⚠ 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 | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL8555531 | 0.97 | — | — | |
| Water SCHEMBL4737329 | 0.97 | — | — | |
| SCHEMBL28366269 | 0.97 | — | — | |
| Formaldehyde SCHEMBL11223994 | 0.94 | ALDH1A1 (0.41) | — | |
| SCHEMBL28370523 | 0.94 | ALDH1A1 (0.41) | — | |
| Methyl Alcohol SCHEMBL1615268 | 0.94 | HMGCR (0.48) | — | |
| Benzene SCHEMBL1935095 | 0.94 | ALDH1A1 (0.41) | — | |
| Acetone SCHEMBL1591738 | 0.91 | HMGCR (0.46) | — | |
| Acetic Acid SCHEMBL1591292 | 0.91 | HMGCR (0.46) | — | |
| Cyclohexane SCHEMBL7317750 | 0.91 | ALDH1A1 (0.39) | — |
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 1024 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-120114534-A | Ginseng and tortoise body resistance-strengthening wine and quality detection method and application thereof | 常熟雷允上制药有限公司 | 2025-06-10 | — | — | CN | claimed |
| CN-118258945-A | Radix angelicae pubescentis adulterated thin layer identification method for finished product and raw material of angelica formula granule | 华润三九(六安)中药材产业发展有限公司 | 2024-06-28 | — | — | CN | claimed |
| CN-118063390-A | Diamine with naphthyridone structure, thermosetting polyimide resin and preparation method thereof | 西北工业大学 | 2024-05-24 | — | — | CN | claimed |
| CN-117887086-A | Application of halogen functionalized metal organic framework material in storage and delivery of fluorine-containing electron special gas | 华为技术有限公司 | 2024-04-16 | — | — | CN | claimed |
| WO-2024074141-A1 | POROUS MATERIAL AND APPLICATION THEREOF | 华为技术有限公司 | 2024-04-11 | — | — | WO | claimed |
| CN-117783407-A | Quality control method of yang-warming and diuresis-promoting pharmaceutical composition | 康普药业股份有限公司 | 2024-03-29 | — | — | CN | claimed |
| CN-116854913-A | Preparation method of high-impact-resistance bismaleimide resin | 西北工业大学 | 2023-10-10 | — | — | CN | claimed |
| CN-116854679-A | Novel epoxy resin containing imide unit and preparation method thereof | 西北工业大学 | 2023-10-10 | — | — | CN | claimed |
| EP-2887061-B1 | METHOD FOR BIOMOLECULE ANALYSIS USING RAMAN SPECTROSCOPY | JAPAN SCIENCE & TECH AGENCY (JP) | 2023-09-27 | — | — | EP | claimed |
| CN-116693997-A | Oil-resistant high-low temperature-resistant UV-resistant cable sheath material and preparation method thereof | 镇江市华银仪表电器有限公司 | 2023-09-05 | — | — | CN | claimed |
| US-20030195365-A1 | CC-1065 analog synthesis | IMMUNOGEN INC. | 2003-10-16 | — | — | US | claimed |
| US-6586618-B1 | Amination 1,3-dihydoxynaphthalene, then blocking, iodination, alkylation, cyclization and deblocking to give (5-hydroxy-3-amino-1-(S)-(chloromethyl)-1,2-dihydro-3H-benz(e)indole), used as chemical intermediates of antitumor agents | IMMUNOGEN INC. | 2003-07-01 | — | — | US | claimed |
| US-6534660-B1 | Halogenation, alkylation and ring-closure of protected 2-amino-4-hydroxynaphthalene under suitable conditions to provide desired racemate, isolating (-) isomer, removing protecting groups | IMMUNOGEN, INC. | 2003-03-18 | — | — | US | claimed |
| EP-1104424-A4 | PROCESS FOR THE SYNTHESIS OF CARBAPENEM INTERMEDIATES, AND COMPOUNDS PRODUCED | MERCK & CO INC (US) | 2002-01-23 | — | — | EP | claimed |
| EP-1104424-A1 | PROCESS FOR THE SYNTHESIS OF CARBAPENEM INTERMEDIATES, AND COMPOUNDS PRODUCED | Merck & Co., Inc. (US) | 2001-06-06 | — | — | EP | claimed |
| WO-1999065921-A1 | PROCESS FOR THE SYNTHESIS OF CARBAPENEM INTERMEDIATES, AND COMPOUNDS PRODUCED | MERCK & CO., INC. (US) | 1999-12-23 | — | — | WO | claimed |
| EP-0244167-B1 | IMPROVED PROCESS FOR PREPARING POLY (ARYL ETHERS) AND POLY (ARYL ETHER KETONES) | AMOCO CORPORATION (US) | 1990-04-04 | — | — | EP | claimed |
| US-4748227-A | Process for preparing poly(aryl ether)ketones using a sodium carbonate/organic acid salt catalyst | AMOCO CORPORATION (US) | 1988-05-31 | — | — | US | claimed |
| EP-0244167-A1 | Improved process for preparing poly (aryl ethers) and poly (aryl ether ketones) | AMOCO CORPORATION (US) | 1987-11-04 | — | — | EP | claimed |
| US-4565657-A | Process for the production of 17α-acyloxy-6-chloro-1α,2α-m | SCHERING AKTIENGESELLSCHAFT (DE) | 1986-01-21 | — | — | US | claimed |