Predicted protein targets (top 16)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | ALDH1A1 | P00352 | 4/20 | 0.54 |
| ▸ | GAA | P10253 | 2/20 | 0.54 |
| ▸ | L3MBTL1 | Q9Y468 | 1/20 | 0.53 |
| ▸ | KMT2A | Q03164 | 2/20 | 0.52 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.51 |
| ▸ | LMNA | P02545 | 4/20 | 0.50 |
| ▸ | PPARA | Q07869 | 1/20 | 0.50 |
| ▸ | CYP2D6 | P10635 | 1/20 | 0.50 |
| ▸ | SRC | P12931 | 1/20 | 0.50 |
| ▸ | PKM | P14618 | 1/20 | 0.50 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.50 |
| ▸ | KEAP1 | Q14145 | 1/20 | 0.50 |
| ▸ | NFE2L2 | Q16236 | 1/20 | 0.50 |
| ▸ | RECQL | P46063 | 1/20 | 0.49 |
| ▸ | CYP3A4 | P08684 | 1/20 | 0.48 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.48 |
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 | |
|---|---|---|---|---|
| SCHEMBL104518 | 1.00 | ALDH1A1 (0.54) | ALDH1A1GAAL3MBTL1KMT2ASMN1; SMN2 | |
| SCHEMBL155984 | 1.00 | ALDH1A1 (0.54) | ALDH1A1GAAL3MBTL1KMT2ASMN1; SMN2 | |
| SCHEMBL28215185 | 0.98 | ALDH1A1 (0.53) | ALDH1A1GAAL3MBTL1KMT2ASMN1; SMN2 | |
| Bromide SCHEMBL6042642 | 0.98 | ALDH1A1 (0.53) | ALDH1A1GAAL3MBTL1KMT2ASMN1; SMN2 | |
| Hydrochloric Acid SCHEMBL6178991 | 0.98 | ALDH1A1 (0.53) | ALDH1A1GAAL3MBTL1KMT2ASMN1; SMN2 | |
| Ammonia Solution, Strong SCHEMBL38660904 | 0.98 | ALDH1A1 (0.53) | ALDH1A1GAAL3MBTL1KMT2ASMN1; SMN2 | |
| Methane SCHEMBL9122539 | 0.98 | ALDH1A1 (0.53) | ALDH1A1GAAL3MBTL1KMT2ASMN1; SMN2 | |
| Bromide SCHEMBL6043492 | 0.96 | ALDH1A1 (0.51) | ALDH1A1GAAL3MBTL1KMT2ASMN1; SMN2 | |
| SCHEMBL6043499 | 0.92 | KEAP1 (0.49) | ALDH1A1GAAL3MBTL1KMT2ASMN1; SMN2 | |
| Alcohol SCHEMBL2312710 | 0.92 | PKM (0.49) | ALDH1A1GAAL3MBTL1KMT2ASMN1; SMN2 |
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 672 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119707698-A | Process method for synthesizing (S) - (+) -1-aminoindene | 大连双硼医药化工有限公司 | 2025-03-28 | — | — | CN | claimed |
| EP-4401725-A1 | PREPARATION OF OPTICALLY ACTIVE ENANTIOMERS OF PIPERONYL AMINES BY RESOLUTION OF THE DIASTEREOMERIC SALTS | atai Life Sciences AG (DE) | 2024-07-24 | — | — | EP | claimed |
| US-11999741-B2 | Process for the synthesis of 6-((3S,4S)-4-methyl-1-(pyrimidin-2-ylmethyl)pyrrolidin-3-yl)-3-(tetrahydropyran-4-yl-7H-imidazo[1,5-a]pyrazin-8-one | CARDURION PHARMACEUTICALS, INC. (US) | 2024-06-04 | — | — | US | claimed |
| US-11760750-B1 | Process for preparing levoketoconazole | NURAY CHEMICALS PRIVATE LIMITED (IN) | 2023-09-19 | — | — | US | claimed |
| US-20230109467-A1 | PREPARATION OF OPTICALLY ACTIVE ENANTIOMERS OF PIPERONYL AMINES BY RESOLUTION OF THE DIASTEREOMERIC SALTS | ATAI Life Sciences AG (DE) | 2023-04-06 | — | — | US | claimed |
| CN-115876826-A | Method for judging absolute configuration of oseltamivir | 北京格林意锐医药科技有限责任公司 | 2023-03-31 | — | — | CN | claimed |
| WO-2023044027-A1 | PREPARATION OF OPTICALLY ACTIVE ENANTIOMERS OF PIPERONYL AMINES BY RESOLUTION OF THE DIASTEREOMERIC SALTS | ATAI Life Sciences AG (DE) | 2023-03-23 | — | — | WO | claimed |
| EP-2155756-B1 | PROCESSES FOR THE PREPARATION OF CLOPIDOGREL | WOCKHARDT LTD (IN) | 2015-08-05 | — | — | EP | claimed |
| WO-2015063795-A2 | NOVEL PROCESS FOR PREPARATION OF OPTICALLY PURE NOREPHEDRINE AND ITS DERIVATIVES | LAURUS LABS PRIVATE LIMITED (IN) | 2015-05-07 | — | — | WO | claimed |
