Known targets — ChEMBL curated mechanism
ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4
The experimentally established mechanism targets of Methoxymethane. 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 | |
|---|---|---|---|---|
| Methoxymethane SCHEMBL27502533 | 1.00 | — | — | |
| Methoxymethane SCHEMBL29243163 | 0.91 | — | — | |
| Methoxymethane SCHEMBL27699680 | 0.91 | — | — | |
| Methoxymethane SCHEMBL28440367 | 0.91 | — | — | |
| Methoxymethane SCHEMBL868 | 0.89 | — | — | |
| Methoxymethane SCHEMBL16998540 | 0.89 | — | — | |
| Methoxymethane SCHEMBL5707121 | 0.89 | — | — | |
| Methoxymethane SCHEMBL12190176 | 0.89 | — | — | |
| Methoxymethane SCHEMBL23803961 | 0.80 | — | — | |
| Methoxymethane SCHEMBL727682 | 0.80 | — | — |
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 40 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-120201913-A | Perovskite solar cell and preparation method thereof | 晶澳太阳能有限公司 | 2025-06-24 | — | — | CN | claimed |
| CN-115491190-B | Luminous film and preparation method and application thereof | 五邑大学 | 2025-02-07 | — | — | CN | claimed |
| CN-109694350-B | Compound containing fluoromethyl and preparation method thereof | 中国科学院上海有机化学研究所 | 2023-05-09 | — | — | CN | claimed |
| CN-115491190-A | Luminescent film and preparation method and application thereof | 五邑大学 | 2022-12-20 | — | — | CN | claimed |
| CN-115275025-A | Two-dimensional large-area organic-inorganic hybrid perovskite, preparation method thereof and photoelectric detector | 华中科技大学 | 2022-11-01 | — | — | CN | claimed |
| CN-114497431-A | Quasi-two-dimensional film preparation method | 吉林大学 | 2022-05-13 | — | — | CN | claimed |
| CN-111916561-A | Perovskite solar cell, tandem solar cell and battery pack | 隆基绿能科技股份有限公司 | 2020-11-10 | — | — | CN | claimed |
| CN-108624953-B | Preparation method of ultrathin perovskite single crystal material | 苏州大学 | 2020-07-28 | — | — | CN | claimed |
| CN-120201913-A | Perovskite solar cell and preparation method thereof | 晶澳太阳能有限公司 | 2025-06-24 | — | — | CN | disclosed |
| CN-114008065-B | Glycyrrhetinic acid derivatives for the treatment of hyperkalemia | 阿德利克斯股份有限公司 | 2025-03-11 | — | — | CN | disclosed |
| CN-115491190-B | Luminous film and preparation method and application thereof | 五邑大学 | 2025-02-07 | — | — | CN | disclosed |
| CN-119156385-A | Fused bicyclic heteroaromatic compounds and their use in the treatment of cancer | 阿斯利康(瑞典)有限公司 | 2024-12-17 | — | — | CN | disclosed |
| CN-222090033-U | Stacked solar cell and electricity utilization device | 天合光能股份有限公司 | 2024-11-29 | — | — | CN | disclosed |
| CN-118974037-A | Benzobicyclo compound and preparation method and application thereof | 广州市联瑞制药有限公司 | 2024-11-15 | — | — | CN | disclosed |
| CN-108624953-B | Preparation method of ultrathin perovskite single crystal material | 苏州大学 | 2020-07-28 | — | — | CN | disclosed |
| US-7645894-B2 | Direct process for making cyclic dimethylsiloxane oligomers | BERNARD KANNER (US) | 2010-01-12 | — | — | US | disclosed |
| WO-2007124031-A2 | NOVEL DIRECT PROCESS | BERNARD KANNER AND GEORGE A. SKOLER, PARTNERSHIP (US) | 2007-11-01 | — | — | WO | disclosed |
| US-20070249855-A1 | By reacting in situ methyl bromide, dimethyl ether and activated silicon particles; copper catalyst; fluidization | BERNARD KANNER AND GEORGE A. SKOLER, PARTNERSHIP (US) | 2007-10-25 | — | — | US | disclosed |
| US-5315017-A | Peroxidation and eicosanoid biosynthesis inhibition | ADIR ET COMPAGNIE (FR) | 1994-05-24 | — | — | US | disclosed |
| CN-86107486-A | The synthetic method of Biphenylylmethylcarbinol | — | 1988-05-11 | — | — | CN | disclosed |