Predicted protein targets (top 11)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 4/20 | 0.52 |
| ▸ | ABCC4 | O15439 | 1/20 | 0.44 |
| ▸ | MAPT | P10636 | 1/20 | 0.44 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.43 |
| ▸ | LMNA | P02545 | 2/20 | 0.43 |
| ▸ | TRPA1 | O75762 | 3/20 | 0.41 |
| ▸ | LPAR3 | Q9UBY5 | 2/20 | 0.38 |
| ▸ | LPAR2 | Q9HBW0 | 1/20 | 0.38 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.34 |
| ▸ | USP2 | O75604 | 1/20 | 0.34 |
| ▸ | HPGD | P15428 | 1/20 | 0.34 |
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 | |
|---|---|---|---|---|
| SCHEMBL724224 | 1.00 | TSHR (0.52) | TSHRABCC4MAPTALDH1A1LMNA | |
| SCHEMBL5575307 | 1.00 | TSHR (0.52) | TSHRABCC4MAPTALDH1A1LMNA | |
| SCHEMBL517698 | 1.00 | TSHR (0.52) | TSHRABCC4MAPTALDH1A1LMNA | |
| SCHEMBL9299210 | 1.00 | TSHR (0.52) | TSHRABCC4MAPTALDH1A1LMNA | |
| SCHEMBL5574427 | 1.00 | TSHR (0.52) | TSHRABCC4MAPTALDH1A1LMNA | |
| SCHEMBL25220704 | 1.00 | TSHR (0.52) | TSHRABCC4MAPTALDH1A1LMNA | |
| SCHEMBL5571446 | 1.00 | TSHR (0.52) | TSHRABCC4MAPTALDH1A1LMNA | |
| SCHEMBL5405862 | 1.00 | TSHR (0.52) | TSHRABCC4MAPTALDH1A1LMNA | |
| SCHEMBL8834879 | 1.00 | TSHR (0.52) | TSHRABCC4MAPTALDH1A1LMNA | |
| SCHEMBL346392 | 1.00 | — | — |
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 794 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122011773-A | Dynamic reworkable high-heat-conductivity low-dielectric composite material and preparation method and application thereof | 华东理工大学 | 2026-05-12 | — | — | CN | claimed |
| CN-118440018-A | Photo-curing cross-linking agent and preparation method and application thereof | 中国科学院兰州化学物理研究所 | 2024-08-06 | — | — | CN | claimed |
| US-20230399477-A1 | ANION EXCHANGE MEMBRANE AND METHODS OF MAKING AND USING THE SAME | U.S. DEPARTMENT OF ENERGY | 2023-12-14 | — | — | US | claimed |
| US-20230399425-A1 | SOLUTION PROCESS FOR PRODUCTION OF HALIDE- OR TERTIARY AMINE- FUNCTIONALIZED POLYOLEFINS | SABIC GLOBAL TECHNOLOGIES B.V. (NL) | 2023-12-14 | — | — | US | claimed |
| CN-117003688-A | Fluorescent monomer based on tetraphenyl ethylene and preparation method and application thereof | 中山大学 | 2023-11-07 | — | — | CN | claimed |
| EP-4247865-A1 | SOLUTION PROCESS FOR PRODUCTION OF HALIDE- OR TERTIARY AMINE- FUNCTIONALIZED POLYOLEFINS | SABIC Global Technologies B.V. (NL) | 2023-09-27 | — | — | EP | claimed |
| CN-116804143-A | Photo-curing hyperbranched moisture-proof sealant and preparation method thereof | 常州大学 | 2023-09-26 | — | — | CN | claimed |
| CN-116640262-B | Thickening agent for acidification and synthesis method thereof | 东营市宝泽能源科技有限公司 | 2023-09-19 | — | — | CN | claimed |
| CN-116640262-A | Thickening agent for acidification and synthesis method thereof | 东营市宝泽能源科技有限公司 | 2023-08-25 | — | — | CN | claimed |
| CN-116082648-B | Functionalized star-shaped solution polymerized styrene-butadiene rubber, preparation method thereof and application thereof in new energy automobile tires | 广东粤港澳大湾区黄埔材料研究院 | 2023-08-08 | — | — | CN | claimed |
| WO-2011139817-A2 | PHOTOCHEMICAL CROSS-LINKABLE POLYMERS, METHODS OF MARKING PHOTOCHEMICAL CROSS-LINKABLE POLYMERS, METHODS OF USING PHOTOCHEMICAL CROSS-LINKABLE POLYMERS, AND METHODS OF MAKING ARTICLES CONTAINING PHOTOCHEMICAL CROSS-LINKABLE POLYMERS | UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) | 2011-11-10 | — | — | WO | claimed |
| WO-2000015613-A1 | METHOD OF MAKING TERTIARY HINDERED AMINES | ARISTECH CHEMICAL CORPORATION (US) | 2000-03-23 | — | — | WO | claimed |
| EP-0848693-A4 | ISOMERIZATION OF BISPHENOLS | DOW CHEMICAL CO (US) | 1999-03-17 | — | — | EP | claimed |
| US-5856491-A | REACTING SECONDARY AMINE WITH TERMINALLY UNSATURATED ELECTROPHILIC COMPOUND IN PRESENCE OF N-METHYLPYRROLIDINONE SOLVENT | ARISTECH CHEMICAL CORP. (US) | 1999-01-05 | — | — | US | claimed |
| CN-1200105-A | Isomerization of bisphenols | DOW CHEMICAL CO (US) | 1998-11-25 | — | — | CN | claimed |
| EP-0848693-A1 | ISOMERIZATION OF BISPHENOLS | THE DOW CHEMICAL COMPANY (US) | 1998-06-24 | — | — | EP | claimed |
| WO-1997008122-A1 | ISOMERIZATION OF BISPHENOLS | THE DOW CHEMICAL COMPANY (US) | 1997-03-06 | — | — | WO | claimed |
| EP-0725771-A1 | PROCESS FOR MAKING POLYPHENOLS FROM KETONES OR ALDEHYDES AND PHENOLS | THE DOW CHEMICAL COMPANY (US) | 1996-08-14 | — | — | EP | claimed |
| WO-1996006819-A1 | PROCESS FOR MAKING POLYPHENOLS FROM KETONES OR ALDEHYDES AND PHENOLS | THE DOW CHEMICAL COMPANY (US) | 1996-03-07 | — | — | WO | claimed |
| US-5463140-A | Condensing aldehyde or ketone with phenol in presence of soluble or insoluble mercaptosulfonic acid compound to form geminal bisphenol moiety at each aldehyde or ketone moiety | THE DOW CHEMICAL COMPANY (US) | 1995-10-31 | — | — | US | claimed |