Predicted protein targets (top 14)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | TSHR | P16473 | 1/20 | 0.46 |
| ▸ | HPGD | P15428 | 1/20 | 0.45 |
| ▸ | LMNA | P02545 | 2/20 | 0.38 |
| ▸ | ADRA2A | P08913 | 1/20 | 0.37 |
| ▸ | ADRA2C | P18825 | 1/20 | 0.37 |
| ▸ | HIF1A | Q16665 | 1/20 | 0.37 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.37 |
| ▸ | NOS2 | P35228 | 1/20 | 0.36 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.36 |
| ▸ | MEN1 | O00255 | 1/20 | 0.36 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.36 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.36 |
| ▸ | SRC | P12931 | 1/20 | 0.36 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.35 |
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 | |
|---|---|---|---|---|
| SCHEMBL10645733 | 0.78 | TSHR (0.48) | TSHRHPGDLMNAMEN1KMT2A | |
| SCHEMBL10984767 | 0.78 | TSHR (0.48) | TSHRHPGDLMNAADRA2AADRA2C | |
| SCHEMBL356020 | 0.76 | LMNA (0.47) | TSHRHPGDLMNACYP3A4MEN1 | |
| SCHEMBL16560504 | 0.76 | TSHR (0.46) | TSHRHPGDLMNAADRA2AADRA2C | |
| SCHEMBL1950755 | 0.76 | LMNA (0.43) | TSHRHPGDLMNAALDH1A1 | |
| SCHEMBL9272891 | 0.75 | SRC (0.50) | HPGDLMNAADRA2AADRA2CHIF1A | |
| SCHEMBL9806266 | 0.75 | HPGD (0.48) | HPGDLMNAADRA2AADRA2CHIF1A | |
| SCHEMBL13849535 | 0.73 | HPGD (0.63) | TSHRHPGDLMNAADRA2AADRA2C | |
| SCHEMBL2249346 | 0.73 | HPGD (0.63) | TSHRHPGDLMNAADRA2AADRA2C | |
| SCHEMBL12468637 | 0.73 | HPGD (0.63) | TSHRHPGDLMNAADRA2AADRA2C |
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 39 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-0344021-B1 | Para-alkylstyrene/isoolefin copolymers | EXXONMOBIL CHEM PATENTS INC (US) | 2001-11-07 | — | — | EP | disclosed |
| EP-0609737-B1 | Process for producing a halogenated butyl rubber | BAYER INC (CA) | 2000-06-07 | — | — | EP | disclosed |
| US-5959049-A | COPOLYMERIZATION IN THE PRESENCE OF A DILUENT, AND A LEWIS ACID CATALYST, AND MAINTAINING THE COPOLYMERIZATION REACTOR SUBSTANTIALLY FREE OF IMPURITIES WHICH CAN COMPLEX WITH THE CATALYST OR COPOLYMERIZE WITH THE ISOOLEFIN OR THE | EXXON CHEMICAL PATENTS INC (US) | 1999-09-28 | — | — | US | disclosed |
| US-5654379-A | USING FREE RADICAL CATALYST | EXXON CHEMICALS PATENT, INC. (US) | 1997-08-05 | — | — | US | disclosed |
| EP-0566682-B1 | ENTANGLEMENT-INHIBITED MACROMOLECULES | EXXON CHEMICAL PATENTS INC (US) | 1997-01-22 | — | — | EP | disclosed |
| US-5591551-A | UV/EB curable butyl copolymers for lithographic and corrosion-resistant coating applications | EXXON CHEMICAL PATENTS INC. (US) | 1997-01-07 | — | — | US | disclosed |
| US-5587261-A | UV/EB curable butyl copolymers for lithographic and corrosion-resistant coating | EXXON CHEMICAL PATENTS INC. (US) | 1996-12-24 | — | — | US | disclosed |
| US-5585416-A | ULTRAVIOLET OR ELECTRON BEAM CROSSLINKING; COPOLYMER OF ISOOLEFIN AND PARA-ALKYLSTYRENE | EXXON CHEMICAL PATENTS INC. (US) | 1996-12-17 | — | — | US | disclosed |
| US-5585225-A | P-ALKYLSTYRENE FUNCTIONALIZED WITH RADIATION REACTIVE GROUP TO IMPART RADIATION CURABILITY | EXXON CHEMICAL PATENTS INC. (US) | 1996-12-17 | — | — | US | disclosed |
| EP-0497758-B1 | FUNCTIONALIZED COPOLYMERS OF PARA-ALKYLSTYRENE/ISOOLEFIN PREPARED BY NUCLEOPHILIC SUBSTITUTION | EXXON CHEMICAL PATENTS INC (US) | 1996-10-09 | — | — | EP | disclosed |
| WO-1992011322-A2 | UV/EB CURABLE BUTYL COPOLYMERS FOR LITHOGRAPHIC AND CORROSION-RESISTANT COATING APPLICATIONS | EXXON CHEMICAL PATENTS INC. (US) | 1992-07-09 | — | — | WO | disclosed |
| WO-1991004992-A1 | FUNCTIONALIZED COPOLYMERS OF PARA-ALKYLSTYRENE/ISOOLEFIN PREPARED BY NUCLEOPHILIC SUBSTITUTION | EXXON CHEMICAL PATENTS INC. (US) | 1991-04-18 | — | — | WO | disclosed |
| EP-0360829-A1 | DEHYDROBROMINATION OF SUBSTITUTED ALPHA-HALOCUMENE. | DOW CHEMICAL CO (US) | 1990-04-04 | — | — | EP | disclosed |
| EP-0344021-A2 | Para-alkylstyrene/isoolefin copolymers | EXXON CHEMICAL PATENTS INC. (US) | 1989-11-29 | — | — | EP | disclosed |
| WO-1988009319-A1 | DEHYDROBROMINATION OF SUBSTITUTED alpha-HALOCUMENE | THE DOW CHEMICAL COMPANY (US) | 1988-12-01 | — | — | WO | disclosed |
| US-4543216-A | REACTING A VINYL BENZYL HALIDE WITH AN AMINO ACID OR AMINO SULFONIC ACID | NIPPON PAINT CO., LTD. (JP) | 1985-09-24 | — | — | US | disclosed |
| US-4493884-A | O-NAPHTHOQUINONEDIAZIDE AND AROMATIC POLYMER | FUJI PHOTO FILM CO., LTD. (JP) | 1985-01-15 | — | — | US | disclosed |
| US-4151341-A | LOW MOLECULAR WEIGHT ADDITION-CONDENSATION COPOLYMERS AS DISPERSANTS | THE DOW CHEMICAL COMPANY (US) | 1979-04-24 | — | — | US | disclosed |
| US-4074035-A | ISOBUTYLENE AND PARA AND META CHLOROMETHYL STYRENE | EXXON RESEARCH & ENGINEERING CO. (US) | 1978-02-14 | — | — | US | disclosed |
| US-4020005-A | Gelled reagent materials | LANG JOHN L | 1977-04-26 | — | — | US | disclosed |