Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | MIF | P14174 | 8/20 | 0.38 |
| ▸ | MMP2 | P08253 | 2/20 | 0.34 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.34 |
| ▸ | MMP3 | P08254 | 1/20 | 0.34 |
| ▸ | MMP7 | P09237 | 1/20 | 0.34 |
| ▸ | MMP9 | P14780 | 1/20 | 0.34 |
| ▸ | MMP8 | P22894 | 1/20 | 0.34 |
| ▸ | MMP14 | P50281 | 1/20 | 0.34 |
| ▸ | HDAC6 | Q9UBN7 | 1/20 | 0.34 |
| ▸ | MMP1 | P03956 | 1/20 | 0.33 |
| ▸ | MAOA | P21397 | 1/20 | 0.33 |
| ▸ | MAOB | P27338 | 1/20 | 0.33 |
| ▸ | ESR2 | Q92731 | 3/20 | 0.33 |
| ▸ | ESR1 | P03372 | 2/20 | 0.33 |
| ▸ | CA12 | O43570 | 1/20 | 0.33 |
| ▸ | CA1 | P00915 | 1/20 | 0.33 |
| ▸ | CA2 | P00918 | 1/20 | 0.33 |
| ▸ | CA7 | P43166 | 1/20 | 0.33 |
| ▸ | CA9 | Q16790 | 1/20 | 0.33 |
| ▸ | CA14 | Q9ULX7 | 1/20 | 0.33 |
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 | |
|---|---|---|---|---|
| Phenol SCHEMBL9863953 | 0.88 | TDP1 (0.36) | MMP2KMT2AMMP1ESR1 | |
| Ether SCHEMBL11884826 | 0.82 | SMN1; SMN2 (0.36) | MMP2MMP1 | |
| Ether SCHEMBL17373053 | 0.81 | SMN1; SMN2 (0.41) | MIFKMT2AESR2ESR1 | |
| Ether SCHEMBL6580311 | 0.77 | MIF (0.34) | MIFKMT2AHDAC6ESR2ESR1 | |
| Ether SCHEMBL371586 | 0.75 | ESR1 (0.58) | KMT2AMMP3ESR2ESR1CA12 | |
| Propane SCHEMBL28322219 | 0.74 | SMN1; SMN2 (0.43) | MIFKMT2AESR2ESR1 | |
| SCHEMBL2898358 | 0.72 | ESR1 (0.44) | ESR2ESR1 | |
| Ether SCHEMBL6575659 | 0.71 | KMT2A (0.40) | KMT2AESR2ESR1CA12CA1 | |
| Diallylsulfone SCHEMBL5866729 | 0.71 | KMT2A (0.36) | KMT2AESR2ESR1CA12CA1 | |
| Methane SCHEMBL28842587 | 0.71 | ESR1 (0.42) | ESR2ESR1 |
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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-7049388-B2 | Process for manufacturing an α-dihydroxy derivative and epoxy resins prepared therefrom | DOW GLOBAL TECHNOLOGIES INC. (US) | 2006-05-23 | — | — | US | claimed |
| EP-1080084-B1 | PROCESS FOR EPOXIDATION OF ARYL ALLYL ETHERS | DOW GLOBAL TECHNOLOGIES INC (US) | 2004-05-06 | — | — | EP | claimed |
| US-6646102-B2 | Epoxidizing an alpha - halohydrin intermediate produced from a halide substitution of an alpha -dihydroxy derivative which has been obtained by a dihydroxylation reaction of an aryl allyl ether, oxidation catalysts | DOW GLOBAL TECHNOLOGIES INC. | 2003-11-11 | — | — | US | claimed |
| US-20030105268-A1 | Process for manufacturing an alpha-dihydroxy derivative and epoxy resins prepared therefrom | DOW GLOBAL TECHNOLOGIES INC. | 2003-06-05 | — | — | US | claimed |
| JP-2002517387-A | — | — | 2002-06-18 | — | — | JP | claimed |
| EP-1080084-A2 | PROCESS FOR EPOXIDATION OF ARYL ALLYL ETHERS | THE DOW CHEMICAL COMPANY (US) | 2001-03-07 | — | — | EP | claimed |
