Known targets — ChEMBL curated mechanism
MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Dimethylformamide. 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 | |
|---|---|---|---|---|
| Dimethylformamide SCHEMBL28317966 | 0.97 | TSHR (0.60) | — | |
| Dimethylformamide SCHEMBL11302637 | 0.97 | — | — | |
| Dimethylformamide SCHEMBL2678657 | 0.97 | TSHR (0.60) | — | |
| Dimethylformamide SCHEMBL3457497 | 0.97 | — | — | |
| Dimethylformamide SCHEMBL10405953 | 0.91 | TSHR (0.53) | — | |
| Dimethylformamide SCHEMBL11264821 | 0.88 | TSHR (0.50) | — | |
| Dimethylformamide SCHEMBL8801229 | 0.87 | — | — | |
| Dimethylformamide SCHEMBL23282482 | 0.86 | TSHR (0.47) | — | |
| Ether SCHEMBL8913501 | 0.86 | TSHR (0.47) | — | |
| Dimethylformamide SCHEMBL28282130 | 0.86 | TSHR (0.47) | — |
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 573 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| WO-2023206726-A1 | PREPARATION METHOD FOR LITHIUM HEXAFLUOROPHOSPHATE | 福建省龙德新能源有限公司 | 2023-11-02 | — | — | WO | claimed |
| CN-116742023-A | Nitrogen-doped carbon nano-tube supported metal alloy nitrogen-doped carbon nano-sheet catalyst and preparation method and application thereof | 浙江理工大学 | 2023-09-12 | — | — | CN | claimed |
| CN-114737206-B | Preparation method of lithium hexafluorophosphate | 福建省龙德新能源有限公司 | 2022-11-11 | — | — | CN | claimed |
| CN-113185557-B | Iridium complex organic photovoltaic material and preparation method and application thereof | 南京工业大学 | 2022-08-30 | — | — | CN | claimed |
| CN-114737206-A | Preparation method of lithium hexafluorophosphate | 福建省龙德新能源有限公司 | 2022-07-12 | — | — | CN | claimed |
| CN-114685869-A | Preparation method of antibacterial nitrile butadiene rubber based on surface rapid crosslinking and curing | 厦门赋源高科技有限公司 | 2022-07-01 | — | — | CN | claimed |
| CN-114524829-A | Preparation method of imidazo [2,1-b ] thiazole derivative | 新疆大学 | 2022-05-24 | — | — | CN | claimed |
| CN-112795829-B | Fine-grain hard alloy and preparation method thereof | 广东正信硬质材料技术研发有限公司 | 2022-03-15 | — | — | CN | claimed |
| CN-109593164-B | Active polymer microsphere with hollow structure and preparation method thereof | 南开大学 | 2021-08-17 | — | — | CN | claimed |
| CN-108888763-B | Porous carbon composite material containing copper-based particles and preparation method and application thereof | 中国科学院理化技术研究所 | 2021-07-27 | — | — | CN | claimed |
| CN-105802273-A | Fluorescent recognition dye based on Nile blue matrix, and preparation method and application thereof | 大连理工大学 | 2016-07-27 | — | — | CN | claimed |
| CN-102733007-A | Nanometer fibrous material used for detecting NOX gas and preparation method thereof | FAW GROUP CORP | 2012-10-17 | — | — | CN | claimed |
| CN-102070549-A | 5-substituted-2-(4-substituted phenyl)benzoxazole derivatives and preparation method and application thereof | UNIV SHANDONG | 2011-05-25 | — | — | CN | claimed |
| CN-1260230-C | Production process of camptothecin | KEY LAB OF CHEMISTRY FOR NATUR (CN) | 2006-06-21 | — | — | CN | claimed |
| US-20050222326-A1 | OLIGOMERS CONTAINING N-ACETYL GLUCOSAMINE (NAG) | COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH | 2005-10-06 | — | — | US | claimed |
| CN-1621406-A | Production process of camptothecin | KEY LAB OF CHEMISTRY FOR NATUR (CN) | 2005-06-01 | — | — | CN | claimed |
| EP-0991793-B1 | METHOD FOR PREPARING 2-ARYL OR 2-HETEROCYCLYL CHIRAL PROPIONIC ACIDS AND THEIR ESTERS | CT NAT DE BR LA RECH SCIENT (FR) | 2001-12-05 | — | — | EP | claimed |
| US-6294069-B1 | MIXTURE OF PROPIONIC ACID DERIVATIVE IS ELECTROCHEMICALLY REDUCED IN THE PRESENCE OF NICKEL COMPLEX CATALYST AND SUPPORTING ELECTROLYTE IN ELECTROLYSIS CELL PROVIDED WITH ELECTRODES, PRODUCT IS HYDROLYZED OR TRANSESTERIFIED | CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) | 2001-09-25 | — | — | US | claimed |
| EP-0991793-A1 | METHOD FOR PREPARING 2-ARYL OR 2-HETEROCYCLYL CHIRAL PROPIONIC ACIDS AND THEIR ESTERS | CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) | 2000-04-12 | — | — | EP | claimed |
| WO-1999000535-A1 | METHOD FOR PREPARING 2-ARYL OR 2-HETEROCYCLYL CHIRAL PROPIONIC ACIDS AND THEIR ESTERS | CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) | 1999-01-07 | — | — | WO | claimed |