SCHEMBL237090

SCHEMBL237090

C[C@H](CC(=O)O)c1ccccc1

nearest known ligand 0.70

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
FFAR1 O14842 2/20 0.70
GABBR2 O75899 1/20 0.53
GABBR1 Q9UBS5 1/20 0.53
HPGD P15428 3/20 0.53
CYP2C19 P33261 2/20 0.53
CYP3A4 P08684 1/20 0.53
RAB9A P51151 1/20 0.53
TAAR1 Q96RJ0 2/20 0.52
POLB P06746 2/20 0.51
BCHE P06276 1/20 0.51
TRPA1 O75762 2/20 0.50
ALDH1A1 P00352 2/20 0.50
MAPT P10636 1/20 0.47

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
SCHEMBL237091 1.00 FFAR1 (0.70) FFAR1GABBR2GABBR1HPGDCYP2C19
SCHEMBL1149768 1.00 FFAR1 (0.70) FFAR1GABBR2GABBR1HPGDCYP2C19
Hydrochloric Acid SCHEMBL2005345 0.98 FFAR1 (0.68) FFAR1GABBR2GABBR1HPGDCYP2C19
SCHEMBL28324934 0.98 FFAR1 (0.68) FFAR1GABBR2GABBR1HPGDCYP2C19
SCHEMBL2899426 0.98 FFAR1 (0.68) FFAR1GABBR2GABBR1HPGDCYP2C19
Acetic Acid SCHEMBL159740 0.96 FFAR1 (0.66) FFAR1GABBR2GABBR1HPGDCYP2C19
Glycine SCHEMBL8726564 0.92 FFAR1 (0.62) FFAR1GABBR2GABBR1HPGDCYP2C19
Azetidine SCHEMBL28247623 0.89 FFAR1 (0.58) FFAR1GABBR2GABBR1HPGDCYP2C19
SCHEMBL7858991 0.88 FFAR1 (0.67) FFAR1
SCHEMBL21237780 0.88 FFAR1 (0.67) FFAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2377930-B1 A group of esterases for the enantioselective production of fine and speciality chemicals BRAIN BIOTECHNOLOGY RES & INFORMATION NETWORK AG (DE) 2015-12-02 EP claimed
EP-1638505-A4 AMPHIPHILIC PYRIDINIUM COMPOUNDS, METHOD OF MAKING AND USE THEREOF JACKSON H M FOUND MILITARY MED (US) 2009-01-07 EP claimed
US-20070105916-A1 Amphiphilic pyridinium compounds, method of making and use thereof THE HENRY M. JACKSON FOUNDATION FOR THE ADVANCEMENT OF MILITARY MEDICINE, INC. 2007-05-10 US claimed
EP-1638505-A2 AMPHIPHILIC PYRIDINIUM COMPOUNDS, METHOD OF MAKING AND USE THEREOF HENRY M. JACKSON FOUNDATION FOR THE ADVANCEMENT OF MILITARY MEDICINE, INC. (US) 2006-03-29 EP claimed
WO-2005002519-A2 AMPHIPHILIC PYRIDINIUM COMPOUNDS, METHOD OF MAKING AND USE THEREOF HENRY M.JACKSON FOUNDATION FOR THE ADVANCEMENT OF MILITARY MEDICINE, INC. (US) 2005-01-13 WO claimed
US-12486218-B2 Compounds advantageous in the treatment of central nervous system diseases and disorders AURIMMED PHARMA, INC. (US) 2025-12-02 US disclosed
US-12466805-B2 Pharmaceutical compounds ALMAC DISCOVERY LIMITED (GB) 2025-11-11 US disclosed
US-12168648-B2 Opioid receptor modulators EPIODYNE, INC. (US) 2024-12-17 US disclosed
CN-112867705-B Opioid receptor modulators and products and methods related thereto 埃皮欧黛公司 2024-08-20 CN disclosed
EP-3774722-B1 OPIOID RECEPTOR MODULATORS AND PRODUCTS AND METHODS RELATED THERETO EPIODYNE INC (US) 2024-07-24 EP disclosed
US-20240239739-A1 COMPOUNDS ADVANTAGEOUS IN THE TREATMENT OF CENTRAL NERVOUS SYSTEM DISEASES AND DISORDERS AURIMMED PHARMA, INC. 2024-07-18 US disclosed
US-20240239739-A1 COMPOUNDS ADVANTAGEOUS IN THE TREATMENT OF CENTRAL NERVOUS SYSTEM DISEASES AND DISORDERS AURIMMED PHARMA, INC. 2024-07-18 US disclosed
EP-0409435-B1 Heteroaryl piperazine antipsychotic agents PFIZER (US) 1994-10-26 EP disclosed
US-5350747-A Heteroaryl piperazine antipsychotic agents PFIZER INC (US) 1994-09-27 US disclosed
WO-1991000863-A1 HETEROARYL PIPERAZINE ANTIPSYCHOTIC AGENTS PFIZER INC. (US) 1991-01-24 WO disclosed
EP-0409435-A1 Heteroaryl piperazine antipsychotic agents PFIZER INC. (US) 1991-01-23 EP disclosed
US-4438033-A Steroidal chiral phosphines, methods for their preparation, catalytic systems containing them and catalytic processes in which they are used CONSIGLIO NAZIONALE DELLE RICERCHE (IT) 1984-03-20 US disclosed
EP-0081149-A1 New steroidal chiral phosphines, methods for their preparation, catalytic systems containing them and catalytic processes in which they are used CONSIGLIO NAZIONALE DELLE RICERCHE (IT) 1983-06-15 EP disclosed
US-4198519-A Anti-inflammatory compounds BEECHAM GROUP LIMITED (GB) 1980-04-15 US disclosed
US-4153718-A Anti-inflammatory compounds BEECHAM GROUP LIMITED (GB) 1979-05-08 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 (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-12168648-B2 Opioid receptor modulators OPRM1, OPRK1, OPRL1 FFAR1 235/4885GABBR2 343/4885GABBR1 397/4885
US-12486218-B2 Compounds advantageous in the treatment of central nervous system diseases and disorders SMN1; SMN2, HDAC6, CTSA FFAR1 543/4885GABBR2 132/4885GABBR1 130/4885
US-12466805-B2 Pharmaceutical compounds USP19, USP18, UBE2I FFAR1 4027/4885GABBR2 2603/4885GABBR1 3078/4885
US-20070105916-A1 Amphiphilic pyridinium compounds, method of making and use thereof CXCL8, IL18, CCR8 FFAR1 1062/4885GABBR2 3199/4885GABBR1 3603/4885
US-20240239739-A1 COMPOUNDS ADVANTAGEOUS IN THE TREATMENT OF CENTRAL NERVOUS SYSTEM DISEASES AND DISORDERS SMN1; SMN2, HDAC6, CTSA FFAR1 543/4885GABBR2 132/4885GABBR1 130/4885

“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.