Predicted protein targets (top 16)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CYP1A2 | P05177 | 3/20 | 0.63 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.59 |
| ▸ | BACE1 | P56817 | 2/20 | 0.59 |
| ▸ | LMNA | P02545 | 1/20 | 0.59 |
| ▸ | POLB | P06746 | 1/20 | 0.59 |
| ▸ | CASP6 | P55212 | 1/20 | 0.59 |
| ▸ | CYP2A6 | P11509 | 1/20 | 0.43 |
| ▸ | KDM1A | O60341 | 1/20 | 0.42 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.42 |
| ▸ | RAB9A | P51151 | 2/20 | 0.41 |
| ▸ | NPC1 | O15118 | 1/20 | 0.41 |
| ▸ | GAA | P10253 | 1/20 | 0.41 |
| ▸ | CCR1 | P32246 | 1/20 | 0.41 |
| ▸ | CCR5 | P51681 | 1/20 | 0.41 |
| ▸ | PTPN1 | P18031 | 1/20 | 0.41 |
| ▸ | PSMB5 | P28074 | 1/20 | 0.41 |
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 | |
|---|---|---|---|---|
| Iodomethane SCHEMBL28083725 | 0.96 | CYP1A2 (0.59) | CYP1A2KDM4EBACE1LMNAPOLB | |
| SCHEMBL2222111 | 0.84 | CYP1A2 (0.61) | CYP1A2KDM4EBACE1LMNAPOLB | |
| SCHEMBL30390874 | 0.84 | CYP1A2 (0.61) | CYP1A2KDM4EBACE1LMNAPOLB | |
| SCHEMBL14894660 | 0.78 | BACE1 (0.53) | CYP1A2KDM4EBACE1LMNAPOLB | |
| SCHEMBL29444268 | 0.77 | CYP1A2 (1.00) | CYP1A2KDM4EBACE1LMNAPOLB | |
| SCHEMBL161703 | 0.77 | CYP1A2 (1.00) | CYP1A2KDM4EBACE1LMNAPOLB | |
| SCHEMBL7265492 | 0.77 | BACE1 (0.63) | CYP1A2KDM4EBACE1POLBCYP2A6 | |
| SCHEMBL1914302 | 0.77 | BACE1 (0.63) | CYP1A2KDM4EBACE1CYP2A6ALDH1A1 | |
| SCHEMBL30527824 | 0.77 | BACE1 (0.63) | CYP1A2KDM4EBACE1CYP2A6ALDH1A1 | |
| SCHEMBL10259445 | 0.76 | CYP1A2 (0.68) | CYP1A2KDM4ELMNAPOLBCASP6 |
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 494 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119707791-A | Double-response fluorescent probe for simultaneously imaging myelin and Abeta aggregates in AD brain, and preparation method and application thereof | 南京师范大学 | 2025-03-28 | — | — | CN | claimed |
| CN-115947720-B | Design, preparation and application of beta 3 adrenergic receptor anchoring probe | 南京师范大学 | 2024-03-29 | — | — | CN | claimed |
| CN-115947720-A | Design of beta 3 adrenergic receptor anchoring probe and preparation method and application thereof | 南京师范大学 | 2023-04-11 | — | — | CN | claimed |
| CN-114426534-B | Reversible fluorescent probe for detecting copper ions and preparation method thereof | 南京师范大学 | 2023-01-31 | — | — | CN | claimed |
| CN-114426534-A | Reversible fluorescent probe for detecting copper ions and preparation method thereof | 南京师范大学 | 2022-05-03 | — | — | CN | claimed |
| CN-109111397-B | Quinoline aromatic ethylene derivative and preparation method and application thereof | 广东工业大学 | 2021-12-10 | — | — | CN | claimed |
| CN-113754583-A | 2- ([2, 2' -biquinolyl ] -3-ether) -1-ethanol and derivative and synthetic method thereof | 湖南工程学院 | 2021-12-07 | — | — | CN | claimed |
| CN-110606839-B | Green synthesis method of polysubstituted quinazoline derivative | 南方医科大学 | 2021-10-08 | — | — | CN | claimed |
| CN-109111396-B | Quinoline aromatic vinyl derivative and preparation method and application thereof | 广东工业大学 | 2021-09-03 | — | — | CN | claimed |
| CN-113234067-A | 2, 5-disubstituted thiophene compounds and synthetic method thereof | 湘潭大学 | 2021-08-10 | — | — | CN | claimed |
| CN-112979619-A | Method for catalyzing dehydrogenation coupling reaction of nitrogen heteroaromatic ring compound and cyclic ether by using Bronsted acid | 青岛职业技术学院 | 2021-06-18 | — | — | CN | claimed |
| CN-109776406-B | Method for cross coupling of ether compound and quinoline derivative | 湘潭大学 | 2021-05-04 | — | — | CN | claimed |
| CN-104447539-B | A kind of two grades, the synthetic method of three-level aromatic amides | 湖南大学 | 2017-09-15 | — | — | CN | claimed |
| CN-106565600-A | Deuterated aza aromatic compound and synthesis method thereof | 湖南大学 | 2017-04-19 | — | — | CN | claimed |
| CN-104447539-A | Method for synthesizing binary and ternary aryl amide compounds | UNIV HUNAN | 2015-03-25 | — | — | CN | claimed |
| CN-104447540-A | Synthetic method of primary aryl amide compounds | UNIV HUNAN | 2015-03-25 | — | — | CN | claimed |
| CN-101591291-B | Synthesis method of 2-ethenyl quinoline compound | INST MATERIA MEDICA CAMS | 2012-07-18 | — | — | CN | claimed |
| CN-101591291-A | The synthetic method of 2-ethenyl quinoline compound | INST MATERIA MEDICA CAMS (CN) | 2009-12-02 | — | — | CN | claimed |
| US-20260138998-A1 | GLP-1 RECEPTOR AGONISTS AND METHODS OF USE | MERCK SHARP & DOHME LLC (US) | 2026-05-21 | — | — | US | disclosed |
| EP-0014929-A1 | Diagnostic means, process for its preparation and its use in determining leucocytes in body fluids | Roche Diagnostics GmbH (DE) | 1980-09-03 | — | — | EP | 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-20260138998-A1 | GLP-1 RECEPTOR AGONISTS AND METHODS OF USE | GLP1R, GIPR, GPR119 | CYP1A2 2666/4885KDM4E 2314/4885BACE1 3772/4885 |
“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.