Potential Irritation of Abametapir Lotion |
| NCT02117752 | PHASE1 | COMPLETED | Dermal Tolerability of Dapsone Gel in Healthy Volunteers |
| NCT02227069 | PHASE1 | COMPLETED | Skin Safety Study to Evaluate the Irritation Potential in Healthy Volunteers |
| NCT02256930 | PHASE1 | COMPLETED | Skin Safety Study to Evaluate the Sensitizing Potential in Healthy Volunteers |
| NCT03502434 | PHASE1 | COMPLETED | A Repeat Insult Patch Test (RIPT) Study Evaluating the Sensitization Potential of Topical SM04755 Solution in Healthy Volunteers |
| NCT01501409 | Not specified | COMPLETED | Effect of Sodium Lauryl Sulfate on Recurrent Aphthous Stomatitis |
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
- In clinical trials for: allergic disease