SCHEMBL345517

SCHEMBL345517

COc1ccc2c(c1)CCC(C(=O)O)C2

nearest known ligand 0.59

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
CA1 P00915 3/20 0.56
CA2 P00918 3/20 0.56
ACHE P22303 3/20 0.56
MTNR1A P48039 1/20 0.53
MTNR1B P49286 1/20 0.53
DRD2 P14416 2/20 0.51
DRD3 P35462 2/20 0.51
CYP26A1 O43174 1/20 0.51
FAAH O00519 7/20 0.49
CYP19A1 P11511 1/20 0.48
CYP1A2 P05177 1/20 0.48
GAA P10253 1/20 0.47
FFAR1 O14842 1/20 0.46

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
SCHEMBL8074259 1.00 CA1 (0.56) CA1CA2ACHEMTNR1AMTNR1B
SCHEMBL8603749 1.00 CA1 (0.56) CA1CA2ACHEMTNR1AMTNR1B
SCHEMBL345882 0.94 MTNR1A (0.60) CA1CA2ACHEMTNR1AMTNR1B
SCHEMBL345881 0.94 MTNR1A (0.60) CA1CA2ACHEMTNR1AMTNR1B
SCHEMBL8603880 0.94 MTNR1A (0.60) CA1CA2ACHEMTNR1AMTNR1B
SCHEMBL970670 0.88 CA1 (0.56) CA1CA2ACHEMTNR1AMTNR1B
SCHEMBL10225789 0.87 MTNR1A (0.51) CA1CA2ACHEMTNR1AMTNR1B
SCHEMBL8066286 0.87 CA1 (0.59) CA1CA2ACHEMTNR1AMTNR1B
SCHEMBL9361562 0.87 CA1 (0.55) CA1CA2ACHEMTNR1AMTNR1B
SCHEMBL8076235 0.87 CA1 (0.55) CA1CA2ACHEMTNR1AMTNR1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2215054-A1 AMIDE DERIVATIVES AS ION-CHANNEL LIGANDS AND PHARMACEUTICAL COMPOSITIONS AND METHODS OF USING THE SAME Renovis, Inc. (US) 2010-08-11 EP claimed
WO-2009064449-A1 AMIDE DERIVATIVES AS ION-CHANNEL LIGANDS AND PHARMACEUTICAL COMPOSITIONS AND METHODS OF USING THE SAME RENOVIS, INC. (US) 2009-05-22 WO claimed
US-4374148-A HYPOGLYCEMIC AGENTS PFIZER INC. (US) 1983-02-15 US claimed
US-12565483-B2 Oxopyrrolidine urea FPR2 agonists BRISTOL-MYERS SQUIBB COMPANY (US) 2026-03-03 US disclosed
US-20240109832-A1 RAPID CONSTRUCTION OF TETRALIN, CHROMANE, AND INDANE MOTIFS VIA CYCLATIVE C-H/C-H COUPLING: FOUR-STEP TOTAL SYNTHESIS OF (±)-RUSSUJAPONOL F NATIONAL INSTITUTES OF HEALTH 2024-04-04 US disclosed
US-20230303513-A1 OXOPYRROLIDINE UREA FPR2 AGONISTS BRISTOL MYERS SQUIBB CO (US) 2023-09-28 US disclosed
US-20230303513-A1 OXOPYRROLIDINE UREA FPR2 AGONISTS BRISTOL MYERS SQUIBB CO (US) 2023-09-28 US disclosed
US-20230303513-A1 OXOPYRROLIDINE UREA FPR2 AGONISTS BRISTOL MYERS SQUIBB CO (US) 2023-09-28 US disclosed
CN-116568658-A Rapid construction of tetrahydronaphthalenes, chromanes and indane motifs via cyclized C-H/C-H couplings 斯克里普斯研究学院 2023-08-08 CN disclosed
EP-4196471-A1 OXOPYRROLIDINE UREA FPR2 AGONISTS Bristol-Myers Squibb Company (US) 2023-06-21 EP disclosed
CN-116057055-A Oxo-pyrrolidine urea FPR2 agonists 百时美施贵宝公司 2023-05-02 CN disclosed
US-20020032189-A1 For therapy and prophylaxis of neurodegenerative diseases such as Alzheimer's disease, Down's syndrome, Parkinson's disease, Creutzfeldt-Jacob disease, amyotrophic sclerosis on lateral fasciculus, multiple sclerosis, and neurological disorders THE UNIVERSITY OF TOKYO (JP) 2002-03-14 US disclosed
US-6310107-B1 (+)-6-(4-BIPHENYLYL)METHOXY-2-(2-(N,N-DIMETHYLAMINO)ETHYL)TETR ALIN, OR A SALT IS USEFUL FOR INHIBITING PRODUCTION AND/OR SECRETION OF AMYLOID-BETA PROTEIN TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2001-10-30 US disclosed
US-5130339-A Intestine and uterine motility modulators for reduction of intraocular pressure for glaucoma treatment SANOFI (FR) 1992-07-14 US disclosed
EP-0284359-B1 1,4-DISUBSTITUTED PIPERAZINE COMPOUNDS, THEIR PRODUCTION AND USE Takeda Chemical Industries, Ltd. (JP) 1992-01-08 EP disclosed
US-4880809-A HYPOTENSIVE AGENTS, AMIDE DERIVATIVES TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1989-11-14 US disclosed
EP-0284359-A1 1,4-Disubstituted piperazine compounds, their production and use Takeda Chemical Industries, Ltd. (JP) 1988-09-28 EP disclosed
US-4530919-A A 1,2,3,4-tetrahydronaphthalene carboxylic acid PFIZER INC. (US) 1985-07-23 US disclosed
US-4374148-A HYPOGLYCEMIC AGENTS PFIZER INC. (US) 1983-02-15 US disclosed
US-4305955-A ORAL HYPOGLYCEMIC AGENTS, CHROMAN-4-CARBOXYLIC ACID OR THIOCHROMAN-4-CARBOXYLIC ACID PFIZER INC. (US) 1981-12-15 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 (4 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-20230303513-A1 OXOPYRROLIDINE UREA FPR2 AGONISTS FPR1, FPR2, FPR3 CA1 4808/4885CA2 4020/4885ACHE 4625/4885
US-12565483-B2 Oxopyrrolidine urea FPR2 agonists FPR1, FPR2, FPR3 CA1 4259/4885CA2 2726/4885ACHE 4848/4885
US-20020032189-A1 For therapy and prophylaxis of neurodegenerative diseases such as Alzheimer's disease, Down's syndrome, Parkinson's disease, Creutzfeldt-Jacob disease, amyotrophic sclerosis on lateral fasciculus, multiple sclerosis, and neurological disorders PARK7, PSEN1, PRNP CA1 3139/4885CA2 3174/4885ACHE 1381/4885
US-20240109832-A1 RAPID CONSTRUCTION OF TETRALIN, CHROMANE, AND INDANE MOTIFS VIA CYCLATIVE C-H/C-H COUPLING: FOUR-STEP TOTAL SYNTHESIS OF (±)-RUSSUJAPONOL F HCCS, TAC3, CTRC CA1 1578/4885CA2 2470/4885ACHE 3614/4885

“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.