Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MAPT | P10636 | 4/20 | 0.52 |
| ▸ | ALDH1A1 | P00352 | 5/20 | 0.48 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.48 |
| ▸ | IDO1 | P14902 | 1/20 | 0.46 |
| ▸ | HTT | P42858 | 1/20 | 0.46 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.46 |
| ▸ | TSHR | P16473 | 3/20 | 0.44 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.44 |
| ▸ | ALOX15 | P16050 | 2/20 | 0.44 |
| ▸ | ALOX12 | P18054 | 2/20 | 0.44 |
| ▸ | HSD17B10 | Q99714 | 2/20 | 0.44 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.44 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.44 |
| ▸ | ESR1 | P03372 | 1/20 | 0.43 |
| ▸ | ACP1 | P24666 | 1/20 | 0.43 |
| ▸ | DNM1 | Q05193 | 1/20 | 0.42 |
| ▸ | ADRB2 | P07550 | 1/20 | 0.41 |
| ▸ | ADRB1 | P08588 | 1/20 | 0.41 |
| ▸ | ADRB3 | P13945 | 1/20 | 0.41 |
| ▸ | L3MBTL1 | Q9Y468 | 2/20 | 0.41 |
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 | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL17710400 | 0.98 | MAPT (0.50) | MAPTALDH1A1TDP1IDO1HTT | |
| Ammonia Solution, Strong SCHEMBL6702357 | 0.98 | MAPT (0.50) | MAPTALDH1A1TDP1IDO1HTT | |
| Iodide SCHEMBL29028129 | 0.98 | MAPT (0.50) | MAPTALDH1A1TDP1IDO1HTT | |
| SCHEMBL809618 | 0.91 | ALDH1A1 (0.56) | MAPTALDH1A1TDP1IDO1HTT | |
| SCHEMBL146034 | 0.87 | IDO1 (0.45) | MAPTALDH1A1TDP1IDO1SMN1; SMN2 | |
| SCHEMBL7163224 | 0.87 | FNTA (0.58) | MAPTALDH1A1IDO1SMN1; SMN2ACP1 | |
| SCHEMBL7386242 | 0.82 | MGLL (0.46) | ACP1ADRB2ADRB1ADRB3 | |
| SCHEMBL10359189 | 0.81 | MAPT (0.48) | MAPTALDH1A1TDP1HTTSMN1; SMN2 | |
| SCHEMBL11848304 | 0.81 | MAPT (0.48) | MAPTALDH1A1TDP1HTTSMN1; SMN2 | |
| SCHEMBL16197831 | 0.81 | MAPT (0.58) | MAPTALDH1A1TDP1HTTSMN1; SMN2 |
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 636 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-115322132-B | N-substituted indole compound and synthesis method thereof | 陕西科技大学 | 2024-05-28 | — | — | CN | claimed |
| CN-115322132-A | N-substituted indole compound and synthetic method thereof | 陕西科技大学 | 2022-11-11 | — | — | CN | claimed |
| CN-110590844-A | Preparation method for synthesizing tenofovir alafenamide by two-step method | 江西农业大学 | 2019-12-20 | — | — | CN | claimed |
| CN-110551153-A | Preparation method for synthesizing tenofovir alafenamide by three-step method | UNIV JIANGXI AGRICULTURAL | 2019-12-10 | — | — | CN | claimed |
| CN-108727695-A | A kind of automobile cover plate composite material | 宁波帅特龙集团有限公司 | 2018-11-02 | — | — | CN | claimed |
| CN-107445846-A | The technique of isobutyl-aniline between a kind of synthesis | 江苏广域化学有限公司 | 2017-12-08 | — | — | CN | claimed |
| US-9527042-B2 | Separation membrane for water treatment and production method for same | TORAY INDUSTRIES, INC. (JP) | 2016-12-27 | — | — | US | claimed |
| EP-2313481-A2 | PRODUCTION PROCESS OF UNLEADED HIGH OCTANE NUMBER GASOLINE, AND SO OBTAINED GASOLINES | CHIMEC S.P.A. (IT) | 2011-04-27 | — | — | EP | claimed |
| WO-2010001341-A2 | PRODUCTION PROCESS OF UNLEADED HIGH OCTANE NUMBER GASOLINE, AND SO OBTAINED GASOLINES | CHIMEC S.P.A. (IT) | 2010-01-07 | — | — | WO | claimed |
| US-20080244963-A1 | Lead-Free Aviation Fuel | TOTAL FRANCE (FR) | 2008-10-09 | — | — | US | claimed |
| EP-1971668-A1 | LEAD-FREE AVIATION FUEL | Total France (FR) | 2008-09-24 | — | — | EP | claimed |
| WO-2007074226-A1 | LEAD-FREE AVIATION FUEL | TOTAL FRANCE (FR) | 2007-07-05 | — | — | WO | claimed |
| EP-0979264-B1 | The use of a lubricant in a two-stroke mtorcycle | CASTROL LTD (GB) | 2005-01-05 | — | — | EP | claimed |
| CN-1405631-A | Self-sensitizing type super-branched polyimide photo-sensitive material and its preparing method | UNIV SHANGHAI JIAOTONG (CN) | 2003-03-26 | — | — | CN | claimed |
| US-20020049316-A1 | Protease inhibitors | HALBERT STACIE MARIE (US) | 2002-04-25 | — | — | US | claimed |
| US-6281173-B1 | MINERAL OIL FROM A NAPHTHENIC CRUDE SOURCE HAVING A VISCOSITY OF 100 DEGREES C. OF LESS THAN 4 CST AND A POUR POINT BELOW -30 DEGREES C., TO IMPROVE DETERGENCY, REDUCE BLOCKING OF EXHAUSTS AND CATALYSTS, AND PRODUCE LOW LEVELS OF SMOKE | CASTROL LIMITED (GB) | 2001-08-28 | — | — | US | claimed |
| CN-1261276-A | Protease inhibitors | SMITHKLINE BEECHAM CORP (US) | 2000-07-26 | — | — | CN | claimed |
| US-5026912-A | High selectivity to ortho-alkylated amines | AIR PRODUCTS AND CHEMICALS, INC. (US) | 1991-06-25 | — | — | US | claimed |
| EP-4678620-A1 | FAST-CURING ANCHOR SYSTEM WITH OPTIMIZED HARDENER DISTRIBUTION | Hilti Aktiengesellschaft (LI) | 2026-01-14 | — | — | EP | disclosed |
| US-3992405-A | ESPECIALLY FOR DYEING POLYACRYLIC FIBERS | BAYER AKTIENGESELLSCHAFT (DT) | 1976-11-16 | — | — | 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 (1 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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20020049316-A1 | Protease inhibitors | CTSK, CTSZ, CTSG | MAPT 796/4885ALDH1A1 2831/4885TDP1 1308/4885 |
“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.