Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | LMNA | P02545 | 1/20 | 0.65 |
| ▸ | MAPT | P10636 | 1/20 | 0.65 |
| ▸ | HTT | P42858 | 1/20 | 0.65 |
| ▸ | BLM | P54132 | 1/20 | 0.65 |
| ▸ | MAOB | P27338 | 2/20 | 0.56 |
| ▸ | AHR | P35869 | 3/20 | 0.54 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.54 |
| ▸ | MEN1 | O00255 | 2/20 | 0.50 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.50 |
| ▸ | NPC1 | O15118 | 1/20 | 0.50 |
| ▸ | CASP3 | P42574 | 1/20 | 0.50 |
| ▸ | RAB9A | P51151 | 1/20 | 0.50 |
| ▸ | SENP7 | Q9BQF6 | 1/20 | 0.50 |
| ▸ | MAOA | P21397 | 1/20 | 0.49 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.48 |
| ▸ | HSD17B10 | Q99714 | 1/20 | 0.48 |
| ▸ | TDP1 | Q9NUW8 | 1/20 | 0.48 |
| ▸ | ABCG2 | Q9UNQ0 | 1/20 | 0.48 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.47 |
| ▸ | HSP90AA1 | P07900 | 1/20 | 0.46 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
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 | |
|---|---|---|---|---|
| SCHEMBL29459415 | 1.00 | LMNA (0.65) | LMNAMAPTHTTBLMMAOB | |
| SCHEMBL1136696 | 0.98 | MAPT (0.63) | LMNAMAPTHTTBLMMAOB | |
| SCHEMBL30304403 | 0.98 | MAPT (0.63) | LMNAMAPTHTTBLMMAOB | |
| Methyl Alcohol SCHEMBL28062203 | 0.93 | MAPT (0.59) | LMNAMAPTHTTBLMMAOB | |
| SCHEMBL20741831 | 0.86 | LMNA (0.61) | LMNAMAPTHTTBLMMAOB | |
| SCHEMBL661042 | 0.85 | MAPT (0.87) | LMNAMAPTHTTBLMMAOB | |
| Phenol SCHEMBL27725353 | 0.84 | CYP3A4 (0.55) | LMNAMAPTHTTBLMMAOB | |
| SCHEMBL9037655 | 0.83 | MAPT (0.83) | LMNAMAPTHTTBLMMAOB | |
| SCHEMBL7759290 | 0.82 | CA12 (0.56) | LMNAMAPTHTTBLMMAOB | |
| SCHEMBL21272951 | 0.81 | BLM (0.61) | LMNAMAPTHTTBLMMAOB |
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 1344 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4551680-A2 | METHODS OF MANUFACTURE OF R-MDMA | Mind Medicine, Inc. (US) | 2025-05-14 | — | — | EP | claimed |
| CN-119998433-A | Method for producing R-MDMA | 思维医学股份有限公司 | 2025-05-13 | — | — | CN | claimed |
| CN-116041153-B | Direct cross coupling method of aryl thioether and aryl bromine | 南京工业大学 | 2024-05-24 | — | — | CN | claimed |
| CN-116253623-B | Direct cross-coupling method of aryl fluorine sulfate and aryl bromine | 南京工业大学 | 2024-04-05 | — | — | CN | claimed |
| CN-113527270-B | Medical intermediate of PROTAC molecule targeting monoacylglycerol lipase, preparation method and application | 河南大学 | 2024-03-01 | — | — | CN | claimed |
| WO-2024011067-A2 | METHODS OF MANUFACTURE OF R-MDMA | Mind Medicine, Inc. (US) | 2024-01-11 | — | — | WO | claimed |
| US-20240010628-A1 | METHODS OF MANUFACTURE OF R-MDMA | Mind Medicine, Inc. (US) | 2024-01-11 | — | — | US | claimed |
| CN-114591128-B | Direct cross-coupling method of aryl sulfide salt and aryl bromide | 南京工业大学 | 2023-08-22 | — | — | CN | claimed |
| CN-116573994-A | Direct cross-coupling method of triazine ester and aryl bromide | 南京工业大学 | 2023-08-11 | — | — | CN | claimed |
| CN-116554009-A | Electrophilic cross-coupling reaction method of aryl sulfone or heteroaryl sulfone and aryl bromide | 南京工业大学 | 2023-08-08 | — | — | CN | claimed |
| CN-113999263-A | Synthesis method of tri-substituted phosphine oxide compound | 苏州欣诺科生物科技有限公司 | 2022-02-01 | — | — | CN | claimed |
| CN-215538600-U | Extraction tank for producing 4-bromo-1, 2-methylenedioxybenzene | 苏州兴华高新材料科技有限公司 | 2022-01-18 | — | — | CN | claimed |
| CN-113527270-A | Medicine intermediate of PROTAC molecule of targeted monoacylglycerol lipase, preparation method and application | 河南大学 | 2021-10-22 | — | — | CN | claimed |
| CN-113480513-A | Preparation method of ilexlyamine | 北京斯利安健康科技有限公司 | 2021-10-08 | — | — | CN | claimed |
| CN-110724047-B | Method for preparing aromatic carboxylic acid compound | 中国科学院大连化学物理研究所 | 2020-10-30 | — | — | CN | claimed |
| CN-110724047-A | Method for preparing aromatic carboxylic acid compound | 中国科学院大连化学物理研究所 | 2020-01-24 | — | — | CN | claimed |
| CN-102329199-B | Method for synthesizing biphenyl compounds under composite catalytic actions of Pd/C and crown ether | UNIV HEILONGJIANG | 2014-04-02 | — | — | CN | claimed |
| CN-101243030-B | Method for producing 4-halocatechol compound | UBE INDUSTRIES, LTD. (JP) | 2012-02-01 | — | — | CN | claimed |
| CN-101243030-A | Method for producing 4-halocatechol compound | UBE INDUSTRIES (JP) | 2008-08-13 | — | — | CN | claimed |
| US-4605749-A | R)ACTING AN ORGANIC HALIDE WITH CARBON MONOXIDE USING A TRAN>ITION METAL CATALYST, A HYDROGEN DONOR, AND A BASE AT LOW PRESSURE | STATE OF ISRAEL, PRIME MINISTER'S OFFICE, ATOMIC ENERGY COMMISSION (IL) | 1986-08-12 | — | — | US | claimed |