Known targets — ChEMBL curated mechanism
ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1
The experimentally established mechanism targets of Ether. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
⚠ 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 | |
|---|---|---|---|---|
| Ether SCHEMBL4690980 | 1.00 | ALDH1A1 (0.41) | — | |
| Ether SCHEMBL11292739 | 0.90 | — | — | |
| Ether SCHEMBL12501209 | 0.90 | — | — | |
| Ether SCHEMBL1375446 | 0.90 | — | — | |
| Ether SCHEMBL2812813 | 0.90 | — | — | |
| Ether SCHEMBL4855472 | 0.90 | — | — | |
| Ether SCHEMBL11335832 | 0.90 | — | — | |
| Ether SCHEMBL21406 | 0.89 | ALDH1A1 (0.47) | — | |
| Ether SCHEMBL8160191 | 0.89 | ALDH1A1 (0.47) | — | |
| Ether SCHEMBL9248046 | 0.89 | ALDH1A1 (0.47) | — |
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 790 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119365444-A | Synthesis of duloxetine fumarate | 渤健马萨诸塞州股份有限公司 | 2025-01-24 | — | — | CN | claimed |
| CN-117700440-A | Preparation method of functional disiloxane with atypical fluorescence | 山东大学 | 2024-03-15 | — | — | CN | claimed |
| CN-117700750-A | Preparation method of functional polysiloxane with atypical fluorescence | 山东大学 | 2024-03-15 | — | — | CN | claimed |
| CN-117209767-A | Preparation method of amphiphilic functionalized poly (siloxane-thioether) with atypical fluorescence | 山东大学 | 2023-12-12 | — | — | CN | claimed |
| CN-114957247-A | Synthesis method of Rimegepant and intermediate thereof | 上海鼎雅药物化学科技有限公司 | 2022-08-30 | — | — | CN | claimed |
| CN-113185701-B | Metal porphyrin-based porous polymer, preparation thereof and application thereof in catalyzing addition reaction of carbon dioxide and epoxide ring | 浙江理工大学 | 2022-05-27 | — | — | CN | claimed |
| CN-113185701-A | Metal porphyrin-based porous polymer, preparation thereof and application thereof in catalyzing addition reaction of carbon dioxide and epoxide ring | 浙江理工大学 | 2021-07-30 | — | — | CN | claimed |
| CN-108440488-B | Organic porous copolymer multifunctional bionic heterogeneous catalyst and preparation method thereof | 中国科学院大连化学物理研究所 | 2021-06-01 | — | — | CN | claimed |
| CN-108440485-B | Production method of cyclic carbonate | 中国科学院大连化学物理研究所 | 2021-06-01 | — | — | CN | claimed |
| CN-108586514-B | Synthesis method of diisopropylamine silane | 浙江博瑞电子科技有限公司 | 2020-11-10 | — | — | CN | claimed |
| US-20080255170-A1 | Process for the Synthesis of Rosuvastatin Calcium | LEK PHARMACEUTICALS D.D (SI) | 2008-10-16 | — | — | US | claimed |
| EP-1912953-A1 | PROCESS FOR THE SYNTHESIS OF ROSUVASTATIN CALCIUM | LEK Pharmaceuticals D.D. (SI) | 2008-04-23 | — | — | EP | claimed |
| WO-2007017117-A1 | PROCESS FOR THE SYNTHESIS OF ROSUVASTATIN CALCIUM | LEK PHARMACEUTICALS D.D. (SI) | 2007-02-15 | — | — | WO | claimed |
| CN-1191230-C | Method for preparing neuraminidase inhibitor RO-64-0796 | HOFFMANN LA ROCHE (CH) | 2005-03-02 | — | — | CN | claimed |
| CN-1277957-A | Method for preparing neuraminidase inhibitor RO-64-0796 | HOFFMANN LA ROCHE (CH) | 2000-12-27 | — | — | CN | claimed |
| US-5681951-A | REACTING PENICILLIN DERIVATIVE HAVING SULFINYL OR SULFONYL GROUP IN 2 POSITION WITH SUBSTITUTED MERCAPTAN IN PRESENCE OF SALT OF GROUP IIA OR IIIA ELEMENT | SANKYO COMPANY, LIMITED (JP) | 1997-10-28 | — | — | US | claimed |
| EP-0403150-B1 | Process for the preparation of tigogenin beta-cellobioside | PFIZER (US) | 1994-11-17 | — | — | EP | claimed |
| US-5010185-A | Processes for tigogenin beta-cellobioside | PFIZER INC. (US) | 1991-04-23 | — | — | US | claimed |
| EP-0403150-A2 | Process for the preparation of tigogenin beta-cellobioside | PFIZER INC. (US) | 1990-12-19 | — | — | EP | claimed |
| CN-86104224-A | The preparation method of imidazo [2, the 1-b] thiazole that pyridyl replaces | — | 1987-02-11 | — | — | CN | claimed |