Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | HPGD | P15428 | 4/20 | 0.41 |
| ▸ | GLA | P06280 | 1/20 | 0.41 |
| ▸ | RECQL | P46063 | 1/20 | 0.41 |
| ▸ | L3MBTL1 | Q9Y468 | 2/20 | 0.40 |
| ▸ | CYP2C19 | P33261 | 2/20 | 0.40 |
| ▸ | KMT2A | Q03164 | 5/20 | 0.39 |
| ▸ | PKM | P14618 | 2/20 | 0.39 |
| ▸ | POLB | P06746 | 2/20 | 0.39 |
| ▸ | PTPN1 | P18031 | 1/20 | 0.39 |
| ▸ | PTPN7 | P35236 | 1/20 | 0.39 |
| ▸ | BLM | P54132 | 1/20 | 0.39 |
| ▸ | ESR2 | Q92731 | 1/20 | 0.39 |
| ▸ | ALDH1A1 | P00352 | 6/20 | 0.38 |
| ▸ | MEN1 | O00255 | 4/20 | 0.38 |
| ▸ | MAPT | P10636 | 4/20 | 0.38 |
| ▸ | TSHR | P16473 | 1/20 | 0.38 |
| ▸ | NPSR1 | Q6W5P4 | 2/20 | 0.36 |
| ▸ | HTT | P42858 | 1/20 | 0.36 |
| ▸ | MIF | P14174 | 1/20 | 0.35 |
| ▸ | TP53 | P04637 | 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 | |
|---|---|---|---|---|
| SCHEMBL181943 | 0.91 | HPGD (0.46) | HPGDGLARECQLL3MBTL1CYP2C19 | |
| SCHEMBL21117296 | 0.79 | HPGD (0.57) | HPGDGLARECQLL3MBTL1CYP2C19 | |
| SCHEMBL29013573 | 0.74 | KMT2A (0.46) | HPGDGLARECQLL3MBTL1CYP2C19 | |
| SCHEMBL12464824 | 0.73 | MIF (0.43) | HPGDGLARECQLL3MBTL1CYP2C19 | |
| SCHEMBL19133768 | 0.72 | KMT2A (0.46) | HPGDGLARECQLL3MBTL1CYP2C19 | |
| SCHEMBL23201595 | 0.71 | ALOX5 (0.40) | HPGDGLARECQLL3MBTL1CYP2C19 | |
| SCHEMBL826815 | 0.71 | — | — | |
| SCHEMBL8245610 | 0.71 | — | — | |
| SCHEMBL13881159 | 0.71 | — | — | |
| SCHEMBL11738306 | 0.70 | CFTR (0.44) | HPGDGLARECQLL3MBTL1CYP2C19 |
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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2580252-B1 | METHODS FOR PRODUCING TELECHELIC POLYOLEFINS FROM TERPENE INITIATORS | CHEVRON ORONITE CO (US) | 2016-11-09 | — | — | EP | disclosed |
| US-9187581-B2 | Methods for producing telechelic polyolefins from terpene initiators | CHEVRON ORONITE COMPANY LLC (US) | 2015-11-17 | — | — | US | disclosed |
| US-8969484-B2 | Methods of producing mono- and multi-functional polymers from terpene-based initiators | CHEVRON ORONITE COMPANY LLC (US) | 2015-03-03 | — | — | US | disclosed |
| EP-2729503-A2 | METHODS OF PRODUCING MONO- AND MULTI-FUNCTIONAL POLYMERS FROM TERPENE-BASED INITIATORS | Chevron Oronite Company LLC (US) | 2014-05-14 | — | — | EP | disclosed |
| US-20130267669-A1 | METHODS FOR PRODUCING TELECHELIC POLYOLEFINS FROM TERPENE INITIATORS | CHEVRON ORONITE CO (US) | 2013-10-10 | — | — | US | disclosed |
| US-8492491-B2 | Methods for producing telechelic polyolefins from terpene initiators | CHEVRON ORONITE COMPANY LLC (US) | 2013-07-23 | — | — | US | disclosed |
| EP-2580252-A2 | METHODS FOR PRODUCING TELECHELIC POLYOLEFINS FROM TERPENE INITIATORS | Chevron Oronite Company LLC (US) | 2013-04-17 | — | — | EP | disclosed |
| WO-2013009592-A2 | METHODS OF PRODUCING MONO- AND MULTI-FUNCTIONAL POLYMERS FROM TERPENE-BASED INITIATORS | CHEVRON ORONITE COMPANY LLC (US) | 2013-01-17 | — | — | WO | disclosed |
| US-20130012662-A1 | METHODS OF PRODUCING MONO- AND MULTI-FUNCTIONAL POLYMERS FROM TERPENE-BASED INITIATORS | CHEVRON ORONITE COMPANY LLC | 2013-01-10 | — | — | US | disclosed |
| US-20110306738-A1 | METHODS FOR PRODUCING TELECHELIC POLYOLEFINS FROM TERPENE INITIATORS | CHEVRON ORONITE COMPANY LLC | 2011-12-15 | — | — | US | disclosed |
| EP-1135422-A1 | SILYL-FUNCTIONAL LIVING CATIONIC POLYMERS | DOW CORNING CORPORATION (US) | 2001-09-26 | — | — | EP | disclosed |
| US-6194597-B1 | REACTING CATIONICALLY POLYMERIZABLE MONOMER(ISOBUTYLENE, ISOPRENE) WITH SILYL GROUP CONTAINING INITIATOR IN PRESENCE OF LEWIS ACID TO FORM LIVING CATIONIC POLYMER CONTAINING SILIY GROUPS | DOW CORNING CORPORATION | 2001-02-27 | — | — | US | disclosed |
| WO-2000063256-A1 | LIVING CATIONIC POLYMERS PREPARED FROM SILYL-FUNCTIONAL AROMATIC INITIATORS | DOW CORNING CORPORATION (US) | 2000-10-26 | — | — | WO | disclosed |
| EP-1044226-A1 | METHOD FOR COUPLING LIVING CATIONIC POLYMERS | DOW CORNING CORPORATION (US) | 2000-10-18 | — | — | EP | disclosed |
| WO-2000032654-A1 | SILYL-FUNCTIONAL LIVING CATIONIC POLYMERS | DOW CORNING CORPORATION (US) | 2000-06-08 | — | — | WO | disclosed |
| WO-2000032609-A1 | SILYL-FUNCTIONAL INITIATOR FOR LIVING CATIONIC POLYMERIZATION | DOW CORNING CORPORATION (US) | 2000-06-08 | — | — | WO | disclosed |
| US-6051657-A | Silyl-functional living cationic polymers | DOW CORNING ASIA, LTD. (JP) | 2000-04-18 | — | — | US | disclosed |
| US-6046281-A | REACTING A LIVING CATIONIC POLYMER WITH AN ORGANIC COMPOUND HAVING AT LEAST 2 FURAN RINGS IN ITS MOLECULE, SUCH AS DIFURANYLHEXANE IN THE PRESENCE OF A LEWIS ACID | UNIVERSITY OF MASSACHUSETTS LOWELL (US) | 2000-04-04 | — | — | US | disclosed |
| US-5981785-A | Silyl-functional initiator for living cationic polymerization | UNIVERSITY OF MASSACHUSETTS (US) | 1999-11-09 | — | — | US | disclosed |
| WO-1999024480-A1 | METHOD FOR COUPLING LIVING CATIONIC POLYMERS | DOW CORNING CORPORATION (US) | 1999-05-20 | — | — | WO | disclosed |