Known targets — ChEMBL curated mechanism
ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO
The experimentally established mechanism targets of Trimethylammonium. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
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 | |
|---|---|---|---|---|
| Trimethylammonium SCHEMBL2441583 | 1.00 | — | — | |
| Trimethylammonium SCHEMBL11238572 | 1.00 | — | — | |
| Trimethylammonium SCHEMBL6248490 | 1.00 | — | — | |
| Trimethylammonium SCHEMBL50323 | 1.00 | — | — | |
| Trimethylammonium SCHEMBL21990427 | 1.00 | — | — | |
| Trimethylammonium SCHEMBL6248491 | 1.00 | — | — | |
| Trimethylammonium SCHEMBL28598242 | 0.91 | — | — | |
| Trimethylammonium SCHEMBL27275753 | 0.91 | — | — | |
| Trimethylammonium SCHEMBL11309054 | 0.91 | — | — | |
| Trimethylammonium SCHEMBL5871084 | 0.91 | — | — |
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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-1738792-B | Process for preparing gamma-cyhalothrin | SYNGENTA LTD | 2010-05-05 | — | — | CN | claimed |
| CN-1738792-A | Process for preparing gamma-cyhalothrin | SYNGENTA LTD (GB) | 2006-02-22 | — | — | CN | claimed |
| EP-4289869-A1 | PROCESS FOR THE PRODUCTION OF STARCH BETAINATE | Raiz - Instituto De Investigação Da Floresta E Papel (PT) | 2023-12-13 | — | — | EP | disclosed |
| EP-3684898-A1 | ACTIVE SUBSTANCE WAFER | Symrise AG (DE) | 2020-07-29 | — | — | EP | disclosed |
| CN-110032042-A | Negative photoresist composition and its application method for laser ablation | AZ电子材料卢森堡有限公司 | 2019-07-19 | — | — | CN | disclosed |
| CN-109996563-A | The preparation and its preparation and application that the preparation, taste of 4- methyl -5- (pyrazine -2- base) -3H-1,2- dithiole -3- thioketones are improved | ST知识产权控股公司 | 2019-07-09 | — | — | CN | disclosed |
| CN-109996562-A | The preparation and its preparation and application of 4- methyl -5- (pyrazine -2- base) -3H-1,2- dithiole -3- thioketones | ST知识产权控股公司 | 2019-07-09 | — | — | CN | disclosed |
| WO-2019057294-A1 | ACTIVE SUBSTANCE WAFER | SYMRISE AG (DE) | 2019-03-28 | — | — | WO | disclosed |
| CN-108139670-A | Negative photoresist composition for laser ablation and method of use thereof | AZ电子材料卢森堡有限公司 | 2018-06-08 | — | — | CN | disclosed |
| CN-1738792-B | Process for preparing gamma-cyhalothrin | SYNGENTA LTD | 2010-05-05 | — | — | CN | disclosed |
| CN-100543025-C | The midbody compound of synthesizing lamel larin H and derivative thereof and synthetic method | UNIV DALIAN (CN) | 2009-09-23 | — | — | CN | disclosed |
| CN-1948308-A | Intermediate compound for synthesizing lamel larin H and its derivatives and synthesizing method | UNIV DALIAN (CN) | 2007-04-18 | — | — | CN | disclosed |
| US-7157573-B2 | Hydrophobic starch derivatives | COOPERATIE AVEBE U.A. (NL) | 2007-01-02 | — | — | US | disclosed |
| CN-1875012-A | 2-phenylbenzofuran derivatives, method for the production thereof and use thereof | AVENTIS PHARMA GMBH (DE) | 2006-12-06 | — | — | CN | disclosed |
| CN-1738792-A | Process for preparing gamma-cyhalothrin | SYNGENTA LTD (GB) | 2006-02-22 | — | — | CN | disclosed |
| US-20050277768-A1 | Hydrophobic starch derivatives | COOPERATIEVE VERKOOP-EN PRODUCTIEVERENIGING VAN AARDAPPELMEEL EN DERIVATEN AVEBE B.A. | 2005-12-15 | — | — | US | disclosed |
| CN-1262677-A | Preparation of fused polycyclic alkaloids by ring closure of azomethine ylides, novel compounds thereof and their use as chemotherapeutic agents | UNIV AUSTRALIAN (AU) | 2000-08-09 | — | — | CN | disclosed |
| CN-1045791-C | Lubricating oil containing aromatic ether compound | MITSUI PETROCHEMICAL IND (JP) | 1999-10-20 | — | — | CN | disclosed |
| CN-1130398-A | Lubricating oil containing aromatic ether compound | MITSUI PETROCHEMICAL IND (JP) | 1996-09-04 | — | — | CN | disclosed |
| CN-1099409-A | Non-hydrogen evolving siloxane-based lubricant composition | KHONE POULENC SPECIAL CHEMICCO (US) | 1995-03-01 | — | — | CN | disclosed |