Predicted protein targets (top 1)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 1/20 | 0.33 |
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 | |
|---|---|---|---|---|
| SCHEMBL18923972 | 0.87 | — | — | |
| SCHEMBL8505487 | 0.86 | — | — | |
| SCHEMBL6925490 | 0.80 | — | — | |
| SCHEMBL8505869 | 0.80 | — | — | |
| SCHEMBL516582 | 0.79 | TSHR (0.33) | TSHR | |
| SCHEMBL515547 | 0.76 | — | — | |
| SCHEMBL775732 | 0.73 | TSHR (0.35) | TSHR | |
| SCHEMBL25289015 | 0.73 | — | — | |
| SCHEMBL1935002 | 0.73 | — | — | |
| SCHEMBL647354 | 0.73 | — | — |
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 279 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2481760-B1 | INITIATOR SYSTEM FOR CATIONIC POLYMERIZATION AND POLYMERIZATION METHOD USING SAME | CHINA PETROLEUM & CHEM CORP (CN) | 2021-05-05 | — | — | EP | claimed |
| CN-110143886-A | The method of the preparation such as beta-aromatic alkamine drug of tulobuterol, Clorprenaline, isoproterenol and Sotalol | 北京化工大学 | 2019-08-20 | — | — | CN | claimed |
| US-20100222536-A1 | Method for Functionalizating Carbon Naontubes Utilizing Peroxides | WILLIAM MARSH RICE UNIVERSITY (US) | 2010-09-02 | — | — | US | claimed |
| US-20070098620-A1 | Method for functionalizing carbon nanotubes utilizing peroxides | WILLIAM MARSH RICE UNIVERSITY (US) | 2007-05-03 | — | — | US | claimed |
| US-20040223900-A1 | Method for functionalizing carbon nanotubes utilizing peroxides | WILLIAM MARSH RICE UNIVERSITY (US) | 2004-11-11 | — | — | US | claimed |
| US-3966727-A | Manufacture of phthalo-bis-guanamines | BASF AKTIENGESELLSCHAFT (DT) | 1976-06-29 | — | — | US | claimed |
| US-12221595-B2 | Decomposing/cleaning composition, method for cleaning adhesive polymer, and method for producing device wafer | RESONAC CORPORATION (JP) | 2025-02-11 | — | — | US | disclosed |
| US-12100809-B2 | Non-aqueous liquid electrolyte and non-aqueous liquid electrolyte secondary battery | MITSUBISHI CHEMICAL CORPORATION (JP) | 2024-09-24 | — | — | US | disclosed |
| CN-116162188-B | Isobutene polymerization initiation system composition, polymerization method and application | 浙江信汇新材料股份有限公司 | 2024-01-26 | — | — | CN | disclosed |
| CN-113302269-B | Decomposition cleaning composition, method for cleaning adhesive polymer, and method for manufacturing device wafer | 株式会社力森诺科 | 2023-08-01 | — | — | CN | disclosed |
| CN-116162188-A | Isobutene polymerization initiation system composition, polymerization method and application | 浙江信汇新材料股份有限公司 | 2023-05-26 | — | — | CN | disclosed |
| US-20230158005-A1 | Substituted Azole Dione Compounds with Antiviral Activity | STEMLINE THERAPEUTICS, INC. (US) | 2023-05-25 | — | — | US | disclosed |
| CN-115725010-A | Preparation method of polyisobutylene with medium and high molecular weights, initiation system and application thereof | 浙江信汇新材料股份有限公司 | 2023-03-03 | — | — | CN | disclosed |
| EP-0203722-A1 | Bicyclic pyrazolidinones | ELI LILLY AND COMPANY (US) | 1986-12-03 | — | — | EP | disclosed |
| EP-0202046-A1 | 7-Substituted bicyclic pyrazolidinones | ELI LILLY AND COMPANY (US) | 1986-11-20 | — | — | EP | disclosed |
| CN-86102877-A | The method for preparing bicyclic pyrazolidinones | — | 1986-10-29 | — | — | CN | disclosed |
| CN-86103619-A | The preparation method of the bicyclic pyrazolidinones that 7-replaces | — | 1986-10-29 | — | — | CN | disclosed |
| US-4413124-A | 2-Alkyl-5-alkylsulfonyl-4,6-dihalopyrimidines and the production thereof | CIBA-GEIGY CORPORATION (US) | 1983-11-01 | — | — | US | disclosed |
| US-4412074-A | 2-Alkyl-5-alkyl sulfony 1-4,6-dihalopyrimidines and the production thereof | CIBA-GEIGY CORPORATION (US) | 1983-10-25 | — | — | US | disclosed |
| US-3966727-A | Manufacture of phthalo-bis-guanamines | BASF AKTIENGESELLSCHAFT (DT) | 1976-06-29 | — | — | 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-20230158005-A1 | Substituted Azole Dione Compounds with Antiviral Activity | MAVS, DDX18, ZC3HAV1 | TSHR 4570/4885 |
“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.