Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Bromoethanamine. 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 | |
|---|---|---|---|---|
| Bromoethanamine SCHEMBL94211 | 0.94 | — | — | |
| Bromoethanamine SCHEMBL67614 | 0.89 | — | — | |
| Bromoethanamine SCHEMBL27320074 | 0.89 | — | — | |
| Bromoethanamine SCHEMBL9658147 | 0.89 | — | — | |
| Bromoethanamine SCHEMBL11788853 | 0.89 | — | — | |
| Bromoethanamine SCHEMBL28859568 | 0.84 | — | — | |
| Bromoethanamine SCHEMBL7203619 | 0.84 | — | — | |
| Bromoethanamine SCHEMBL3129998 | 0.84 | — | — | |
| Hydrochloric Acid SCHEMBL670126 | 0.77 | — | — | |
| Hydrochloric Acid SCHEMBL11215577 | 0.74 | — | — |
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 223 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119569611-A | Tetramethyl bisphenol F cyanate and preparation method thereof | 扬州天启新材料股份有限公司 | 2025-03-07 | — | — | CN | claimed |
| CN-118046138-A | Water-washing soldering paste, manufacturing method thereof and water-washing soldering paste | 昆山市诺菲尔电子科技有限公司 | 2024-05-17 | — | — | CN | claimed |
| CN-117069668-A | Pleuromutilin compound with triazine side chain, and preparation method and application thereof | 中国农业科学院兰州畜牧与兽药研究所 | 2023-11-17 | — | — | CN | claimed |
| US-11390594-B2 | Procedure for the preparation of 2-cyanoimino-1,3-thiazolidine | BAYER CROPSCIENCE LP (US) | 2022-07-19 | — | — | US | claimed |
| US-20200347024-A1 | PROCEDURE FOR THE PREPARATION OF 2-CYANOIMINO-1,3-THIAZOLIDINE | BAYER CROPSCIENCE LP | 2020-11-05 | — | — | US | claimed |
| CN-110746459-A | Preparation method of Avramide | 上海喀露蓝科技有限公司 | 2020-02-04 | — | — | CN | claimed |
| US-20190152933-A1 | Procedure for the Preparation of 2-Cyanoimino-1,3-Thiazolidine | BAYER CROPSCIENCE LP | 2019-05-23 | — | — | US | claimed |
| EP-3350172-A1 | PROCEDURE FOR THE PREPARATION OF 2-CYANOIMINO-1,3-THIAZOLIDINE | Bayer Cropscience LP (US) | 2018-07-25 | — | — | EP | claimed |
| WO-2017048628-A1 | PROCEDURE FOR THE PREPARATION OF 2-CYANOIMINO-1,3-THIAZOLIDINE | BAYER CROPSCIENCE LP (US) | 2017-03-23 | — | — | WO | claimed |
| EP-1420021-A1 | DNA Methyltransferase inhibitors | The Penn State Research Foundation (US) | 2004-05-19 | — | — | EP | claimed |
| US-20260085077-A1 | HETEROCYCLIC DERIVATIVES AS JANUS KINASE INHIBITORS | CHIESI FARMACEUTICI S.P.A. (IT) | 2026-03-26 | — | — | US | disclosed |
| EP-4583977-A1 | HETEROCYCLIC DERIVATIVES AS JANUS KINASE INHIBITORS | Chiesi Farmaceutici S.p.A. (IT) | 2025-07-16 | — | — | EP | disclosed |
| CN-119569611-A | Tetramethyl bisphenol F cyanate and preparation method thereof | 扬州天启新材料股份有限公司 | 2025-03-07 | — | — | CN | disclosed |
| US-20250011348-A1 | Synthesis Process of X-IPM, Stable Crystal Form and Application Thereof | ASCENTAWITS PHARMACEUTICALS, LTD. (CN) | 2025-01-09 | — | — | US | disclosed |
| CN-119176839-A | Synthesis method of chroman compound with aziridine structure fragment | 深圳艾欣达伟医药科技有限公司 | 2024-12-24 | — | — | CN | disclosed |
| US-4328367-A | HERBICIDE | TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) | 1982-05-04 | — | — | US | disclosed |
| US-4304715-A | Enkephalin analogues | HUDSON DEREK | 1981-12-08 | — | — | US | disclosed |
| US-RE30731-E | Enkephalin analogues | Hudson, Derek (GB) | 1981-09-01 | — | — | US | disclosed |
| US-4198398-A | Enkephalin analogues | HUDSON DEREK (GB) | 1980-04-15 | — | — | US | disclosed |
| US-4017486-A | Cationic alpha-cyano-p-dimethylaminocinnamoyl dyes and paper dyed therewith | AMERICAN CYANAMID COMPANY (US) | 1977-04-12 | — | — | US | disclosed |