Predicted protein targets (top 17)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | IDO1 | P14902 | 2/20 | 0.50 |
| ▸ | TSHR | P16473 | 3/20 | 0.47 |
| ▸ | HSPA5 | P11021 | 1/20 | 0.43 |
| ▸ | HTR1A | P08908 | 1/20 | 0.43 |
| ▸ | MAOB | P27338 | 1/20 | 0.43 |
| ▸ | LTA4H | P09960 | 2/20 | 0.42 |
| ▸ | NR5A1 | Q13285 | 1/20 | 0.42 |
| ▸ | L3MBTL1 | Q9Y468 | 2/20 | 0.41 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.41 |
| ▸ | NPC1 | O15118 | 1/20 | 0.41 |
| ▸ | BRD4 | O60885 | 1/20 | 0.41 |
| ▸ | MITF | O75030 | 1/20 | 0.41 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.41 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.40 |
| ▸ | KEAP1 | Q14145 | 1/20 | 0.40 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.40 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.40 |
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 | |
|---|---|---|---|---|
| SCHEMBL1833480 | 0.95 | IDO1 (0.48) | IDO1TSHRHSPA5HTR1ALTA4H | |
| SCHEMBL1836172 | 0.93 | NR5A1 (0.47) | IDO1TSHRHTR1ALTA4HNR5A1 | |
| SCHEMBL1838765 | 0.93 | NR5A1 (0.47) | IDO1TSHRHTR1ALTA4HNR5A1 | |
| SCHEMBL1835399 | 0.93 | NR5A1 (0.47) | IDO1TSHRHTR1ALTA4HNR5A1 | |
| SCHEMBL1836977 | 0.93 | NR5A1 (0.47) | IDO1TSHRHTR1ALTA4HNR5A1 | |
| SCHEMBL1840225 | 0.93 | NR5A1 (0.47) | IDO1TSHRHTR1ALTA4HNR5A1 | |
| SCHEMBL1837814 | 0.93 | NR5A1 (0.47) | IDO1TSHRHTR1ALTA4HNR5A1 | |
| SCHEMBL1838592 | 0.93 | NR5A1 (0.47) | IDO1TSHRHTR1ALTA4HNR5A1 | |
| SCHEMBL1840002 | 0.89 | IDO1 (0.53) | IDO1TSHRHSPA5HTR1AL3MBTL1 | |
| SCHEMBL647824 | 0.86 | LTA4H (0.45) | TSHRLTA4HNR5A1L3MBTL1TDP1 |
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 57 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-105575775-A | Method of producing layer structure, layer structure, a method of forming patterns and a semiconductor device | SAMSUNG SDI CO LTD | 2016-05-11 | — | — | CN | claimed |
| EP-4446310-A1 | METHOD FOR PRODUCING BLOCKED ISOCYANATE COMPOUND AND METHOD FOR PRODUCING ISOCYANATE COMPOUND | Asahi Kasei Kabushiki Kaisha (JP) | 2024-10-16 | — | — | EP | disclosed |
| CN-118382612-A | Method for producing blocked isocyanate compound and method for producing isocyanate compound | 旭化成株式会社 | 2024-07-23 | — | — | CN | disclosed |
| WO-2023106377-A1 | METHOD FOR PRODUCING BLOCKED ISOCYANATE COMPOUND AND METHOD FOR PRODUCING ISOCYANATE COMPOUND | 旭化成株式会社 | 2023-06-15 | — | — | WO | disclosed |
| EP-3838892-B1 | METHOD FOR PRODUCING ISOCYANATE | ASAHI CHEMICAL IND (JP) | 2022-10-12 | — | — | EP | disclosed |
| EP-3293173-B1 | METHOD FOR PRODUCING ISOCYANATE | ASAHI CHEMICAL IND (JP) | 2021-07-28 | — | — | EP | disclosed |
| EP-3838892-A1 | METHOD FOR PRODUCING ISOCYANATE | Asahi Kasei Kabushiki Kaisha (JP) | 2021-06-23 | — | — | EP | disclosed |
| EP-2980066-B1 | METHOD FOR PRODUCING ISOCYANATE | ASAHI CHEMICAL IND (JP) | 2021-04-21 | — | — | EP | disclosed |
| CN-107266338-B | The manufacturing method of isocyanates | 旭化成株式会社 | 2019-10-11 | — | — | CN | disclosed |
| CN-105575775-B | Layer structure and the method and semiconductor device for manufacturing its method, forming pattern | 三星SDI株式会社 | 2019-08-13 | — | — | CN | disclosed |
| CN-102906189-A | Compositions having phosphorus-containing compounds | DOW GLOBAL TECHNOLOGIES LLC | 2013-01-30 | — | — | CN | disclosed |
| CN-102858786-A | Thermosetting monomers and compositions comprising phosphorus and cyanato groups | DOW GLOBAL TECHNOLOGIES LLC | 2013-01-02 | — | — | CN | disclosed |
| CN-102781950-A | Thermosetting monomers and compositions comprising phosphorus and cyanato groups | DOW GLOBAL TECHNOLOGIES LLC | 2012-11-14 | — | — | CN | disclosed |
| US-20110160476-A1 | N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2011-06-30 | — | — | US | disclosed |
| US-20110133121-A1 | N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, And Composition For Transfer And Storage Of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound | ASAHI KASEI CHEMICALS CORPORATION (JP) | 2011-06-09 | — | — | US | disclosed |
| EP-2322504-A1 | PROCESS FOR THE PREPARATION OF N-SUBSTITUTED CARBAMIC ACID ESTER AND PROCESS FOR THE PREPARATION OF ISOCYANATE USING THE N-SUBSTITUTED CARBAMIC ACID ESTER | Asahi Kasei Chemicals Corporation (JP) | 2011-05-18 | — | — | EP | disclosed |
| US-20090163615-A1 | Uv curable hybridcuring ink jet ink composition and solder mask using the same | CAMTEK LTD. (IL) | 2009-06-25 | — | — | US | disclosed |
| US-20090163615-A1 | Uv curable hybridcuring ink jet ink composition and solder mask using the same | CAMTEK LTD. (IL) | 2009-06-25 | — | — | US | disclosed |
| US-20090110843-A1 | Thermosetting ink formulation for ink-jet applications | CAMTEK LTD. (IL) | 2009-04-30 | — | — | US | disclosed |
| EP-1593520-B1 | Thermal transfer dye-donors sheet for recording by laser. | EASTMAN KODAK CO (US) | 2007-05-30 | — | — | 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 (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-20110133121-A1 | N-Substituted Carbamic Acid Ester Production Method, Isocyanate Production Method Using Such N-Substituted Carbamic Acid Ester, And Composition For Transfer And Storage Of N-Substituted Carbamic Acid Ester Comprising N-Substituted Carbamic Acid Ester and Aromatic Hydroxy Compound | CPS1, ALKBH3, RCC1 | IDO1 2297/4885TSHR 4686/4885HSPA5 2972/4885 |
| US-20110160476-A1 | N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester | ALKBH3, CPS1, APEH | IDO1 1147/4885TSHR 2998/4885HSPA5 2082/4885 |
“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.