Zoniporide

Zoniporide

SCHEMBL6586323

N=C(N)NC(=O)c1cnn(-c2cccc3ncccc23)c1C1CC1.O

nearest known ligand 0.69

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Zoniporide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
OPRM1 known ✓ P35372 1/20 0.68
OPRD1 known ✓ P41143 1/20 0.68
OPRK1 known ✓ P41145 1/20 0.68
SLC9A1 P19634 5/20 0.69
SLC9A2 Q9UBY0 2/20 0.69
MALT1 Q9UDY8 15/20 0.46

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.

Compoundsimilaritytop predictedshared targets
Zoniporide SCHEMBL6312868 1.00 SLC9A1 (0.69) SLC9A1SLC9A2OPRM1OPRD1OPRK1
Zoniporide SCHEMBL6263279 0.99 SLC9A1 (0.70) SLC9A1SLC9A2OPRM1OPRD1OPRK1
Zoniporide SCHEMBL4461125 0.99 SLC9A1 (0.71) SLC9A1SLC9A2OPRM1OPRD1OPRK1
Zoniporide SCHEMBL6313038 0.98 SLC9A1 (0.71) SLC9A1SLC9A2OPRM1OPRD1OPRK1
Zoniporide SCHEMBL6268513 0.94 SLC9A1 (0.65) SLC9A1SLC9A2OPRM1OPRD1OPRK1
Zoniporide SCHEMBL7523119 0.94 SLC9A1 (0.65) SLC9A1SLC9A2OPRM1OPRD1OPRK1
Hydrochloric Acid SCHEMBL6319082 0.94 SLC9A1 (0.66) SLC9A1SLC9A2OPRM1OPRD1OPRK1
SCHEMBL4456213 0.92 SLC9A1 (0.61) SLC9A1SLC9A2OPRM1OPRD1OPRK1
Hydrochloric Acid SCHEMBL6315010 0.91 SLC9A1 (0.61) SLC9A1SLC9A2OPRM1OPRD1OPRK1
SCHEMBL6314100 0.86 SLC9A1 (0.70) SLC9A1SLC9A2OPRM1OPRD1OPRK1

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 3 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1224179-B1 SODIUM-HYDROGEN EXCHANGER TYPE 1 INHIBITOR CRYSTALS PFIZER PROD INC (US) 2004-07-14 EP disclosed
EP-1224179-A2 SODIUM-HYDROGEN EXCHANGER TYPE 1 INHIBITOR CRYSTALS Pfizer Products Inc. (US) 2002-07-24 EP disclosed
WO-2001030759-A2 SODIUM-HYDROGEN EXCHANGER TYPE 1 INHIBITOR CRYSTALS PFIZER PRODUCTS INC. (US) 2001-05-03 WO disclosed