| US-6087513-A | REACTION OF ALLYL ARYL ETHER WITH HYDROGEN PEROXIDE IN THE PRESENCE OF TRANSITION METALS FOR OXIDATION | THE DOW CHEMICAL COMPANY (US) | 2000-07-11 | — | — | US | claimed |
| WO-1999062894-A2 | PROCESS FOR EPOXIDATION OF ARYL ALLYL ETHERS | THE DOW CHEMICAL COMPANY (US) | 1999-12-09 | — | — | WO | claimed |
| US-7807012-B2 | Moldable compositions containing carbinol functional silicone resins or anhydride functional silicone resins | DOW CORNING CORPORATION (US) | 2010-10-05 | — | — | US | disclosed |
| EP-1809701-B1 | MOLDABLE COMPOSITIONS CONTAINING CARBINOL FUNCTIONAL SILICONE REISINS OR ANHYDRIDE FUNCTIONAL SILICONE RESINS | DOW CORNING (US) | 2009-08-05 | — | — | EP | disclosed |
| US-20080105375-A1 | Moldable Compositions Containing Carbinol Functional Silicone Resins or Anhydride Functional Silicone Resins | DOW CORNING CORPORATION (US) | 2008-05-08 | — | — | US | disclosed |
| EP-1809701-A1 | MOLDABLE COMPOSITIONS CONTAINING CARBINOL FUNCTIONAL SILICONE REISINS OR ANHYDRIDE FUNCTIONAL SILICONE RESINS | Dow Corning Corporation (US) | 2007-07-25 | — | — | EP | disclosed |
| US-7049388-B2 | Process for manufacturing an α-dihydroxy derivative and epoxy resins prepared therefrom | DOW GLOBAL TECHNOLOGIES INC. (US) | 2006-05-23 | — | — | US | disclosed |
| WO-2006047318-A1 | MOLDABLE COMPOSITIONS CONTAINING CARBINOL FUNCTIONAL SILICONE REISINS OR ANHYDRIDE FUNCTIONAL SILICONE RESINS | DOW CORNING CORPORATION (US) | 2006-05-04 | — | — | WO | disclosed |
| EP-1406885-B1 | PROCESS FOR MANUFACTURING AN A-DIHYDROXY DERIVATIVE AND EPOXY RESINS PREPARED THEREFROM | DOW GLOBAL TECHNOLOGIES INC (US) | 2006-01-18 | — | — | EP | disclosed |
| EP-1406885-A1 | PROCESS FOR MANUFACTURING AN A-DIHYDROXY DERIVATIVE AND EPOXY RESINS PREPARED THEREFROM | DOW GLOBAL TECHNOLOGIES INC. (US) | 2004-04-14 | — | — | EP | disclosed |
| US-20040049004-A1 | Process for manufacturing an alpha-dihydroxy derivative and epoxy resins prepared therefrom | THE DOW CHEMICAL COMPANY | 2004-03-11 | — | — | US | disclosed |
| US-6646102-B2 | Epoxidizing an alpha - halohydrin intermediate produced from a halide substitution of an alpha -dihydroxy derivative which has been obtained by a dihydroxylation reaction of an aryl allyl ether, oxidation catalysts | DOW GLOBAL TECHNOLOGIES INC. | 2003-11-11 | — | — | US | disclosed |
| US-20030105268-A1 | Process for manufacturing an alpha-dihydroxy derivative and epoxy resins prepared therefrom | DOW GLOBAL TECHNOLOGIES INC. | 2003-06-05 | — | — | US | disclosed |
| WO-2003004481-A1 | PROCESS FOR MANUFACTURING AN A-DIHYDROXY DERIVATIVE AND EPOXY RESINS PREPARED THEREFROM | DOW GLOBAL TECHNOLOGIES INC. (US) | 2003-01-16 | — | — | WO | disclosed |