Phenadoxone

Phenadoxone

SCHEMBL11319633

CCC(=O)C(CC(C)N1CCOCC1)(c1ccccc1)c1ccccc1.Cl.O=CO

nearest known ligand 0.57

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
OPRM1 known ✓ P35372 4/20 0.57
OPRD1 known ✓ P41143 2/20 0.57
GRIN2D known ✓ O15399 2/20 0.49
GRIN1 known ✓ Q05586 2/20 0.49
GRIN2A known ✓ Q12879 2/20 0.49
GRIN2B known ✓ Q13224 2/20 0.49
GRIN2C known ✓ Q14957 2/20 0.49
DRD3 known ✓ P35462 2/20 0.49
CACNA1F known ✓ O60840 1/20 0.49
DRD4 known ✓ P21917 1/20 0.49
OPRK1 known ✓ P41145 1/20 0.49
CACNA1D known ✓ Q01668 1/20 0.49
KCNH2 known ✓ Q12809 1/20 0.49
CACNA1S known ✓ Q13698 1/20 0.49
CACNA1C known ✓ Q13936 1/20 0.49
KCNA5 known ✓ P22460 2/20 0.43
DRD2 known ✓ P14416 1/20 0.40
ABCB1 P08183 1/20 0.49
CYP2B6 P20813 1/20 0.49
MRGPRX2 Q96LB1 1/20 0.49

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
Phenadoxone SCHEMBL2032631 0.95 OPRM1 (0.62) OPRM1OPRD1GRIN2DGRIN1GRIN2A
Phenadoxone SCHEMBL25165 0.94 OPRM1 (0.63) OPRM1OPRD1GRIN2DGRIN1GRIN2A
Phenadoxone SCHEMBL9858401 0.93 OPRM1 (0.59) OPRM1OPRD1GRIN2DGRIN1GRIN2A
Dipipanone SCHEMBL392119 0.83 OPRM1 (0.56) OPRM1OPRD1GRIN2DGRIN1GRIN2A
Dipipanone SCHEMBL25367 0.82 OPRM1 (0.57) OPRM1OPRD1GRIN2DGRIN1GRIN2A
Phenadoxone SCHEMBL6912655 0.79 TSHR (0.48) OPRM1OPRD1SMN1; SMN2ALDH1A1MEN1
Dextromoramide SCHEMBL29395675 0.78 SMN1; SMN2 (0.51) OPRM1OPRD1KCNA5SMN1; SMN2ALDH1A1
SCHEMBL9917093 0.76 OPRM1 (0.50) OPRM1OPRD1GRIN2DGRIN1GRIN2A
Dextromoramide SCHEMBL29581857 0.73 SMN1; SMN2 (0.46) OPRM1OPRD1KCNA5SMN1; SMN2ALDH1A1
SCHEMBL9917096 0.70 SLC6A2 (0.43) OPRM1OPRD1GRIN2DGRIN1GRIN2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4258175-A BY REACTING A HALOGENATED DIPHENOXY COMPOUND AND AN ALKYLENE DIHALIDE; REACTING THE HALOARYETHER WITH A HALOGENATED PHENOL VELSICOL CHEMICAL CORPORATION (US) 1981-03-24 US disclosed