Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | PTPN1 | P18031 | 3/20 | 0.42 |
| ▸ | TSHR | P16473 | 2/20 | 0.41 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.41 |
| ▸ | CA1 | P00915 | 1/20 | 0.39 |
| ▸ | CA2 | P00918 | 1/20 | 0.39 |
| ▸ | CA5A | P35218 | 1/20 | 0.39 |
| ▸ | CA9 | Q16790 | 1/20 | 0.39 |
| ▸ | CES1 | P23141 | 2/20 | 0.37 |
| ▸ | ALDH1A1 | P00352 | 3/20 | 0.36 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.36 |
| ▸ | GPR3 | P46089 | 1/20 | 0.34 |
| ▸ | HSD11B1 | P28845 | 1/20 | 0.34 |
| ▸ | SRC | P12931 | 1/20 | 0.33 |
| ▸ | HTR6 | P50406 | 1/20 | 0.33 |
| ▸ | POLB | P06746 | 1/20 | 0.32 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.32 |
| ▸ | FAAH | O00519 | 1/20 | 0.32 |
| ▸ | PRSS1 | P07477 | 1/20 | 0.32 |
| ▸ | PRSS2 | P07478 | 1/20 | 0.32 |
| ▸ | ELANE | P08246 | 1/20 | 0.32 |
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 | |
|---|---|---|---|---|
| Trifluoromethanesulfonic Acid SCHEMBL29587491 | 1.00 | PTPN1 (0.42) | PTPN1TSHRSMN1; SMN2CA1CA2 | |
| Trifluoromethanesulfonic Acid SCHEMBL31473545 | 0.88 | PTPN1 (0.53) | PTPN1CA1CA2CA9 | |
| Trifluoromethanesulfonic Acid SCHEMBL562439 | 0.86 | IDO1 (0.48) | PTPN1TSHRSMN1; SMN2CES1ALDH1A1 | |
| Benzenethiol SCHEMBL11884916 | 0.83 | TSHR (0.46) | TSHRSMN1; SMN2CA1CA2CA5A | |
| Biphenyl SCHEMBL27775707 | 0.83 | MMP3 (0.47) | PTPN1 | |
| Trifluoromethanesulfonic Acid SCHEMBL17907399 | 0.83 | CA1 (0.44) | PTPN1TSHRSMN1; SMN2CA1CA2 | |
| Trifluoromethanesulfonic Acid SCHEMBL17835417 | 0.83 | MMP13 (0.41) | PTPN1TSHRSMN1; SMN2CA1CA2 | |
| Benzenethiol SCHEMBL11884719 | 0.83 | TSHR (0.50) | TSHRSMN1; SMN2CA1CA2CA5A | |
| Biphenyl SCHEMBL1993781 | 0.82 | PTPN1 (0.44) | PTPN1SMN1; SMN2CA1CA2CA5A | |
| Biphenyl SCHEMBL1050411 | 0.81 | PTPN1 (0.58) | PTPN1TSHRSMN1; SMN2CA1CA2 |
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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20250354031-A1 | Transparent Omniphobic Coatings | UNIV KINGSTON (CA) | 2025-11-20 | — | — | US | disclosed |
| US-20240369924-A1 | RESIST COMPOSITION AND RESIST FILM FORMING METHOD USING SAME | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 2024-11-07 | — | — | US | disclosed |
| CN-115368494-B | Monomer copolymer containing hexafluoroisopropanol, preparation method thereof, chemical amplification type photoresist and application thereof | 瑞红(苏州)电子化学品股份有限公司 | 2024-03-29 | — | — | CN | disclosed |
| CN-111234236-B | Siloxane polymer containing isocyanuric acid and polyether skeleton, photosensitive resin composition, and pattern formation method | 信越化学工业株式会社 | 2023-03-24 | — | — | CN | disclosed |
| CN-108388082-B | Photosensitive resin composition, photosensitive dry film, photosensitive resin coating and pattern forming method | 信越化学工业株式会社（JP） | 2023-01-13 | — | — | CN | disclosed |
