Predicted protein targets (top 15)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | DPP4 | P27487 | 2/20 | 0.50 |
| ▸ | SCN4A | P35499 | 2/20 | 0.50 |
| ▸ | F2 | P00734 | 1/20 | 0.50 |
| ▸ | HTR2A | P28223 | 1/20 | 0.46 |
| ▸ | TAAR1 | Q96RJ0 | 1/20 | 0.46 |
| ▸ | GRIN2D | O15399 | 1/20 | 0.45 |
| ▸ | GRIN3B | O60391 | 1/20 | 0.45 |
| ▸ | GRIN1 | Q05586 | 1/20 | 0.45 |
| ▸ | GRIN2A | Q12879 | 1/20 | 0.45 |
| ▸ | GRIN2B | Q13224 | 1/20 | 0.45 |
| ▸ | GRIN2C | Q14957 | 1/20 | 0.45 |
| ▸ | GRIN3A | Q8TCU5 | 1/20 | 0.45 |
| ▸ | TRPA1 | O75762 | 2/20 | 0.45 |
| ▸ | ADRA2A | P08913 | 1/20 | 0.44 |
| ▸ | ADRA2C | P18825 | 1/20 | 0.44 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL176645 | 1.00 | DPP4 (0.50) | DPP4SCN4AF2HTR2ATAAR1 | |
| SCHEMBL30559582 | 1.00 | DPP4 (0.50) | DPP4SCN4AF2HTR2ATAAR1 | |
| SCHEMBL101140 | 1.00 | DPP4 (0.50) | DPP4SCN4AF2HTR2ATAAR1 | |
| Hydrochloric Acid SCHEMBL20972918 | 0.97 | SCN4A (0.48) | DPP4SCN4AF2HTR2ATAAR1 | |
| Ammonia Solution, Strong SCHEMBL13737655 | 0.97 | SCN4A (0.48) | DPP4SCN4AF2HTR2ATAAR1 | |
| Hydrochloric Acid SCHEMBL19554902 | 0.97 | SCN4A (0.48) | DPP4SCN4AF2HTR2ATAAR1 | |
| Hydrochloric Acid SCHEMBL30450135 | 0.95 | GRIN2D (0.47) | DPP4SCN4AF2HTR2ATAAR1 | |
| Hydrochloric Acid SCHEMBL30450281 | 0.95 | GRIN2D (0.47) | DPP4SCN4AF2HTR2ATAAR1 | |
| Isopropyl Alcohol SCHEMBL4065314 | 0.91 | KDM4E (0.54) | TAAR1TRPA1ADRA2AADRA2C | |
| Phenol SCHEMBL28231638 | 0.91 | CA12 (0.48) | DPP4SCN4AF2GRIN2DGRIN3B |
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
Appears in 5782 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20260138972-A1 | PREPARATION METHOD AND CHIRAL SIEVING APPLICATION OF NOVEL 12-CROWN-4 COVALENT ORGANIC FRAMEWORKS | CHONGQING UNIV OF ARTS AND SCIENCES (CN) | 2026-05-21 | — | — | US | claimed |
| CN-119656869-A | Method for realizing diastereomeric crystallization mother liquor regeneration and reuse of amine chiral compound by utilizing unconventional electrodialysis | 湖南科技大学 | 2025-03-21 | — | — | CN | claimed |
| WO-2025019172-A1 | ANTIMICROBIAL EXTRACTANT FORMED FROM COPPER-CONTAINING SOURCE | CORNING INCORPORATED (US) | 2025-01-23 | — | — | WO | claimed |
| CN-119119087-A | Chiral binuclear copper complex with benzo [ c ] cinnoline skeleton and preparation method thereof | 中国科学院上海有机化学研究所 | 2024-12-13 | — | — | CN | claimed |
| CN-119110654-A | Method for constructing artificial vision system based on cluster heterojunction and application | 中国科学院化学研究所 | 2024-12-10 | — | — | CN | claimed |
| US-20240052394-A1 | BIOPRODUCTION OF ENANTIOPURE (R)- AND (S)-2-PHENYLGLYCINOL FROM STYRENE AND RENEWABLE FEEDSTOCKS VIA ARTIFICIAL ENZYME CASCADE | NATIONAL UNIVERSITY OF SINGAPORE (SG) | 2024-02-15 | — | — | US | claimed |
| CN-115626891-B | Synthesis method of nilaparib key intermediate | 四川轻化工大学 | 2024-01-26 | — | — | CN | claimed |
| CN-116829726-A | Biological production of enantiomerically pure (R) -and (S) -2-phenylglycinol from styrene and renewable raw materials by artificial enzyme cascade | 新加坡国立大学 | 2023-09-29 | — | — | CN | claimed |
| US-20230048657-A1 | PROCESS FOR THE PREPARATION OF (9S)-2-BROMO-9-(2,3,4-TRIFLUOROPHENYL)-6,7,8,9-TETRAHYDRO-5H-[1,2,4]TRIAZOLO[1,5-A]AZEPINE | HOFFMANN-LA ROCHE INC. (US) | 2023-02-16 | — | — | US | claimed |
| US-20230033510-A1 | Compounds and Methods for Treatment of Visceral Pain | ARENA PHARMACEUTICALS, INC. | 2023-02-02 | — | — | US | claimed |
| EP-0824531-A1 | METHOD FOR PREPARING AN OPTICALLY PURE BENZOFURAN CARBOXYLIC ACID AND USE THEREOF FOR PREPARING EFAROXAN | PIERRE FABRE MEDICAMENT (FR) | 1998-02-25 | — | — | EP | claimed |
| EP-0433897-B1 | Process for preparing an optically active cyclobutane nucleoside | SQUIBB & SONS INC (US) | 1997-10-01 | — | — | EP | claimed |
| WO-1997020842-A1 | NOVEL PURINE DERIVATIVES HAVING, IN PARTICULAR, ANTIPROLIFERATIVE PROPERTIES, AND BIOLOGICAL USES THEREOF | CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N.R.S.) (FR) | 1997-06-12 | — | — | WO | claimed |
| WO-1996035682-A1 | METHOD FOR PREPARING AN OPTICALLY PURE BENZOFURAN CARBOXYLIC ACID AND USE THEREOF FOR PREPARING EFAROXAN | PIERRE FABRE MEDICAMENT (FR) | 1996-11-14 | — | — | WO | claimed |
| EP-0485069-B1 | Process for producing optically active amines | SUMITOMO CHEMICAL CO (JP) | 1995-02-15 | — | — | EP | claimed |
| US-5200561-A | PROCESS FOR PRODUCING OPTICALLY ACTIVE AMINES | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1993-04-06 | — | — | US | claimed |
| EP-0485069-A1 | Process for producing optically active amines | SUMITOMO CHEMICAL COMPANY, LIMITED (JP) | 1992-05-13 | — | — | EP | claimed |
| EP-0484843-A1 | An optically active cyclobutyl pyrimidine | E.R. SQUIBB & SONS, INC. (US) | 1992-05-13 | — | — | EP | claimed |
| US-5064961-A | PROCESS FOR PREPARING AN OPTICALLY ACTIVE CYCLOBUTANE NUCLEOSIDE | E. R. SQUIBB & SONS, INC. (US) | 1991-11-12 | — | — | US | claimed |
| EP-0433897-A2 | Process for preparing an optically active cyclobutane nucleoside | E.R. SQUIBB & SONS, INC. (US) | 1991-06-26 | — | — | EP | claimed |