Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MAOB | P27338 | 2/20 | 0.64 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.50 |
| ▸ | MAPT | P10636 | 1/20 | 0.50 |
| ▸ | ESR1 | P03372 | 1/20 | 0.48 |
| ▸ | ESR2 | Q92731 | 1/20 | 0.48 |
| ▸ | ACHE | P22303 | 1/20 | 0.45 |
| ▸ | APP | P05067 | 1/20 | 0.44 |
| ▸ | ALOX5 | P09917 | 1/20 | 0.43 |
| ▸ | PTGS2 | P35354 | 1/20 | 0.43 |
| ▸ | TUBB1 | Q9H4B7 | 1/20 | 0.43 |
| ▸ | MEN1 | O00255 | 1/20 | 0.42 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.42 |
| ▸ | CAPN1 | P07384 | 1/20 | 0.42 |
| ▸ | PARP1 | P09874 | 1/20 | 0.42 |
| ▸ | MAOA | P21397 | 1/20 | 0.42 |
| ▸ | CTSL | P07711 | 1/20 | 0.42 |
| ▸ | CTSB | P07858 | 1/20 | 0.42 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.42 |
| ▸ | RET | P07949 | 1/20 | 0.42 |
| ▸ | KIF5B | P33176 | 1/20 | 0.42 |
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 | |
|---|---|---|---|---|
| SCHEMBL29427137 | 1.00 | MAOB (0.64) | MAOBCYP3A4MAPTESR1ESR2 | |
| Hydrazine SCHEMBL10758378 | 0.96 | MAOB (0.59) | MAOBCYP3A4MAPTESR1ESR2 | |
| SCHEMBL23861426 | 0.83 | MAOB (0.48) | MAOBCYP3A4ESR1ESR2ACHE | |
| SCHEMBL263095 | 0.81 | MAOB (0.58) | MAOBCYP3A4MAPTESR1ESR2 | |
| SCHEMBL31703288 | 0.81 | MAOB (0.58) | MAOBCYP3A4MAPTESR1ESR2 | |
| SCHEMBL30514387 | 0.80 | MAOB (0.70) | MAOBCYP3A4MAPTESR1ESR2 | |
| SCHEMBL119396 | 0.80 | MAOB (0.70) | MAOBCYP3A4MAPTESR1ESR2 | |
| SCHEMBL16542012 | 0.80 | ALDH1A1 (0.49) | MAOBCYP3A4MAPTESR1ESR2 | |
| SCHEMBL16542009 | 0.80 | MAOB (0.43) | MAOBESR1ESR2TUBB1CTSL | |
| SCHEMBL16542013 | 0.80 | TUBB1 (0.57) | MAOBCYP3A4MAPTESR1ESR2 |
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 240 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119350185-A | Biphenyl hydroxamic derivative and preparation method and application thereof | 聊城大学 | 2025-01-24 | — | — | CN | claimed |
| CN-114181047-A | Method for preparing biphenol from cresol | 中国科学院大连化学物理研究所 | 2022-03-15 | — | — | CN | claimed |
| CN-107089898-B | Method for synthesizing cyclohexanol compounds by catalytic hydrogenation of biomass phenolic compounds | 浙江工业大学 | 2020-06-23 | — | — | CN | claimed |
| CN-107089898-A | A kind of method of biomass phenolic compound catalytic hydrogenation synthesizing cyclohexane 1 alcohols compound | 浙江工业大学 | 2017-08-25 | — | — | CN | claimed |
| US-4968759-A | Phenolic polymer and production thereof | HITACHI CHEMICAL COMPANY, LTD. (JP) | 1990-11-06 | — | — | US | claimed |
| WO-2025217099-A1 | INHIBITORS FOR HYDROGEN EMBRITTLEMENT AND METHODS | CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) | 2025-10-16 | — | — | WO | disclosed |
| WO-2025217091-A1 | ODORANTS FOR FLUIDS, ODORIZED FLUIDS, METHODS, AND SYSTEMS | CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) | 2025-10-16 | — | — | WO | disclosed |
| EP-3947365-B1 | SUBSTITUTED-N-HETEROARYL COMPOUNDS AND USES THEREOF | BIONOMICS LTD (AU) | 2025-10-01 | — | — | EP | disclosed |
| CN-119350185-A | Biphenyl hydroxamic derivative and preparation method and application thereof | 聊城大学 | 2025-01-24 | — | — | CN | disclosed |
| US-12162871-B2 | Inhibitors of VAP-1 | ACUCELA INC. (US) | 2024-12-10 | — | — | US | disclosed |
| US-12139473-B2 | Substituted-N-heteroaryl compounds and uses thereof | BIONOMICS LIMITED (AU) | 2024-11-12 | — | — | US | disclosed |
| EP-4217062-B1 | CYCLOBUTYL AMIDE MONOACYLGLYCEROL LIPASE MODULATORS | JANSSEN PHARMACEUTICA NV (BE) | 2024-10-09 | — | — | EP | disclosed |
| EP-1675814-A1 | PHENOXYETHER DERIVATIVES AS PPAR MODULATORS | ELI LILLY AND COMPANY (US) | 2006-07-05 | — | — | EP | disclosed |
| US-20050201265-A1 | Phthalocyanine compound, process for producing the same, and optical recording medium containing the same | MITSUI CHEMICALS, INC. (JP) | 2005-09-15 | — | — | US | disclosed |
| WO-2005037763-A1 | PHENOXYETHER DERIVATIVES AS PPAR MODULATORS | ELI LILLY AND COMPANY (US) | 2005-04-28 | — | — | WO | disclosed |
| EP-1482013-A1 | PHTHALOCYANINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND OPTICAL RECORDING MEDIUM CONTAINING THE SAME | MITSUI CHEMICALS, INC. (JP) | 2004-12-01 | — | — | EP | disclosed |
| US-5102962-A | Phenolic polymer and production thereof | HITACHI CHEMICAL COMPANY, LTD. (JP) | 1992-04-07 | — | — | US | disclosed |
| US-4897438-A | BLEND WITH A PHENOLIC RESIN | HITACHI CHEMICAL COMPANY, LTD. (JP) | 1990-01-30 | — | — | US | disclosed |
| US-4772742-A | POLYESTER INTERMEDIATES | AMOCO CORPORATION (US) | 1988-09-20 | — | — | US | disclosed |
| US-4709080-A | POLYESTERS | STANDARD OIL COMPANY (US) | 1987-11-24 | — | — | 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-12139473-B2 | Substituted-N-heteroaryl compounds and uses thereof | SCN3A, KCND3, GRIN3A | MAOB 2112/4885CYP3A4 2075/4885MAPT 379/4885 |
| US-12162871-B2 | Inhibitors of VAP-1 | VAPB, VAPA, TOE1 | MAOB 1440/4885CYP3A4 4363/4885MAPT 2213/4885 |
“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.