| CN-115368494-A | Hexafluoroisopropanol-containing monomer copolymer, preparation method thereof, chemical amplification type photoresist and application | 瑞红(苏州)电子化学品股份有限公司 | 2022-11-22 | — | — | CN | disclosed |
| EP-2384457-B1 | COATING COMPOSITIONS | MERCK PATENT GMBH (DE) | 2022-07-06 | — | — | EP | disclosed |
| US-11118082-B2 | Composition, insulating material, and method for preparing an insulating material | INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) | 2021-09-14 | — | — | US | disclosed |
| US-10927135-B2 | Metal-free direct arylation of dialkyl phosphonates for the synthesis of mixed alkyl aryl phosphonates | THE BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION ON BEHALF OF THE UNIVERSITY OF NEVADA, LAS VEGAS (US) | 2021-02-23 | — | — | US | disclosed |
| US-20200255461-A1 | METAL-FREE DIRECT ARYLATION OF DIALKYL PHOSPHONATES FOR THE SYNTHESIS OF MIXED ALKYL ARYL PHOSPHONATES | THE BOARD OF REGENTS OF THE NEVADA SYSTEM OF HIGHER EDUCATION ON BEHALF OF THE UNIVERSITY OF NEVADA, LAS VEGAS | 2020-08-13 | — | — | US | disclosed |
| US-6136783-A | Antifungal compositions | MERCK & CO., INC. (US) | 2000-10-24 | — | — | US | disclosed |
| US-6132644-A | Energy sensitive electrically conductive admixtures | INTERNATIONAL BUSINESS MACHINES CORPORATION (US) | 2000-10-17 | — | — | US | disclosed |
| US-5952300-A | CYCLIC PEPTIDE FUNGICIDE FOR INTRAVENOUS ADMINISTRATION | MERCK & CO., INC. (US) | 1999-09-14 | — | — | US | disclosed |
| US-5936062-A | Process for preparing certain aza cyclohexapeptides | MERCK & CO., INC. (US) | 1999-08-10 | — | — | US | disclosed |
| EP-0912603-A1 | A PROCESS FOR PREPARING CERTAIN AZA CYCLOHEXAPEPTIDES | Merck & Co., Inc. (US) | 1999-05-06 | — | — | EP | disclosed |
| WO-1997047645-A1 | A PROCESS FOR PREPARING CERTAIN AZA CYCLOHEXAPEPTIDES | MERCK & CO., INC. (US) | 1997-12-18 | — | — | WO | disclosed |
| EP-0808330-A1 | A PROCESS FOR PREPARING CERTAIN AZA CYCLOHEXAPEPTIDES | Merck & Co., Inc. (US) | 1997-11-26 | — | — | EP | disclosed |
| US-5552521-A | REDUCTION OF PRIMARY AMIDE, STEREOSELECTIVE AMINATION | MERCK & CO., INC. (US) | 1996-09-03 | — | — | US | disclosed |
| WO-1996024613-A1 | A PROCESS FOR PREPARING CERTAIN AZA CYCLOHEXAPEPTIDES | MERCK & CO., INC. (US) | 1996-08-15 | — | — | WO | disclosed |
| EP-0377175-A2 | Pattern forming composition and process for forming pattern using the same | HITACHI, LTD. (JP) | 1990-07-11 | — | — | EP | 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 (2 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-20200255461-A1 | METAL-FREE DIRECT ARYLATION OF DIALKYL PHOSPHONATES FOR THE SYNTHESIS OF MIXED ALKYL ARYL PHOSPHONATES | SLC35B2, PPIP5K2, PPA1 | PTPN1 184/4885TSHR 733/4885SMN1; SMN2 4720/4885 |
| US-10927135-B2 | Metal-free direct arylation of dialkyl phosphonates for the synthesis of mixed alkyl aryl phosphonates | SLC35B2, PPIP5K2, PPA1 | PTPN1 184/4885TSHR 733/4885SMN1; SMN2 4720/4885 |
“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.