Predicted protein targets (top 4)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 1/20 | 0.38 |
| ▸ | ADRA2A | P08913 | 1/20 | 0.30 |
| ▸ | ADRA1A | P35348 | 1/20 | 0.30 |
| ▸ | GAA | P10253 | 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 | |
|---|---|---|---|---|
| SCHEMBL18826713 | 0.85 | DGKA (0.39) | TSHR | |
| SCHEMBL27473319 | 0.83 | DGKA (0.47) | TSHR | |
| SCHEMBL43519 | 0.83 | ALDH1A1 (0.33) | — | |
| SCHEMBL28096696 | 0.82 | DGKA (0.50) | TSHR | |
| SCHEMBL1811295 | 0.82 | DGKA (0.33) | TSHRGAA | |
| SCHEMBL20285671 | 0.81 | KDM4E (0.30) | — | |
| SCHEMBL25236913 | 0.80 | — | — | |
| SCHEMBL24813044 | 0.80 | PAOX (0.44) | TSHR | |
| SCHEMBL28697666 | 0.80 | TSHR (0.38) | TSHRADRA2AADRA1AGAA | |
| SCHEMBL27814498 | 0.79 | GAA (0.46) | GAA |
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 55 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2723750-B1 | DIKETOPYRROLOPYRROLE OLIGOMERS FOR USE IN ORGANIC SEMICONDUCTOR DEVICES | CLAP CO LTD (KR) | 2022-08-10 | — | — | EP | disclosed |
| EP-2751855-B1 | DIKETOPYRROLOPYRROLE OLIGOMERS AND COMPOSITIONS, COMPRISING DIKETOPYRROLOPYRROLE OLIGOMERS | BASF SE (DE) | 2020-10-28 | — | — | EP | disclosed |
| EP-2216312-B1 | PROCESS FOR PRODUCING ORGANIC COMPOUND | M TECHNIQUE CO LTD (JP) | 2019-05-01 | — | — | EP | disclosed |
| EP-2184109-B1 | METHOD FOR PRODUCING NANOPARTICLES BY FORCED ULTRA-THIN FILM ROTARY PROCESSING | M TECHNIQUE CO LTD (JP) | 2017-08-23 | — | — | EP | disclosed |
| US-9362508-B2 | Diketopyrrolopyrrole oligomers for use in organic semiconductor devices | BASF SE (DE) | 2016-06-07 | — | — | US | disclosed |
| US-9211510-B2 | Method for producing nanoparticles by forced ultrathin film rotary processing | M. TECHNIQUE CO., LTD. (JP) | 2015-12-15 | — | — | US | disclosed |
| US-9209412-B2 | Diketopyrrolopyrrole oligomers and compositions, comprising diketopyrrolopyrrole oligomers | BASF SE (DE) | 2015-12-08 | — | — | US | disclosed |
| US-8883889-B2 | Pigment compositions comprising pyrrolo[3,4-c]pyrroles | BASF SE (DE) | 2014-11-11 | — | — | US | disclosed |
| US-20140217329-A1 | DIKETOPYRROLOPYRROLE OLIGOMERS AND COMPOSITIONS, COMPRISING DIKETOPYRROLOPYRROLE OLIGOMERS | UNIVERSITE LIBRE DE BRUXELLES (BE) | 2014-08-07 | — | — | US | disclosed |
| EP-2751855-A1 | DIKETOPYRROLOPYRROLE OLIGOMERS AND COMPOSITIONS, COMPRISING DIKETOPYRROLOPYRROLE OLIGOMERS | BASF SE (DE) | 2014-07-09 | — | — | EP | disclosed |
| US-20020010331-A1 | Reacting succinic diester with nitrile | CLARIANT GMBH | 2002-01-24 | — | — | US | disclosed |
| US-6057449-A | HEATING A DISUCCINATE WITH A NITRILE IN THE PRESENCE OF BASE | CIBA SPECIALTY CHEMICALS CORPORATION (US) | 2000-05-02 | — | — | US | disclosed |
| EP-0962499-A2 | Direct preparation of pigmentary pyrrolo-(3,4-C)pyrroles | Ciba SC Holding AG (CH) | 1999-12-08 | — | — | EP | disclosed |
| US-5514677-A | Hydroxamic acid based collagenase inhibitors | BRITISH BIOTECH PHARMACEUTICALS LIMITED (GB) | 1996-05-07 | — | — | US | disclosed |
| US-5492564-A | HIGH OPACITY, COLORFASTNESS | CIBA-GEIGY CORPORATION (US) | 1996-02-20 | — | — | US | disclosed |
| US-5304604-A | Treating diseases involving tissue degradation, promoting wound healing | BRITISH BIO-TECHNOLOGY LIMITED (GB) | 1994-04-19 | — | — | US | disclosed |
| US-4749795-A | Phenyl substituted pyrrolinones | CIBA-GEIGY CORPORATION (US) | 1988-06-07 | — | — | US | disclosed |
| US-4720305-A | Mixtures of pigments | CIBA-GEIGY CORPORATION (US) | 1988-01-19 | — | — | US | disclosed |
| US-4681971-A | Phenyl substituted aminodicarboxylate esters | CIBA-GEIGY CORPORATION (US) | 1987-07-21 | — | — | US | disclosed |
| US-4579949-A | REACTING DISUCCINATE WITH NITRILES | CIBA-GEIGY CORPORATION (US) | 1986-04-01 | — | — | 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 (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-20020010331-A1 | Reacting succinic diester with nitrile | SDHA, QDPR, SDHB | TSHR 3768/4885ADRA2A 3754/4885ADRA1A 4206/4885 |
“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.