Sudapyridine

drug
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Also known as Wx-081

Summary

Sudapyridine (CHEMBL5314931) is a phase-3 clinical-stage small molecule; indicated across 2 conditions including tuberculosis and pulmonary tuberculosis.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • Indications: 2 conditions
  • Clinical trials: 5
  • Chemistry: 537.1 Da · C34H33ClN2O2

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL5314931
NameSudapyridine
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID156777270
Molecular formulaC34H33ClN2O2
Molecular weight537.1
InChIKeyMMUCHWPQRGEHDV-ZFEZZJPFSA-N

SMILES: CN(C)CC[C@@](C1=CC=CC2=CC=CC=C21)([C@H](C3=CC=CC=C3)C4=C(N=CC(=C4)C5=CC=C(C=C5)Cl)OC)O

IUPAC name: (1R,2S)-1-[5-(4-chlorophenyl)-2-methoxy-3-pyridinyl]-4-(dimethylamino)-2-naphthalen-1-yl-1-phenylbutan-2-ol

Also known as: Sudapyridine, Wx-081, SUDAPYRIDINE

Parent form; salt/anhydrous children: CHEMBL5316189

Patent coverage: 1 distinct patent families (1 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

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

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)PhaseMONDOEFO
tuberculosis3MONDO:0018076MONDO:0018076
pulmonary tuberculosis2MONDO:0006052EFO:1000049

Clinical trials

Total trials: 5.

Phase distribution

PhaseTrials
PHASE13
PHASE31
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05824871PHASE3RECRUITINGA Phase III Study of Oral Sudapyridine (WX-081) Tablets in Rifampicin-Resistant Pulmonary Tuberculosis Patients
NCT04608955PHASE2COMPLETEDEvaluation of Early Bactericidal Activity and Safety in Pulmonary Tuberculosis With WX-081
NCT06701110PHASE1RECRUITINGPharmacokinetic Study of Sudapyridine(WX-081)in Healthy Chinese Subjects
NCT06701136PHASE1NOT_YET_RECRUITINGDrug-Drug Interaction and Food Effect of Sudapyridine(WX-081) With Itraconazole and Rifampin in Healthy Chinese Adults
NCT06117514PHASE1COMPLETEDSudapyridine (WX-081) in Healthy Volunteers

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).