Predicted protein targets (top 16)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.68 |
| ▸ | ENPP3 | O14638 | 2/20 | 0.68 |
| ▸ | ENPP1 | P22413 | 2/20 | 0.68 |
| ▸ | ENPP2 | Q13822 | 1/20 | 0.68 |
| ▸ | KMT2A | Q03164 | 4/20 | 0.60 |
| ▸ | MEN1 | O00255 | 3/20 | 0.60 |
| ▸ | ALPL | P05186 | 1/20 | 0.51 |
| ▸ | ALPI | P09923 | 1/20 | 0.51 |
| ▸ | CA2 | P00918 | 4/20 | 0.50 |
| ▸ | CA1 | P00915 | 2/20 | 0.50 |
| ▸ | CA9 | Q16790 | 2/20 | 0.50 |
| ▸ | CA12 | O43570 | 2/20 | 0.50 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.50 |
| ▸ | MAPT | P10636 | 1/20 | 0.50 |
| ▸ | HTT | P42858 | 1/20 | 0.50 |
| ▸ | PPARG | P37231 | 1/20 | 0.50 |
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 | |
|---|---|---|---|---|
| SCHEMBL12584886 | 1.00 | TDP1 (0.68) | TDP1ENPP3ENPP1ENPP2KMT2A | |
| SCHEMBL17287655 | 0.95 | ENPP3 (0.63) | TDP1ENPP3ENPP1ENPP2KMT2A | |
| Chlorfenson SCHEMBL7194888 | 0.90 | TDP1 (0.81) | TDP1ENPP3ENPP1ENPP2KMT2A | |
| Chlorfenson SCHEMBL116752 | 0.90 | TDP1 (0.81) | TDP1ENPP3ENPP1ENPP2KMT2A | |
| SCHEMBL9852204 | 0.90 | MEN1 (0.60) | TDP1ENPP3ENPP1ENPP2KMT2A | |
| SCHEMBL18179825 | 0.90 | MEN1 (0.60) | TDP1ENPP3ENPP1ENPP2KMT2A | |
| SCHEMBL4126086 | 0.90 | MEN1 (0.60) | TDP1ENPP3ENPP1ENPP2KMT2A | |
| Iodide SCHEMBL22068772 | 0.88 | CA2 (0.59) | TDP1ENPP3ENPP1ENPP2KMT2A | |
| SCHEMBL4084466 | 0.85 | MEN1 (0.53) | TDP1ENPP3ENPP1ENPP2KMT2A | |
| SCHEMBL941647 | 0.85 | GAA (0.64) | TDP1ENPP3ENPP1ENPP2KMT2A |
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 20 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118715015-A | Selective PHD1 inhibitor compounds, compositions and methods of use | 阿克比治疗有限公司 | 2024-09-27 | — | — | CN | disclosed |
| US-10463391-B2 | Magnetic ferrocenyl-functionalized nanoparticle | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2019-11-05 | — | — | US | disclosed |
| US-10370397-B2 | Phosphine substituted ferrocenyl complex | Kind Fahd University of Petroleum and Minerals (SA) | 2019-08-06 | — | — | US | disclosed |
| US-20190031697-A1 | PHOSPHINE SUBSTITUTED FERROCENYL COMPLEX | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2019-01-31 | — | — | US | disclosed |
| US-20190029718-A1 | MAGNETIC FERROCENYL-FUNCTIONALIZED NANOPARTICLE | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2019-01-31 | — | — | US | disclosed |
| US-10150109-B2 | Palladium(II)-silica supported catalyst | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-12-11 | — | — | US | disclosed |
| US-10150111-B2 | Method for catalytic synthesis of cinnamic acid with catalyst recycle | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-12-11 | — | — | US | disclosed |
| US-10150110-B2 | Method for making and using a solid-supported catalyst | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-12-11 | — | — | US | disclosed |
| US-20180326409-A1 | METHOD FOR MAKING AND USING A SOLID-SUPPORTED CATALYST | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-11-15 | — | — | US | disclosed |
| US-20180326410-A1 | METHOD FOR CATALYTIC SYNTHESIS OF CINNAMIC ACID WITH CATALYST RECYCLE | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-11-15 | — | — | US | disclosed |
| US-10125159-B2 | Functionalized magnetic nanoparticle, a catalyst, a method for forming C—C bonds | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-11-13 | — | — | US | disclosed |
| US-10058856-B2 | Method for palladium-catalyzed cinammic acid formation | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-08-28 | — | — | US | disclosed |
