Predicted protein targets (top 9)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LSS | P48449 | 7/20 | 0.35 |
| ▸ | CNR2 | P34972 | 1/20 | 0.34 |
| ▸ | MEN1 | O00255 | 2/20 | 0.32 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.32 |
| ▸ | ALOX15 | P16050 | 2/20 | 0.32 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.32 |
| ▸ | MAPT | P10636 | 2/20 | 0.31 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.31 |
| ▸ | UGT1A1 | P22309 | 1/20 | 0.31 |
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 | |
|---|---|---|---|---|
| SCHEMBL9650230 | 1.00 | LSS (0.35) | LSSCNR2MEN1CYP3A4ALOX15 | |
| SCHEMBL10629087 | 1.00 | LSS (0.35) | LSSCNR2MEN1CYP3A4ALOX15 | |
| SCHEMBL11001883 | 1.00 | LSS (0.35) | LSSCNR2MEN1CYP3A4ALOX15 | |
| SCHEMBL4053634 | 0.90 | KMT2A (0.49) | LSSMEN1CYP3A4ALOX15KMT2A | |
| Tetrahydrothiophene SCHEMBL27901474 | 0.89 | LSS (0.30) | LSS | |
| SCHEMBL28586778 | 0.85 | LSS (0.36) | LSSCNR2ALOX15ALDH1A1 | |
| SCHEMBL14518213 | 0.85 | LSS (0.35) | LSSCNR2KMT2A | |
| SCHEMBL15164669 | 0.85 | LSS (0.35) | LSSCNR2KMT2A | |
| SCHEMBL17705183 | 0.83 | LSS (0.34) | LSSCNR2 | |
| SCHEMBL11342582 | 0.83 | LSS (0.34) | LSSCNR2 |
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 656 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-12496370-B2 | Freshening compositions comprising controlled release modulators | Arylessence, Inc. (US) | 2025-12-16 | — | — | US | claimed |
| US-11806448-B2 | Freshening compositions comprising controlled release modulators | Arylessence, Inc. (US) | 2023-11-07 | — | — | US | claimed |
| EP-4257663-A1 | FOOD CONTACT SURFACE SANITIZING LIQUID | The Procter & Gamble Company (US) | 2023-10-11 | — | — | EP | claimed |
| EP-3416729-B1 | PRO-FRAGRANCE COMPOSITION | AQDOT LTD (GB) | 2023-09-20 | — | — | EP | claimed |
| EP-3658655-B1 | ORGANIC COMPOUNDS | GIVAUDAN SA (CH) | 2022-11-23 | — | — | EP | claimed |
| US-11447724-B2 | Compositions that include siloxane compounds having pendant silyl ether moieties | THE PROCTER & GAMBLE COMPANY (US) | 2022-09-20 | — | — | US | claimed |
| EP-3935101-A1 | COMPOSITIONS THAT INCLUDE SILOXANE COMPOUNDS HAVING PENDANT SILYL ETHER MOIETIES | The Procter & Gamble Company (US) | 2022-01-12 | — | — | EP | claimed |
| CN-113557261-A | Compositions comprising siloxane compounds having pendant silyl ether moieties | 宝洁公司 | 2021-10-26 | — | — | CN | claimed |
| US-10899996-B2 | Organic compounds | GIVAUDAN SA (CH) | 2021-01-26 | — | — | US | claimed |
| WO-2020185481-A1 | COMPOSITIONS THAT INCLUDE SILOXANE COMPOUNDS HAVING PENDANT SILYL ETHER MOIETIES | THE PROCTER & GAMBLE COMPANY (US) | 2020-09-17 | — | — | WO | claimed |
| CN-102335492-A | Odorant for fire suppression system | KIDDE TECH INC | 2012-02-01 | — | — | CN | claimed |
| CN-102176818-A | Antimicrobial gel formulations | NOVABAY PHARMACEUTICALS INC | 2011-09-07 | — | — | CN | claimed |
| CN-101528063-A | Solid unit dose, sweetening compositions | MC NEIL NUTRITIONALS LLC (US) | 2009-09-09 | — | — | CN | claimed |
| CN-101299928-A | Sweetener and aroma compositions | MCNEIL NUTRITIONALS LLC (US) | 2008-11-05 | — | — | CN | claimed |
| US-7166728-B2 | Process for preparation of nerol oxide | COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) | 2007-01-23 | — | — | US | claimed |
| WO-2006070383-A1 | PROCESS FOR THE PREPARATION OF NEROL OXIDE | COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) | 2006-07-06 | — | — | WO | claimed |
| US-20060142450-A1 | By haloalkoxylating nerol to produce a 7-alkoxy-3,7-dimethyl-6-halo-2-octenol, dehydrohalogenating the product to produce a 7-alkoxy-3,7-dimethyl-octa-2,5-dien-1-ol, which is cyclized, especially using dilute mineral acid, lewis acid or an acidic resin to produce racemic nerol oxide | COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) | 2006-06-29 | — | — | US | claimed |
| EP-0659721-B1 | Method for the photooxidation of terpene olefins | HAARMANN & REIMER GMBH (DE) | 1998-06-10 | — | — | EP | claimed |
| US-5620569-A | Process for the photooxidation of terpene olefins | HAARMANN & REIMER GMBH (DE) | 1997-04-15 | — | — | US | claimed |
| EP-0325869-B1 | NOVEL PROCESSES AND INTERMEDIATES | MERRELL DOW PHARMACEUTICALS INC. (US) | 1992-11-25 | — | — | EP | claimed |