Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 2/20 | 0.41 |
| ▸ | THRB | P10828 | 1/20 | 0.41 |
| ▸ | FDPS | P14324 | 11/20 | 0.37 |
| ▸ | GGPS1 | O95749 | 7/20 | 0.37 |
| ▸ | SMPD1 | P17405 | 3/20 | 0.37 |
| ▸ | LMNA | P02545 | 1/20 | 0.35 |
| ▸ | CES2 | O00748 | 1/20 | 0.34 |
| ▸ | LPAR1 | Q92633 | 1/20 | 0.34 |
| ▸ | LPAR3 | Q9UBY5 | 1/20 | 0.34 |
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 | |
|---|---|---|---|---|
| SCHEMBL7189663 | 0.97 | TSHR (0.47) | TSHRTHRBFDPSGGPS1SMPD1 | |
| SCHEMBL30381193 | 0.97 | TSHR (0.47) | TSHRTHRBFDPSGGPS1SMPD1 | |
| SCHEMBL28571235 | 0.97 | TSHR (0.47) | TSHRTHRBFDPSGGPS1SMPD1 | |
| SCHEMBL8470352 | 0.97 | TSHR (0.47) | TSHRTHRBFDPSGGPS1SMPD1 | |
| SCHEMBL571523 | 0.94 | TSHR (0.44) | TSHRTHRBFDPSGGPS1SMPD1 | |
| SCHEMBL571531 | 0.92 | TSHR (0.42) | TSHRTHRBFDPSGGPS1SMPD1 | |
| SCHEMBL28728010 | 0.92 | TSHR (0.42) | TSHRTHRBFDPSGGPS1SMPD1 | |
| SCHEMBL19862 | 0.90 | TSHR (0.38) | TSHRTHRBFDPSLMNA | |
| SCHEMBL9233911 | 0.88 | TSHR (0.37) | TSHRTHRBFDPSGGPS1SMPD1 | |
| SCHEMBL130209 | 0.88 | TSHR (0.37) | TSHRTHRBFDPSGGPS1SMPD1 |
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 23 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2086915-B1 | TRITYL CHLORIDE RECOVERY | TATE & LYLE TECHNOLOGY LTD (GB) | 2015-04-29 | — | — | EP | claimed |
| US-8153849-B2 | Triarylmethylating sucrose in presence of amine to form 6,1',6'-tri-O-triarylmethylsucrose and byproducts, acylating to form 6,1',6'-tri-O-triarylmethylsucrose pentaester, separating, washing with hydrogen halide to remove amine | TATE & LYLE TECHNOLOGY LTD. (GB) | 2012-04-10 | — | — | US | claimed |
| EP-2086915-A2 | TRITYL CHLORIDE RECOVERY | Tate & Lyle Technology Limited (GB) | 2009-08-12 | — | — | EP | claimed |
| US-20080234526-A1 | Triarylmethylating sucrose in presence of amine to form 6,1',6'-tri-O-triarylmethylsucrose and byproducts, acylating to form 6,1',6'-tri-O-triarylmethylsucrose pentaester, separating, washing with hydrogen halide to remove amine | TATE & LYLE TECHNOLOGY LIMITED (GB) | 2008-09-25 | — | — | US | claimed |
| WO-2008070043-A2 | TRITYL CHLORIDE RECOVERY | TATE & LYLE TECHNOLOGY LTD. (GB) | 2008-06-12 | — | — | WO | claimed |
| US-20070172755-A1 | Positive photoresist and method for producing structure | SEKISUI CHECMICAL CO., LTD. (JP) | 2007-07-26 | — | — | US | claimed |
| EP-2086915-B1 | TRITYL CHLORIDE RECOVERY | TATE & LYLE TECHNOLOGY LTD (GB) | 2015-04-29 | — | — | EP | disclosed |
| US-8153849-B2 | Triarylmethylating sucrose in presence of amine to form 6,1',6'-tri-O-triarylmethylsucrose and byproducts, acylating to form 6,1',6'-tri-O-triarylmethylsucrose pentaester, separating, washing with hydrogen halide to remove amine | TATE & LYLE TECHNOLOGY LTD. (GB) | 2012-04-10 | — | — | US | disclosed |
| EP-2086915-A2 | TRITYL CHLORIDE RECOVERY | Tate & Lyle Technology Limited (GB) | 2009-08-12 | — | — | EP | disclosed |
| US-20080234526-A1 | Triarylmethylating sucrose in presence of amine to form 6,1',6'-tri-O-triarylmethylsucrose and byproducts, acylating to form 6,1',6'-tri-O-triarylmethylsucrose pentaester, separating, washing with hydrogen halide to remove amine | TATE & LYLE TECHNOLOGY LIMITED (GB) | 2008-09-25 | — | — | US | disclosed |
| WO-2008070043-A2 | TRITYL CHLORIDE RECOVERY | TATE & LYLE TECHNOLOGY LTD. (GB) | 2008-06-12 | — | — | WO | disclosed |
| US-20070172755-A1 | Positive photoresist and method for producing structure | SEKISUI CHECMICAL CO., LTD. (JP) | 2007-07-26 | — | — | US | disclosed |
| US-6946575-B2 | for DNA analysis via fluorescent in situ hybridization (FISH) | ISIS INNOVATION LTD. (GB) | 2005-09-20 | — | — | US | disclosed |
| EP-1268706-A1 | TRITYL-TYPE COMPOUNDS AND THEIR USE | ISIS INNOVATION LIMITED (GB) | 2003-01-02 | — | — | EP | disclosed |
| WO-2001072926-A1 | TRITYL-TYPE COMPOUNDS AND THEIR USE | ISIS INNOVATION LIMITED (GB) | 2001-10-04 | — | — | WO | disclosed |
| EP-1070052-A1 | FUNGICIDE COMPOSITIONS COMPRISING A HYDROXIMIC OR HYDRAZONIC GROUP | AVENTIS CROPSCIENCE S.A. (FR) | 2001-01-24 | — | — | EP | disclosed |
| WO-1999051579-A1 | FUNGICIDE COMPOSITIONS COMPRISING A HYDROXIMIC OR HYDRAZONIC GROUP | AVENTIS CROPSCIENCE S.A. (FR) | 1999-10-14 | — | — | WO | disclosed |
| US-4943626-A | Primary polyether active hydrogen compounds which are prepared from linked, protectively initiated polyalkyleneoxides | THE DOW CHEMICAL COMPANY (US) | 1990-07-24 | — | — | US | disclosed |
| EP-0352819-A2 | Primary polyether active hydrogen compounds and process for preparing the same | THE DOW CHEMICAL COMPANY (US) | 1990-01-31 | — | — | EP | disclosed |
| EP-0315097-A2 | Acyl labdane derivatives, process for their preparation and their use as medicines | HOECHST AKTIENGESELLSCHAFT (DE) | 1989-05-10 | — | — | EP | disclosed |