Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | IDO1 | P14902 | 2/20 | 0.58 |
| ▸ | MTNR1A | P48039 | 1/20 | 0.56 |
| ▸ | MTNR1B | P49286 | 1/20 | 0.56 |
| ▸ | RECQL | P46063 | 2/20 | 0.50 |
| ▸ | SMN1; SMN2 | Q16637 | 2/20 | 0.50 |
| ▸ | HPGD | P15428 | 2/20 | 0.50 |
| ▸ | MEN1 | O00255 | 2/20 | 0.50 |
| ▸ | NPC1 | O15118 | 2/20 | 0.50 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.50 |
| ▸ | HTT | P42858 | 2/20 | 0.50 |
| ▸ | RAB9A | P51151 | 2/20 | 0.50 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.50 |
| ▸ | POLB | P06746 | 1/20 | 0.50 |
| ▸ | MAPT | P10636 | 1/20 | 0.50 |
| ▸ | PKM | P14618 | 1/20 | 0.50 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.50 |
| ▸ | CYP1A2 | P05177 | 1/20 | 0.49 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.49 |
| ▸ | CYP2C19 | P33261 | 1/20 | 0.49 |
| ▸ | TTR | P02766 | 1/20 | 0.49 |
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 | |
|---|---|---|---|---|
| Bicarbonate SCHEMBL5277147 | 0.96 | IDO1 (0.55) | IDO1MTNR1AMTNR1BRECQLSMN1; SMN2 | |
| Hydroquinone SCHEMBL15387408 | 0.95 | IDO1 (0.53) | IDO1MTNR1AMTNR1BRECQLSMN1; SMN2 | |
| SCHEMBL16776780 | 0.87 | IDO1 (0.46) | IDO1MTNR1AMTNR1BRECQLSMN1; SMN2 | |
| SCHEMBL18398576 | 0.87 | IDO1 (0.56) | IDO1MTNR1AMTNR1BRECQLSMN1; SMN2 | |
| SCHEMBL10827236 | 0.87 | IDO1 (0.56) | IDO1MTNR1AMTNR1BRECQLSMN1; SMN2 | |
| SCHEMBL1030014 | 0.87 | IDO1 (0.56) | IDO1MTNR1AMTNR1BRECQLSMN1; SMN2 | |
| SCHEMBL31072414 | 0.87 | IDO1 (0.56) | IDO1MTNR1AMTNR1BRECQLSMN1; SMN2 | |
| SCHEMBL10834706 | 0.87 | IDO1 (0.49) | IDO1MTNR1AMTNR1BRECQLSMN1; SMN2 | |
| SCHEMBL2296213 | 0.85 | MEN1 (0.58) | IDO1MTNR1AMTNR1BRECQLSMN1; SMN2 | |
| SCHEMBL113807 | 0.85 | IDO1 (0.59) | IDO1MTNR1AMTNR1BRECQLSMN1; SMN2 |
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 1058 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4605443-A1 | PROCESS FOR MAKING TRANSPARENT POLYMER-BASED MATERIALS FOR SOLAR PANELS | Saudi Arabian Oil Company (SA) | 2025-08-27 | — | — | EP | claimed |
| CN-120077082-A | Method for producing transparent polymer-based material for solar panels | 沙特阿拉伯石油公司 | 2025-05-30 | — | — | CN | claimed |
| WO-2024191025-A1 | COSMETIC COMPOSITION COMPRISING CAPSULES OR BEADS | 한국콜마주식회사 | 2024-09-19 | — | — | WO | claimed |
| US-20240228701-A9 | PROCESS FOR MAKING TRANSPARENT POLYMER-BASED MATERIALS FOR SOLAR PANELS | SAUDI ARABIAN OIL COMPANY (SA) | 2024-07-11 | — | — | US | claimed |
| WO-2024086343-A1 | PROCESS FOR MAKING TRANSPARENT POLYMER-BASED MATERIALS FOR SOLAR PANELS | SAUDI ARABIAN OIL COMPANY (SA) | 2024-04-25 | — | — | WO | claimed |
| US-20240132663-A1 | PROCESS FOR MAKING TRANSPARENT POLYMER-BASED MATERIALS FOR SOLAR PANELS | SAUDI ARABIAN OIL COMPANY (SA) | 2024-04-25 | — | — | US | claimed |
| CN-107075121-B | Polysiloxane copolymers or terpolymers and polymers made therefrom | 莫门蒂夫性能材料股份有限公司 | 2021-01-22 | — | — | CN | claimed |
| CN-106471043-B | UV-active chromophore functionalized polysiloxanes and copolymers made therefrom | 莫门蒂夫性能材料股份有限公司 | 2021-01-12 | — | — | CN | claimed |
| CN-107075124-B | Alpha, omega-functionalized polyoxyalkylene-siloxane polymers and copolymers prepared therefrom | 莫门蒂夫性能材料股份有限公司 | 2020-10-23 | — | — | CN | claimed |
| CN-107406592-B | Reactive polysiloxanes and copolymers made therefrom | 莫门蒂夫性能材料股份有限公司 | 2020-09-22 | — | — | CN | claimed |
| US-6608164-B2 | Diaryl carbonate reacted with dihydroxy aromatic compounds in the presence of a transesterification catalyst; furan diol derivative is dimethyl 3,4-dihydroxy-2,5-furandiacarboxylate disodium salt | GENERAL ELECTRIC COMPANY | 2003-08-19 | — | — | US | claimed |
| US-6600004-B1 | Preparing polyestercarbonates is presented in which a mixture of at least one activated diaryl carbonate is reacted under melt polymerization conditions with at least one aromatic dihydroxy compound together with at least one dicarboxylic | GENERAL ELECTRIC COMPANY | 2003-07-29 | — | — | US | claimed |
| US-20030139529-A1 | Method of making block copolymers by solid state polymerization | GENERAL ELECTRIC COMPANY | 2003-07-24 | — | — | US | claimed |
| US-6583258-B1 | Transesterification catalyst is a salt of adenosine 5'-monophosphate or 2-deoxy-6-phosphogluconic acid; diaryl carbonate with a dihydroxy aromatic compound; bisphenol A with diphenyl carbonate | GENERAL ELECTRIC COMPANY | 2003-06-24 | — | — | US | claimed |
| US-20030114633-A1 | Salts of heterocyclic diols as catalysts for melt polycarbonate | GENERAL ELECTRIC COMPANY | 2003-06-19 | — | — | US | claimed |
| US-6569986-B1 | Multistage process; using tetraalkylphosphonium compound and basic catalyst | GENERAL ELECTRIC COMPANY | 2003-05-27 | — | — | US | claimed |
| WO-2003040208-A1 | METHOD OF MAKING BLOCK COPOLYMERS BY SOLID STATE POLYMERIZATION | GENERAL ELECTRIC COMPANY (US) | 2003-05-15 | — | — | WO | claimed |
| WO-2003010220-A1 | EXTRUSION METHOD FOR MAKING POLYCARBONATE | GENERAL ELECTRIC COMPANY (US) | 2003-02-06 | — | — | WO | claimed |
| US-6506871-B1 | Ester interchange of bis(methyl salicyl) carbonate and bisphenol A in presence of tetrabutylphosphonium acetate catalyst | GENERAL ELECTRIC COMPANY | 2003-01-14 | — | — | US | claimed |
| US-6399739-B1 | PROCESS CONTROL USING COMPUTERS | GENERAL ELECTRIC COMPANY | 2002-06-04 | — | — | US | claimed |