⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| Methane SCHEMBL5484517 | 1.00 | — | — | |
| SCHEMBL28132514 | 0.97 | — | — | |
| SCHEMBL20168 | 0.97 | — | — | |
| Ethane SCHEMBL28170087 | 0.95 | — | — | |
| SCHEMBL22462258 | 0.95 | — | — | |
| SCHEMBL25397062 | 0.95 | — | — | |
| SCHEMBL27650623 | 0.95 | — | — | |
| SCHEMBL2229944 | 0.95 | — | — | |
| SCHEMBL28086676 | 0.95 | — | — | |
| SCHEMBL28226535 | 0.95 | — | — |
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 51 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4217181-B1 | METHOD AND 3D PRINTING METHOD FOR LAYER-BY-LAYER FABRICATION OF OBJECTS USING LAYER TRANSFER PRINTING | WACKER CHEMIE AG (DE) | 2024-03-06 | — | — | EP | disclosed |
| US-11903320-B2 | Method for applying at least one silicone layer by laser transfer printing | WACKER CHEMIE AG (DE) | 2024-02-13 | — | — | US | disclosed |
| EP-4284865-A1 | SILICON-CONTAINING THERMALLY CONDUCTIVE PASTES | Wacker Chemie AG (DE) | 2023-12-06 | — | — | EP | disclosed |
| EP-4139389-B1 | OPTICAL BONDING SILICONE WITH UV BLOCKER FOR OUTDOOR APPLICATION | WACKER CHEMIE AG (DE) | 2023-11-29 | — | — | EP | disclosed |
| WO-2023143730-A1 | LIGHT-METAL ALLOY-CONTAINING THERMAL PASTES | WACKER CHEMIE AG (DE) | 2023-08-03 | — | — | WO | disclosed |
| WO-2023143728-A1 | ALUMINUM-CONTAINING THERMAL PASTES | WACKER CHEMIE AG (DE) | 2023-08-03 | — | — | WO | disclosed |
| EP-4217181-A1 | METHOD AND 3D PRINTING METHOD FOR LAYER-BY-LAYER FABRICATION OF OBJECTS USING LAYER TRANSFER PRINTING | Wacker Chemie AG (DE) | 2023-08-02 | — | — | EP | disclosed |
| EP-4077491-B1 | SILICONE PARTICLES WITH A CROSS-LINKED CORE AND PREPARATION THEREOF | WACKER CHEMIE AG (DE) | 2023-06-14 | — | — | EP | disclosed |
| US-20230142071-A1 | OPTICAL BONDING SILICONE WITH UV BLOCKER FOR OUTDOOR APPLICATION | WACKER CHEMIE AG (DE) | 2023-05-11 | — | — | US | disclosed |
| WO-2023061585-A1 | ANTIMICROBIAL COMPOSITION AND METHOD FOR MAKING THE SAME | WACKER CHEMIE AG (DE) | 2023-04-20 | — | — | WO | disclosed |
| US-7291670-B2 | Cross-linking silicone elastomers, method for the production thereof, and use of the cross-linkable masses | WACKER CHEMIE AG (DE) | 2007-11-06 | — | — | US | disclosed |
| US-7129309-B2 | Use of rhodium-crosslinking silicone elastomers for producing baking molds | WACKER-CHEMIE GMBH (DE) | 2006-10-31 | — | — | US | disclosed |
| US-7053141-B2 | Organosilicone compounds having alkynol groups and the use thereof in crosslinkable materials | WACKER-CHEMIE GMBH (DE) | 2006-05-30 | — | — | US | disclosed |
| US-20060058484-A1 | Cross-linking silicone elastomers, method for the production thereof, and use of the cross-linkable masses | WACKER-CHEMIE GMBH (DE) | 2006-03-16 | — | — | US | disclosed |
| US-20040116566-A1 | Organosilicone compounds having alkynol groups and the use thereof in crosslinkable materials | WACKER-CHEMIE GMBH (DE) | 2004-06-17 | — | — | US | disclosed |
| US-20040022978-A1 | Use of rhodium-crosslinking silicone elstomers for producing baking molds | WACKER-CHEMIE GMBH (DE) | 2004-02-05 | — | — | US | disclosed |
| US-6566430-B2 | Crosslinking; molding materials | WACKER-CHEMIE GMBH (DE) | 2003-05-20 | — | — | US | disclosed |
| US-20020111426-A1 | Curable organopolysiloxane compositions | WACKER-CHEMIE GMBH (DE) | 2002-08-15 | — | — | US | disclosed |
| US-6359098-B1 | SHELF LIFE AS ONE-COMPONENT ADDITION-CURABLE ORGANOPOLYSILOXANES, AND EXTENDED POT LIFE FOR TWO-COMPONENT ADDITION-CURABLE ORGANOPOLYSILOXANES, WITHOUT COMPROMISING CROSSLINKING RATES OR LEVELS | WACKER-CHEMIE GMBH (DE) | 2002-03-19 | — | — | US | disclosed |
| US-6187890-B1 | CROSSLINK BY REACTION OF ALIPHATICALLY UNSATURATED GROUPS WITH SI-BONDED HYDROGEN (HYDROSILYLATION) IN THE PRESENCE OF A CATALYST, TYPICALLY A PLATINUM COMPOUND | WACKER-CHEMIE GMBH (DE) | 2001-02-13 | — | — | US | disclosed |