Predicted protein targets (top 12)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TAAR1 | Q96RJ0 | 3/20 | 0.61 |
| ▸ | SLC6A2 | P23975 | 1/20 | 0.61 |
| ▸ | PCNA | P12004 | 1/20 | 0.56 |
| ▸ | LIG1 | P18858 | 1/20 | 0.56 |
| ▸ | SLC7A5 | Q01650 | 1/20 | 0.55 |
| ▸ | OPRK1 | P41145 | 1/20 | 0.55 |
| ▸ | ESR1 | P03372 | 4/20 | 0.48 |
| ▸ | ESR2 | Q92731 | 4/20 | 0.48 |
| ▸ | SLC6A4 | P31645 | 1/20 | 0.48 |
| ▸ | ABAT | P80404 | 1/20 | 0.48 |
| ▸ | CA2 | P00918 | 1/20 | 0.46 |
| ▸ | EPHX1 | P07099 | 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 | |
|---|---|---|---|---|
| SCHEMBL2992550 | 1.00 | TAAR1 (0.61) | TAAR1SLC6A2PCNALIG1SLC7A5 | |
| SCHEMBL80783 | 1.00 | TAAR1 (0.61) | TAAR1SLC6A2PCNALIG1SLC7A5 | |
| Hydrochloric Acid SCHEMBL1168215 | 0.98 | TAAR1 (0.59) | TAAR1SLC6A2PCNALIG1SLC7A5 | |
| SCHEMBL1255741 | 0.98 | TAAR1 (0.59) | TAAR1SLC6A2PCNALIG1SLC7A5 | |
| Hydrochloric Acid SCHEMBL1168213 | 0.98 | TAAR1 (0.59) | TAAR1SLC6A2PCNALIG1SLC7A5 | |
| Iodide SCHEMBL9393026 | 0.98 | TAAR1 (0.59) | TAAR1SLC6A2PCNALIG1SLC7A5 | |
| Biphenyl SCHEMBL7890864 | 0.88 | EPHX1 (0.52) | TAAR1SLC6A2PCNALIG1SLC7A5 | |
| SCHEMBL2617270 | 0.85 | TAAR1 (0.61) | TAAR1SLC6A2PCNALIG1SLC7A5 | |
| SCHEMBL8503457 | 0.84 | OPRK1 (0.62) | TAAR1SLC6A2SLC7A5OPRK1ESR1 | |
| SCHEMBL22153161 | 0.84 | OPRK1 (0.62) | TAAR1SLC6A2SLC7A5OPRK1ESR1 |
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 654 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-12534571-B2 | Amphiphilic block copolymer, preparation method thereof and nanomicelle drug-loading system | SHANGHAI BEST-LINK BIOSCIENCE, LLC (CN) | 2026-01-27 | — | — | US | claimed |
| US-20250223406-A1 | EFFICIENT METHOD FOR BRANCHED AMINO AND CARBOXYLATED NATURAL OILS WITH CHOLINE CHLORIDE | Ohio Soybean Council | 2025-07-10 | — | — | US | claimed |
| EP-3753966-B1 | AMPHIPHILIC BLOCK COPOLYMER, PREPARATION METHOD THEREOF AND NANOMICELLE DRUG-LOADING SYSTEM | SHANGHAI BEST LINK BIOSCIENCE LLC (CN) | 2022-05-25 | — | — | EP | claimed |
| US-20220098367-A1 | AMPHIPHILIC BLOCK COPOLYMER, PREPARATION METHOD THEREOF AND NANOMICELLE DRUG-LOADING SYSTEM | SHANGHAI BEST-LINK BIOSCIENCE, LLC (CN) | 2022-03-31 | — | — | US | claimed |
| US-11225551-B2 | Amphiphilic block copolymer, preparation method thereof and nanomicelle drug-loading system | SELECTION BIOSCIENCE LLC (CN) | 2022-01-18 | — | — | US | claimed |
| US-20210047467-A1 | AMPHIPHILIC BLOCK COPOLYMER, PREPARATION METHOD THEREOF AND NANOMICELLE DRUG-LOADING SYSTEM | SHANGHAI BEST-LINK BIOSCIENCE, LLC (CN) | 2021-02-18 | — | — | US | claimed |
| EP-3753966-A1 | AMPHIPHILIC BLOCK COPOLYMER, PREPARATION METHOD THEREOF AND NANOMICELLE DRUG-LOADING SYSTEM | Selection Bioscience LLC (CN) | 2020-12-23 | — | — | EP | claimed |
| US-10604742-B2 | Adsorptive membranes for trapping viruses | WISCONSIN ALUMNI RESEARCH FOUNDATION (US) | 2020-03-31 | — | — | US | claimed |
| EP-2043767-B1 | ADSORPTIVE MEMBRANES FOR TRAPPING VIRUSES | WISCONSIN ALUMNI RES FOUND (US) | 2020-03-25 | — | — | EP | claimed |
| US-20190249150-A1 | ADSORPTIVE MEMBRANES FOR TRAPPING VIRUSES | WISCONSIN ALUMNI RESEARCH FOUNDATION (US) | 2019-08-15 | — | — | US | claimed |
| US-20070142648-A1 | Hydrogenation method for producing optically active alcohols or carboxylic acids | BASF AKTIENGESELLSCHAFT (DE) | 2007-06-21 | — | — | US | claimed |
