⚠ 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 | |
|---|---|---|---|---|
| Acetone SCHEMBL10855260 | 1.00 | LMNA (0.60) | — | |
| Acetone SCHEMBL8505655 | 1.00 | LMNA (0.60) | — | |
| Acetone SCHEMBL29098211 | 1.00 | LMNA (0.60) | — | |
| Acetone SCHEMBL10768381 | 1.00 | LMNA (0.60) | — | |
| Acetone SCHEMBL2783426 | 0.95 | — | — | |
| Acetone SCHEMBL9790224 | 0.95 | — | — | |
| Acetone SCHEMBL28533561 | 0.95 | LMNA (0.55) | — | |
| Acetone SCHEMBL2347196 | 0.95 | — | — | |
| Acetone SCHEMBL28768895 | 0.95 | LMNA (0.55) | — | |
| Acetone SCHEMBL970686 | 0.95 | LMNA (0.55) | — |
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 1786 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118108575-A | Method for preparing acetone isopropanol by low-temperature oxidation of propane | 西北大学 | 2024-05-31 | — | — | CN | claimed |
| CN-115108955-B | Separation and purification method of calcitriol related impurity PZB | 南京海融制药有限公司 | 2024-05-07 | — | — | CN | claimed |
| WO-2024080956-A1 | A METHOD FOR OBTAINING A DEVICE USED IN BIOMARKER DETECTION | BILKENT UNIVERSITESI ULUSAL NANOTEKNOLOJI ARASTIRMA MERKEZI (TR) | 2024-04-18 | — | — | WO | claimed |
| CN-114099462-B | Duloxetine delayed release pharmaceutical composition and preparation method thereof | 宁波高新区美诺华医药创新研究院有限公司 | 2023-11-17 | — | — | CN | claimed |
| WO-2023209033-A1 | METHOD FOR CRYSTALLIZING TAPENTADOL INTERMEDIATE, TAPENTADOL INTERMEDIATE OF HIGH PURITY, METHOD OF MAKING TAPENTADOL AND TAPENTADOL OF HIGH PURITY | KRKA, D.D., NOVO MESTO (SI) | 2023-11-02 | — | — | WO | claimed |
| EP-4269384-A1 | METHOD FOR CRYSTALLIZING TAPENTADOL INTERMEDIATE, TAPENTADOL INTERMEDIATE OF HIGH PURITY, METHOD OF MAKING TAPENTADOL AND TAPENTADOL OF HIGH PURITY | KRKA, d.d., Novo mesto (SI) | 2023-11-01 | — | — | EP | claimed |
| CN-115376926-A | Special method for preparing rare earth element doped two-dimensional transition metal chalcogenide heterojunction | 天津理工大学 | 2022-11-22 | — | — | CN | claimed |
| CN-114927618-A | Multi-band composite photoelectric detector based on Bayer model and preparation method thereof | 江苏大学 | 2022-08-19 | — | — | CN | claimed |
| US-11390637-B2 | Salts of antiviral phosphonate analogues and process for preparation thereof | CIPLA LIMITED (IN) | 2022-07-19 | — | — | US | claimed |
| CN-114099462-A | Duloxetine delayed release pharmaceutical composition and preparation method thereof | 宁波高新区美诺华医药创新研究院有限公司 | 2022-03-01 | — | — | CN | claimed |
| WO-2001079342-A2 | CROSS-LINKED COLLAGEN MATRICES AND METHODS FOR THEIR PREPARATION | COLBAR R & D LTD. (IL) | 2001-10-25 | — | — | WO | claimed |
| EP-0877742-B1 | METHOD OF PRODUCTION OF LOVASTATIN | BALKANPHARMA RAZGRAD AD (BG) | 2001-08-16 | — | — | EP | claimed |
| WO-1998056750-A1 | A PROCESS FOR THE PREPARATION OF DIACEREIN | SYNTECO S.R.L. (IT) | 1998-12-17 | — | — | WO | claimed |
| US-5069700-A | method of manufacturing gradient-index glass | PRESIDENT OF TOKYO INSTITUTE OF TECHNOLOGY (JP) | 1991-12-03 | — | — | US | claimed |
| EP-0101570-B1 | METHOD FOR THE RESOLUTION OF RACEMIC 2-CP-DIFLUOROMETHOXY PHENYL)-3-METHYLBUTYRIC ACID | AMERICAN CYANAMID COMPANY (US) | 1988-01-27 | — | — | EP | claimed |
| EP-0145840-B1 | MONOESTER OF CELIPROLOL COMPRISING OPTICALLY ACTIVE, DISUBSTITUTED TARTARIC ACIDS, THEIR PREPARATION AND USE | CHEMIE LINZ AG (AT) | 1987-05-06 | — | — | EP | claimed |
| EP-0145840-A1 | Monoester of celiprolol comprising optically active, disubstituted tartaric acids, their preparation and use | CHEMIE LINZ AG (AT) | 1985-06-26 | — | — | EP | claimed |
| EP-0101570-A1 | Method for the resolution of racemic 2-CP-difluoromethoxy phenyl)-3-methylbutyric acid | AMERICAN CYANAMID COMPANY (US) | 1984-02-29 | — | — | EP | claimed |
| US-4407760-A | ETHERFICATION OF A PHENOL WITH CHLORODIFLUOROMETHANE | AMERICAN CYANAMID COMPANY (US) | 1983-10-04 | — | — | US | claimed |
| US-4405529-A | FROM CHLORODIFLUOROMETHANE AND PHENOL, 2-PROPANOL LAND ACETONE OR ACETONITRILE SOLVENT | AMERICAN CYANAMID COMPANY (US) | 1983-09-20 | — | — | US | claimed |