SCHEMBL2292396

SCHEMBL2292396

CCCC(CC(=O)O)c1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ GABBR2 O75899 4/20 0.61
▸ GABBR1 Q9UBS5 4/20 0.61
▸ MAPT P10636 1/20 0.54
▸ FNTA P49354 6/20 0.47
▸ FNTB P49356 6/20 0.47
▸ MEN1 O00255 2/20 0.46
▸ KMT2A Q03164 2/20 0.46
▸ KDM4E B2RXH2 1/20 0.46
▸ RECQL P46063 1/20 0.46
▸ POLB P06746 1/20 0.44
▸ LMNA P02545 2/20 0.43
▸ CYP2C9 P11712 2/20 0.43
▸ CYP2C19 P33261 2/20 0.43
▸ CYP3A4 P08684 1/20 0.43
▸ ADORA3 P0DMS8 1/20 0.43
▸ NFKB1 P19838 1/20 0.43
▸ DRD3 P35462 1/20 0.43
▸ BLM P54132 1/20 0.43
▸ CYP1A2 P05177 1/20 0.43
▸ CYP2D6 P10635 1/20 0.43

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
SCHEMBL28346014 1.00 GABBR2 (0.61) GABBR2GABBR1MAPTFNTAFNTB
SCHEMBL2289954 0.89 GABBR2 (0.58) GABBR2GABBR1MAPTFNTAFNTB
SCHEMBL28642990 0.89 GABBR2 (0.47) GABBR2GABBR1MAPTPOLBLMNA
SCHEMBL7663044 0.87 GABBR2 (0.56) GABBR2GABBR1MAPTPOLB
SCHEMBL4403980 0.86 GABBR2 (0.54) GABBR2GABBR1MAPT
SCHEMBL3242852 0.86 GABBR2 (0.54) GABBR2GABBR1MAPT
SCHEMBL27688433 0.86 GABBR2 (0.54) GABBR2GABBR1MAPT
SCHEMBL184884 0.85 ALDH1A1 (0.54) GABBR2GABBR1MAPTPOLBLMNA
SCHEMBL15614666 0.85 ALDH1A1 (0.54) GABBR2GABBR1MAPTPOLBLMNA
SCHEMBL3879432 0.85 ESR1 (0.59) GABBR2GABBR1MAPTFNTAFNTB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240173227-A1 A FRAGRANCE MIXTURE CONTAINING ISOCITRONELLOL SYMRISE AG (DE) 2024-05-30 — — US claimed
WO-2009131692-A1 SUBSTRATES FOR DELIVERY OF PHYSIOLOGICALLY ACTIVE AGENTS THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ALABAMA (US) 2009-10-29 — — WO claimed
EP-0244167-B1 IMPROVED PROCESS FOR PREPARING POLY (ARYL ETHERS) AND POLY (ARYL ETHER KETONES) AMOCO CORPORATION (US) 1990-04-04 — — EP claimed
CN-119875109-A Low-odor hydrolysis-resistant mercaptan curing agent and preparation method and application thereof 益丰新材料股份有限公司 2025-04-25 — — CN disclosed
CN-110590552-B Synthetic method of acetate compound 青岛农业大学 2022-02-08 — — CN disclosed
CN-110590552-A Synthetic method of acetate compound 青岛农业大学 2019-12-20 — — CN disclosed
US-9371296-B2 Bicyclic 1,3,4-oxadiazole derivatives as sphingosine-1-phosphate receptors' modulators ALLERGAN, INC. (US) 2016-06-21 — — US disclosed
US-20160137616-A1 BICYCLIC 1,3,4-OXADIAZOLE DERIVATIVES AS SPHINGOSINE-1-PHOSPHATE RECEPTORS' MODULATORS ALLERGAN, INC. 2016-05-19 — — US disclosed
WO-2015134467-A1 METHODS AND COMPOSITIONS FOR DIRECT RADIOACTIVE LABELING OF BIO-ACTIVE MOLECULES AND BUILDING BLOCKS THE TRUSTEES OF PRINCETON UNIVERSITY (US) 2015-09-11 — — WO disclosed
WO-2015108577-A1 DIPHENYL UREA DERIVATIVES AS FORMYL PEPTIDE RECEPTOR MODULATORS ALLERGAN, INC. (US) 2015-07-23 — — WO disclosed
US-8304223-B2 Isoforms of pig liver esterase ENZYMICALS AG (DE) 2012-11-06 — — US disclosed
US-20070286842-A1 Organic Compounds and Their Uses NOVARTIS AG (CH) 2007-12-13 — — US disclosed
US-7229817-B2 Recombinant porcine liver esterases, their use and a method for the production thereof DEGUSSA AG (DE) 2007-06-12 — — US disclosed
CN-1806206-A Photosensitive resin composition AZ ELECTRONIC MATERIALS JAPAN (JP) 2006-07-19 — — CN disclosed
EP-0738269-B1 PIPERIDINE DERIVATIVES WITH PAF ANTAGONIST ACTIVITY URIACH & CIA SA J (ES) 2000-04-26 — — EP disclosed
US-5705504-A PLATELET ACTIVATING FACTOR J. URIACH & CIA, S.A. (ES) 1998-01-06 — — US disclosed
US-4537871-A Carbonylation catalyst THE HALCON SD GROUP, INC. (US) 1985-08-27 — — US disclosed
US-4483803-A Preparation of carboxylic acid anhydrides THE HALCON SD GROUP, INC. (US) 1984-11-20 — — US disclosed
US-4335058-A Preparation of carboxylic acid anhydrides HALCON RESEARCH AND DEVELOPMENT CORP. (US) 1982-06-15 — — US disclosed
US-4273873-A BONDING SYNTHETIC FIBRINOLYTIC COMPOUND OR ENZYME UNITIKA LTD. (JP) 1981-06-16 — — 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-20070286842-A1 Organic Compounds and Their Uses OAT, OTC, AOX1 GABBR2 993/4885GABBR1 746/4885MAPT 1444/4885
US-20160137616-A1 BICYCLIC 1,3,4-OXADIAZOLE DERIVATIVES AS SPHINGOSINE-1-PHOSPHATE RECEPTORS' MODULATORS S1PR3, S1PR1, S1PR4 GABBR2 537/4885GABBR1 495/4885MAPT 3562/4885
US-20240173227-A1 A FRAGRANCE MIXTURE CONTAINING ISOCITRONELLOL IPO5, OR51E2, FDFT1 GABBR2 2842/4885GABBR1 2773/4885MAPT 3448/4885

“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.

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