Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Morpholine. 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 | |
|---|---|---|---|---|
| Morpholine SCHEMBL17336349 | 1.00 | — | — | |
| Morpholine SCHEMBL29440831 | 1.00 | MEN1 (0.85) | — | |
| Morpholine SCHEMBL4620513 | 1.00 | — | — | |
| Morpholine SCHEMBL10782491 | 1.00 | MEN1 (0.85) | — | |
| Morpholine SCHEMBL25338784 | 0.96 | — | — | |
| Morpholine SCHEMBL2164566 | 0.96 | — | — | |
| Morpholine SCHEMBL15789175 | 0.96 | — | — | |
| Morpholine SCHEMBL31312337 | 0.96 | — | — | |
| Hydrochloric Acid SCHEMBL8586805 | 0.96 | KDM4E (0.92) | — | |
| Morpholine SCHEMBL27466765 | 0.96 | — | — |
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 1539 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122057566-A | Ionic liquid catalyst for preparing methacrolein and preparation method thereof | 中国科学院过程工程研究所 | 2026-05-19 | — | — | CN | claimed |
| CN-120022522-A | Drug-loaded microneedle, drug-loaded microneedle patch and electrically-controlled drug release microneedle system | 成都邦迈医创科技有限公司 | 2025-05-23 | — | — | CN | claimed |
| CN-119978822-A | Antistatic silicone rubber composition and preparation method thereof | 杭州之江有机硅化工有限公司 | 2025-05-13 | — | — | CN | claimed |
| CN-118684636-B | Synthesis process of 4-morpholine-1-phenylmercapto-2-butanone | 上海优合贝德医药科技有限公司 | 2025-03-11 | — | — | CN | claimed |
| CN-118684636-A | Synthesis process of 4-morpholine-1-phenylmercapto-2-butanone | 上海优合贝德医药科技有限公司 | 2024-09-24 | — | — | CN | claimed |
| WO-2024105225-A1 | SYNERGISTIC COMBINATIONS OF A SIGMA RECEPTOR 1 (S1R) ANTAGONIST AND A SOLUBLE EPOXIDE HYDROLASE INHIBITOR (SEHI) AND THEIR USE IN THE TREATMENT OF PAIN | UNIVERSITAT DE BARCELONA (ES) | 2024-05-23 | — | — | WO | claimed |
| CN-118028412-A | Extraction processing technology of rice protein | 安徽稼仙金佳粮集团股份有限公司 | 2024-05-14 | — | — | CN | claimed |
| CN-117986139-A | Synthesis method of 1- (biphenyl-4-yl) -2-methyl-2-aminopropane-1-ketone | 深圳有为技术控股集团有限公司 | 2024-05-07 | — | — | CN | claimed |
| EP-4315482-A1 | HALOGEN COMPLEXING AGENTS BOUND TO THE CATHODE SURFACE IN A STATIC ZINC HALIDE BATTERY | EOS Energy Technology Holdings, LLC (US) | 2024-02-07 | — | — | EP | claimed |
| CN-108350005-B | Chiral agent for preparing homogeneous oligomer | 卫材R&D管理有限公司 | 2024-02-06 | — | — | CN | claimed |
| EP-0843592-A1 | DEHALOGENATION OF HALOGENATED HYDROCARBONS IN AQUEOUS COMPOSITIONS | MONSANTO COMPANY (US) | 1998-05-27 | — | — | EP | claimed |
| CN-1171398-A | Process for preparing morpholine hydrochloride as precursor of monoxydine hydrochloride | LU XINGHAI (CN) | 1998-01-28 | — | — | CN | claimed |
| WO-1997004868-A1 | DEHALOGENATION OF HALOGENATED HYDROCARBONS IN AQUEOUS COMPOSITIONS | MONSANTO COMPANY (US) | 1997-02-13 | — | — | WO | claimed |
| US-4915169-A | Method for controlling the pH of steam fluids using heterocyclic, multifunctional, nitrogen-containing compounds | CHEVRON RESEARCH COMPANY (US) | 1990-04-10 | — | — | 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 |
| EP-0209274-A2 | Furanone derivatives | ELI LILLY AND COMPANY (US) | 1987-01-21 | — | — | EP | claimed |
| CN-86104450-A | The preparation method of furanone derivatives | — | 1986-12-31 | — | — | CN | claimed |
| US-4287284-A | AND A DEVELOPER OF BUTYL METHACRYLATE-STYRENE RESIN OR BUTADIENE-STYRENE RESIN WITH CARBON BLACK, AND A CARRIER OF POLYVINYLIDENE FLUORIDE COATED STEEL | XEROX CORPORATION (US) | 1981-09-01 | — | — | US | claimed |
| US-4097479-A | FROM ORGANIC NITRILE AND AZIDE ANION, AMINE SOLVENT | MILES LABORATORIES, INC. (US) | 1978-06-27 | — | — | US | claimed |