Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TYMS | P04818 | 5/20 | 0.41 |
| ▸ | ALOX15 | P16050 | 1/20 | 0.38 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.38 |
| ▸ | TSHR | P16473 | 1/20 | 0.37 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.34 |
| ▸ | MEN1 | O00255 | 1/20 | 0.30 |
| ▸ | POLB | P06746 | 1/20 | 0.30 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.30 |
| ▸ | BCL2 | P10415 | 1/20 | 0.30 |
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 | |
|---|---|---|---|---|
| SCHEMBL4904796 | 0.92 | TSHR (0.39) | TYMSALOX15TDP1TSHRALDH1A1 | |
| SCHEMBL29768809 | 0.92 | TSHR (0.42) | TYMSALOX15TDP1TSHRALDH1A1 | |
| SCHEMBL127904 | 0.92 | TSHR (0.42) | TYMSALOX15TDP1TSHRALDH1A1 | |
| SCHEMBL127961 | 0.90 | TSHR (0.41) | TYMSALOX15TDP1TSHRALDH1A1 | |
| SCHEMBL127148 | 0.85 | TSHR (0.46) | TYMSALOX15TDP1TSHR | |
| SCHEMBL13713810 | 0.81 | TSHR (0.34) | TYMSALOX15TDP1TSHR | |
| SCHEMBL127867 | 0.79 | TSHR (0.54) | TYMSALOX15TDP1TSHRALDH1A1 | |
| SCHEMBL32670397 | 0.79 | TYMS (0.41) | TYMSALOX15TDP1ALDH1A1MEN1 | |
| SCHEMBL29580210 | 0.79 | TYMS (0.41) | TYMSALOX15TDP1ALDH1A1MEN1 | |
| SCHEMBL4324585 | 0.79 | TYMS (0.41) | TYMSALOX15TDP1ALDH1A1MEN1 |
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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2023167234-A1 | COMPOUND, ORGANIC THIN FILM, PHOTOELECTRIC CONVERSION ELEMENT, IMAGING ELEMENT, PHOTOSENSOR AND SOLID-STATE IMAGING DEVICE | 三菱瓦斯化学株式会社 | 2023-09-07 | — | — | WO | disclosed |
| US-20150123090-A1 | METHOD FOR THE DEPOSITION OF AN ORGANIC MATERIAL | BASF SE (DE) | 2015-05-07 | — | — | US | disclosed |
| US-20150123090-A1 | METHOD FOR THE DEPOSITION OF AN ORGANIC MATERIAL | BASF SE (DE) | 2015-05-07 | — | — | US | disclosed |
| US-8912535-B2 | Naphthalene-diimide-heterocycle-naphthalene diimide oligomers as organic semiconductors and transistors therefrom | GEORGIA TECH RESEARCH CORPORATION (US) | 2014-12-16 | — | — | US | disclosed |
| US-20140021448-A1 | NAPHTHALENE-DIIMIDE-HETEROCYCLE-NAPHTHALENE DIIMIDE OLIGOMERS AS ORGANIC SEMICONDUCTORS AND TRANSISTORS THEREFROM | GEORGIA TECH RESEARCH CORPORATION (US) | 2014-01-23 | — | — | US | disclosed |
| WO-2013164761-A1 | METHOD FOR THE DEPOSITION OF AN ORGANIC MATERIAL | BASF SE (DE) | 2013-11-07 | — | — | WO | disclosed |
| EP-2532663-A1 | Naphthalenecarboxylic acid derivatives and their use as semiconductors | BASF SE (DE) | 2012-12-12 | — | — | EP | disclosed |
| US-8309728-B2 | Naphthalenetetracarboxylic acid derivatives and their use as semiconductors | BASF AKTIENGESELLSCHAFT (DE) | 2012-11-13 | — | — | US | disclosed |
| US-20120059168-A1 | NAPHTHALENETETRACARBOXYLIC ACID DERIVATIVES AND THEIR USE AS SEMICONDUCTORS | BASF SE (DE) | 2012-03-08 | — | — | US | disclosed |
| US-8084603-B2 | Naphthalenetetracarboxylic acid derivatives and their use as semiconductors | BASF AKTIENGESELLSCHAFT (DE) | 2011-12-27 | — | — | US | disclosed |
| US-20080300405-A1 | Naphthalenetetracarboxylic Aicd Derivatives and their Use as Semiconductors | BASF SE (DE) | 2008-12-04 | — | — | US | disclosed |
| US-20080300405-A1 | Naphthalenetetracarboxylic Aicd Derivatives and their Use as Semiconductors | BASF SE (DE) | 2008-12-04 | — | — | US | disclosed |
| US-7405030-B2 | Imide compound and optical recording media made by using the same | MITSUI CHEMICALS, INC. (JP) | 2008-07-29 | — | — | US | disclosed |
| US-7405030-B2 | Imide compound and optical recording media made by using the same | MITSUI CHEMICALS, INC. (JP) | 2008-07-29 | — | — | US | disclosed |
| EP-1930339-A2 | Imide compound | MITSUI CHEMICALS, INC. (JP) | 2008-06-11 | — | — | EP | disclosed |
| US-20070259151-A1 | Imide compound and optical recording media made by using the same | MITSUI CHEMICALS, INC. (JP) | 2007-11-08 | — | — | US | disclosed |
| US-20070259151-A1 | Imide compound and optical recording media made by using the same | MITSUI CHEMICALS, INC. (JP) | 2007-11-08 | — | — | US | disclosed |
| US-7259260-B2 | Imide compound and optical recording media made by using the same | MITSUI CHEMICALS, INC. (JP) | 2007-08-21 | — | — | US | disclosed |
| US-7259260-B2 | Imide compound and optical recording media made by using the same | MITSUI CHEMICALS, INC. (JP) | 2007-08-21 | — | — | US | disclosed |
| WO-2007074137-A1 | NAPHTHALENETETRACARBOXYLIC ACID DERIVATIVES AND THEIR USE AS SEMICONDUCTORS | BASF SE (DE) | 2007-07-05 | — | — | WO | 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-20120059168-A1 | NAPHTHALENETETRACARBOXYLIC ACID DERIVATIVES AND THEIR USE AS SEMICONDUCTORS | TST, NANS, NCDN | TYMS 328/4885ALOX15 2912/4885TDP1 4130/4885 |
| US-20080300405-A1 | Naphthalenetetracarboxylic Aicd Derivatives and their Use as Semiconductors | ADSL, ALAD, EED | TYMS 173/4885ALOX15 2871/4885TDP1 4282/4885 |
“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.