⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL20436910 | 1.00 | — | — | |
| Formamide SCHEMBL26614879 | 0.90 | — | — | |
| Tert-Butyl Formate SCHEMBL28044015 | 0.81 | TDP1 (0.41) | — | |
| SCHEMBL28311545 | 0.76 | — | — | |
| SCHEMBL10076030 | 0.75 | — | — | |
| SCHEMBL13465078 | 0.75 | — | — | |
| SCHEMBL21850852 | 0.74 | — | — | |
| SCHEMBL22193773 | 0.74 | — | — | |
| SCHEMBL9691031 | 0.73 | — | — | |
| SCHEMBL5850298 | 0.73 | HTR1A (0.36) | — |
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 92 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119875044-A | Preparation method and application of super-alkali-resistant bipiperidinium cross-linked anion exchange membrane | 宿迁时代储能科技有限公司 | 2025-04-25 | — | — | CN | claimed |
| CN-115548397-A | Preparation method and application of cross-linked anion exchange membrane | 宿迁时代储能科技有限公司 | 2022-12-30 | — | — | CN | claimed |
| CN-1125053-C | Method of preparing norbenzomorphane as an intermediate in the preparation of pharmaceutically useful benzomorphane derivatives, in particular (-)-(1R, 5S, 2'R')-3'-hydroxy-2-(2-methoxypropyl)-5,..... | BOEHRINGER INGELHEIM KG (DE) | 2003-10-22 | — | — | CN | claimed |
| CN-119875044-A | Preparation method and application of super-alkali-resistant bipiperidinium cross-linked anion exchange membrane | 宿迁时代储能科技有限公司 | 2025-04-25 | — | — | CN | disclosed |
| US-20240124447-A1 | INHIBITORS OF THE MENIN-MLL INTERACTION | VITAE PHARMACEUTICALS, LLC (US) | 2024-04-18 | — | — | US | disclosed |
| CN-115232129-B | PARP1 selective inhibitor and preparation method and application thereof | 上海闻耐医药科技有限公司 | 2023-12-01 | — | — | CN | disclosed |
| US-11739085-B2 | Inhibitors of the menin-MLL interaction | VITAE PHARMACEUTICALS, LLC (US) | 2023-08-29 | — | — | US | disclosed |
| CN-114456286-B | Catalyst system for olefin polymerization and application thereof | 中国石油化工股份有限公司 | 2023-08-15 | — | — | CN | disclosed |
| CN-114456290-B | Catalyst system for olefin polymerization and prepolymerized catalyst composition | 中国石油化工股份有限公司 | 2023-07-21 | — | — | CN | disclosed |
| US-20230192700-A1 | PYRAZOLOPYRAZINES ACTING ON CANCERS VIA INHIBITION OF CDK12 | BAYER AKTIENGESELLSCHAFT (DE) | 2023-06-22 | — | — | US | disclosed |
| EP-4114837-A1 | PYRAZOLOPYRAZINES ACTING ON CANCERS VIA INHIBITION OF CDK12 | Bayer Aktiengesellschaft (DE) | 2023-01-11 | — | — | EP | disclosed |
| WO-1997047302-A1 | INHIBITION OF SEROTONIN REUPTAKE | ELI LILLY AND COMPANY (US) | 1997-12-18 | — | — | WO | disclosed |
| EP-0724570-A1 | AMIDINO DERIVATIVES USEFUL AS NITRIC OXIDE SYNTHASE INHIBITORS | G.D. SEARLE & CO. (US) | 1996-08-07 | — | — | EP | disclosed |
| WO-1995011231-A1 | AMIDINO DERIVATIVES USEFUL AS NITRIC OXIDE SYNTHASE INHIBITORS | G. D. SEARLE & CO. (US) | 1995-04-27 | — | — | WO | disclosed |
| EP-0094018-B1 | 4-ARYL-4-PIPERIDINECARBINOLS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1988-03-09 | — | — | EP | disclosed |
| EP-0119558-B1 | STEREOSELECTIVE REDUCTION OF 2- OR 3-SUBSTITUTED 4-PIPERIDONES WITH SODIUM BOROHYDRIDE | HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) | 1987-06-24 | — | — | EP | disclosed |
| US-4496732-A | LOW TEMPERATURE; USING INORGANIC ACID | HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) | 1985-01-29 | — | — | US | disclosed |
| US-4485109-A | 4-Aryl-4-piperidinecarbinols | E. I. DU PONT DE NEMOURS AND COMPANY (US) | 1984-11-27 | — | — | US | disclosed |
| EP-0119558-A1 | Stereoselective reduction of 2- or 3-substituted 4-piperidones with sodium borohydride | HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) | 1984-09-26 | — | — | EP | disclosed |
| EP-0094018-A2 | 4-Aryl-4-piperidinecarbinols | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1983-11-16 | — | — | EP | disclosed |