Predicted protein targets (top 13)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | HPRT1 | P00492 | 1/20 | 0.36 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.31 |
| ▸ | CYP2A6 | P11509 | 1/20 | 0.31 |
| ▸ | TSHR | P16473 | 1/20 | 0.31 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.31 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.31 |
| ▸ | LMNA | P02545 | 1/20 | 0.31 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.31 |
| ▸ | MAPT | P10636 | 1/20 | 0.31 |
| ▸ | APEX1 | P27695 | 1/20 | 0.31 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.31 |
| ▸ | PMP22 | Q01453 | 1/20 | 0.31 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.30 |
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 | |
|---|---|---|---|---|
| SCHEMBL7951420 | 0.84 | HPRT1 (0.32) | HPRT1 | |
| SCHEMBL6433447 | 0.80 | HPRT1 (0.41) | HPRT1ALDH1A1CYP2A6TSHRHSD17B10 | |
| SCHEMBL7935709 | 0.73 | HPRT1 (0.35) | HPRT1ALDH1A1CYP2A6TSHRHSD17B10 | |
| SCHEMBL7635425 | 0.73 | HPRT1 (0.50) | HPRT1ALDH1A1CYP2A6TSHRHSD17B10 | |
| SCHEMBL8194253 | 0.72 | ALDH1A1 (0.42) | HPRT1ALDH1A1CYP2A6TSHRHSD17B10 | |
| SCHEMBL7926905 | 0.72 | HPRT1 (0.36) | HPRT1ALDH1A1CYP2A6TSHRHSD17B10 | |
| SCHEMBL5179240 | 0.70 | CYP11B2 (0.34) | — | |
| SCHEMBL7148640 | 0.68 | TRIM24 (0.32) | CYP2A6TSHRMAPT | |
| SCHEMBL30565795 | 0.68 | HPRT1 (0.48) | HPRT1ALDH1A1CYP2A6TSHRHSD17B10 | |
| Hydrochloric Acid SCHEMBL6764889 | 0.68 | CYP11B2 (0.33) | — |
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 11 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1208155-B1 | POLYMER COMPOSITIONS | DOW GLOBAL TECHNOLOGIES INC (US) | 2005-02-09 | — | — | EP | disclosed |
| EP-1171295-B1 | MULTILAYER STRUCTURES | DOW GLOBAL TECHNOLOGIES INC (US) | 2004-11-17 | — | — | EP | disclosed |
| EP-1054910-B1 | IMPROVED OLEFIN POLYMERIZATION PROCESS | DOW GLOBAL TECHNOLOGIES INC (US) | 2004-09-22 | — | — | EP | disclosed |
| EP-1124834-B1 | PREPARATION OF TITANIUM(II) OR ZIRCONIUM(II) COMPLEXES | DOW CHEMICAL CO (US) | 2002-11-06 | — | — | EP | disclosed |
| US-6329486-B1 | PHYSICAL PROPERTIES | THE DOW CHEMICAL COMPANY | 2001-12-11 | — | — | US | disclosed |
| US-6323294-B1 | CONTACTING C.SUB.2-100,000 OLEFIN/S UNDER POLYMERIZATION CONDITIONS WITH CATALYST SYSTEM COMPRISING METAL COMPLEX AND ACTIVATING COCATALYST OR REACTION PRODUCT OF METAL COMPLEX AND COCATALYST TO FORM ADDITION POLYMER | THE DOW CHEMICAL COMPANY | 2001-11-27 | — | — | US | disclosed |
| US-6310256-B1 | REDUCING 1-CARBOHYDROCARBYLOXY-2-KETO-4-HYDROXY-5-CYCLOPENTENE COMPOUND BY CONTACTING WITH ZINC AND DECARBOXYLATING THE RESULTING REACTION PRODUCT BY CONTACTING THE REACTION MIXTURE WITH A MIXTURE OF AN ORGANIC ACID AND INORGANIC HALIDE | THE DOW CHEMICAL COMPANY | 2001-10-30 | — | — | US | disclosed |
| US-6258902-B1 | USING A METAL COMPLEX CATALYST AND AN ALKENYL CONTAINING HYDROCARBYLSILANE | THE DOW CHEMICAL COMPANY | 2001-07-10 | — | — | US | disclosed |
| US-6090962-A | Preparation of titanium(II) or zirconium(II) complexes | THE DOW CHEMICAL COMPANY (US) | 2000-07-18 | — | — | US | disclosed |
| EP-1017701-A1 | CYCLOPENTAPHENANTHRENEYL METAL COMPLEXES AND POLYMERIZATION PROCESS | THE DOW CHEMICAL COMPANY (US) | 2000-07-12 | — | — | EP | disclosed |
| WO-1999014221-A1 | CYCLOPENTAPHENANTHRENEYL METAL COMPLEXES AND POLYMERIZATION PROCESS | THE DOW CHEMICAL COMPANY (US) | 1999-03-25 | — | — | WO | disclosed |