Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA2 | P00918 | 2/20 | 0.59 |
| ▸ | TAAR1 | Q96RJ0 | 2/20 | 0.56 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.55 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.50 |
| ▸ | HTR3E | A5X5Y0 | 1/20 | 0.50 |
| ▸ | HTR3B | O95264 | 1/20 | 0.50 |
| ▸ | HTR3A | P46098 | 1/20 | 0.50 |
| ▸ | HTR3D | Q70Z44 | 1/20 | 0.50 |
| ▸ | HTR3C | Q8WXA8 | 1/20 | 0.50 |
| ▸ | IGF1R | P08069 | 1/20 | 0.48 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.48 |
| ▸ | MAOB | P27338 | 1/20 | 0.48 |
| ▸ | IDO1 | P14902 | 3/20 | 0.48 |
| ▸ | AOC3 | Q16853 | 1/20 | 0.46 |
| ▸ | CA12 | O43570 | 1/20 | 0.46 |
| ▸ | CA1 | P00915 | 1/20 | 0.46 |
| ▸ | CA4 | P22748 | 1/20 | 0.46 |
| ▸ | CA6 | P23280 | 1/20 | 0.46 |
| ▸ | CA5A | P35218 | 1/20 | 0.46 |
| ▸ | CA7 | P43166 | 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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL28309115 | 0.95 | CA2 (0.54) | CA2TAAR1TDP1L3MBTL1HTR3E | |
| SCHEMBL11000396 | 0.93 | MAOB (0.59) | CA2TAAR1TDP1L3MBTL1HTR3E | |
| SCHEMBL10789850 | 0.93 | CA2 (0.52) | CA2TAAR1TDP1L3MBTL1HTR3E | |
| Alcohol SCHEMBL5328957 | 0.93 | CA2 (0.52) | CA2TAAR1TDP1L3MBTL1HTR3E | |
| SCHEMBL11127235 | 0.89 | CA2 (0.48) | CA2TAAR1TDP1L3MBTL1HTR3E | |
| SCHEMBL1396008 | 0.89 | CA2 (0.48) | CA2TAAR1TDP1L3MBTL1HTR3E | |
| Phenylethyl Alcohol SCHEMBL21802430 | 0.87 | TDP1 (0.76) | CA2TAAR1TDP1L3MBTL1TSHR | |
| SCHEMBL2773286 | 0.87 | LTA4H (0.49) | CA2TAAR1IGF1RALOX15MAOB | |
| SCHEMBL40656 | 0.85 | CA2 (0.77) | CA2TAAR1TDP1L3MBTL1HTR3A | |
| SCHEMBL8822598 | 0.85 | SRD5A2 (0.55) | CA2L3MBTL1ALOX15TSHRALDH1A1 |
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 1253 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119591964-A | Breathable film containing polystyrene and preparation method thereof | 衢州瑞兴新材料有限责任公司 | 2025-03-11 | — | — | CN | claimed |
| CN-119491240-A | Method for preparing benzyl carboxylic acid compound by taking carbon dioxide as raw material | 哈尔滨工业大学（深圳） | 2025-02-21 | — | — | CN | claimed |
| CN-114315658-B | Preparation method of sulfonate alkane ester | 宁波南大光电材料有限公司 | 2023-06-30 | — | — | CN | claimed |
| CN-115784911-A | Synthetic method of 1- [2- (4-chlorophenyl) -ethylamino ] -2-propanol | 山东省药学科学院 | 2023-03-14 | — | — | CN | claimed |
| CN-111393264-B | Synthetic method of p-hydroxyphenylethanol | 杭州盛弗泰新材料科技有限公司 | 2022-07-15 | — | — | CN | claimed |
| CN-114315658-A | Preparation method of sulfonate alkane ester | 宁波南大光电材料有限公司 | 2022-04-12 | — | — | CN | claimed |
| CN-113333018-A | Preparation method and application of supported catalyst for preparing halogenated styrene | 中触媒新材料股份有限公司 | 2021-09-03 | — | — | CN | claimed |
| CN-110776422-B | Method for preparing ester by irradiating halogenated aromatic hydrocarbon, alcohol and carbonyl source by ultraviolet light | 福州大学 | 2021-07-27 | — | — | CN | claimed |
| CN-107814687-B | Synthetic method of p-chlorophenylethanol | 湖北朗昕生化药业有限公司 | 2021-02-26 | — | — | CN | claimed |
| CN-112358406-A | Preparation method of lorcaserin intermediate | 山东省药学科学院 | 2021-02-12 | — | — | CN | claimed |
| EP-0449975-B1 | NON-TIN-BASED, LOW TOXICITY ANTI-FOULING AGENTS | BATTELLE MEMORIAL INSTITUTE (US) | 1997-04-23 | — | — | EP | claimed |
| US-5441743-A | In thermoplastic or thermosetting binder | BATTELLE MEMORIAL INSTITUTE (US) | 1995-08-15 | — | — | US | claimed |
| EP-0251369-B1 | PHARMACEUTICAL COMPOSITIONS ENDOWED WITH SEQUESTERING ACTIVITY FOR THE BILIARY ACIDS, CONTAINING COLESTYRAMIN AS THEIR ACTIVE PRINCIPLE, AND PROCESS FOR PREPARING THEM | FARKEMO S.r.l. (IT) | 1992-05-20 | — | — | EP | claimed |
| WO-1990006975-A1 | NON-TIN-BASED, LOW TOXICITY ANTI-FOULING AGENTS | BATTELLE MEMORIAL INSTITUTE (US) | 1990-06-28 | — | — | WO | claimed |
| US-4902501-A | ANTICHOLESTEROL AGENTS | PRODOTTI FORMENTI S.R.L. (IT) | 1990-02-20 | — | — | US | claimed |
| EP-0122151-B1 | PRODUCTION OF PRIMARY OR SECONDARY ALCOHOL DERIVATIVES OF PHOSPHOLIPIDS BY THE ENZYMATIC TECHNIQUE | MEITO SANGYO KABUSHIKI KAISHA (JP) | 1989-02-15 | — | — | EP | claimed |
| US-4783402-A | Production of primary or secondary alcohol derivatives of phospholipids by the enzymatic technique | MEITO SANGYO KABUSHIKI KAISHA (JP) | 1988-11-08 | — | — | US | claimed |
| EP-0251369-A2 | Pharmaceutical compositions endowed with sequestering activity for the biliary acids, containing colestyramin as their active principle, and process for preparing them | FARKEMO S.r.l. (IT) | 1988-01-07 | — | — | EP | claimed |
| EP-0122151-A2 | Production of primary or secondary alcohol derivatives of phospholipids by the enzymatic technique | MEITO SANGYO KABUSHIKI KAISHA (JP) | 1984-10-17 | — | — | EP | claimed |
| US-4338437-A | Cephalosporin antibiotics | MERCK & CO., INC. (US) | 1982-07-06 | — | — | US | claimed |