Predicted protein targets (top 14)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LMNA | P02545 | 2/20 | 0.52 |
| ▸ | MIF | P14174 | 1/20 | 0.42 |
| ▸ | TAAR1 | Q96RJ0 | 4/20 | 0.41 |
| ▸ | HTR2A | P28223 | 4/20 | 0.41 |
| ▸ | HRH1 | P35367 | 3/20 | 0.41 |
| ▸ | HKDC1 | Q2TB90 | 1/20 | 0.41 |
| ▸ | TRPA1 | O75762 | 1/20 | 0.41 |
| ▸ | AOC3 | Q16853 | 1/20 | 0.39 |
| ▸ | NOS3 | P29474 | 1/20 | 0.39 |
| ▸ | NOS2 | P35228 | 1/20 | 0.39 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.39 |
| ▸ | POLB | P06746 | 1/20 | 0.38 |
| ▸ | MEN1 | O00255 | 1/20 | 0.38 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.38 |
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 | |
|---|---|---|---|---|
| SCHEMBL3477567 | 0.80 | AOC3 (0.46) | LMNATAAR1HTR2AHRH1AOC3 | |
| SCHEMBL29308038 | 0.80 | LMNA (0.43) | LMNAMIFTAAR1HTR2AHRH1 | |
| SCHEMBL10935767 | 0.79 | TAAR1 (0.40) | LMNATAAR1HTR2AHRH1TDP1 | |
| SCHEMBL31190174 | 0.78 | HRH1 (0.46) | LMNATAAR1HTR2AHRH1 | |
| SCHEMBL169508 | 0.78 | LMNA (0.56) | LMNAMIFTAAR1HTR2AHRH1 | |
| SCHEMBL8741675 | 0.77 | CHRNA7 (0.41) | LMNAHTR2ATDP1MEN1KMT2A | |
| SCHEMBL5034682 | 0.77 | POLB (0.45) | LMNAHTR2AHRH1AOC3POLB | |
| SCHEMBL2376253 | 0.76 | TAAR1 (0.42) | LMNATAAR1HTR2AHRH1 | |
| Ammonia Solution, Strong SCHEMBL1640901 | 0.76 | LMNA (0.54) | LMNAMIFTAAR1HTR2AHRH1 | |
| SCHEMBL5167170 | 0.75 | AOC3 (0.38) | LMNAAOC3TDP1MEN1KMT2A |
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 69 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116406213-A | Chemical method for inhibiting ion diffusion in perovskite battery | 华东理工大学 | 2023-07-07 | — | — | CN | claimed |
| CN-111954848-B | Photosensitive resin composition, cured product, insulating material, resin material for solder resist, and resist member | DIC株式会社 | 2024-05-03 | — | — | CN | disclosed |
| CN-114394923-B | Preparation method of N-acyl-2-alkyl indoline compound | 浙江工业大学 | 2024-02-06 | — | — | CN | disclosed |
| US-20230367214-A1 | CHEMICALLY AMPLIFIED POSITIVE RESIST COMPOSITION AND RESIST PATTERN FORMING PROCESS | SHIN-ETSU CHEMICAL CO., LTD. (JP) | 2023-11-16 | — | — | US | disclosed |
| WO-2023220439-A1 | COMPOSITIONS USEFUL FOR MODULATING SPLICING | SKYHAWK THERAPEUTICS, INC. (US) | 2023-11-16 | — | — | WO | disclosed |
| CN-117042473-A | Perovskite solar cell and preparation method and application thereof | 深圳现象光伏科技有限公司 | 2023-11-10 | — | — | CN | disclosed |
| CN-116396137-A | Thermodynamically unstable substituted cyclohexane compound and synthesis method thereof | 武汉大学 | 2023-07-07 | — | — | CN | disclosed |
| US-20230194986-A1 | CHEMICALLY AMPLIFIED POSITIVE RESIST COMPOSITION AND RESIST PATTERN FORMING PROCESS | SHIN-ETSU CHEMICAL CO., LTD. (JP) | 2023-06-22 | — | — | US | disclosed |
| CN-116209334-A | Method for preparing red, green and blue color perovskite pixel array by ink-jet printing and application thereof | 华南理工大学 | 2023-06-02 | — | — | CN | disclosed |
| US-11407772-B2 | Optically-active cyclopentenone derivatives | TOHOKU UNIVERSITY (JP) | 2022-08-09 | — | — | US | disclosed |
| US-6462248-B1 | THROUGH CONVERSION, ISOMERIZATION AND/OR ADSORPTIVE SEPARATION OF AROMATIC COMPOUNDS | TORAY INDUSTRIES, INC. (JP) | 2002-10-08 | — | — | US | disclosed |
| WO-2001087849-A2 | MODULATORS OF TNF- ALPHA SIGNALING | GENZYME CORPORATION (US) | 2001-11-22 | — | — | WO | disclosed |
| EP-0985649-A2 | Method for producing an aromatic compound having an alkyl group with at least three carbon atoms | TORAY INDUSTRIES, INC. (JP) | 2000-03-15 | — | — | EP | disclosed |
| EP-0848693-A4 | ISOMERIZATION OF BISPHENOLS | DOW CHEMICAL CO (US) | 1999-03-17 | — | — | EP | disclosed |
| EP-0848693-A1 | ISOMERIZATION OF BISPHENOLS | THE DOW CHEMICAL COMPANY (US) | 1998-06-24 | — | — | EP | disclosed |
| WO-1997008122-A1 | ISOMERIZATION OF BISPHENOLS | THE DOW CHEMICAL COMPANY (US) | 1997-03-06 | — | — | WO | disclosed |
| EP-0682662-A1 | BICYCLIC CARBOXYLIC ACID LEUKOTRIENE B 4? ANTAGONISTS | F. HOFFMANN-LA ROCHE AG (CH) | 1995-11-22 | — | — | EP | disclosed |
| WO-1995015956-A1 | BICYCLIC CARBOXYLIC ACID LEUKOTRIENE B4 ANTAGONISTS | F. HOFFMANN-LA ROCHE AG (CH) | 1995-06-15 | — | — | WO | disclosed |
| EP-0534511-A1 | HIV protease inhibitors useful for the treatment of aids | MERCK & CO. INC. (US) | 1993-03-31 | — | — | EP | disclosed |
| US-4087426-A | Oxybisberberine and a process for its production | RESEARCH CORPORATION (US) | 1978-05-02 | — | — | 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-11407772-B2 | Optically-active cyclopentenone derivatives | PTGIS, PTGES, PTGES2 | LMNA 2200/4885MIF 2413/4885TAAR1 4061/4885 |
“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.