| US-20070135648-A1 | Decarboxylation/hydroxylation without the release of carbon monoxide by using a mixed-oxide, supported, hydrogenation catalyst based on rhenium oxide with an absense of ruthenium and, in some cases, platinum and palladium; autoclaving malic acid to obtain hydroxybutyrolactone and 1,2,4-butanetriol | BASF AKTIENGESELLSCHAFT (DE) | 2007-06-14 | — | — | US | claimed |
| US-20070123578-A1 | Hexahydro-cycloheptapyrazole cannabinoid modulators | JANSSEN PHARMACEUTICA N.V. (BE) | 2007-05-31 | — | — | US | claimed |
| EP-1716091-A1 | METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOLS OR CARBOXYLIC ACIDS | BASF AKTIENGESELLSCHAFT (DE) | 2006-11-02 | — | — | EP | claimed |
| EP-1716090-A1 | HYDROGENATION METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOLS OR CARBOXYLIC ACIDS | BASF AKTIENGESELLSCHAFT (DE) | 2006-11-02 | — | — | EP | claimed |
| WO-2005077870-A1 | HYDROGENATION METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOLS OR CARBOXYLIC ACIDS | BASF AKTIENGESELLSCHAFT (DE) | 2005-08-25 | — | — | WO | claimed |
| WO-2005077871-A1 | METHOD FOR PRODUCING OPTICALLY ACTIVE ALCOHOLS OR CARBOXYLIC ACIDS | BASF AKTIENGESELLSCHAFT (DE) | 2005-08-25 | — | — | WO | claimed |
| EP-0941212-B1 | ENANTIOSELECTIVE CATALYTIC REDUCTION OF KETONES | DEGUSSA (DE) | 2001-03-21 | — | — | EP | claimed |
| US-4397779-A | RADIOIMMUNOASSAY OF THEOPHYLLINE AND DERIVATIVES; IODINATION | BAXTER TRAVENOL LABORATORIES, INC. (US) | 1983-08-09 | — | — | US | claimed |
| US-4244939-A | RADIOIMMUNOASSAY | BAXTER TRAVENOL LABORATORIES, INC. (US) | 1981-01-13 | — | — | US | claimed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (7 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-20070142648-A1 | Hydrogenation method for producing optically active alcohols or carboxylic acids | HAO2, PPARG, ADH1A | TAAR1 90/4885SLC6A2 3454/4885PCNA 813/4885 |
| US-20210047467-A1 | AMPHIPHILIC BLOCK COPOLYMER, PREPARATION METHOD THEREOF AND NANOMICELLE DRUG-LOADING SYSTEM | TNF, IAPP, ABCE1 | TAAR1 1264/4885SLC6A2 1357/4885PCNA 1137/4885 |
| US-20070135648-A1 | Decarboxylation/hydroxylation without the release of carbon monoxide by using a mixed-oxide, supported, hydrogenation catalyst based on rhenium oxide with an absense of ruthenium and, in some cases, platinum and palladium; autoclaving malic acid to obtain hydroxybutyrolactone and 1,2,4-butanetriol | ALDH7A1, HAO2, OGDH | TAAR1 2917/4885SLC6A2 4671/4885PCNA 82/4885 |
| US-12534571-B2 | Amphiphilic block copolymer, preparation method thereof and nanomicelle drug-loading system | NR0B1, ABCE1, LDLR | TAAR1 467/4885SLC6A2 1770/4885PCNA 1945/4885 |
| US-20220098367-A1 | AMPHIPHILIC BLOCK COPOLYMER, PREPARATION METHOD THEREOF AND NANOMICELLE DRUG-LOADING SYSTEM | TNF, IAPP, ABCE1 | TAAR1 1264/4885SLC6A2 1357/4885PCNA 1137/4885 |
| US-11225551-B2 | Amphiphilic block copolymer, preparation method thereof and nanomicelle drug-loading system | TNF, IAPP, ABCE1 | TAAR1 1264/4885SLC6A2 1357/4885PCNA 1137/4885 |
| US-20070123578-A1 | Hexahydro-cycloheptapyrazole cannabinoid modulators | CNR2, CNR1, FAAH | TAAR1 271/4885SLC6A2 758/4885PCNA 4525/4885 |
“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.