⚠ 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 | |
|---|---|---|---|---|
| Tromethamine SCHEMBL11423310 | 0.84 | PPARD (0.38) | — | |
| Diethyl Hydrogen Phosphate SCHEMBL31413319 | 0.83 | TP53 (0.52) | — | |
| Diethyl Hydrogen Phosphate SCHEMBL93056 | 0.83 | — | — | |
| Diethyl Hydrogen Phosphate SCHEMBL27294237 | 0.83 | TSHR (0.56) | — | |
| Diethyl Hydrogen Phosphate SCHEMBL4948463 | 0.80 | TSHR (0.53) | — | |
| Diethyl Hydrogen Phosphate SCHEMBL906759 | 0.80 | TSHR (0.53) | — | |
| Diethyl Hydrogen Phosphate SCHEMBL11745053 | 0.80 | TSHR (0.53) | — | |
| Diethyl Hydrogen Phosphate SCHEMBL11752938 | 0.80 | TSHR (0.53) | — | |
| Diethyl Hydrogen Phosphate SCHEMBL3133022 | 0.80 | TSHR (0.53) | — | |
| Diethyl Hydrogen Phosphate SCHEMBL11757040 | 0.80 | TSHR (0.53) | — |
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 35 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118852239-A | Method for preparing perfluorophosphonate vinyl ether monomer from perfluorovinyl ether halide in one step | 山东东岳未来氢能材料股份有限公司 | 2024-10-29 | — | — | CN | claimed |
| US-6093758-A | REACTING AN ARYLOXY-HYDROXY FUNCTIONAL PHOSPHAZENE WITH A HALOGENATED CHLOROPHOSPHATE SELECTED FROM THE GROUP CONSISTING OF ALIPHATIC AND AROMATIC CHLOROPHOSPHATES TO FORM PHOSPHORYLATED PHOSPHAZENES WITH IMPROVED HEAT RESISTANCE | THE PENN STATE RESEARCH FOUNDATION (US) | 2000-07-25 | — | — | US | claimed |
| CN-118852239-A | Method for preparing perfluorophosphonate vinyl ether monomer from perfluorovinyl ether halide in one step | 山东东岳未来氢能材料股份有限公司 | 2024-10-29 | — | — | CN | disclosed |
| CN-118852239-A | Method for preparing perfluorophosphonate vinyl ether monomer from perfluorovinyl ether halide in one step | 山东东岳未来氢能材料股份有限公司 | 2024-10-29 | — | — | CN | disclosed |
| US-11898082-B1 | Fire resistant phosphate cyanate esters | THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY OF THE NAVY (US) | 2024-02-13 | — | — | US | disclosed |
| CN-116728924-B | PVC decorative film containing thermal transfer printing gold and silver patterns | 广东瀚泰装饰材料有限公司 | 2023-12-08 | — | — | CN | disclosed |
| CN-116728924-A | PVC decorative film containing thermal transfer printing gold and silver patterns | 广东瀚泰装饰材料有限公司 | 2023-09-12 | — | — | CN | disclosed |
| CN-114685559-B | Preparation method of lithium bistrifluoromethyl phosphate | 多氟多新材料股份有限公司 | 2023-07-18 | — | — | CN | disclosed |
| CN-114685559-B | Preparation method of lithium bistrifluoromethyl phosphate | 多氟多新材料股份有限公司 | 2023-07-18 | — | — | CN | disclosed |
| CN-114685559-A | Preparation method of bis (trifluoromethyl) lithium phosphate | 多氟多新材料股份有限公司 | 2022-07-01 | — | — | CN | disclosed |
| CN-114685559-A | Preparation method of bis (trifluoromethyl) lithium phosphate | 多氟多新材料股份有限公司 | 2022-07-01 | — | — | CN | disclosed |
| WO-2006014828-A1 | SYNTHESIS OF 6,7-DIHYDRO-5H-IMIDAZO[1,2-A]IMIDAZOLE-3-SULFONIC ACID AMIDES | BOEHRINGER INGELHEIM INTERNATIONAL, GMBH (DE) | 2006-02-09 | — | — | WO | disclosed |
| US-20060025447-A1 | Synthesis of 6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-sulfonic acid amides | BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) | 2006-02-02 | — | — | US | disclosed |
| CN-1143855-C | I (ortho)-anthranilamide derivatives as anti-coagulants | ���ֹɷݹ�˾ | 2004-03-31 | — | — | CN | disclosed |
| EP-1070061-A4 | OXIDATION PROCESS USING PERIODIC ACID | MERCK & CO INC (US) | 2001-11-07 | — | — | EP | disclosed |
| CN-1282329-A | I (ortho)-anthranilamide derivatives as anti-coagulants | SCHERING AG (DE) | 2001-01-31 | — | — | CN | disclosed |
| EP-1070061-A1 | OXIDATION PROCESS USING PERIODIC ACID | Merck & Co., Inc. (US) | 2001-01-24 | — | — | EP | disclosed |
| US-6093758-A | REACTING AN ARYLOXY-HYDROXY FUNCTIONAL PHOSPHAZENE WITH A HALOGENATED CHLOROPHOSPHATE SELECTED FROM THE GROUP CONSISTING OF ALIPHATIC AND AROMATIC CHLOROPHOSPHATES TO FORM PHOSPHORYLATED PHOSPHAZENES WITH IMPROVED HEAT RESISTANCE | THE PENN STATE RESEARCH FOUNDATION (US) | 2000-07-25 | — | — | US | disclosed |
| WO-1999052899-A1 | OXIDATION PROCESS USING PERIODIC ACID | MERCK & CO., INC. (US) | 1999-10-21 | — | — | WO | disclosed |
| US-5010201-A | Process for the preparation of substituted 2-chloropyridines | BAYER AKTIENGESELLSCHAFT (DE) | 1991-04-23 | — | — | US | disclosed |