Fexofenadine

Fexofenadine

SCHEMBL4900

CC(C)(C(=O)O)c1ccc(C(O)CCCN2CCC(C(O)(c3ccccc3)c3ccccc3)CC2)cc1

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 Fexofenadine. 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 6/20 1.00
KCNH2 Q12809 4/20 1.00
LMNA P02545 3/20 1.00
DRD3 P35462 3/20 1.00
HTR2A P28223 2/20 1.00
HTR2B P41595 2/20 1.00
BLM P54132 2/20 1.00
CNR1 P21554 1/20 1.00
APEX1 P27695 1/20 1.00
PDE4A P27815 1/20 1.00
PDE3A Q14432 1/20 1.00
DRD2 P14416 2/20 0.98
ALOX15 P16050 1/20 0.98
HSD17B10 Q99714 1/20 0.98
CYP2J2 P51589 3/20 0.80
MEN1 O00255 1/20 0.80
NPC1 O15118 1/20 0.80
CACNA1F O60840 1/20 0.80
GMNN O75496 1/20 0.80
USP2 O75604 1/20 0.80

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
Fexofenadine SCHEMBL4901 1.00 HRH1 (1.00) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL1972366 1.00 HRH1 (1.00) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL7104316 1.00 HRH1 (1.00) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL1561082 1.00 HRH1 (1.00) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL3178320 1.00 HRH1 (1.00) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL9943444 0.99 HRH1 (0.98) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL16651410 0.99 HRH1 (0.98) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL16652202 0.99 HRH1 (0.98) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL1395674 0.99 HRH1 (0.98) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL20531399 0.99 HRH1 (0.98) HRH1KCNH2LMNADRD3HTR2A

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 32218 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6436924-B1 None US claimed
US-20260139860-A1 PRODUCTS OF MANUFACTURE FOR THE TREATMENT, PREVENTION AND AMELIORATION OF MICROBIAL INFECTIONS CENTRE FOR DIGESTIVE DISEASES (AU) 2026-05-21 US 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-117209417-B Fexofenadine Process for the preparation of isomers 梯尔希(南京)药物研发有限公司 2026-05-15 CN claimed
EP-4734952-A1 ORAL TABLET WITH IMPROVED UNIFORMITY OF CONTENT OF ACTIVES Fertin Pharma A/S (DK) 2026-05-06 EP claimed
EP-4736841-A1 A MUCOADHESIVE LAYER FOR BUCCAL ADMINISTRATION OF AN ACTIVE PHARMACEUTICAL INGREDIENT IQ medical GmbH (DE) 2026-05-06 EP claimed
US-20260118349-A1 METHODS AND KITS FOR PREDICTING INFUSION REACTION RISK AND ANTIBODY MEDIATED LOSS OF RESPONSE BY MONITORING SERUM URIC ACID DURING PEGYLATED URICASE THERAPY HORIZON THERAPEUTICS USA, INC. (US) 2026-04-30 US claimed
US-20260109705-A1 COMPOUNDS AND METHODS FOR THE TREATMENT OF OCULAR DISORDERS Azura Ophthalmics Ltd. (IL) 2026-04-23 US claimed
EP-4724049-A1 MODIFIED RELEASE FILL COMPOSITIONS FOR DOSAGE FORMS AND METHODS OF PREPARATION AND USE THEREOF Catalent Ontario Limited (CA) 2026-04-15 EP claimed
US-20260069593-A1 METHODS FOR TREATING CANCER AMGEN INC (US) 2026-03-12 US claimed
WO-1998048839-A1 TOPICAL NASAL ANTIINFLAMMATORY COMPOSITIONS WARNER-LAMBERT COMPANY (US) 1998-11-05 WO claimed
WO-1998022114-A1 A METHOD FOR PROMOTING TISSUE REPAIR DUMEX-ALPHARMA A/S (DK) 1998-05-28 WO 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-0759904-A1 PROCESS AND DIASTEREOMERIC SALTS USEFUL FOR THE OPTICAL RESOLUTION OF RACEMIC ALPHA-[4-(1,1-DIMETHYLETHYL)PHENYL]-4-(HYDROXYDIPHENYLMETHYL)-1-PIPERIDINEBUTANOL AND DERIVATIVE COMPOUNDS MERRELL PHARMACEUTICALS INC. (US) 1997-03-05 EP claimed
WO-1995031436-A1 PROCESS AND DIASTEREOMERIC SALTS USEFUL FOR THE OPTICAL RESOLUTION OF RACEMIC α-[4-(1,1-DIMETHYLETHYL)PHENYL]-4-(HYDROXYDIPHENYLMETHYL)-1-PIPERIDINEBUTANOL AND DERIVATIVE COMPOUNDS MERRELL PHARMACEUTICALS INC. (US) 1995-11-23 WO claimed
EP-0675924-A1 CYCLIC-SUBSTITUTED UNSYMMETRICAL CYANINE DYES MOLECULAR PROBES, INC. (US) 1995-10-11 EP claimed
EP-0639976-A1 USE OF TERFENADINE DERIVATIVES AS ANTIHISTAMINICS IN A HEPATICALLY IMPAIRED PATIENT MERRELL PHARMACEUTICALS INC. (US) 1995-03-01 EP claimed
WO-1994024213-A1 CYCLIC-SUBSTITUTED UNSYMMETRICAL CYANINE DYES MOLECULAR PROBES, INC. (US) 1994-10-27 WO claimed
WO-1993023047-A1 USE OF TERFENADINE DERIVATIVES AS ANTIHISTAMINICS IN A HEPATICALLY IMPAIRED PATIENT MERRELL DOW PHARMACEUTICALS INC. (US) 1993-11-25 WO claimed
US-4254129-A ANTIALLERGENS, BRONCHODILATORS, ANTIHISTAMINES; 4-DIPHENYLMETHYL PIPERIDINO-ALKANOLS RICHARDSON-MERRELL INC. (US) 1981-03-03 US claimed