Terfenadine

Terfenadine

SCHEMBL137824

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

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HRH1

The experimentally established mechanism targets of Terfenadine. 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 3/20 0.94
KCNH2 Q12809 3/20 0.94
LMNA P02545 3/20 0.94
DRD3 P35462 3/20 0.94
HTR2A P28223 2/20 0.94
HTR2B P41595 2/20 0.94
BLM P54132 2/20 0.94
DRD2 P14416 2/20 0.94
CYP2J2 P51589 2/20 0.94
MEN1 O00255 1/20 0.94
NPC1 O15118 1/20 0.94
CACNA1F O60840 1/20 0.94
GMNN O75496 1/20 0.94
USP2 O75604 1/20 0.94
EGFR P00533 1/20 0.94
CYP1A2 P05177 1/20 0.94
FYN P06241 1/20 0.94
CHRM2 P08172 1/20 0.94
ABCB1 P08183 1/20 0.94
CYP3A4 P08684 1/20 0.94

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
Terfenadine SCHEMBL5998456 0.97 KCNH2 (1.00) KCNH2LMNAHRH1DRD3HTR2A
Terfenadine SCHEMBL5152 0.97 KCNH2 (1.00) KCNH2LMNAHRH1DRD3HTR2A
Terfenadine SCHEMBL5999024 0.97 KCNH2 (1.00) KCNH2LMNAHRH1DRD3HTR2A
R-Terfenadine SCHEMBL155924 0.97 KCNH2 (1.00) KCNH2LMNAHRH1DRD3HTR2A
SCHEMBL11857869 0.97 KCNH2 (1.00) KCNH2LMNAHRH1DRD3HTR2A
Terfenadine SCHEMBL5999023 0.97 KCNH2 (1.00) KCNH2LMNAHRH1DRD3HTR2A
R-Terfenadine SCHEMBL17732284 0.96 KCNH2 (0.98) KCNH2LMNAHRH1DRD3HTR2A
Terfenadine SCHEMBL27965234 0.96 KCNH2 (0.98) KCNH2LMNAHRH1DRD3HTR2A
Terfenadine SCHEMBL11546558 0.96 KCNH2 (0.98) KCNH2LMNAHRH1DRD3HTR2A
Terfenadine SCHEMBL17732283 0.96 KCNH2 (0.98) KCNH2LMNAHRH1DRD3HTR2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240217966-A1 PHARMACEUTICAL COMPOSITION CONTAINING GLP-1 RECEPTOR AGONIST HAVING FUSED RING SHIONOGI & CO., LTD. (JP) 2024-07-04 US disclosed
US-12024519-B2 Fused ring derivative having MGAT-2 inhibitory activity SHIONOGI & CO., LTD. (JP) 2024-07-02 US disclosed
EP-3957627-B1 6-MEMBERED HETEROCYCLIC DERIVATIVE AND PHARMACEUTICAL COMPOSITION COMPRISING SAME SHIONOGI & CO (JP) 2024-06-19 EP disclosed
US-20240182463-A1 SUBSTITUTED POLYCYCLIC CARBAMOYL PYRIDONE DERIVATIVE PRODRUG SHIONOGI & CO., LTD. (JP) 2024-06-06 US disclosed
EP-4219508-B1 SUBSTITUTED POLYCYCLIC PYRIDONE DERIVATIVE AND PRODRUG THEREOF SHIONOGI & CO (JP) 2024-06-05 EP disclosed
CN-117999257-A Bicyclic heterocyclic derivatives having virus proliferation inhibitory activity and pharmaceutical compositions containing the same 盐野义制药株式会社 2024-05-07 CN disclosed
CN-113501821-B Fused ring derivatives having MGAT-2 inhibitory activity 盐野义制药株式会社 2024-04-09 CN disclosed
CN-111801330-B Fused ring compounds having dopamine D3 receptor antagonism 盐野义制药株式会社 2024-04-05 CN disclosed
WO-2024063143-A1 FUSED RING COMPOUND HAVING GLP-1 RECEPTOR AGONIST EFFECT 塩野義製薬株式会社 2024-03-28 WO disclosed
WO-2024063140-A1 MONOCYCLIC COMPOUND HAVING GLP-1 RECEPTOR AGONIST ACTIVITY 塩野義製薬株式会社 2024-03-28 WO disclosed
EP-1019042-A1 ANTI-FIRST-PASS EFFECT COMPOUNDS Bioavailability Systems, L.L.C. (US) 2000-07-19 EP disclosed
US-6063809-A Anti-first-pass effect compounds BIOAVAILABILITY SYSTEMS, LLC (US) 2000-05-16 US disclosed
US-6054477-A Anti-first-pass effect compounds BIOAVAILABILITY SYSTEMS, LLC (US) 2000-04-25 US disclosed
US-5990154-A Anti-first-pass effect compounds and citrus extract BIOAVAILABILITY SYSTEMS, L.L.C. (US) 1999-11-23 US disclosed
US-5962044-A Citrus extract BIOAVAILABILITY SYSTEMS, L.L.C. (US) 1999-10-05 US disclosed
WO-1999009976-A1 ANTI-FIRST-PASS EFFECT COMPOUNDS BIOAVAILABILITY SYSTEMS, L.L.C. (US) 1999-03-04 WO disclosed
WO-1998053658-A2 ANTI-FIRST-PASS EFFECT COMPOUNDS AND CITRUS EXTRACT BIOAVAILABILITY SYSTEMS, L.L.C. (US) 1998-12-03 WO disclosed
US-5820915-A Method for the preparation of a first-pass effective citrus-derived substance and product thereof BIOAVAILABILITY SYSTEMS, L.L.C. (US) 1998-10-13 US disclosed
WO-1998024316-A1 ANTI-FIRST-PASS EFFECT COMPOUNDS AND CITRUS EXTRACT HARRIS JAMES W (US) 1998-06-11 WO disclosed
WO-1997049301-A1 CITRUS EXTRACT AND METHOD OF MAKING BIOAVAILABILITY SYSTEMS, L.L.C. (US) 1997-12-31 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 (3 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-20240217966-A1 PHARMACEUTICAL COMPOSITION CONTAINING GLP-1 RECEPTOR AGONIST HAVING FUSED RING GLP1R, GIPR, GCGR HRH1 139/4885KCNH2 676/4885LMNA 3263/4885
US-20240182463-A1 SUBSTITUTED POLYCYCLIC CARBAMOYL PYRIDONE DERIVATIVE PRODRUG PREP, UNG, DPP4 HRH1 2463/4885KCNH2 3392/4885LMNA 1238/4885
US-12024519-B2 Fused ring derivative having MGAT-2 inhibitory activity MGAT2, MGAT1, ACAT2 HRH1 3574/4885KCNH2 3212/4885LMNA 4291/4885

“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.