| US-20180200705-A1 | METHOD FOR PALLADIUM-CATALYZED CINAMMIC ACID FORMATION | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-07-19 | — | — | US | disclosed |
| US-20180200706-A1 | PALLADIUM(II)-SILICA SUPPORTED CATALYST | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-07-19 | — | — | US | disclosed |
| US-9956550-B2 | Solid-supported palladium(II) complex for catalyzing Mizoroki-Heck coupling reactions and a method thereof | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-05-01 | — | — | US | disclosed |
| US-20180099987-A1 | FUNCTIONALIZED MAGNETIC NANOPARTICLE, A CATALYST, A METHOD FOR FORMING C-C BONDS | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-04-12 | — | — | US | disclosed |
| US-20180065117-A1 | SOLID-SUPPORTED PALLADIUM(II) COMPLEX FOR CATALYZING MIZOROKI-HECK COUPLING REACTIONS AND A METHOD THEREOF | KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) | 2018-03-08 | — | — | US | disclosed |
| US-5049558-A | Quaternized nitrogen-heterocycle substituted | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1991-09-17 | — | — | US | disclosed |
| EP-0164944-B1 | CEPHALOSPORIN DERIVATIVES | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1990-07-11 | — | — | EP | disclosed |
| EP-0164944-A1 | Cephalosporin derivatives | IMPERIAL CHEMICAL INDUSTRIES PLC (GB) | 1985-12-18 | — | — | 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 (13 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-10150109-B2 | Palladium(II)-silica supported catalyst | PDK2, SIK2, SIK1 | TDP1 4356/4885ENPP3 3759/4885ENPP1 3952/4885 |
| US-20180099987-A1 | FUNCTIONALIZED MAGNETIC NANOPARTICLE, A CATALYST, A METHOD FOR FORMING C-C BONDS | MSN, COIL, NSFL1C | TDP1 4863/4885ENPP3 3953/4885ENPP1 4451/4885 |
| US-20180326409-A1 | METHOD FOR MAKING AND USING A SOLID-SUPPORTED CATALYST | AOC1, SOD1, PDK2 | TDP1 3883/4885ENPP3 3414/4885ENPP1 3546/4885 |
| US-20180326410-A1 | METHOD FOR CATALYTIC SYNTHESIS OF CINNAMIC ACID WITH CATALYST RECYCLE | DDT, PDK2, CLK2 | TDP1 4209/4885ENPP3 3088/4885ENPP1 3194/4885 |
| US-10058856-B2 | Method for palladium-catalyzed cinammic acid formation | ME1, CLK2, DDT | TDP1 4162/4885ENPP3 4040/4885ENPP1 4058/4885 |
| US-10370397-B2 | Phosphine substituted ferrocenyl complex | FECH, PHOSPHO1, FTH1 | TDP1 4869/4885ENPP3 2460/4885ENPP1 2917/4885 |
| US-20190031697-A1 | PHOSPHINE SUBSTITUTED FERROCENYL COMPLEX | FECH, FOLR1, FOLR2 | TDP1 4655/4885ENPP3 2188/4885ENPP1 2539/4885 |
| US-20180200706-A1 | PALLADIUM(II)-SILICA SUPPORTED CATALYST | PDK2, SIK2, SIK1 | TDP1 4356/4885ENPP3 3759/4885ENPP1 3952/4885 |
| US-20180200705-A1 | METHOD FOR PALLADIUM-CATALYZED CINAMMIC ACID FORMATION | ME1, CLK2, DDT | TDP1 4162/4885ENPP3 4040/4885ENPP1 4058/4885 |
| US-10150111-B2 | Method for catalytic synthesis of cinnamic acid with catalyst recycle | DDT, PDK2, CLK2 | TDP1 4209/4885ENPP3 3088/4885ENPP1 3194/4885 |
| US-20180065117-A1 | SOLID-SUPPORTED PALLADIUM(II) COMPLEX FOR CATALYZING MIZOROKI-HECK COUPLING REACTIONS AND A METHOD THEREOF | DDT, PDK2, DNAJA2 | TDP1 4207/4885ENPP3 3612/4885ENPP1 3813/4885 |
| US-10150110-B2 | Method for making and using a solid-supported catalyst | AOC1, SOD1, PDK2 | TDP1 3883/4885ENPP3 3414/4885ENPP1 3546/4885 |
| US-10125159-B2 | Functionalized magnetic nanoparticle, a catalyst, a method for forming C—C bonds | MSN, COIL, CORO1C | TDP1 4867/4885ENPP3 3904/4885ENPP1 4447/4885 |
“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.