Orvepitant

Orvepitant

SCHEMBL1421784

Cc1cc(F)ccc1[C@H]1C[C@@H](N2CCN3C(=O)CC[C@H]3C2)CCN1C(=O)N(C)[C@H](C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

TACR1

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

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
TACR1 known ✓ P25103 19/20 1.00
SIGMAR1 Q99720 2/20 1.00
PTAFR P25105 1/20 1.00
CYP3A4 P08684 2/20 0.74

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
Orvepitant SCHEMBL21931158 1.00 TACR1 (1.00) TACR1SIGMAR1PTAFRCYP3A4
Orvepitant SCHEMBL2483270 1.00 TACR1 (1.00) TACR1SIGMAR1PTAFRCYP3A4
Orvepitant SCHEMBL29373789 1.00 TACR1 (1.00) TACR1SIGMAR1PTAFRCYP3A4
Orvepitant SCHEMBL2484579 1.00 TACR1 (1.00) TACR1SIGMAR1PTAFRCYP3A4
Orvepitant SCHEMBL19581227 1.00 TACR1 (1.00) TACR1SIGMAR1PTAFRCYP3A4
Orvepitant SCHEMBL23895405 1.00 TACR1 (1.00) TACR1SIGMAR1PTAFRCYP3A4
Orvepitant SCHEMBL19117640 1.00 TACR1 (1.00) TACR1SIGMAR1PTAFRCYP3A4
Orvepitant SCHEMBL2179896 1.00 TACR1 (1.00) TACR1SIGMAR1PTAFRCYP3A4
Orvepitant SCHEMBL5360752 0.99 TACR1 (0.99) TACR1SIGMAR1PTAFRCYP3A4
Orvepitant SCHEMBL30110395 0.99 TACR1 (0.99) TACR1SIGMAR1PTAFRCYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1615641-A1 COMBINATIONS OF PAROXETINE AND 2-(R)-(4-FLUORO-2-METHYL-PHENYL)-4-(S)-((8AS)-6-OXO-HEXAHYDRO-PYRROLO 1,2-A -PYRAZIN-2-YL)-PIPERIDINE-1-CARBOXYLIC ACID 1-(R)-(3,5-BIS-TRIFLUOROMETHYL-PHENYL)-ETHYL -METHYLAMIDE FOR TREATMENT OF DEPRESSION/ANXIETY GLAXO GROUP LIMITED (GB) 2006-01-18 EP claimed
WO-2004091615-A1 COMBINATIONS OF PAROXETINE AND 2-(R)-(4-FLUORO-2-METHYL-PHENYL)-4-(S)-((8AS)-6-OXO-HEXAHYDRO-PYRROLO[1,2-A]-PYRAZIN-2-YL)-PIPERIDINE-1-CARBOXYLIC ACID[1-(R)-(3,5-BIS-TRIFLUOROMETHYL-PHENYL)-ETHYL]-METHYLAMIDE FOR TREATMENT OF DEPRESSION/ANXIETY GLAXO GROUP LIMITED (GB) 2004-10-28 WO claimed
WO-2026090360-A1 FUSED PYRIMIDINE COMPOUNDS FOR TREATMENT OF TINNITUS, HEARING LOSS, AND MENIERE'S DISEASE OVID THERAPEUTICS INC. (US) 2026-04-30 WO disclosed
US-20260108529-A1 FUSED AMINO PYRIMIDINE COMPOUNDS FOR TREATMENT OF TINNITUS, ACUTE SENSORINEURAL HEARING LOSS, AGE-RELATED HEARING LOSS, AND MENIERE'S DISEASE OVID THERAPEUTICS INC (US) 2026-04-23 US disclosed
EP-4426280-B1 PROTECTION AGAINST ARTHROPOD PARASITES WITH PURINERGIC RECEPTOR (OPR) ANTAGONISTS GURBA ALEXANDRE (CH) 2026-03-18 EP disclosed
US-20250302821-A1 SYNERGISTIC ANTIFUNGAL COMPOSITION AND METHOD ST. JUDE CHILDREN'S RESEARCH HOSPITAL, INC. 2025-10-02 US disclosed
US-20250195459-A1 USE OF (1S,3S)-3-AMINO-4-(DIFLUOROMETHYLIDENE) CYCLOPENTANE-1-CARBOXYLIC ACID AND (S)-3-AMINO-4-(DIFLUOROMETHYLENYL)CYCLOPENT-1-ENE-1-CARBOXYLIC ACID IN THE TREATMENT OF TINNITUS, ACUTE SENSORINEURAL HEARING LOSS, MENIERE’S DISEASE, TOURETTE’S SYNDROME, ATTENTION DEFICIT HYPERACTIVITY DISORDER AND ADDICTION OVID THERAPEUTICS INC. 2025-06-19 US disclosed
US-20250057791-A1 PROTECTION AGAINST ARTHROPOD PARASITES WITH PURINERGIC RECEPTOR (OPR) ANTAGONISTS GURBA ALEXANDRE (CH) 2025-02-20 US disclosed
