⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL16231365 | 1.00 | — | — | |
| SCHEMBL4919210 | 1.00 | — | — | |
| SCHEMBL1053407 | 0.97 | — | — | |
| SCHEMBL18707170 | 0.97 | TP53 (0.46) | — | |
| SCHEMBL1056494 | 0.97 | — | — | |
| SCHEMBL11165174 | 0.97 | TP53 (0.46) | — | |
| SCHEMBL18706728 | 0.97 | TP53 (0.46) | — | |
| SCHEMBL4731258 | 0.97 | TP53 (0.46) | — | |
| SCHEMBL5195 | 0.97 | — | — | |
| SCHEMBL8086336 | 0.97 | TP53 (0.46) | — |
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 543 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2648675-A1 | HAIR RELAXING AND STRAIGHTENING COMPOSITIONS | International Flora Technologies, Ltd. (US) | 2013-10-16 | — | — | EP | claimed |
| US-20120148517-A1 | Hair Relaxing and Straightening Compositions | INTERNATIONAL FLORA TECHNOLOGIES, LTD. (US) | 2012-06-14 | — | — | US | claimed |
| WO-2012078658-A1 | HAIR RELAXING AND STRAIGHTENING COMPOSITIONS | INTERNATIONAL FLORA TECHNOLOGIES, LTD. (US) | 2012-06-14 | — | — | WO | claimed |
| CN-101712665-B | Method for synthesizing butyrolactone and butyrolactone obtained by same | BEIJING PEKING UNIVERSITY ZOTEQ CO LTD | 2012-01-11 | — | — | CN | claimed |
| CN-101712665-A | Method for synthesizing butyrolactone and butyrolactone obtained by same | BEIJING PEKING UNIVERSITY ZOTE | 2010-05-26 | — | — | CN | claimed |
| CN-1235851-C | Method for producing alkenyl ethers | BASF AG (DE) | 2006-01-11 | — | — | CN | claimed |
| EP-1268380-B1 | METHOD FOR PRODUCING ALKENYL ETHERS | BASF AG (DE) | 2003-09-17 | — | — | EP | claimed |
| US-20030114715-A1 | Method for producing alkenyl ethers | BOETTCHER ARND (DE) | 2003-06-19 | — | — | US | claimed |
| US-12486248-B2 | 2,4,5-trisubstituted 1,2,4-triazolones useful as inhibitors of DHODH | BAYER AKTIENGESELLSCHAFT (DE) | 2025-12-02 | — | — | US | disclosed |
| CN-115557907-B | 2,4, 5-Trisubstituted 1,2, 4-triazolones as DHODH inhibitors | 拜耳股份有限公司 | 2024-12-06 | — | — | CN | disclosed |
| EP-4182301-B1 | AMIDO CYCLOHEXANE ACID DERIVATIVES AS LPA RECEPTOR INHIBITORS | CHIESI FARM SPA (IT) | 2024-09-04 | — | — | EP | disclosed |
| US-20240229063-A1 | TRANSGENIC CORN EVENT ZM_CSM63715 AND METHODS FOR DETECTION AND USES THEREOF | MONSANTO TECHNOLOGY LLC (US) | 2024-07-11 | — | — | US | disclosed |
| EP-4396163-A1 | HERBICIDAL MALONAMIDES CONTAINING MONOCYCLIC HETEROAROMATIC RINGS | BASF SE (DE) | 2024-07-10 | — | — | EP | disclosed |
| EP-4396173-A1 | HERBICIDAL MALONAMIDES CONTAINING A CONDENSED RING SYSTEM | BASF SE (DE) | 2024-07-10 | — | — | EP | disclosed |
| US-4177302-A | DIGLYCIDYL ETHER OF HYDANTOIN COMPOUND, POLYAMIDOAMINE, CURING | CIBA-GEIGY CORPORATION (US) | 1979-12-04 | — | — | US | disclosed |
| US-4118573-A | ANTIVIRAL AGENTS | ELI LILLY AND COMPANY (US) | 1978-10-03 | — | — | US | disclosed |
| US-4025638-A | ANTHELMINTICS | SMITHKLINE CORPORATION (US) | 1977-05-24 | — | — | US | disclosed |
| US-4018790-A | VIRICIDES | ELI LILLY AND COMPANY (US) | 1977-04-19 | — | — | US | disclosed |
| US-4008243-A | Antiviral thiazolinyl or thiazinyl benzimidazole esters | ELI LILLY AND COMPANY (US) | 1977-02-15 | — | — | US | disclosed |
| US-3957883-A | PROCESS FOR OXIDIZING ORGANIC COMPOUNDS TO PEROXIDES | ATLANTIC RESEARCH CORPORATION (US) | 1976-05-18 | — | — | US | disclosed |