Fexofenadine

Fexofenadine

SCHEMBL48729

CC(C)(C(=O)O)c1ccc(C(O)CCCN2CCC(C(O)(c3ccccc3)c3ccccc3)CC2)cc1.Cl.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
LMNA P02545 3/20 0.98
DRD3 P35462 3/20 0.98
DRD2 P14416 2/20 0.98
ALOX15 P16050 1/20 0.98
HSD17B10 Q99714 1/20 0.98
KCNH2 Q12809 4/20 0.96
HTR2A P28223 2/20 0.96
HTR2B P41595 2/20 0.96
BLM P54132 2/20 0.96
CNR1 P21554 1/20 0.96
APEX1 P27695 1/20 0.96
PDE4A P27815 1/20 0.96
PDE3A Q14432 1/20 0.96
CYP2J2 P51589 3/20 0.77
MEN1 O00255 1/20 0.77
NPC1 O15118 1/20 0.77
CACNA1F O60840 1/20 0.77
GMNN O75496 1/20 0.77
USP2 O75604 1/20 0.77

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 SCHEMBL1395627 1.00 HRH1 (0.98) HRH1LMNADRD3DRD2ALOX15
Fexofenadine SCHEMBL9943442 0.99 HRH1 (0.98) HRH1LMNADRD3DRD2ALOX15
Fexofenadine SCHEMBL29562068 0.99 HRH1 (1.00) HRH1LMNADRD3DRD2ALOX15
Fexofenadine SCHEMBL40914 0.99 HRH1 (1.00) HRH1LMNADRD3DRD2ALOX15
Fexofenadine SCHEMBL1395675 0.99 HRH1 (0.98) HRH1LMNADRD3DRD2ALOX15
Fexofenadine SCHEMBL9943444 0.99 HRH1 (0.98) HRH1LMNADRD3DRD2ALOX15
Fexofenadine SCHEMBL40915 0.99 HRH1 (1.00) HRH1LMNADRD3DRD2ALOX15
Fexofenadine SCHEMBL1395674 0.99 HRH1 (0.98) HRH1LMNADRD3DRD2ALOX15
Fexofenadine SCHEMBL3543634 0.98 HRH1 (0.98) HRH1LMNADRD3DRD2ALOX15
Fexofenadine SCHEMBL3178320 0.98 HRH1 (1.00) HRH1LMNADRD3DRD2ALOX15

