Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TDP1 | Q9NUW8 | 4/20 | 0.41 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.41 |
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.40 |
| ▸ | CA1 | P00915 | 3/20 | 0.38 |
| ▸ | CA2 | P00918 | 3/20 | 0.38 |
| ▸ | CA4 | P22748 | 2/20 | 0.37 |
| ▸ | CA7 | P43166 | 2/20 | 0.37 |
| ▸ | CA14 | Q9ULX7 | 2/20 | 0.37 |
| ▸ | ORAI1 | Q96D31 | 2/20 | 0.37 |
| ▸ | ORAI2 | Q96SN7 | 2/20 | 0.37 |
| ▸ | ORAI3 | Q9BRQ5 | 2/20 | 0.37 |
| ▸ | TRPV6 | Q9H1D0 | 2/20 | 0.37 |
| ▸ | CA6 | P23280 | 1/20 | 0.37 |
| ▸ | CA5A | P35218 | 1/20 | 0.37 |
| ▸ | ENPP2 | Q13822 | 1/20 | 0.37 |
| ▸ | CA5B | Q9Y2D0 | 1/20 | 0.37 |
| ▸ | PCSK9 | Q8NBP7 | 1/20 | 0.37 |
| ▸ | TSHR | P16473 | 4/20 | 0.35 |
| ▸ | CA9 | Q16790 | 2/20 | 0.35 |
| ▸ | ALOX12 | P18054 | 2/20 | 0.35 |
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 | |
|---|---|---|---|---|
| Phenol SCHEMBL4184679 | 0.96 | TDP1 (0.44) | TDP1CYP3A4ALDH1A1CA1CA2 | |
| Phenol SCHEMBL150379 | 0.92 | TDP1 (0.41) | TDP1CYP3A4ALDH1A1CA1CA2 | |
| Phenol SCHEMBL12477517 | 0.92 | TDP1 (0.41) | TDP1CYP3A4ALDH1A1CA1CA2 | |
| Phenol SCHEMBL17060450 | 0.92 | TDP1 (0.41) | TDP1CYP3A4ALDH1A1CA1CA2 | |
| Phenol SCHEMBL17709449 | 0.92 | — | — | |
| Phenol SCHEMBL3806092 | 0.92 | — | — | |
| Phenol SCHEMBL9187012 | 0.92 | TDP1 (0.41) | TDP1CYP3A4ALDH1A1CA1CA2 | |
| Phenol SCHEMBL9442373 | 0.92 | TDP1 (0.41) | TDP1CYP3A4ALDH1A1CA1CA2 | |
| Phenol SCHEMBL11214345 | 0.92 | TDP1 (0.41) | TDP1CYP3A4ALDH1A1CA1CA2 | |
| Phenol SCHEMBL264361 | 0.92 | TDP1 (0.41) | TDP1CYP3A4ALDH1A1CA1CA2 |
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 65 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4600734-A1 | PATTERN FORMING METHOD AND LAMINATE | Shin-Etsu Chemical Co., Ltd. (JP) | 2025-08-13 | — | — | EP | disclosed |
| US-20250246429-A1 | Pattern Forming Method And Laminate | SHIN-ETSU CHEMICAL CO., LTD. (JP) | 2025-07-31 | — | — | US | disclosed |
| CN-111856882-B | Composition for forming silicon-containing resist underlayer film and pattern forming method | 信越化学工业株式会社 | 2024-11-29 | — | — | CN | disclosed |
| CN-110021744-B | Preparation method of nano niobium dioxide/carbon lithium ion battery cathode material | 中国科学院宁波材料技术与工程研究所 | 2022-08-12 | — | — | CN | disclosed |
| CN-111856882-A | Composition for forming silicon-containing resist underlayer film and pattern forming method | 信越化学工业株式会社 | 2020-10-30 | — | — | CN | disclosed |
| EP-2278643-B1 | CONDUCTIVE LITHIUM STORAGE ELECTRODE | MASSACHUSETTS INSTITUTE OF TECH MIT (US) | 2018-03-28 | — | — | EP | disclosed |
| US-9745194-B2 | Method of producing cathode active material for lithium secondary battery | SHOWA DENKO K.K. (JP) | 2017-08-29 | — | — | US | disclosed |
| US-9624356-B2 | Ultraviolet absorber, composition for forming a resist under layer film, and patterning process | SHIN-ETSU CHEMIAL CO., LTD (JP) | 2017-04-18 | — | — | US | disclosed |
| EP-1456895-B1 | CONDUCTIVE LITHIUM STORAGE ELECTRODE | MASSACHUSETTS INST TECHNOLOGY (US) | 2017-03-29 | — | — | EP | disclosed |
| US-9577249-B2 | Cathode material for lithium secondary battery, and method of producing said cathode material | SHOWA DENKO K.K. (JP) | 2017-02-21 | — | — | US | disclosed |
| EP-0328101-A2 | Process for producing alkylenamines | Tosoh Corporation (JP) | 1989-08-16 | — | — | EP | disclosed |
| EP-0256516-A2 | Process for preparation of alkyleneamines | Tosoh Corporation (JP) | 1988-02-24 | — | — | EP | disclosed |
| EP-0101877-B1 | PROCESS FOR THE PREPARATION OF N-ALLYL-O-ALKYL-THIONCARBAMATES | AMERICAN CYANAMID COMPANY (US) | 1986-11-26 | — | — | EP | disclosed |
| US-4590323-A | Conversion of paraffins to aromatics over zeolites modified with oxides of group IIIA, IVA and VA elements | MOBIL OIL CORPORATION (US) | 1986-05-20 | — | — | US | disclosed |
| EP-0051346-B1 | SHAPE SELECTIVE REACTIONS UTILIZING ZEOLITES MODIFIED WITH GROUP V A METALS | MOBIL OIL CORPORATION (US) | 1984-11-28 | — | — | EP | disclosed |
| US-4456560-A | A TRANSITION METAL COMPOUND AS CATALYST FOR REACTING AN ALCOHOL AND AN ALLYL ISOTHIOCYANATE | AMERICAN CYANAMID COMPANY (US) | 1984-06-26 | — | — | US | disclosed |
| EP-0101877-A1 | Process for the preparation of N-allyl-o-alkyl-thioncarbamates | AMERICAN CYANAMID COMPANY (US) | 1984-03-07 | — | — | EP | disclosed |
| US-4371457-A | ALKYLATION CATALYSTS | MOBIL OIL CORPORATION (US) | 1983-02-01 | — | — | US | disclosed |
| EP-0051346-A1 | Shape selective reactions utilizing zeolites modified with group V A metals | MOBIL OIL CORPORATION (US) | 1982-05-12 | — | — | EP | disclosed |
| US-4302621-A | ALKYLATION AND DISPROPORTIONATION OF ALKYLAROMATIC COMPOUNDS; CATALYST SELECTIVITY | MOBIL OIL CORPORATION (US) | 1981-11-24 | — | — | US | disclosed |