⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL49393 | 0.89 | — | — | |
| Fluoride SCHEMBL28471604 | 0.80 | — | — | |
| Water SCHEMBL436199 | 0.80 | — | — | |
| SCHEMBL17036073 | 0.80 | — | — | |
| SCHEMBL9480550 | 0.80 | — | — | |
| Ammonia Solution, Strong SCHEMBL2467040 | 0.80 | — | — | |
| SCHEMBL439983 | 0.60 | — | — | |
| SCHEMBL301805 | 0.55 | — | — | |
| Methane Boronic Acid SCHEMBL80533 | 0.55 | — | — | |
| SCHEMBL15576727 | 0.55 | — | — |
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 39 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-112645284-A | Preparation method of diborane | 山东国邦药业有限公司 | 2021-04-13 | — | — | CN | claimed |
| CN-115836041-B | Process for producing optically active compound | 住友化学株式会社 | 2024-09-17 | — | — | CN | disclosed |
| CN-115836041-A | Process for producing optically active compound | 住友化学株式会社 | 2023-03-21 | — | — | CN | disclosed |
| CN-112645284-A | Preparation method of diborane | 山东国邦药业有限公司 | 2021-04-13 | — | — | CN | disclosed |
| US-10888845-B1 | Graphene-tungsten oxide-metal boride/hydroxide photocatalysts, and methods for organic pollutant degradation and hydrogen production | KING ABDULAZIZ UNIVERSITY (SA) | 2021-01-12 | — | — | US | disclosed |
| US-7572303-B2 | A symmetrical dialkyl carbonate, a metal, borong, silicon, or group 7 compound, a hydrogen or hydrocarbon-based fuel, an oxidizer, and a metallic cocatalyst; minimized hydrolysis; improved combustion and storage stability | OCTANE INTERNATIONAL, LTD. (US) | 2009-08-11 | — | — | US | disclosed |
| CN-101437811-A | Quinoline derivatives | ASTRAZENECA AB (SE) | 2009-05-20 | — | — | CN | disclosed |
| EP-1500659-B1 | Selective, catalytic, thermal functionalization of secondary or aromatic C-H bonds in cyclic hydrocarbons | SHELL INT RESEARCH (NL) | 2008-09-24 | — | — | EP | disclosed |
| CN-1882576-A | Quinazoline derivatives | ASTRAZENECA AB (SE) | 2006-12-20 | — | — | CN | disclosed |
| EP-0954558-B1 | FUEL COMPOSITIONS EXHIBITING IMPROVED FUEL STABILITY | ORR WILLIAM C (US) | 2006-06-14 | — | — | EP | disclosed |
| EP-0954558-A1 | FUEL COMPOSITIONS EXHIBITING IMPROVED FUEL STABILITY | ORR, William C. (US) | 1999-11-10 | — | — | EP | disclosed |
| WO-1998026028-A1 | FUEL COMPOSITIONS EXHIBITING IMPROVED FUEL STABILITY | ORR WILLIAM C (US) | 1998-06-18 | — | — | WO | disclosed |
| US-5557027-A | METAL COMPLEX WITH CYCLIC PHOSPHORANE LIGAND, PREPARATION OF LINEAR ALPHA-OLEFINS | SHELL OIL COMPANY (US) | 1996-09-17 | — | — | US | disclosed |
| US-5439862-A | Comprising transition metal complexed with a five coordinate phosphorus compound, such as a phosphorane; producing linear ethylene oligomers | SHELL OIL COMPANY | 1995-08-08 | — | — | US | disclosed |
| EP-0254277-B1 | OLIGOMERIZATION CATALYST AND OLIGOMERIZATION PROCESS | UNION CARBIDE CORPORATION (US) | 1993-03-17 | — | — | EP | disclosed |
| US-4822915-A | METAL COMPLEXES AS POLYMERIZATION CATALYST FOR THE OLIGOMERIZATION OF ETHYLENE; CATALYST SELECTIVITY | UNION CARBIDE CORPORATION (US) | 1989-04-18 | — | — | US | disclosed |
| US-4716138-A | REACTION PRODUCT OF TRANSITION METAL COMPOUND AND ORGANOPHOSPHORUS SULFONATE | UNION CARBIDE CORPORATION (US) | 1987-12-29 | — | — | US | disclosed |
| US-4689437-A | ETHYLENE OR ETHYLENE-PROPYLENE, CATALYST FROM TRANSITION METAL COMPOUND, ACTIVATOR, ORGANOPHOSPHORUS SULFONATE LIGAND | UNION CARBIDE CORPORATION (US) | 1987-08-25 | — | — | US | disclosed |
| US-4085267-A | Process for the suspension polymerization of vinyl chloride with low polymer buildup | THE B. F. GOODRICH COMPANY (US) | 1978-04-18 | — | — | US | disclosed |
| US-3932383-A | MICROBIOCIDES | ABBOTT LABORATORIES (US) | 1976-01-13 | — | — | US | disclosed |