⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL14175014 | 1.00 | — | — | |
| SCHEMBL283751 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL20605479 | 0.97 | — | — | |
| Hydrochloric Acid SCHEMBL631154 | 0.97 | — | — | |
| SCHEMBL26622824 | 0.82 | KDM4E (0.32) | — | |
| SCHEMBL235759 | 0.81 | KDM4E (0.36) | — | |
| SCHEMBL317785 | 0.81 | KDM4E (0.36) | — | |
| SCHEMBL516493 | 0.79 | TSHR (0.32) | — | |
| SCHEMBL12779438 | 0.78 | — | — | |
| Hydrochloric Acid SCHEMBL10694337 | 0.77 | KDM4E (0.34) | — |
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 137 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-114539195-A | Ludartin derivative, pharmaceutical composition thereof, preparation method and application thereof | 中国科学院昆明植物研究所 | 2022-05-27 | — | — | CN | claimed |
| US-11094526-B2 | Liquid composition for imparting alcohol-repellency to semiconductor substrate material, and method for treating surface of semiconductor substrate using said liquid composition | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 2021-08-17 | — | — | US | claimed |
| EP-3404700-B1 | LIQUID COMPOSITION FOR IMPARTING ALCOHOL-REPELLENCY TO SEMICONDUCTOR SUBSTRATE MATERIAL, AND METHOD FOR TREATING SURFACE OF SEMICONDUCTOR SUBSTRATE USING SAID LIQUID COMPOSITION | MITSUBISHI GAS CHEMICAL CO (JP) | 2020-05-13 | — | — | EP | claimed |
| US-20190019672-A1 | LIQUID COMPOSITION FOR IMPARTING ALCOHOL-REPELLENCY TO SEMICONDUCTOR SUBSTRATE MATERIAL, AND METHOD FOR TREATING SURFACE OF SEMICONDUCTOR SUBSTRATE USING SAID LIQUID COMPOSITION | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 2019-01-17 | — | — | US | claimed |
| EP-3404700-A1 | LIQUID COMPOSITION FOR IMPARTING ALCOHOL-REPELLENCY TO SEMICONDUCTOR SUBSTRATE MATERIAL, AND METHOD FOR TREATING SURFACE OF SEMICONDUCTOR SUBSTRATE USING SAID LIQUID COMPOSITION | Mitsubishi Gas Chemical Company, Inc. (JP) | 2018-11-21 | — | — | EP | claimed |
| CN-102869367-A | Novel cyclic peptides | SCYNEXIS INC | 2013-01-09 | — | — | CN | claimed |
| CN-102775356-A | 4-aminoquinazoline derivative and application thereof | JIANGSU HENGYI PHARMACEUTICAL CO LTD | 2012-11-14 | — | — | CN | claimed |
| CN-102083852-A | Cyclosporin analogs and their use in the treatment of HCV infections | SCYNEXIS INC | 2011-06-01 | — | — | CN | claimed |
| EP-2061776-A1 | ARYL SULFAMIDE DERIVATIVES AND METHODS OF THEIR USE | Wyeth a Corporation of the State of Delaware (US) | 2009-05-27 | — | — | EP | claimed |
| WO-2008073459-A1 | ARYL SULFAMIDE DERIVATIVES AND METHODS OF THEIR USE | WYETH (US) | 2008-06-19 | — | — | WO | claimed |
| WO-2024026056-A2 | HETEROARYL COMPOUNDS AS EGFR INHIBITORS AND THEIR USES | ACCUTAR BIOTECHNOLOGY, INC. (US) | 2024-02-01 | — | — | WO | disclosed |
| WO-2023227125-A1 | NEW FUSED-HETEROCYCLIC COMPOUND AS CDK INHIBITOR AND USE THEREOF | 杭州德睿智药科技有限公司 | 2023-11-30 | — | — | WO | disclosed |
| EP-3705478-B1 | TRIAZINE COMPOUND AND PHARMACEUTICALLY ACCEPTABLE SALT THEREOF | SHENZHEN FORWARD PHARMACEUTICALS CO LTD (CN) | 2023-10-04 | — | — | EP | disclosed |
| EP-3670513-B1 | FGFR INHIBITOR AND MEDICAL APPLICATION THEREOF | CSPC ZHONGQI PHARMACEUTICAL TECH SHIJIAZHUANG CO LTD (CN) | 2023-09-20 | — | — | EP | disclosed |
| US-20230227472-A1 | FUSED PYRIDONE COMPOUND, AND PREPARATION METHOD THEREFOR AND USE THEREOF | SHANGHAI JEMINCARE PHARMACEUTICALS CO., LTD (CN) | 2023-07-20 | — | — | US | disclosed |
| US-4026945-A | REACTION PRODUCT OF DIFUNCTIONAL TERTIARY AMINES AND 1,4-DIHALO-2-BUTENE | MILLMASTER ONYX CORPORATION (US) | 1977-05-31 | — | — | US | disclosed |
| US-4025617-A | Anti-microbial quaternary ammonium co-polymers | MILLMASTER ONYX CORPORATION (US) | 1977-05-24 | — | — | US | disclosed |
| US-3966904-A | Quaternary ammonium co-polymers for controlling the proliferation of bacteria | MILLMASTER ONYX CORPORATION (US) | 1976-06-29 | — | — | US | disclosed |
| US-3961042-A | BACTERICIDES | MILLMASTER ONYX CORPORATION (US) | 1976-06-01 | — | — | US | disclosed |
| US-3933812-A | ANTIMICROBIAL QUATERNARY AMMONIUM COPOLYMERS | MILLMASTER ONYX CORPORATION (US) | 1976-01-20 | — | — | US | disclosed |