Predicted protein targets (top 4)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CYP1A2 | P05177 | 1/20 | 0.33 |
| ▸ | CA1 | P00915 | 1/20 | 0.31 |
| ▸ | CA2 | P00918 | 1/20 | 0.31 |
| ▸ | CA4 | P22748 | 1/20 | 0.31 |
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 | |
|---|---|---|---|---|
| SCHEMBL301104 | 0.97 | CYP1A2 (0.37) | CYP1A2CA1CA2CA4 | |
| SCHEMBL7535948 | 0.97 | CYP1A2 (0.37) | CYP1A2CA1CA2CA4 | |
| Ammonia Solution, Strong SCHEMBL4079351 | 0.95 | CYP1A2 (0.36) | CYP1A2 | |
| SCHEMBL27824835 | 0.89 | CYP1A2 (0.32) | CYP1A2 | |
| SCHEMBL28901892 | 0.89 | CYP1A2 (0.32) | CYP1A2 | |
| SCHEMBL1324543 | 0.84 | CYP1A2 (0.41) | CYP1A2 | |
| SCHEMBL1324612 | 0.84 | CYP1A2 (0.41) | CYP1A2 | |
| SCHEMBL9017493 | 0.82 | CYP1A2 (0.44) | CYP1A2 | |
| SCHEMBL1324548 | 0.82 | CYP1A2 (0.39) | CYP1A2 | |
| SCHEMBL1323174 | 0.82 | CYP1A2 (0.39) | CYP1A2 |
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 49 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-111518145-A | Cyanide-bridged metal organic compound with intramolecular magnetic transformation, and preparation method and application thereof | 荆楚理工学院 | 2020-08-11 | — | — | CN | claimed |
| US-7067654-B2 | Preparation of polyisocyanates containing uretdione groups | BAYER MATERIALSCIENCE AG (DE) | 2006-06-27 | — | — | US | claimed |
| US-20040110915-A1 | for production of polyurethanes via catalytic polymerization with trimethylphosphine; improved storage stability | BAYER AKTIENGESELLSCHAFT (DE) | 2004-06-10 | — | — | US | claimed |
| US-20040106789-A1 | Preparation of polyisocyanates containing uretdione groups | COVESTRO DEUTSCHLAND AG (DE) | 2004-06-03 | — | — | US | claimed |
| US-12492281-B2 | Polyisocyanurate materials as electrical potting compounds | COVESTRO DEUTSCHLAND AG (DE) | 2025-12-09 | — | — | US | disclosed |
| CN-113631545-B | Polyisocyanurate materials as electrical potting compounds | 科思创德国股份有限公司 | 2025-01-07 | — | — | CN | disclosed |
| CN-111518145-B | Cyano-bridged metal organic compound with intramolecular magnetic transformation and preparation method and application thereof | 荆楚理工学院 | 2023-06-20 | — | — | CN | disclosed |
| CN-108884010-B | Process for preparing unsaturated carboxylic acid salts | 巴斯夫欧洲公司 | 2022-11-08 | — | — | CN | disclosed |
| EP-3794049-B1 | METHOD FOR PRODUCING A POLYISOCYANATE POLYMER AND A POLYISOCYANURATE PLASTIC | COVESTRO INTELLECTUAL PROPERTY GMBH & CO KG (DE) | 2022-06-08 | — | — | EP | disclosed |
| US-11319402-B2 | Method for producing a polyisocyanate polymer and a polyisocyanurate plastic | COVESTRO INTELLECTUAL PROPERTY GMBH & CO. KG (DE) | 2022-05-03 | — | — | US | disclosed |
| US-20220127407-A1 | POLYISOCYANURATE MATERIALS AS ELECTRICAL POTTING COMPOUNDS | COVESTRO DEUTSCHLAND AG (DE) | 2022-04-28 | — | — | US | disclosed |
| CN-106458823-B | Process for preparing unsaturated carboxylic acid salts | 巴斯夫欧洲公司 | 2022-04-19 | — | — | CN | disclosed |
| US-20060173152-A1 | Uretdione formation in solution | BAYER MATERIALSCIENCE AG | 2006-08-03 | — | — | US | disclosed |
| EP-1683818-A2 | Uretdione formation in solution | Bayer MaterialScience AG (DE) | 2006-07-26 | — | — | EP | disclosed |
| US-7067654-B2 | Preparation of polyisocyanates containing uretdione groups | BAYER MATERIALSCIENCE AG (DE) | 2006-06-27 | — | — | US | disclosed |
| US-20040110915-A1 | for production of polyurethanes via catalytic polymerization with trimethylphosphine; improved storage stability | BAYER AKTIENGESELLSCHAFT (DE) | 2004-06-10 | — | — | US | disclosed |
| EP-1426393-A2 | Low monomer urethdione-groups containing polyisocyanates | Bayer MaterialScience AG (DE) | 2004-06-09 | — | — | EP | disclosed |
| US-20040106789-A1 | Preparation of polyisocyanates containing uretdione groups | COVESTRO DEUTSCHLAND AG (DE) | 2004-06-03 | — | — | US | disclosed |
| EP-1422223-A1 | Preparation of polyisocyanates containing uretdione groups with cycloalkylphosphines as catalysts | Bayer MaterialScience AG (DE) | 2004-05-26 | — | — | EP | disclosed |
| US-4595701-A | Reacting carbon monoxide and hydrogen in liquid phase in the presence of a rhodium and trialkylphosphine catalyst | AGENCY OF INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) | 1986-06-17 | — | — | 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-20040106789-A1 | Preparation of polyisocyanates containing uretdione groups | UROD, PUF60, UTS2R | CYP1A2 905/4885CA1 3661/4885CA2 3625/4885 |
“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.