Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of N-Methylpiperidine. 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 | |
|---|---|---|---|---|
| N-Methylpiperidine SCHEMBL571891 | 1.00 | — | — | |
| N-Methylpiperidine SCHEMBL9042504 | 0.96 | — | — | |
| N-Methylpiperidine SCHEMBL28226735 | 0.96 | — | — | |
| N-Methylpiperidine SCHEMBL31425141 | 0.96 | — | — | |
| N-Methylpiperidine SCHEMBL1920 | 0.96 | — | — | |
| N-Methyl Pyrrolidine (Nmp) SCHEMBL3633193 | 0.96 | — | — | |
| N-Methylpiperidine SCHEMBL6660565 | 0.96 | HRH3 (0.37) | — | |
| SCHEMBL21960469 | 0.96 | HRH3 (0.37) | — | |
| SCHEMBL12952612 | 0.96 | HRH3 (0.37) | — | |
| SCHEMBL12316976 | 0.96 | HRH3 (0.37) | — |
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 18 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2155152-A2 | COLOURING COMPOSITION COMPRISING AN AMINOPYRAZOLOPYRIDINE OXIDATION BASE AND EXHIBITING AN ACIDIC PH | L'Oreal (FR) | 2010-02-24 | — | — | EP | claimed |
| WO-2008138845-A2 | COLOURING COMPOSITION COMPRISING AN AMINOPYRAZOLOPYRIDINE OXIDATION BASE AND EXHIBITING AN ACIDIC PH | L'OREAL (FR) | 2008-11-20 | — | — | WO | claimed |
| CN-107056681-A | A kind of support method replaces the preparation method of cloth intermediate | 广州白云山光华制药股份有限公司 | 2017-08-18 | — | — | CN | disclosed |
| EP-2155152-A2 | COLOURING COMPOSITION COMPRISING AN AMINOPYRAZOLOPYRIDINE OXIDATION BASE AND EXHIBITING AN ACIDIC PH | L'Oreal (FR) | 2010-02-24 | — | — | EP | disclosed |
| WO-2008138845-A2 | COLOURING COMPOSITION COMPRISING AN AMINOPYRAZOLOPYRIDINE OXIDATION BASE AND EXHIBITING AN ACIDIC PH | L'OREAL (FR) | 2008-11-20 | — | — | WO | disclosed |
| CN-1189476-C | Thrombin inhibitors, their preparation and use | BASF AG (DE) | 2005-02-16 | — | — | CN | disclosed |
| CN-1090188-C | Benzonaphthyridines as inhibitors of HIV | BYK GULDEN LOMBERG CHEM FAB (DE) | 2002-09-04 | — | — | CN | disclosed |
| CN-1053893-C | Process for the manufacture of dicarboxamides | HOFFMANN LA ROCHE (CH) | 2000-06-28 | — | — | CN | disclosed |
| CN-1038839-C | Process for preparation of cyclic amine compounds | EISAI CO LTD (JP) | 1998-06-24 | — | — | CN | disclosed |
| CN-1154114-A | New thrombin inhibitors, their preparation and use | BASF AG (DE) | 1997-07-09 | — | — | CN | disclosed |
| CN-1034015-C | Process to prepare cycloamine compounds | EISAI CO LTD (JP) | 1997-02-12 | — | — | CN | disclosed |
| CN-1117488-A | Process for the manufacture of dicarboxamides | HOFFMANN LA ROCHE (CH) | 1996-02-28 | — | — | CN | disclosed |
| CN-1024547-C | Preparation method of cyclic amine compound | EISAI CO LTD (JP) | 1994-05-18 | — | — | CN | disclosed |
| CN-1073939-A | A kind of preparation method of cyclic amine compound | EISAI CO LTD (JP) | 1993-07-07 | — | — | CN | disclosed |
| CN-1071417-A | The preparation method of cyclic amine compound | EISAI CO LTD (JP) | 1993-04-28 | — | — | CN | disclosed |
| CN-1019973-C | Piperidine derivative and pharmaceutical composition containing the same | EISAI CO LTD (JP) | 1993-03-03 | — | — | CN | disclosed |
| CN-1030752-A | Preparation method of cyclic amine compound | EISAI CO LTD (JP) | 1989-02-01 | — | — | CN | disclosed |
| CN-87100928-A | Piperidine derivatives and pharmaceutical compositions thereof | — | 1987-09-09 | — | — | CN | disclosed |