Known targets — ChEMBL curated mechanism
ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1
The experimentally established mechanism targets of Methyl Alcohol. 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 | |
|---|---|---|---|---|
| Methyl Alcohol SCHEMBL9716190 | 0.89 | — | — | |
| Methyl Alcohol SCHEMBL1077779 | 0.89 | — | — | |
| Methyl Alcohol SCHEMBL29123034 | 0.80 | — | — | |
| Methyl Alcohol SCHEMBL9306151 | 0.80 | — | — | |
| Methyl Alcohol SCHEMBL29230035 | 0.80 | — | — | |
| Methyl Alcohol SCHEMBL950847 | 0.80 | — | — | |
| Methyl Alcohol SCHEMBL368033 | 0.80 | — | — | |
| Methyl Alcohol SCHEMBL10877885 | 0.80 | — | — | |
| Methyl Alcohol SCHEMBL5177518 | 0.80 | — | — | |
| Methyl Alcohol SCHEMBL8413048 | 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-117720591-A | Synthesis method of 14-methyl ether epirubicin | 浙江亚瑟医药有限公司 | 2024-03-19 | — | — | CN | claimed |
| CN-117088813-A | Azaanthracene fluorescent dye and preparation method thereof | 岱纳科技(北京)有限公司 | 2023-11-21 | — | — | CN | claimed |
| CN-116120759-A | Method for synthesizing anthracene fluorescent dye | 岱纳科技(北京)有限公司 | 2023-05-16 | — | — | CN | claimed |
| CN-114085145-B | Preparation method of R- (+) -2- (4-hydroxyphenoxy) methyl propionate | 苏州开元民生科技股份有限公司 | 2022-11-08 | — | — | CN | claimed |
| CN-114085145-A | Environment-friendly preparation method of R- (+) -2- (4-hydroxyphenoxy) methyl propionate | 苏州开元民生科技股份有限公司 | 2022-02-25 | — | — | CN | claimed |
| CN-101781305-A | Method for artificially synthesizing galanthamine | TAIZHOU JINZHAO WEIYE FINE CHE | 2010-07-21 | — | — | CN | claimed |
| CN-100389877-C | Supported catalyst for preparing chiral secondary alcohol under normal pressure and method for preparing the same | UNIV FUDAN (CN) | 2008-05-28 | — | — | CN | claimed |
| CN-1827216-A | Supported catalyst for preparing chiral secondary alcohol under normal pressure and method for preparing the same | UNIV FUDAN (CN) | 2006-09-06 | — | — | CN | claimed |
| CN-117720591-A | Synthesis method of 14-methyl ether epirubicin | 浙江亚瑟医药有限公司 | 2024-03-19 | — | — | CN | disclosed |
| CN-117088813-A | Azaanthracene fluorescent dye and preparation method thereof | 岱纳科技(北京)有限公司 | 2023-11-21 | — | — | CN | disclosed |
| CN-116120760-A | Sulfur-containing anthracene fluorescent dye and synthesis method thereof | 岱纳科技(北京)有限公司 | 2023-05-16 | — | — | CN | disclosed |
| CN-116120759-A | Method for synthesizing anthracene fluorescent dye | 岱纳科技(北京)有限公司 | 2023-05-16 | — | — | CN | disclosed |
| CN-114085145-B | Preparation method of R- (+) -2- (4-hydroxyphenoxy) methyl propionate | 苏州开元民生科技股份有限公司 | 2022-11-08 | — | — | CN | disclosed |
| CN-114685399-A | Preparation method of urapidil intermediate 1- (2-methoxyphenyl) piperazine and salt thereof | 河北广祥制药有限公司 | 2022-07-01 | — | — | CN | disclosed |
| US-20100087418-A1 | BENZOXAZEPINE DERIVATIVES AND USE THEREOF | TAKEDA PHARMACEUTICAL COMPANY LIMITED | 2010-04-08 | — | — | US | disclosed |
| EP-2123644-A1 | BENZOXAZEPINE DERIVATIVES AND USE THEREOF | Takeda Pharmaceutical Company Limited (JP) | 2009-11-25 | — | — | EP | disclosed |
| CN-100389877-C | Supported catalyst for preparing chiral secondary alcohol under normal pressure and method for preparing the same | UNIV FUDAN (CN) | 2008-05-28 | — | — | CN | disclosed |
| CN-1827216-A | Supported catalyst for preparing chiral secondary alcohol under normal pressure and method for preparing the same | UNIV FUDAN (CN) | 2006-09-06 | — | — | CN | disclosed |
| CN-1031055-C | Process for preparing dideoxycarbocyclic nucleosides | UNIV MINNESOTA (US) | 1996-02-21 | — | — | CN | disclosed |
| CN-1036015-A | The preparation method of dideoxycarbocyclic nucleosides | UNIV MINNESOTA (US) | 1989-10-04 | — | — | CN | disclosed |