Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Ethylamine. 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 | |
|---|---|---|---|---|
| Ethylamine SCHEMBL674041 | 1.00 | — | — | |
| Ethylamine SCHEMBL28837475 | 1.00 | — | — | |
| Ethylamine SCHEMBL3412953 | 1.00 | DNM1 (0.40) | — | |
| Ethylamine SCHEMBL30458185 | 1.00 | DNM1 (0.40) | — | |
| Ethylamine SCHEMBL1331914 | 1.00 | — | — | |
| Ethylamine SCHEMBL124697 | 1.00 | DNM1 (0.40) | — | |
| Ethylamine SCHEMBL674042 | 1.00 | — | — | |
| Ethylamine SCHEMBL3412956 | 1.00 | — | — | |
| Ethylamine SCHEMBL23910301 | 0.94 | — | — | |
| Ethylamine SCHEMBL5507383 | 0.94 | — | — |
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
Appears in 9176 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20260130139-A1 | LOW TEMPERATURE SI-CONTAINING FILMS DEPOSITED FROM CHLOROSILANE AND AMINOSILANE REACTIONS | VERSUM MAT US LLC (US) | 2026-05-07 | — | — | US | claimed |
| WO-2025245379-A1 | SUPERCRITICAL FLUIDS REGENERATION OF PFAS-CONTAMINATED SPENT MEDIA AND WATER TREATMENT TRAIN | UNIVERSITY OF WASHINGTON (US) | 2025-11-27 | — | — | WO | claimed |
| US-20250297351-A1 | LASER-ASSISTED REAGENT ACTIVATION AND PROPERTY MODIFICATION OF SELF-PASSIVATING METALS | SWAGELOK COMPANY | 2025-09-25 | — | — | US | claimed |
| CN-120192237-A | Synthesis and application of novel non-classical solid phase synthesis carrier | 瑞博(苏州)制药有限公司 | 2025-06-24 | — | — | CN | claimed |
| US-20250177885-A1 | COMPOSITION, SYSTEM AND METHOD FOR REMOVAL OF DETERGENTS FROM AQUEOUS SOLUTIONS | DNA GENOTEK INC. (CA) | 2025-06-05 | — | — | US | claimed |
| CN-120082611-A | Mutant of aminotransferase and application thereof | 上海合全药业股份有限公司 | 2025-06-03 | — | — | CN | claimed |
| CN-120058561-A | Method for preparing high-purity acetonitrile by separating mixture containing acetonitrile and water through high-purity acetonitrile and extractive distillation | 中国石油化工股份有限公司 | 2025-05-30 | — | — | CN | claimed |
| CN-120060408-A | Method for carrying out subcritical hydrolysis alkaline DES treatment on castor straw cellulose enzyme hydrolysis with associated xylooligosaccharide and micro-nano lignin | 齐鲁工业大学(山东省科学院) | 2025-05-30 | — | — | CN | claimed |
| CN-120004697-A | Preparation method of OrgVO material and application of OrgVO material as secondary battery anode material | 同济大学 | 2025-05-16 | — | — | CN | claimed |
| WO-2025088249-A1 | SOLUTION PROCESSABLE METALLO-ORGANIC COMPLEXES AND USES THEREOF | PIBOND OY (FI) | 2025-05-01 | — | — | WO | claimed |
| EP-0038972-A1 | Process for the preparation of ethers of alkyl-aryl ketoximes | BASF Aktiengesellschaft (DE) | 1981-11-04 | — | — | EP | claimed |
| US-4283343-A | HEAT TREATMENT TO PRODUCE STEREOISOMERS | NIPPON ZEON CO. LTD. (JP) | 1981-08-11 | — | — | US | claimed |
| EP-0023913-A4 | DEHYDROHALOGENATION OF A DIPHENYL TRICHLOROETHANE. | GEN ELECTRIC (US) | 1981-06-26 | — | — | EP | claimed |
| EP-0023913-A1 | DEHYDROHALOGENATION OF A DIPHENYL TRICHLOROETHANE | GENERAL ELECTRIC COMPANY (US) | 1981-02-18 | — | — | EP | claimed |
| US-4228308-A | IN METHYLAMINE AND A SALT | GENERAL ELECTRIC COMPANY (US) | 1980-10-14 | — | — | US | claimed |
| WO-1980001687-A1 | DEHYDROHALOGENATION OF A DIPHENYL TRICHLOROETHANE | GEN ELECTRIC (US) | 1980-08-21 | — | — | WO | claimed |
| US-4192957-A | DEHYDROCHLORINATION OF 1,1,1-TRICHLORO-2,2-BIS(4-HYDROXYPHENYL)ETHANE TO 1,1-DICHLORO-2,2-BIS(4-HYDROXYPHENYL)ETHYLENE WITH LIQUID AMMONIA AND ALKYL AMINE HYDROHALIDE PROMOTER | GENERAL ELECTRIC COMPANY (US) | 1980-03-11 | — | — | US | claimed |
| US-4069384-A | CYCLIC ANHYDRIDE; QUATERNARY AMMONIUM SALTS OR HALOGEN ACID SALTS AS CATALYSTS | THE GOODYEAR TIRE & RUBBER COMPANY (US) | 1978-01-17 | — | — | US | claimed |
| US-4051165-A | Preparation of biuret polyisocyanates | BAYER AKTIENGESELLSCHAFT (DT) | 1977-09-27 | — | — | US | claimed |
| US-4042605-A | Process for the production of 1,4-diaminoanthraquinone-2,3-dinitrile | BASF AKTIENGESELLSCHAFT (DT) | 1977-08-16 | — | — | US | claimed |