Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LMNA | P02545 | 1/20 | 0.68 |
| ▸ | MAOA | P21397 | 1/20 | 0.61 |
| ▸ | PTGS1 | P23219 | 1/20 | 0.61 |
| ▸ | MAPT | P10636 | 2/20 | 0.59 |
| ▸ | POLB | P06746 | 1/20 | 0.59 |
| ▸ | HPGD | P15428 | 1/20 | 0.59 |
| ▸ | XBP1 | P17861 | 1/20 | 0.59 |
| ▸ | MEN1 | O00255 | 1/20 | 0.54 |
| ▸ | ALOX12 | P18054 | 1/20 | 0.54 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.54 |
| ▸ | SCN4A | P35499 | 2/20 | 0.54 |
| ▸ | MTNR1A | P48039 | 3/20 | 0.53 |
| ▸ | MTNR1B | P49286 | 3/20 | 0.53 |
| ▸ | CYP2D6 | P10635 | 3/20 | 0.53 |
| ▸ | ADRB2 | P07550 | 1/20 | 0.53 |
| ▸ | ADRB1 | P08588 | 1/20 | 0.53 |
| ▸ | ADRB3 | P13945 | 1/20 | 0.53 |
| ▸ | KCNA3 | P22001 | 1/20 | 0.50 |
| ▸ | NPC1 | O15118 | 1/20 | 0.47 |
| ▸ | MTOR | P42345 | 1/20 | 0.47 |
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 | |
|---|---|---|---|---|
| SCHEMBL9178337 | 1.00 | LMNA (0.68) | LMNAMAOAPTGS1MAPTPOLB | |
| Ammonia Solution, Strong SCHEMBL28834669 | 0.98 | LMNA (0.65) | LMNAMAOAPTGS1MAPTPOLB | |
| Ethylene Glycol SCHEMBL6560927 | 0.91 | LMNA (0.64) | LMNAMAOAPTGS1MAPTPOLB | |
| Ether SCHEMBL7051516 | 0.89 | LMNA (0.57) | LMNAMAOAPTGS1MAPTPOLB | |
| SCHEMBL10583987 | 0.88 | LMNA (0.55) | LMNAMAOAPTGS1MAPTPOLB | |
| Propylene Glycol SCHEMBL6558972 | 0.88 | LMNA (0.71) | LMNAMAOAPTGS1MAPTPOLB | |
| SCHEMBL123415 | 0.87 | MAPT (0.55) | LMNAMAOAPTGS1MAPTPOLB | |
| SCHEMBL14672093 | 0.87 | MAPT (0.57) | LMNAMAOAPTGS1MAPTPOLB | |
| SCHEMBL20385241 | 0.86 | LMNA (0.63) | LMNAMAOAPTGS1MAPTPOLB | |
| SCHEMBL13385106 | 0.85 | LMNA (0.68) | LMNAMAOAPTGS1SCN4AMTNR1A |
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 867 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119656881-B | Reverse osmosis membrane with coralloid structure and preparation method and application thereof | 苏州实验室 | 2025-05-23 | — | — | CN | claimed |
| CN-119841982-A | Catalyst for olefin polymerization and olefin polymerization method | 中国石油化工股份有限公司 | 2025-04-18 | — | — | CN | claimed |
| CN-119841979-A | Catalyst for olefin polymerization and olefin polymerization method | 中国石油化工股份有限公司 | 2025-04-18 | — | — | CN | claimed |
| CN-119841980-A | Catalyst for olefin polymerization and olefin polymerization method | 中国石油化工股份有限公司 | 2025-04-18 | — | — | CN | claimed |
| CN-119656881-A | Reverse osmosis membrane with coralloid structure and preparation method and application thereof | 苏州实验室 | 2025-03-21 | — | — | CN | claimed |
| CN-119613599-A | Hydrophilic-hydrophobic heterogeneous pleated polymer microsphere and preparation method and application thereof | 南方医科大学 | 2025-03-14 | — | — | CN | claimed |
| CN-111018688-B | Method for preparing 3-hydroxypropionaldehyde and method for preparing 1,3-propylene glycol | 上海华谊能源化工有限公司 | 2022-10-11 | — | — | CN | claimed |
| CN-110002971-B | P-alkoxy phenyl fullerene and preparation method and application thereof | 西南科技大学 | 2022-04-01 | — | — | CN | claimed |
| CN-109574951-A | A kind of preparation method of Febuxostat | 安徽省庆云医药股份有限公司 | 2019-04-05 | — | — | CN | claimed |
| CN-108250087-A | A kind of synthetic method of 4- isobutoxies benzylamine | 常州大学 | 2018-07-06 | — | — | CN | claimed |
| US-20080244963-A1 | Lead-Free Aviation Fuel | TOTAL FRANCE (FR) | 2008-10-09 | — | — | US | claimed |
| EP-1971668-A1 | LEAD-FREE AVIATION FUEL | Total France (FR) | 2008-09-24 | — | — | EP | claimed |
| WO-2007074226-A1 | LEAD-FREE AVIATION FUEL | TOTAL FRANCE (FR) | 2007-07-05 | — | — | WO | claimed |
| US-20040059165-A1 | Synthesis of aliphatic 1,3-diols utilizing reduced ligand concentration and water extraction | POWELL JOSEPH BROUN (US) | 2004-03-25 | — | — | US | claimed |
| US-6660892-B2 | Catalytic hydroformylation, hydrogenation of oxirane | SHELL OIL COMPANY | 2003-12-09 | — | — | US | claimed |
| US-20030166977-A1 | Synthesis of aliphatic 1, 3-diols utilizing reduced ligand concentration and water extraction | SHELL OIL COMPANY | 2003-09-04 | — | — | US | claimed |
| US-6384273-B1 | REACTING A CARBOCYCLIC AROMATIC DERIVATIVE WITH AN ALKALINE METAL IN THE PRESENCE OF A HALOGEN COMPOUND | RHODIA CHIMIE (FR) | 2002-05-07 | — | — | US | claimed |
| EP-1077911-A1 | METHOD FOR ORTHOMETALATION OF A CARBOCYCLIC AROMATIC DERIVATIVE BEARING AT LEAST AN ELECTRON DONOR GROUP | RHODIA CHIMIE (FR) | 2001-02-28 | — | — | EP | claimed |
| WO-1999059941-A1 | METHOD FOR ORTHOMETALATION OF A CARBOCYCLIC AROMATIC DERIVATIVE BEARING AT LEAST AN ELECTRON DONOR GROUP | RHODIA CHIMIE (FR) | 1999-11-25 | — | — | WO | claimed |
| US-4473713-A | Hydrolysis of aryl-aliphatic ethers | RHONE-POULENC SPECIALITES CHIMIQUES (FR) | 1984-09-25 | — | — | US | claimed |
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-20030166977-A1 | Synthesis of aliphatic 1, 3-diols utilizing reduced ligand concentration and water extraction | OXGR1, OXER1, ADH1A | LMNA 4335/4885MAOA 772/4885PTGS1 218/4885 |
| US-20040059165-A1 | Synthesis of aliphatic 1,3-diols utilizing reduced ligand concentration and water extraction | OXGR1, OXER1, ADH1A | LMNA 4335/4885MAOA 772/4885PTGS1 218/4885 |
“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.