| CN-102898397-B | Synthesis method of (4aR,10bR)-3,4,4a,5,6,10b-hexahydro-2H-naphtho[1,2-b][1,4]oxazine-9-ol substance and hydrochloride thereof | JIANGSU HUAYI TECHNOLOGY CO LTD | 2014-12-10 | — | — | CN | claimed |
| EP-1413565-A2 | Method for optical resolution of 3-aminopentanenitrile | Bayer Chemicals AG (DE) | 2004-04-28 | — | — | EP | claimed |
| US-20040034080-A1 | Method for producing 3,3-diarylpropylamines | UCB PHARMA GMBH (DE) | 2004-02-19 | — | — | US | claimed |
| US-20040030145-A1 | Optically active B-aminoketones, optically active 1,3-amino alcohols and processes for preparing them | AVENTIS PHARMA DEUTSCHLAND GMBH (DE) | 2004-02-12 | — | — | US | claimed |
| US-6657065-B2 | Which are useful as microsomal triglyceride transfer protein (MTP) inhibitors | PFIZER INC | 2003-12-02 | — | — | US | claimed |
| CN-1441771-A | Process for producing 3, 3-diarylpropylamines | SANOL ARZNEI SCHWARZ GMBH (DE) | 2003-09-10 | — | — | CN | claimed |
| US-20030082830-A1 | Synthesis of combinatorial libraries of compounds reminiscent of natural products | NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT | 2003-05-01 | — | — | US | claimed |
| US-20020161233-A1 | Methods of making quinoline amides | TOM NORMA J (US) | 2002-10-31 | — | — | US | claimed |
| US-6448443-B1 | GENERATED FROM DIVERSIFIABLE SCAFFOLDS SYNTHESIZED FROM THE PYRIDINE-BASED TEMPLATE ISONICOTINAMIDE; ALSO PROVIDES A NOVEL ORTHO-NITROBENZYL PHOTOLINKER; SYNTHESIZED FROM A SHIKIMIC ACID BASED EPOXYOL TEMPLATE | PRESIDENT AND FELLOWS OF HARVARD COLLEGE | 2002-09-10 | — | — | US | claimed |
| US-20020042516-A1 | Methods of making quinoline amides | TOM NORMA J (US) | 2002-04-11 | — | — | US | claimed |
| US-4973750-A | Preparation of (threo)-1-aryl-2-acylamido-3-fluoro-1-propanols | SCHERING CORPORATION (US) | 1990-11-27 | — | — | US | claimed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (8 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20020161233-A1 | Methods of making quinoline amides | CETP, MTTP, LCAT | ALDH1A1 721/4885GAA 336/4885L3MBTL1 3175/4885 |
| US-20020042516-A1 | Methods of making quinoline amides | CETP, MTTP, LCAT | ALDH1A1 721/4885GAA 336/4885L3MBTL1 3175/4885 |
| US-20040034080-A1 | Method for producing 3,3-diarylpropylamines | HNMT, CYP1A1, HRH3 | ALDH1A1 121/4885GAA 3558/4885L3MBTL1 3487/4885 |
| US-11999741-B2 | Process for the synthesis of 6-((3S,4S)-4-methyl-1-(pyrimidin-2-ylmethyl)pyrrolidin-3-yl)-3-(tetrahydropyran-4-yl-7H-imidazo[1,5-a]pyrazin-8-one | CDK8, PRMT8, RPS8 | ALDH1A1 2636/4885GAA 1985/4885L3MBTL1 3371/4885 |
| US-20040030145-A1 | Optically active B-aminoketones, optically active 1,3-amino alcohols and processes for preparing them | ORMDL3, OR10J3, BCAT2 | ALDH1A1 59/4885GAA 3204/4885L3MBTL1 1700/4885 |
| US-20230109467-A1 | PREPARATION OF OPTICALLY ACTIVE ENANTIOMERS OF PIPERONYL AMINES BY RESOLUTION OF THE DIASTEREOMERIC SALTS | PRLHR, SRM, ADRB1 | ALDH1A1 139/4885GAA 2644/4885L3MBTL1 2345/4885 |
| US-20030082830-A1 | Synthesis of combinatorial libraries of compounds reminiscent of natural products | TKFC, NISCH, PTGIS | ALDH1A1 568/4885GAA 3302/4885L3MBTL1 4342/4885 |
| US-11760750-B1 | Process for preparing levoketoconazole | KHK, KYAT3, PLK3 | ALDH1A1 2659/4885GAA 576/4885L3MBTL1 2109/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.