Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MEN1 | O00255 | 6/20 | 0.53 |
| ▸ | KMT2A | Q03164 | 6/20 | 0.53 |
| ▸ | USP2 | O75604 | 3/20 | 0.53 |
| ▸ | CASP1 | P29466 | 2/20 | 0.53 |
| ▸ | BRCA1 | P38398 | 1/20 | 0.53 |
| ▸ | CASP7 | P55210 | 1/20 | 0.53 |
| ▸ | CASP3 | P42574 | 1/20 | 0.48 |
| ▸ | HPGD | P15428 | 4/20 | 0.47 |
| ▸ | MAPT | P10636 | 2/20 | 0.47 |
| ▸ | DDB1 | Q16531 | 1/20 | 0.47 |
| ▸ | CRBN | Q96SW2 | 1/20 | 0.47 |
| ▸ | POLB | P06746 | 2/20 | 0.44 |
| ▸ | ALDH1A1 | P00352 | 5/20 | 0.43 |
| ▸ | KDM4E | B2RXH2 | 4/20 | 0.43 |
| ▸ | KEAP1 | Q14145 | 2/20 | 0.43 |
| ▸ | NFE2L2 | Q16236 | 2/20 | 0.43 |
| ▸ | ATM | Q13315 | 1/20 | 0.43 |
| ▸ | GAA | P10253 | 1/20 | 0.43 |
| ▸ | CA1 | P00915 | 1/20 | 0.43 |
| ▸ | CA2 | P00918 | 1/20 | 0.43 |
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 | |
|---|---|---|---|---|
| SCHEMBL30725964 | 1.00 | MEN1 (0.53) | MEN1KMT2AUSP2CASP1BRCA1 | |
| SCHEMBL27322335 | 0.78 | CASP3 (0.38) | MEN1KMT2AUSP2CASP1BRCA1 | |
| SCHEMBL9279014 | 0.78 | DDB1 (0.44) | MEN1KMT2ADDB1CRBNATM | |
| SCHEMBL13239551 | 0.78 | MEN1 (0.54) | MEN1KMT2AUSP2CASP1BRCA1 | |
| SCHEMBL2036747 | 0.78 | MEN1 (0.58) | MEN1KMT2AUSP2CASP1BRCA1 | |
| SCHEMBL3218263 | 0.76 | ANPEP (0.54) | MEN1KMT2AUSP2CASP1BRCA1 | |
| SCHEMBL1500604 | 0.76 | ALDH1A1 (0.56) | MEN1KMT2AUSP2CASP1BRCA1 | |
| SCHEMBL30725967 | 0.76 | MEN1 (0.53) | MEN1KMT2AUSP2CASP1BRCA1 | |
| SCHEMBL30788074 | 0.76 | ANPEP (0.54) | MEN1KMT2AUSP2CASP1BRCA1 | |
| SCHEMBL133067 | 0.76 | MEN1 (0.53) | MEN1KMT2AUSP2CASP1BRCA1 |
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 23 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119504556-A | Bisphenol phthaloyl Process for producing imine | 潍坊弘润石化科技有限公司 | 2025-02-25 | — | — | CN | disclosed |
| WO-2022133551-A1 | HISTONE DEACETYLASE INHIBITORS | THE UNIVERSITY OF QUEENSLAND (AU) | 2022-06-30 | — | — | WO | disclosed |
| US-11276825-B2 | Organic molecules for use in organic devices | CYNORA GMBH (DE) | 2022-03-15 | — | — | US | disclosed |
| EP-3658551-B1 | BENZOXAZINONE DERIVATIVES USEFUL AS HERBICIDES | REDAG CROP PROT LTD (GB) | 2022-01-19 | — | — | EP | disclosed |
| US-20210184134-A1 | ORGANIC MOLECULES FOR USE IN ORGANIC DEVICES | SAMSUNG DISPLAY CO., LTD. (KR) | 2021-06-17 | — | — | US | disclosed |
| CN-108117645-B | Method for preparing polyaryl imide and production device thereof | 北京鼎益新材科技有限公司 | 2020-08-14 | — | — | CN | disclosed |
| EP-3279193-B1 | COMPOUNDS COMPRISING A PHTHALIMIDE GROUP AND CARBAZOLE OR ITS ANALOGUES FOR USE IN ORGANIC OPTOELECTRONIC DEVICES | CYNORA GMBH (DE) | 2019-05-08 | — | — | EP | disclosed |
| WO-2019020987-A1 | BENZOXAZINONE DERIVATIVES USEFUL AS HERBICIDES | REDAG CROP PROTECTION LTD. (GB) | 2019-01-31 | — | — | WO | disclosed |
| WO-2018024723-A1 | PHTHALIMIDE AND CARBAZOLE OR ANALOGS THEREOF CONTAINING COMPOUNDS FOR USE IN ORGANIC OPTOELECTRONIC DEVICES | CYNORA GMBH (DE) | 2018-02-08 | — | — | WO | disclosed |
| EP-3279193-A1 | COMPOUNDS COMPRISING PHTHALIMIDE AND CARBAZOLE OR ITS ANALOGUES FOR USE IN ORGANIC OPTOELECTRONIC DEVICES | CYNORA GMBH (DE) | 2018-02-07 | — | — | EP | disclosed |
| US-4960903-A | Aromatic compounds having sulfonyl groups | TOA NENRYO KOGYO KABUSHIKI KAISHA (JP) | 1990-10-02 | — | — | US | disclosed |
| EP-0233409-B1 | AROMATIC SULFONYL COMPOUNDS | Tonen Corporation (JP) | 1990-09-26 | — | — | EP | disclosed |
| EP-0233409-A2 | Aromatic sulfonyl compounds | Tonen Corporation (JP) | 1987-08-26 | — | — | EP | disclosed |
| US-4476309-A | Method for making aromatic etherimides | GENERAL ELECTRIC COMPANY (US) | 1984-10-09 | — | — | US | disclosed |
| EP-0119576-A1 | Method for making aromatic etherimides | GENERAL ELECTRIC COMPANY (US) | 1984-09-26 | — | — | EP | disclosed |
| US-4471125-A | Method for making aromatic ether imides | GENERAL ELECTRIC COMPANY (US) | 1984-09-11 | — | — | US | disclosed |
| US-4302616-A | Method for making alkali metal bisphenoxide salts and bisimides derived therefrom | GENERAL ELECTRIC COMPANY (US) | 1981-11-24 | — | — | US | disclosed |
| US-4273712-A | PHASE TRANSFER CATALYSTS | GENERAL ELECTRIC COMPANY (US) | 1981-06-16 | — | — | US | disclosed |
| US-4257953-A | Method for making bisphenoxide salts and bisimides derived therefrom | GENERAL ELECTRIC COMPANY (US) | 1981-03-24 | — | — | US | disclosed |
| US-3992407-A | Preparation of aromatic bisimides | GENERAL ELECTRIC COMPANY (US) | 1976-11-16 | — | — | 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-20210184134-A1 | ORGANIC MOLECULES FOR USE IN ORGANIC DEVICES | CHRM1, C1S, DNMT3L | MEN1 887/4885KMT2A 1260/4885USP2 3112/4885 |
| US-11276825-B2 | Organic molecules for use in organic devices | AOX1, OR10J3, L1CAM | MEN1 2728/4885KMT2A 4062/4885USP2 4145/4885 |
“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.