Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Piperidine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | CA2 known ✓ | P00918 | 1/20 | 0.39 |
| ▸ | SLC6A1 known ✓ | P30531 | 2/20 | 0.32 |
| ▸ | GABRP known ✓ | O00591 | 1/20 | 0.32 |
| ▸ | GABRD known ✓ | O14764 | 1/20 | 0.32 |
| ▸ | GABRA1 known ✓ | P14867 | 1/20 | 0.32 |
| ▸ | GABRB1 known ✓ | P18505 | 1/20 | 0.32 |
| ▸ | GABRG2 known ✓ | P18507 | 1/20 | 0.32 |
| ▸ | GABRB3 known ✓ | P28472 | 1/20 | 0.32 |
| ▸ | GABRA5 known ✓ | P31644 | 1/20 | 0.32 |
| ▸ | GABRA3 known ✓ | P34903 | 1/20 | 0.32 |
| ▸ | GABRA2 known ✓ | P47869 | 1/20 | 0.32 |
| ▸ | GABRB2 known ✓ | P47870 | 1/20 | 0.32 |
| ▸ | GABRA4 known ✓ | P48169 | 1/20 | 0.32 |
| ▸ | GABRE known ✓ | P78334 | 1/20 | 0.32 |
| ▸ | GABRA6 known ✓ | Q16445 | 1/20 | 0.32 |
| ▸ | GABRG1 known ✓ | Q8N1C3 | 1/20 | 0.32 |
| ▸ | GABRG3 known ✓ | Q99928 | 1/20 | 0.32 |
| ▸ | GABRQ known ✓ | Q9UN88 | 1/20 | 0.32 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.56 |
| ▸ | KDM4E | B2RXH2 | 2/20 | 0.41 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Piperidine SCHEMBL7344752 | 0.97 | ALDH1A1 (0.60) | ALDH1A1KDM4EKMT2AMAPTATM | |
| Piperidine SCHEMBL3283269 | 0.97 | ALDH1A1 (0.60) | ALDH1A1KDM4EKMT2AMAPTATM | |
| Pyrrolidine SCHEMBL28527711 | 0.94 | ALDH1A1 (0.53) | ALDH1A1KDM4EKMT2AMAPTATM | |
| Pyrrolidine SCHEMBL1800837 | 0.94 | — | — | |
| Piperidine SCHEMBL3873742 | 0.91 | ALDH1A1 (0.53) | ALDH1A1KDM4EKMT2AMAPTATM | |
| Piperidine SCHEMBL11283067 | 0.88 | ALDH1A1 (0.56) | ALDH1A1KDM4EKMT2AMAPTATM | |
| Piperidine SCHEMBL10778074 | 0.88 | ALDH1A1 (0.56) | ALDH1A1KDM4EKMT2AMAPTATM | |
| Azepane SCHEMBL11282804 | 0.88 | ALDH1A1 (0.56) | ALDH1A1KDM4EKMT2AMAPTATM | |
| Piperidine SCHEMBL1793471 | 0.88 | ALDH1A1 (0.56) | ALDH1A1KDM4EKMT2AMAPTATM | |
| Piperidine SCHEMBL8761997 | 0.88 | ALDH1A1 (0.56) | ALDH1A1KDM4EKMT2AMAPTATM |
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 14 patents. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-101659668-A | Process to prepare camptothecin derivatives and novel intermediate and compounds thereof | CHATHAM BIOTEC LTD | 2010-03-03 | — | — | CN | claimed |
| CN-1434043-B | Novel intermediate for preparing camptothecin derivative (CPT-11) and correlated compound and method thereof | PHARMACIA & UPJOHN CO LLC (US) | 2010-04-28 | — | — | CN | disclosed |
| CN-101659668-A | Process to prepare camptothecin derivatives and novel intermediate and compounds thereof | CHATHAM BIOTEC LTD | 2010-03-03 | — | — | CN | disclosed |
| CN-100537538-C | Nove intermediate for preparing camptothecin derivative (CPT-11) and correlated compound and method thereof | PHARMACIA & UPJOHN CO LLC (US) | 2009-09-09 | — | — | CN | disclosed |
| CN-100396682-C | Novel intermediate for preparing camptothecin derivative (CPT-11) and correlated compound and method thereof | PHARMACIA & UPJOHN CO LLC (US) | 2008-06-25 | — | — | CN | disclosed |
| CN-1241926-C | Novel intermediate for preparing camptothecin derivative (CPT-11) and correlated compound and method thereof | PHARMACIA & UPJOHN CO LLC (US) | 2006-02-15 | — | — | CN | disclosed |
| CN-1434044-A | Novel intermediate for preparing camptothecin derivative (CPT-11) and correlated compound and method thereof | PHARMACIA & UPJOHN CO LLC (US) | 2003-08-06 | — | — | CN | disclosed |
| CN-1434037-A | Nove intermediate for preparing camptothecin derivative (CPT-11) and correlated compound and method thereof | PHARMACIA & UPJOHN CO LLC (US) | 2003-08-06 | — | — | CN | disclosed |
| CN-1434046-A | Novel intermediate for preparing camptothecin derivative (CPT-11) and correlated compound and method thereof | PHARMACIA & UPJOHN CO LLC (US) | 2003-08-06 | — | — | CN | disclosed |
| CN-1434043-A | Novel intermediate for preparing camptothecin derivative (CPT-11) and correlated compound and method thereof | PHARMACIA & UPJOHN CO LLC (US) | 2003-08-06 | — | — | CN | disclosed |
| CN-1398247-A | Colchicol derivatives as vascular damaging agents | ANGIOGENE PHARM LTD (GB) | 2003-02-19 | — | — | CN | disclosed |
| CN-1100058-C | Intermediates and processes for the preparation of camptothecin derivatives (CPT-11) and related compounds | UPJOHN CO (US) | 2003-01-29 | — | — | CN | disclosed |
| CN-1181083-A | Novel intermediates and processes for the preparation of camptothecin derivatives (CPT-11) and related compounds | UPJOHN CO (US) | 1998-05-06 | — | — | CN | disclosed |
| CN-1131417-A | Substituted 4-carbamoyl pyrrolin-2-one and dihydrofuran-2-one derivatives and their use as pesticides | BAYER AG (DE) | 1996-09-18 | — | — | CN | disclosed |