Fexofenadine

Fexofenadine

SCHEMBL1395674

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

nearest known ligand 0.98

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 0.98
KCNH2 Q12809 4/20 0.98
LMNA P02545 3/20 0.98
DRD3 P35462 3/20 0.98
HTR2A P28223 2/20 0.98
HTR2B P41595 2/20 0.98
BLM P54132 2/20 0.98
CNR1 P21554 1/20 0.98
APEX1 P27695 1/20 0.98
PDE4A P27815 1/20 0.98
PDE3A Q14432 1/20 0.98
DRD2 P14416 2/20 0.96
ALOX15 P16050 1/20 0.96
HSD17B10 Q99714 1/20 0.96
CYP2J2 P51589 3/20 0.79
MEN1 O00255 1/20 0.79
NPC1 O15118 1/20 0.79
CACNA1F O60840 1/20 0.79
GMNN O75496 1/20 0.79
USP2 O75604 1/20 0.79

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 SCHEMBL9943442 1.00 HRH1 (0.98) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL1395675 1.00 HRH1 (0.98) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL9943444 1.00 HRH1 (0.98) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL1395627 0.99 HRH1 (0.98) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL48729 0.99 HRH1 (0.98) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL3178320 0.99 HRH1 (1.00) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL1972366 0.99 HRH1 (1.00) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL1561082 0.99 HRH1 (1.00) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL4901 0.99 HRH1 (1.00) HRH1KCNH2LMNADRD3HTR2A
Fexofenadine SCHEMBL7104316 0.99 HRH1 (1.00) 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

Claimed or disclosed in 16 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070129401-A1 PROCESSES FOR PREPARING ANHYDROUS AND HYDRATE FORMS OF ANTIHISTAMINIC PIPERIDINE DERIVATIVES, POLYMORPHS AND PSEUDOMORPHS THEREOF AVENTIS PHARMACEUTICALS, INC. 2007-06-07 US claimed
US-20050090528-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof AVENTIS PHARMACETICALS, INC. 2005-04-28 US claimed
US-20030045722-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HENTON DANIEL R (US) 2003-03-06 US claimed
CN-106806346-B Fexofenadine hydrochloride dry suspension preparation and preparation method thereof 国药集团广东环球制药有限公司 2020-09-11 CN disclosed
CN-106806346-A A kind of fexofenadine hydrochloride dry suspensoid agent preparation and preparation method thereof 国药集团广东环球制药有限公司 2017-06-09 CN disclosed
EP-2289878-A1 Fexofenadine polymorphs and process for the preparation thereof Dipharma S.p.A. (IT) 2011-03-02 EP disclosed
WO-2007110884-A3 A PROCESS FOR THE PREPARATION OF HIGHLY PURE ANHYDROUS FEXOFENADINE HYDROCHLORIDE IND SWIFT LAB LTD (IN) 2009-05-28 WO disclosed
US-20090111853-A1 FEXOFENADINE POLYMORPHS AND PROCESS FOR THE PREPARATION THEREOF DIPHARMA S.P.A. (IT) 2009-04-30 US disclosed
WO-2007110884-A2 A PROCESS FOR THE PREPARATION OF HIGHLY PURE ANHYDROUS FEXOFENADINE HYDROCHLORIDE IND-SWIFT LABORATORIES LIMITED (IN) 2007-10-04 WO disclosed
US-20070129401-A1 PROCESSES FOR PREPARING ANHYDROUS AND HYDRATE FORMS OF ANTIHISTAMINIC PIPERIDINE DERIVATIVES, POLYMORPHS AND PSEUDOMORPHS THEREOF AVENTIS PHARMACEUTICALS, INC. 2007-06-07 US disclosed
EP-1614681-A1 Fexofenadine polymorphs and process for the preparation thereof Dipharma S.p.A. (IT) 2006-01-11 EP disclosed
US-20050282860-A1 Fexofenadine polymorphs and process for the preparation thereof DIPHARMA S.P.A. (IT) 2005-12-22 US disclosed
US-20050090528-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof AVENTIS PHARMACETICALS, INC. 2005-04-28 US disclosed
EP-1399422-A2 NOVEL CRYSTALLINE FORMS OF 4-[4-[4-(HYDROXYDIPHENYLMETHYL)-1-PIPERIDINYL] -1-HYDROXYBUTYL] -A,A-DIMETHYLBENZENE ACETIC ACID AND ITS HYDROCHLORIDE Dr. Reddy's Laboratories Ltd. (IN) 2004-03-24 EP disclosed
US-20030045722-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HENTON DANIEL R (US) 2003-03-06 US disclosed
WO-2002102777-A2 NOVEL CRYSTALLINE FORMS OF 4-[4-[4-(HYDROXYDIPHENYLMETHYL)-1-PIPERINDINYL]-1-HYDROXYBUTYL]-α, α-DIMETHYLBENZENE ACETIC ACID AND ITS HYDROCHLORIDE DR. REDDY'S LABORATORIES LTD. (IN) 2002-12-27 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050282860-A1 Fexofenadine polymorphs and process for the preparation thereof CYP4F3, CYP4F2, CYP2C19 HRH1 27/4885KCNH2 739/4885LMNA 3993/4885
US-20090111853-A1 FEXOFENADINE POLYMORPHS AND PROCESS FOR THE PREPARATION THEREOF CYP4F3, CYP4F2, CYP2C19 HRH1 27/4885KCNH2 739/4885LMNA 3993/4885
US-20050090528-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HRH1, HRH2, HRH4 HRH1 1/4885KCNH2 89/4885LMNA 3956/4885
US-20070129401-A1 PROCESSES FOR PREPARING ANHYDROUS AND HYDRATE FORMS OF ANTIHISTAMINIC PIPERIDINE DERIVATIVES, POLYMORPHS AND PSEUDOMORPHS THEREOF HRH1, HRH2, HRH4 HRH1 1/4885KCNH2 89/4885LMNA 3956/4885
US-20030045722-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HRH1, HRH2, HRH4 HRH1 1/4885KCNH2 123/4885LMNA 4081/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.