EP-4461362-A2 NK1-ANTAGONIST COMBINATION AND METHOD FOR TREATING SYNUCLEINOPATHIES Chase Therapeutics Corporation (US) 2024-11-13 EP disclosed
EP-4426280-A1 PROTECTION AGAINST ARTHROPOD PARASITES WITH PURINERGIC RECEPTOR (OPR) ANTAGONISTS Gurba, Alexandre (CH) 2024-09-11 EP disclosed
CN-115427033-B NK-1 receptor antagonists for the treatment of diseases selected from sepsis, septic shock, acute Respiratory Distress Syndrome (ARDS) or Multiple Organ Dysfunction Syndrome (MODS) 尼尔医疗有限公司 2024-08-09 CN disclosed
EP-2297152-A1 ANHYDROUS CRYSTAL FORM OF ORVEPITANT MALEATE Glaxo Group Limited (GB) 2011-03-23 EP disclosed
WO-2009124996-A1 ANHYDROUS CRYSTAL FORM OF ORVEPITANT MALEATE GLAXO GROUP LIMITED (GB) 2009-10-15 WO disclosed
WO-2009124996-A1 ANHYDROUS CRYSTAL FORM OF ORVEPITANT MALEATE GLAXO GROUP LIMITED (GB) 2009-10-15 WO disclosed
EP-1041449-B1 Electrophotographic image-forming method, electrophotographic image-forming apparatus, and process cartridge CANON KK (JP) 2004-10-13 EP disclosed
US-6384099-B1 APPLYING DENTAL MATERIAL INCLUDING MONOMERS AND INITIATOR SENSITIVE TO LIGHT OF PARTICULAR WAVELENGTH TO DENTAL SURFACE, EXPOSING MATERIAL TO LIGHT AT FIRST POWER LEVEL TO INITIATE POLYMERIZATION, EXPOSING TO LIGHT AT SECOND POWER LEVEL LASER MED. INC. 2002-05-07 US disclosed
US-6282013-B1 System for curing polymeric materials, such as those used in dentistry, and for tailoring the post-cure properties of polymeric materials through the use of light source power modulation LASERMED, INC. 2001-08-28 US disclosed
US-6215971-B1 Electrophotographic image-forming method, electrophotographic image-forming apparatus, and process cartridge CANON KABUSHIKI KAISHA (JP) 2001-04-10 US disclosed
EP-1041449-A1 Electrophotographic image-forming method, electrophotographic image-forming apparatus, and process cartridge CANON KABUSHIKI KAISHA (JP) 2000-10-04 EP disclosed
US-6008264-A APPLYING A DENTAL MATERIAL WITH LIGHT SENSITIVE INITIATOR TO A DENTAL SURFACE, EXPOSING TO LIGHT SOURCE AT FIRST POWER LEVEL TO INITIATE POLYMERIZATION, SIMULTANEOUSLY DECREASING LEVEL OF LIGHT, MAINTAINING UNTIL MATERIAL IS POLYMERIZED LASER MED, INC. (US) 1999-12-28 US 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-20250195459-A1 USE OF (1S,3S)-3-AMINO-4-(DIFLUOROMETHYLIDENE) CYCLOPENTANE-1-CARBOXYLIC ACID AND (S)-3-AMINO-4-(DIFLUOROMETHYLENYL)CYCLOPENT-1-ENE-1-CARBOXYLIC ACID IN THE TREATMENT OF TINNITUS, ACUTE SENSORINEURAL HEARING LOSS, MENIERE’S DISEASE, TOURETTE’S SYNDROME, ATTENTION DEFICIT HYPERACTIVITY DISORDER AND ADDICTION SLC6A3, SLC1A2, SLC1A3 TACR1 659/4885SIGMAR1 2610/4885PTAFR 746/4885
US-20260108529-A1 FUSED AMINO PYRIMIDINE COMPOUNDS FOR TREATMENT OF TINNITUS, ACUTE SENSORINEURAL HEARING LOSS, AGE-RELATED HEARING LOSS, AND MENIERE'S DISEASE OTC, MEN1, MT-CO1 TACR1 3463/4885SIGMAR1 4461/4885PTAFR 1986/4885
US-20250057791-A1 PROTECTION AGAINST ARTHROPOD PARASITES WITH PURINERGIC RECEPTOR (OPR) ANTAGONISTS P2RX2, P2RX3, P2RX1 TACR1 34/4885SIGMAR1 257/4885PTAFR 222/4885

“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.