Known targets — ChEMBL curated mechanism
ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol
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 SCHEMBL27853942 | 0.96 | CA2 (0.44) | — | |
| Trimethylammonium SCHEMBL27527228 | 0.96 | CA2 (0.44) | — | |
| SCHEMBL6913509 | 0.91 | — | — | |
| Sulfuric Acid SCHEMBL166792 | 0.86 | CA5A (0.60) | — | |
| Sulfuric Acid SCHEMBL1155575 | 0.86 | — | — | |
| Sulfuric Acid SCHEMBL27867083 | 0.86 | CA5A (0.60) | — | |
| Sulfuric Acid SCHEMBL28249272 | 0.86 | CA5A (0.60) | — | |
| SCHEMBL8596055 | 0.85 | CA2 (0.58) | — | |
| SCHEMBL246838 | 0.85 | CA2 (0.58) | — | |
| SCHEMBL25599 | 0.85 | CA2 (0.58) | — |
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 546 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119753849-A | Second-order nonlinear optical crystal material of trimethylamine methylsulfonate and preparation and application thereof | 同济大学 | 2025-04-04 | — | — | CN | claimed |
| CN-109575676-B | Photosensitive ink for 3D glass, preparation method of photosensitive ink and preparation method of photosensitive coating | 湖南松井新材料股份有限公司 | 2021-12-07 | — | — | CN | claimed |
| CN-109721548-B | Preparation method of azoxystrobin | 南通泰禾化工股份有限公司 | 2020-11-13 | — | — | CN | claimed |
| CN-111393253-A | Synthesis method of compound containing trans-substituted cyclohexyl | 江苏广域化学有限公司 | 2020-07-10 | — | — | CN | claimed |
| EP-3476837-B1 | METHOD FOR PREPARING AZOXYSTROBIN INTERMEDIATES | CAC NANTONG CHEMICAL CO LTD (CN) | 2020-04-08 | — | — | EP | claimed |
| EP-3476838-B1 | METHOD FOR PREPARING AZOXYSTROBIN | CAC NANTONG CHEMICAL CO LTD (CN) | 2019-11-13 | — | — | EP | claimed |
| CN-110028399-A | A kind of preparation method of 2-methyl-4-chlorophenoxyacetic acid | 上海泰禾国际贸易有限公司 | 2019-07-19 | — | — | CN | claimed |
| EP-3476837-A1 | METHOD FOR PREPARING AZOXYSTROBIN INTERMEDIATES | CAC Nantong Chemical Co., Ltd. (CN) | 2019-05-01 | — | — | EP | claimed |
| EP-3476838-A1 | METHOD FOR PREPARING AZOXYSTROBIN | CAC Nantong Chemical Co., Ltd. (CN) | 2019-05-01 | — | — | EP | claimed |
| US-10189793-B1 | Method for preparing azoxystrobin | CAC NANTONG CHEMICAL CO., LTD (CN) | 2019-01-29 | — | — | US | claimed |
| CN-1150175-C | Derivatives of 1,3,4-oxadiazolone | ����˹�ж�-����˹˹������˾ | 2004-05-19 | — | — | CN | claimed |
| CN-1289249-A | Derivatives of 1,3,4-oxadiazolone | BRISTOL MYERS SQUIBB CO (US) | 2001-03-28 | — | — | CN | claimed |
| EP-0577302-B1 | Process for preparing alpha-anomer enriched 2-deoxy-2,2-difluoro-D-ribofuranosyl sulfonates | LILLY CO ELI (US) | 1997-07-16 | — | — | EP | claimed |
| EP-0640614-B1 | Stereoselective process for preparing beta-anomer enriched 2-deoxy-2, 2-difluoro-d-ribofuranosyl-3, 5-hydroxy protected-1-alkyl and aryl sulfonate intermediates | LILLY CO ELI (US) | 1996-12-04 | — | — | EP | claimed |
| US-5424416-A | Sulfonating a lactol, followed with nucleobase anion, forming anomers | ELI LILLY AND COMPANY (US) | 1995-06-13 | — | — | US | claimed |
| EP-0640614-A2 | Stereoselective process for preparing beta-anomer enriched 2-deoxy-2, 2-difluoro-d-ribofuranosyl-3, 5-hydroxy protected-1-alkyl and aryl sulfonate intermediates | ELI LILLY AND COMPANY (US) | 1995-03-01 | — | — | EP | claimed |
| EP-0577302-A1 | Process for preparing alpha-anomer enriched 2-deoxy-2,2-difluoro-D-ribofuranosyl sulfonates | ELI LILLY AND COMPANY (US) | 1994-01-05 | — | — | EP | claimed |
| US-5256798-A | Treating beta-anomer ribofuranosyl sulfonate with source of conjugate anion | ELI LILLY AND COMPANY (US) | 1993-10-26 | — | — | US | claimed |
| US-4845219-A | ANTITUMOR, ANTOCOAGULANT | TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) | 1989-07-04 | — | — | US | claimed |
| EP-0255366-A2 | Nitrogen- and sulfur-containing lipid compound, their production and use | Takeda Chemical Industries, Ltd. (JP) | 1988-02-03 | — | — | EP | claimed |