SCHEMBL65960

SCHEMBL65960

O=CCCc1ccc(F)cc1

nearest known ligand 0.50

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 3/20 0.50
MAOB P27338 2/20 0.43
IDO1 P14902 1/20 0.42
LOXL2 Q9Y4K0 1/20 0.42
AOC3 Q16853 2/20 0.42
L3MBTL1 Q9Y468 1/20 0.41
AOC2 O75106 1/20 0.41
MAOA P21397 1/20 0.41
KDM4E B2RXH2 1/20 0.41
ALDH1A1 P00352 1/20 0.41
FFAR1 O14842 1/20 0.40
CA12 O43570 1/20 0.40
CA1 P00915 1/20 0.40
CA2 P00918 1/20 0.40
CA4 P22748 1/20 0.40
PTGS1 P23219 1/20 0.39
PTGS2 P35354 1/20 0.39

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
SCHEMBL1842465 0.94 MAOB (0.53) TAAR1MAOBIDO1LOXL2AOC3
SCHEMBL9671868 0.87 HIF1A (0.37) ALDH1A1FFAR1CA2
SCHEMBL3242822 0.86 TAAR1 (0.46) TAAR1MAOBIDO1LOXL2AOC3
SCHEMBL5538118 0.85 TAAR1 (0.45) TAAR1MAOB
SCHEMBL5539547 0.83 TAAR1 (0.43) TAAR1MAOB
SCHEMBL15453289 0.83 TAAR1 (0.43) TAAR1MAOB
SCHEMBL26908283 0.83 TAAR1 (0.43) TAAR1MAOB
SCHEMBL25048987 0.81 TAAR1 (0.52) TAAR1L3MBTL1KDM4EALDH1A1CA12
SCHEMBL10012084 0.80 HRH3 (0.41) MAOBFFAR1PTGS1
SCHEMBL16595322 0.80 SLC6A2 (0.46) MAOBMAOA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10787484-B2 Compositions and methods for treating cardiovascular disease GENENTECH, INC. (US) 2020-09-29 US claimed
US-20190177366-A1 COMPOSITIONS AND METHODS FOR TREATING CARDIOVASCULAR DISEASE GENENTECH, INC. (US) 2019-06-13 US claimed
US-7732412-B2 Methods of treatment using novel LHRH antagonists having improved solubility properties ZENTARIS GMBH (DE) 2010-06-08 US claimed
EP-1830818-B1 PROCESS FOR THE MANUFACTURE OF STERILE SUSPENSIONS OR LYOPHILISATES OF LOW-SOLUBLE BASIC PEPTIDE COMPLEXES, PHARMACEUTICAL FORMULATIONS COMPRISING THESE COMPLEXES AND THEIR USE AS MEDICAMENT AETERNA ZENTARIS GMBH (DE) 2010-04-07 EP claimed
US-20060281685-A1 METHODS OF TREATMENT USING NOVEL LHRH ANTAGONISTS HAVING IMPROVED SOLUBILITY PROPERTIES ZENTARIS GMBH (DE) 2006-12-14 US claimed
US-7148195-B2 LHRH antagonists having improved solubility properties ZENTARIS GMBH (DE) 2006-12-12 US claimed
US-20060135405-A1 Process for producing sterile suspensions of slightly soluble basic peptide complexes, sterile suspensions of slightly soluble basic peptide complexes, pharmaceutical formulations containing them, and the use thereof as medicaments ZENTARIS GMBH (DE) 2006-06-22 US claimed
EP-1556361-A2 2-ALKYL-(2-AMINO-3-ARYL-PROPIONYL)-PIPERAZINE DERIVATIVES AND RELATED COMPOUNDS AS MELANOCORTIN RECEPTOR LIGANDS FOR THE TREATMENT OF OBESITY THE PROCTER & GAMBLE COMPANY (US) 2005-07-27 EP claimed
US-20050159335-A1 Pharmaceutical administration form for peptides, process for its preparation, and use AETERNA ZENTARIS GMBH (DE) 2005-07-21 US claimed
CN-1185251-C Novel LHRH-antagonists with improved solubility characteristics ZANTARIS AG (DE) 2005-01-19 CN claimed
CN-1096300-A Isosteric antiherpes peptide derivatives BIO MEGA BOEHRINGER INGELHEIM (CA) 1994-12-14 CN claimed
WO-1994025046-A1 METHOD OF COMBATING ACYCLOVIR-RESISTANT HERPES SIMPLEX VIRAL INFECTIONS BIO-MEGA/BOEHRINGER INGELHEIM RESEARCH INC. (CA) 1994-11-10 WO claimed
WO-1993018056-A1 ISOSTERIC ANTIHERPES PEPTIDE DERIVATIVES BIO-MEGA/BOEHRINGER INGELHEIM RESEARCH INC. (CA) 1993-09-16 WO claimed
EP-0560267-A1 Isosteric antiherpes peptide derivatives BIO-MEGA/BOEHRINGER INGELHEIM RESEARCH INC. (CA) 1993-09-15 EP claimed
US-5140009-A Stable against proteolytic enzymes; anticarcinogenic agents; urogenital disorders TAP PHARMACEUTICALS, INC. (US) 1992-08-18 US claimed
EP-0480918-A1 REDUCED SIZE LHRH ANALOGS ABBOTT LABORATORIES (US) 1992-04-22 EP claimed
EP-0480918-A4 REDUCED SIZE LHRH ANALOGS. ABBOTT LAB (US) 1991-06-04 EP claimed
EP-0417454-A2 Reduced size LHRH analogs ABBOTT LABORATORIES (US) 1991-03-20 EP claimed
WO-1989007451-A1 REDUCED SIZE LHRH ANALOGS ABBOTT LABORATORIES (US) 1989-08-24 WO claimed
EP-0328089-A2 Reduced size LHRH analogs ABBOTT LABORATORIES (US) 1989-08-16 EP 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 (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-20060135405-A1 Process for producing sterile suspensions of slightly soluble basic peptide complexes, sterile suspensions of slightly soluble basic peptide complexes, pharmaceutical formulations containing them, and the use thereof as medicaments VIP, NASP, SPCS2 TAAR1 4469/4885MAOB 4666/4885IDO1 3616/4885
US-20060281685-A1 METHODS OF TREATMENT USING NOVEL LHRH ANTAGONISTS HAVING IMPROVED SOLUBILITY PROPERTIES GNRHR, PRLHR, FSHR TAAR1 3388/4885MAOB 2247/4885IDO1 1152/4885
US-10787484-B2 Compositions and methods for treating cardiovascular disease PCSK9, PCSK7, PCSK6 TAAR1 4623/4885MAOB 1282/4885IDO1 3199/4885
US-20190177366-A1 COMPOSITIONS AND METHODS FOR TREATING CARDIOVASCULAR DISEASE PCSK9, PCSK7, PCSK6 TAAR1 4623/4885MAOB 1282/4885IDO1 3199/4885
US-20050159335-A1 Pharmaceutical administration form for peptides, process for its preparation, and use LHCGR, GNRHR, GHRHR TAAR1 4149/4885MAOB 1848/4885IDO1 4715/4885

“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.