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 100 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2354125-A1 Anhydrous and hydrate polymorphic forms of antihistaminic piperidine derivatives Aventisub II Inc. (US) 2011-08-10 EP claimed
EP-2289878-A1 Fexofenadine polymorphs and process for the preparation thereof Dipharma S.p.A. (IT) 2011-03-02 EP claimed
US-7666881-B2 Methods of treating allergic reactions using hydrated forms of antihistaminic piperidine derivatives Aventis Holdings, Inc. (US) 2010-02-23 US claimed
US-20090111853-A1 FEXOFENADINE POLYMORPHS AND PROCESS FOR THE PREPARATION THEREOF DIPHARMA S.P.A. (IT) 2009-04-30 US claimed
US-20090054486-A1 POLYMORPHIC FORM XVI OF FEXOFENADINE HYDROCHLORIDE TEVA PHARMACEUTICALS USA, INC. 2009-02-26 US claimed
US-20080167471-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof AVENTIS PHARMACEUTICALS INC. 2008-07-10 US claimed
US-20080167469-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof AVENTIS PHARMACEUTICALS INC. 2008-07-10 US claimed
US-20070021461-A1 PROCESSES FOR PREPARING ANHYDROUS AND HYDRATE FORMS OF ANTIHISTAMINIC PIPERIDINE DERIVATIVES, POLYMORPHS AND PSEUDOMORPHS THEREOF AVENTIS PHARMACEUTICALS, INC. (US) 2007-01-25 US claimed
US-7135571-B2 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof AVENTIS PHARMACEUTICALS, INC. (US) 2006-11-14 US claimed
US-20060217557-A1 Polymorphic form XVI of fexofenadine hydrochloride KROCHMAL BARNABA 2006-09-28 US claimed
US-20020193600-A1 Process for preparing anyhdrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HENTON DANIEL R (US) 2002-12-19 US claimed
US-20020193603-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof AVENTISUB II INC. 2002-12-19 US claimed
US-20020193601-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof AVENTISUB II INC. 2002-12-19 US claimed
EP-0766668-B1 PROCESSES FOR PREPARING ANHYDROUS AND HYDRATE FORMS OF ANTIHISTAMINIC PIPERIDINE DERIVATIVES, POLYMORPHS AND PSEUDORMOPHS THEREOF AVENTIS PHARMA INC (US) 2002-07-17 EP claimed
EP-1178041-A1 Process for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives Aventis Pharmaceuticals Inc. (US) 2002-02-06 EP claimed
US-20010025106-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HENTON DANIEL R (US) 2001-09-27 US claimed
US-20010014741-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HENTON DANIEL R (US) 2001-08-16 US claimed
US-20010012896-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HENTON DANIEL R (US) 2001-08-09 US claimed
EP-0766668-A1 PROCESSES FOR PREPARING ANHYDROUS AND HYDRATE FORMS OF ANTIHISTAMINIC PIPERIDINE DERIVATIVES, POLYMORPHS AND PSEUDORMOPHS THEREOF HOECHST MARION ROUSSEL, INC. (US) 1997-04-09 EP claimed
WO-1995031437-A1 PROCESSES FOR PREPARING ANHYDROUS AND HYDRATE FORMS OF ANTIHISTAMINIC PIPERIDINE DERIVATIVES, POLYMORPHS AND PSEUDORMOPHS THEREOF HOECHST MARRION ROUSSEL, INC. (US) 1995-11-23 WO claimed

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

For each of this compound's patents that has machine-readable text (12 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-20090054486-A1 POLYMORPHIC FORM XVI OF FEXOFENADINE HYDROCHLORIDE UBE2V1, XDH, F5 HRH1 67/4885LMNA 3538/4885DRD3 1635/4885
US-20020193603-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HRH1, HRH2, HRH4 HRH1 1/4885LMNA 4081/4885DRD3 451/4885
US-20080167471-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HRH1, HRH2, HRH4 HRH1 1/4885LMNA 3956/4885DRD3 415/4885
US-20090111853-A1 FEXOFENADINE POLYMORPHS AND PROCESS FOR THE PREPARATION THEREOF CYP4F3, CYP4F2, CYP2C19 HRH1 27/4885LMNA 3993/4885DRD3 2586/4885
US-20010012896-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HRH1, HRH2, HRH4 HRH1 1/4885LMNA 4098/4885DRD3 513/4885
US-20070021461-A1 PROCESSES FOR PREPARING ANHYDROUS AND HYDRATE FORMS OF ANTIHISTAMINIC PIPERIDINE DERIVATIVES, POLYMORPHS AND PSEUDOMORPHS THEREOF HRH1, HRH2, HRH4 HRH1 1/4885LMNA 3956/4885DRD3 415/4885
US-20020193600-A1 Process for preparing anyhdrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HRH1, HRH2, HRH4 HRH1 1/4885LMNA 4091/4885DRD3 259/4885
US-20010025106-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HRH1, HRH2, HRH4 HRH1 1/4885LMNA 4081/4885DRD3 451/4885
US-20010014741-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HRH1, HRH2, HRH4 HRH1 1/4885LMNA 4081/4885DRD3 451/4885
US-20060217557-A1 Polymorphic form XVI of fexofenadine hydrochloride UBE2V1, XDH, F5 HRH1 67/4885LMNA 3538/4885DRD3 1635/4885
US-20020193601-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HRH1, HRH2, HRH4 HRH1 1/4885LMNA 4081/4885DRD3 451/4885
US-20080167469-A1 Processes for preparing anhydrous and hydrate forms of antihistaminic piperidine derivatives, polymorphs and pseudomorphs thereof HRH1, HRH2, HRH4 HRH1 1/4885LMNA 3956/4885DRD3 415/4885

“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.