⚠ 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 | |
|---|---|---|---|---|
| SCHEMBL20979388 | 0.73 | — | — | |
| SCHEMBL14252471 | 0.69 | — | — | |
| SCHEMBL16215767 | 0.69 | — | — | |
| SCHEMBL7081098 | 0.69 | — | — | |
| SCHEMBL482706 | 0.69 | — | — | |
| SCHEMBL2137186 | 0.69 | — | — | |
| SCHEMBL4653973 | 0.67 | — | — | |
| SCHEMBL14025857 | 0.67 | — | — | |
| SCHEMBL66164 | 0.67 | — | — | |
| SCHEMBL8928316 | 0.65 | — | — |
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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-120057904-A | Halogen and nitrogen element co-doped graphene composite material loading metal active site, hydrogen evolution electrode, preparation method and application | 上海交通大学 | 2025-05-30 | — | — | CN | claimed |
| EP-0006089-B1 | PREPARATION OF IMPACT RESISTANT POLYSTYRENE HAVING IMPROVED TRANSPARENCY | THE DOW CHEMICAL COMPANY (US) | 1983-03-02 | — | — | EP | claimed |
| EP-0006089-A1 | Preparation of impact resistant polystyrene having improved transparency | THE DOW CHEMICAL COMPANY (US) | 1980-01-09 | — | — | EP | claimed |
| US-4100227-A | Transparent impact-resistant polystyrene structure | THE DOW CHEMICAL COMPANY (US) | 1978-07-11 | — | — | US | claimed |
| US-4100228-A | Transparent impact styrene polymer structure | THE DOW CHEMICAL COMPANY (US) | 1978-07-11 | — | — | US | claimed |
| CN-120057904-A | Halogen and nitrogen element co-doped graphene composite material loading metal active site, hydrogen evolution electrode, preparation method and application | 上海交通大学 | 2025-05-30 | — | — | CN | disclosed |
| US-20180223181-A1 | SILOXANE MONOMER, POLYMER THEREOF, COMPOSITION CONTAINING SAID POLYMER, AND ELECTRONIC ELEMENT | DAINIPPON INK & CHEMICALS (JP) | 2018-08-09 | — | — | US | disclosed |
| US-20110071272-A1 | FLUOROSULFONYL GROUP-CONTAINING MONOMER AND ITS POLYMER, AND SULFONIC ACID GROUP-CONTAINING POLYMER | ASAHI GLASS COMPANY, LIMITED (JP) | 2011-03-24 | — | — | US | disclosed |
| US-7470822-B2 | 2,7-Dimethyl-4-octenedial, which can be efficiently utilized in the synthesis of carotenoid compounds containing the conjugated polyene chain of beta-carotene by the double elimination reaction without going through the Ramberg-Backlund reaction; use in food additives and nutraceuticals | MYONGJI UNIVERSITY INDUSTRY AND ACADEMIA COOPERATION (KR) | 2008-12-30 | — | — | US | disclosed |
| US-20080262271-A1 | 2,7-Dimethyl-4-octenedial, which can be efficiently utilized in the synthesis of carotenoid compounds containing the conjugated polyene chain of beta-carotene by double elimination reaction without going through the Ramberg-Backlund reaction; use in food additives and nutraceuticals | MYONGJI UNIVERSITY INDUSTRY AND ACADEMIA COOPERATION (KP) | 2008-10-23 | — | — | US | disclosed |
| WO-2006038764-A1 | ClO DIALDEHYDE, SYNTHETIC METHOD THEREOF, AND SYNTHETIC METHOD OF BETA-CAROTENE USING THE SAME | KOO SANGHO (KR) | 2006-04-13 | — | — | WO | disclosed |
| US-5616762-A | Process for the preparation of 3-halo-and pseudohalo-alkylsilane esters | HUELS AKTIENGESELLSCHAFT (DE) | 1997-04-01 | — | — | US | disclosed |
| EP-0025846-A1 | Improved process for the preparation of vinylcyclopropane derivatives | NATIONAL DISTILLERS AND CHEMICAL CORPORATION (US) | 1981-04-01 | — | — | EP | disclosed |
| US-4252739-A | ALKYLATING AGENT SUCH AS 1,4-DIHALO-2-BUTENE, AN ACTIVE METHYLENE COMPOUND, A CATALYTIC ONIUM COMPOUND, AN ALKALI METAL COMPOUND AND WATER; ONE STEP | EMERY INDUSTRIES, INC. (US) | 1981-02-24 | — | — | US | disclosed |
| EP-0006089-A1 | Preparation of impact resistant polystyrene having improved transparency | THE DOW CHEMICAL COMPANY (US) | 1980-01-09 | — | — | EP | disclosed |
| EP-0000554-A1 | Process for the preparation of oxiranes substituted by halogen alkyl | BAYER AG (DE) | 1979-02-07 | — | — | EP | disclosed |
| EP-0000555-A1 | Process for the preparation of oxiranes substituted by halogen alkyl | BAYER AG (DE) | 1979-02-07 | — | — | EP | disclosed |
| US-4132741-A | Process for producing haloprene | DENKA CHEMICAL CORPORATION (US) | 1979-01-02 | — | — | US | disclosed |
| US-4100227-A | Transparent impact-resistant polystyrene structure | THE DOW CHEMICAL COMPANY (US) | 1978-07-11 | — | — | US | disclosed |
| US-4100228-A | Transparent impact styrene polymer structure | THE DOW CHEMICAL COMPANY (US) | 1978-07-11 | — | — | US | disclosed |