Epinastine

Epinastine

SCHEMBL18794

NC1=NCC2c3ccccc3Cc3ccccc3N12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HRH1

The experimentally established mechanism targets of Epinastine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HRH1 known ✓ P35367 13/20 0.45
ADRA1A P35348 5/20 1.00
ADRA2A P08913 4/20 1.00
HTR1A P08908 3/20 1.00
OPRM1 P35372 3/20 1.00
DRD1 P21728 2/20 1.00
SLC6A2 P23975 2/20 1.00
SLC6A4 P31645 2/20 1.00
KCNH2 Q12809 2/20 1.00
SLC22A2 O15244 1/20 1.00
GABRA1 P14867 1/20 1.00
GABRA2 P47869 1/20 1.00
GABRB2 P47870 1/20 1.00
SLC47A2 Q86VL8 1/20 1.00
SLC47A1 Q96FL8 1/20 1.00
HTR2A P28223 15/20 0.45
HTR2C P28335 12/20 0.45
DRD2 P14416 4/20 0.43
DRD4 P21917 3/20 0.43
DRD3 P35462 3/20 0.43

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Epinastine SCHEMBL29945140 1.00 ADRA1A (1.00) ADRA1AADRA2AHTR1AOPRM1DRD1
Epinastine SCHEMBL357588 1.00 ADRA1A (1.00) ADRA1AADRA2AHTR1AOPRM1DRD1
Epinastine SCHEMBL122749 0.98 ADRA1A (0.97) ADRA1AADRA2AHTR1AOPRM1DRD1
Epinastine SCHEMBL4292213 0.98 ADRA1A (0.97) ADRA1AADRA2AHTR1AOPRM1DRD1
Epinastine SCHEMBL3989748 0.98 ADRA1A (0.97) ADRA1AADRA2AHTR1AOPRM1DRD1
Epinastine SCHEMBL30678575 0.98 ADRA1A (0.97) ADRA1AADRA2AHTR1AOPRM1DRD1
Epinastine SCHEMBL3989750 0.98 ADRA1A (0.97) ADRA1AADRA2AHTR1AOPRM1DRD1
Epinastine SCHEMBL122751 0.98 ADRA1A (0.97) ADRA1AADRA2AHTR1AOPRM1DRD1
Epinastine SCHEMBL122750 0.97 ADRA1A (0.94) ADRA1AADRA2AHTR1AOPRM1DRD1
Epinastine SCHEMBL16093961 0.90 ADRA1A (0.81) ADRA1AADRA2AHTR1AOPRM1DRD1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Appears in 9497 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122075669-A Composition and application thereof in preparation of drugs for preventing and treating lymphoma 2026-05-26 CN claimed
WO-2026100654-A1 NUCLEIC ACID INTRODUCTION AID, NUCLEIC ACID INTRODUCTION AGENT, AND NUCLEIC ACID INTRODUCTION METHOD 株式会社インファーマシア 2026-05-15 WO claimed
CN-122020554-A Automatic identification method and model for tobacco diseases 昆明学院 2026-05-12 CN claimed
CN-122023992-A Tobacco disease diagnosis method and model based on image processing 昆明学院 2026-05-12 CN claimed
EP-4724079-A2 METHODS AND COMPOSITIONS FOR THE TREATMENT OF AGE-RELATED MACULAR DEGENERATION Stealth BioTherapeutics Inc. (US) 2026-04-15 EP claimed
EP-4704971-A1 GAMMA STIMULATION AND NEUROMODULATOR COMBINATION THERAPY Cognito Therapeutics, Inc. (US) 2026-03-11 EP claimed
US-12569451-B2 Bio-inspired tissue-adhesive hydrogel patch and uses thereof Cellartgen Inc. (KR) 2026-03-10 US claimed
US-20260048096-A1 METHODS AND COMPOSITIONS FOR PRESERVING THE RETINAL OUTER NUCLEAR LAYER (ONL), PHOTORECEPTORS, AND RETINAL THICKNESS STEALTH BIOTHERAPEUTICS INC. (US) 2026-02-19 US claimed
US-12390363-B2 Ophthalmic drug compositions OXULAR LIMITED (GB) 2025-08-19 US claimed
EP-4596049-A2 PEPTIDE FOR USE IN PREVENTING OR TREATING MACULAR DEGENERATION Stealth BioTherapeutics Inc. (US) 2025-08-06 EP claimed
US-5869479-A ADMINISTERING HISTAMINE H1 RECEPTOR ANTAGONISTS AND HISTAMINE H3 RECEPTOR ANTAGONISTS; NASAL DECONGESTANT WITHOUT THE NERVOUS SYSTEM OR CARDIOVASCULAR SIDE EFFECTS SCHERING CORPORATION (US) 1999-02-09 US claimed
CN-1202111-A Use of epinastine in the treatment of pain BOEHRINGER INGELHEIM KG (DE) 1998-12-16 CN claimed
CN-1191535-A Novel pharmaceutical compositions and uses thereof BOEHRINGER INGELHEIM KG (DE) 1998-08-26 CN claimed
WO-1998006394-A1 TREATMENT OF UPPER AIRWAY ALLERGIC RESPONSES WITH A COMBINATION OF HISTAMINE RECEPTOR ANTAGONISTS SCHERING CORPORATION (US) 1998-02-19 WO claimed
EP-0496306-B1 Process for the preparation of 3-amino-9,13b-dihydro-1H-dibenz-[c,f]imidazo[1,5-a]azepine hydrochloride BOEHRINGER INGELHEIM KG (DE) 1995-09-13 EP claimed
US-5312916-A Process for preparing 3-amino-9,13b-dihydro-1H-dibenz(c,f)imidazo(1,5-a)azepine-hydrochloride BOEHRINGER INGELHEIM KG (DE) 1994-05-17 US claimed
EP-0345931-B1 CERTAIN PAF ANTAGONIST/ANTIHISTAMINE COMBINATIONS AND METHODS SCHERING CORPORATION (US) 1993-01-20 EP claimed
EP-0496306-A1 Process for the preparation of 3-amino-9,13b-dihydro-1H-dibenz-[c,f]imidazo[1,5-a]azepine hydrochloride BOEHRINGER INGELHEIM KG (DE) 1992-07-29 EP claimed
EP-0402422-A1 CERTAIN PAF ANTAGONIST ANTIHISTAMINE COMBINATIONS AND METHODS SCHERING CORPORATION (US) 1990-12-19 EP claimed
WO-1989010143-A1 CERTAIN PAF ANTAGONIST ANTIHISTAMINE COMBINATIONS AND METHODS SCHERING CORPORATION (US) 1989-11-02 WO claimed