Predicted protein targets (top 3)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LMNA | P02545 | 1/20 | 0.37 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.33 |
| ▸ | THRB | P10828 | 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 | |
|---|---|---|---|---|
| Ether SCHEMBL9793363 | 1.00 | LMNA (0.37) | LMNAALDH1A1THRB | |
| Ether SCHEMBL8431870 | 0.94 | ALDH1A1 (0.36) | LMNAALDH1A1 | |
| Ether SCHEMBL15135184 | 0.91 | MAPK1 (0.36) | LMNA | |
| Ether SCHEMBL5404357 | 0.91 | TSHR (0.36) | LMNAALDH1A1 | |
| Ether SCHEMBL1325841 | 0.91 | ALDH1A1 (0.41) | LMNAALDH1A1 | |
| Ether SCHEMBL11876258 | 0.88 | ALDH1A1 (0.46) | LMNAALDH1A1 | |
| Hexane SCHEMBL515233 | 0.88 | OPRM1 (0.42) | LMNATHRB | |
| SCHEMBL29239907 | 0.84 | ALDH1A1 (0.41) | LMNAALDH1A1THRB | |
| Ether SCHEMBL9122015 | 0.82 | TSHR (0.46) | THRB | |
| Ether SCHEMBL7738174 | 0.81 | LMNA (0.44) | LMNAALDH1A1THRB |
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 847 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-108602914-B | Method for producing highly reactive isobutene homo-or copolymers | 巴斯夫欧洲公司 | 2021-09-24 | — | — | CN | claimed |
| EP-3416992-B1 | PROCESS FOR PREPARING HIGH-REACTIVITY ISOBUTENE HOMO- OR COPOLYMERS | BASF SE (DE) | 2020-04-15 | — | — | EP | claimed |
| EP-3416992-A1 | PROCESS FOR PREPARING HIGH-REACTIVITY ISOBUTENE HOMO- OR COPOLYMERS | BASF SE (DE) | 2018-12-26 | — | — | EP | claimed |
| CN-108602914-A | Method for producing highly reactive isobutene homo-or copolymers | 巴斯夫欧洲公司 | 2018-09-28 | — | — | CN | claimed |
| WO-2017140603-A1 | PROCESS FOR PREPARING HIGH-REACTIVITY ISOBUTENE HOMO- OR COPOLYMERS | BASF SE (DE) | 2017-08-24 | — | — | WO | claimed |
| CN-103360291-B | With producing the method that high concentration TGA prepared by the O-alkyl-N-alkyl sulfide tail washings by carbamate | 青岛联拓化工有限公司 | 2016-12-07 | — | — | CN | claimed |
| CN-105859770-A | Method of synthesizing alkyl phosphate | 云南云天化以化磷业研究技术有限公司 | 2016-08-17 | — | — | CN | claimed |
| US-20030135041-A1 | Synthesis of ceftiofur intermediate | ORCHID CHEMICALS & PHARMACEUTICALS LIMITED, INDIA (IN) | 2003-07-17 | — | — | US | claimed |
| US-6023005-A | TOTALLY REGENERATING ONLY A PORTION OF THE TOTAL REACTION VOLUME OF CATALYST AND MIXING THE REGENERATED PORTION WITH THE UNREGENERATED TOTAL REACTION VOLUME OF CATALYST. | EXXON CHEMICALS PATENTS INC. (US) | 2000-02-08 | — | — | US | claimed |
| EP-0667337-B1 | Method for preparing fluoroanilines | CLARIANT GMBH (DE) | 1998-01-21 | — | — | EP | claimed |
| EP-0667337-A1 | Method for preparing fluoroanilines | HOECHST AKTIENGESELLSCHAFT (DE) | 1995-08-16 | — | — | EP | claimed |
| CN-113045476-B | Monosubstituted or disubstituted indole derivatives as dengue virus replication inhibitors | 杨森制药公司 | 2024-07-16 | — | — | CN | disclosed |
| US-20240182463-A1 | SUBSTITUTED POLYCYCLIC CARBAMOYL PYRIDONE DERIVATIVE PRODRUG | SHIONOGI & CO., LTD. (JP) | 2024-06-06 | — | — | US | disclosed |
| WO-2023232613-A1 | PROCESS FOR MANUFACTURING OF HIGHER FUNCTIONAL POLYISOBUTENES | BASF SE (DE) | 2023-12-07 | — | — | WO | disclosed |
| CN-113698514-B | Process for preparing highly reactive isobutylene homo-or copolymers | 巴斯夫欧洲公司 | 2023-11-10 | — | — | CN | disclosed |
| US-4035392-A | Prostanoic acid intermediate | CARLO ERBA S.P.A. (IT) | 1977-07-12 | — | — | US | disclosed |
| US-4021477-A | 14-Chloro prostadienoic acid compounds | CARLO-ERBA S.P.A. (IT) | 1977-05-03 | — | — | US | disclosed |
| US-3989724-A | Tetrahydropyran-2-ols | HOFFMANN-LA ROCHE INC. (US) | 1976-11-02 | — | — | US | disclosed |
| US-3944577-A | Novel pregnane-21-oic acid derivatives | SCHERING AKTIENGESELLSCHAFT (DT) | 1976-03-16 | — | — | US | disclosed |
| US-3935254-A | 5C-PROSTEN-13-YNOIC ACIDS | CARLO ERBA S.P.A. (IT) | 1976-01-27 | — | — | 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 (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-20030135041-A1 | Synthesis of ceftiofur intermediate | COASY, ACACA, BCAT1 | LMNA 3789/4885ALDH1A1 215/4885THRB 2228/4885 |
| US-20240182463-A1 | SUBSTITUTED POLYCYCLIC CARBAMOYL PYRIDONE DERIVATIVE PRODRUG | PREP, UNG, DPP4 | LMNA 1238/4885ALDH1A1 1564/4885THRB 3578/4885 |
“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.