Trimethylammonium

Trimethylammonium

SCHEMBL534138

C=C(C)C(=O)OCC(C)O.CN(C)C.Cl

nearest known ligand 0.62

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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.

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.62
THRB P10828 1/20 0.40
ALDH1A1 P00352 2/20 0.38
MAPT P10636 1/20 0.37
POLB P06746 1/20 0.30
APEX1 P27695 1/20 0.30
HTT P42858 1/20 0.30
TDP1 Q9NUW8 1/20 0.30
MAPK1 P28482 1/20 0.30

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.

Compoundsimilaritytop predictedshared targets
Trimethylammonium SCHEMBL5242715 0.98 TSHR (0.64) TSHRTHRBALDH1A1MAPTPOLB
Methacrylic Acid SCHEMBL25184921 0.95 TSHR (0.56) TSHRTHRBALDH1A1MAPTPOLB
Hydrochloric Acid SCHEMBL27495672 0.94 TSHR (0.69) TSHRTHRBALDH1A1MAPTPOLB
SCHEMBL19017 0.92 TSHR (0.72) TSHRTHRBALDH1A1MAPTPOLB
SCHEMBL9695772 0.92 TSHR (0.72) TSHRTHRBALDH1A1MAPTPOLB
Isobutane SCHEMBL28146334 0.90 TSHR (0.69) TSHRTHRBALDH1A1MAPTPOLB
Ammonia Solution, Strong SCHEMBL28645738 0.90 TSHR (0.69) TSHRTHRBALDH1A1MAPTPOLB
Methoxymethane SCHEMBL5841853 0.88 TSHR (0.67) TSHRTHRBALDH1A1MAPTPOLB
Methylamine SCHEMBL27537685 0.88 TSHR (0.67) TSHRTHRBALDH1A1MAPTPOLB
Methacrylic Acid SCHEMBL1076438 0.86 TSHR (0.64) TSHRTHRBALDH1A1MAPTPOLB

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 138 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2828692-B1 HYDROPHILIC MACROMERS AND HYDROGELS COMPRISING THE SAME MOMENTIVE PERFORMANCE MAT INC (US) 2024-02-28 EP claimed
CN-116438252-A Contact lens and method for manufacturing same 晶硕光学股份有限公司 2023-07-14 CN claimed
WO-2023082166-A1 CONTACT LENS AND MANUFACTURING METHOD THEREFOR 晶硕光学股份有限公司 2023-05-19 WO claimed
CN-110431203-B Ionically modified silicones, compositions, and medical devices formed therefrom 莫门蒂夫性能材料股份有限公司 2021-11-02 CN claimed
CN-110494519-B Ionically modified silicones, compositions, and medical devices formed therefrom 莫门蒂夫性能材料股份有限公司 2021-10-26 CN claimed
EP-3583177-B1 IONICALLY MODIFIED SILICONES, COMPOSITIONS, AND MEDICAL DEVICES FORMED THEREFROM MOMENTIVE PERFORMANCE MAT INC (US) 2020-12-23 EP claimed
EP-3583176-B1 IONICALLY MODIFIED SILICONES, COMPOSITIONS, AND MEDICAL DEVICES FORMED THEREFROM MOMENTIVE PERFORMANCE MAT INC (US) 2020-12-16 EP claimed
CN-105334640-B Silicone hydrogel lenses with rich water surface 诺华股份有限公司 2018-12-28 CN claimed
EP-2264486-B1 Ophthalmic, tinted molding composition, molding having high Dk-value and method of its production NOVARTIS AG (CH) 2018-08-22 EP claimed
CN-103298602-A Method for making silicone hydrogel contact lenses NOVARTIS AG 2013-09-11 CN claimed
US-20090269392-A1 Drug Delivery System And Methods Of Use Ocugenics, LLC 2009-10-29 US claimed
US-20090096985-A1 Tinted, high DK ophthalmic molding and a method for making same ALCON INC. (CH) 2009-04-16 US claimed
CN-100374169-C Method of manufacturing antimicrobial medical devices NOVARTIS AG (CH) 2008-03-12 CN claimed
CN-1822867-A antibacterial medical equipment NOVARTIS AG (CH) 2006-08-23 CN claimed
US-20040157276-A1 Agglutination accelerator for immunological measurement WAKO PURE CHEMICALS INDUSTRIES, LTD. (JP) 2004-08-12 US claimed
JP-2004517360-A 2004-06-10 JP claimed
CN-1484771-A A tinted high dk ophthalmic molding and a method for making same ��˹��ŵ�� 2004-03-24 CN claimed
EP-1360527-A2 A TINTED, HIGH DK OPHTHALMIC MOLDING AND A METHOD FOR MAKING SAME Novartis AG (CH) 2003-11-12 EP claimed
WO-2002054136-A2 A TINTED, HIGH DK OPHTHALMIC MOLDING AND A METHOD FOR MAKING SAME NOVARTIS AG (CH) 2002-07-11 WO claimed
EP-0490940-B2 PROCESS FOR GRAFTING OF NITROGEN-CONTAINING POLYMERS, AND POLYMERS THUS OBTAINED SARTORIUS GMBH (DE) 2000-07-05 EP claimed