⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL3111006 | 0.93 | ALDH1A1 (0.54) | — | |
| SCHEMBL630948 | 0.91 | ALDH1A1 (0.52) | — | |
| SCHEMBL11581868 | 0.91 | ALDH1A1 (0.52) | — | |
| SCHEMBL2125096 | 0.91 | ALDH1A1 (0.52) | — | |
| SCHEMBL52421 | 0.91 | ALDH1A1 (0.52) | — | |
| SCHEMBL1300597 | 0.91 | ALDH1A1 (0.52) | — | |
| SCHEMBL8813032 | 0.91 | ALDH1A1 (0.52) | — | |
| SCHEMBL8811545 | 0.91 | ALDH1A1 (0.52) | — | |
| SCHEMBL2124125 | 0.91 | ALDH1A1 (0.52) | — | |
| SCHEMBL8814291 | 0.91 | ALDH1A1 (0.52) | — |
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 291 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119746938-A | Forming method of super-crosslinked phosphine ligand polymer Rh catalyst, formed catalyst and application thereof | 中国科学院青岛生物能源与过程研究所 | 2025-04-04 | — | — | CN | claimed |
| CN-119552076-A | Synthesis method of tomato leaf miner sex pheromone compound | 宁波纽康生物技术有限公司 | 2025-03-04 | — | — | CN | claimed |
| CN-119390566-A | Method for preparing 4-acetoxybutyraldehyde by hydroformylation of allyl acetate | 中国科学院青岛生物能源与过程研究所 | 2025-02-07 | — | — | CN | claimed |
| CN-118993887-A | Method for preparing 4-acetoxybutyraldehyde by hydroformylation | 万华化学集团股份有限公司 | 2024-11-22 | — | — | CN | claimed |
| CN-115772081-B | Preparation method of 4-ethoxy-2-methyl alkenyl butyraldehyde | 万华化学集团营养科技有限公司 | 2024-11-12 | — | — | CN | claimed |
| CN-118666676-A | Preparation method of 2-methylene-4-acetoxyl butyraldehyde | 万华化学集团股份有限公司 | 2024-09-20 | — | — | CN | claimed |
| CN-114605261-B | Preparation method of 4-acetoxyl butyraldehyde | 万华化学集团股份有限公司 | 2023-05-26 | — | — | CN | claimed |
| CN-115772081-A | Preparation method of 4-ethoxy-2-methylal | 万华化学集团股份有限公司 | 2023-03-10 | — | — | CN | claimed |
| CN-113603591-B | Preparation method of 4-acetoxybutyraldehyde | 万华化学集团股份有限公司（CN） | 2023-01-13 | — | — | CN | claimed |
| CN-114920643-A | Method for preparing 4-acetoxy butyraldehyde from allyl acetate | 华东师范大学 | 2022-08-19 | — | — | CN | claimed |
| US-5175162-A | Anxiolytic, antiepilepic agents | YOSHITIOMI PHARMACEUTICAL INDUSTRIES LTD. (JP) | 1992-12-29 | — | — | US | claimed |
| US-4873362-A | REACTING AN ACYLOXYACETALDEHYDE WITH AN ALDEHYDE USING AN AMINE AND ACID CATALYST SYSTEM | BASF AKTIENGESELLSCHAFT (DE) | 1989-10-10 | — | — | US | claimed |
| US-4806678-A | 4-ACYLOXYBUTYRALDEHYDES; PROMOTERS OF GERMANE, DIPHENYL SULFIDE, SUCCINONITRILE OR BIPYRIDINE/2,2*-/ | TEXACO INC. (US) | 1989-02-21 | — | — | US | claimed |
| US-4777302-A | USING RUTHENIUM CATALYST FORMED BY REDUCING ALKALI METAL RUTHENATE WITH METHANOL, FORMALDEHYDE OR FORMIC ACID | MITSUBISHI CHEMICAL INDUSTRIES LIMITED (JP) | 1988-10-11 | — | — | US | claimed |
| EP-0191542-B1 | ARYLCYCLOBUTYLALKYL AMINES AND THEIR USE AS ANTIDEPRESSIVE MEDICINES | The Boots Company PLC (GB) | 1988-06-08 | — | — | EP | claimed |
| US-4058556-A | FROM ALLYL ACETATE, CARBON MONOXIDE AND HYDROGEN, COBALT CARBONYL CATALYST, SOLVENT | BAYER AKTIENGESELLSCHAFT (DT) | 1977-11-15 | — | — | US | claimed |
| US-4035408-A | Process for hydroformylation of allyl acetate or 1-propenyl acetate | GENERAL ELECTRIC COMPANY (US) | 1977-07-12 | — | — | US | claimed |
| US-4016201-A | Process for the preparation of acetoxybutanols | BAYER AKTIENGESELLSCHAFT (DT) | 1977-04-05 | — | — | US | claimed |
| US-3943166-A | Separation of an isomeric mixture of acetoxy-aldehydes by catalytic decomposition of an aldehyde to acetic acid and methacrolein | GENERAL ELECTRIC COMPANY (US) | 1976-03-09 | — | — | US | claimed |
| US-3941851-A | 1,4-Butanediol from hydrogenated hydroformylated allyl acetate | GENERAL ELECTRIC COMPANY (US) | 1976-03-02 | — | — | US | claimed |