Dioxifedrine

Dioxifedrine

SCHEMBL364347

CNC(C)C(O)c1ccc(O)c(O)c1.Cl

nearest known ligand 0.96

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 Dioxifedrine. 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
▸ ADRB2 known ✓ P07550 6/20 0.54
▸ ADRA1A known ✓ P35348 3/20 0.53
▸ ADRA2C known ✓ P18825 2/20 0.53
▸ CHRM2 known ✓ P08172 1/20 0.53
▸ GLA known ✓ P06280 1/20 0.53
▸ HTR2A known ✓ P28223 1/20 0.53
▸ PTGS2 known ✓ P35354 2/20 0.53
▸ OPRK1 known ✓ P41145 1/20 0.53
▸ SLC6A3 known ✓ Q01959 1/20 0.53
▸ ADRB1 known ✓ P08588 4/20 0.51
▸ ADRB3 known ✓ P13945 3/20 0.51
▸ DRD2 known ✓ P14416 2/20 0.51
▸ ADRA1D known ✓ P25100 2/20 0.51
▸ ADRA1B known ✓ P35368 2/20 0.51
▸ DRD3 known ✓ P35462 2/20 0.51
▸ ADRA2A known ✓ P08913 1/20 0.51
▸ ADRA2B known ✓ P18089 1/20 0.51
▸ DRD1 known ✓ P21728 1/20 0.51
▸ GAA known ✓ P10253 1/20 0.51
▸ DRD4 known ✓ P21917 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
Dioxifedrine SCHEMBL250137 0.98 TDP1 (0.61) KDM4ETDP1MAPTRECQLKMT2A
SCHEMBL668000 0.83 KDM4E (0.61) KDM4ETDP1MAPTRECQLKMT2A
SCHEMBL10305119 0.82 ADRA2C (0.57) KDM4ETDP1MAPTRECQLKMT2A
Hydrochloric Acid SCHEMBL11279633 0.81 KDM4E (0.57) KDM4ETDP1MAPTRECQLKMT2A
Dioxethedrin SCHEMBL365011 0.81 KDM4E (0.57) KDM4ETDP1MAPTRECQLKMT2A
Racepinephrine SCHEMBL9227820 0.80 KDM4E (0.69) KDM4ETDP1MAPTRECQLKMT2A
Dioxethedrin SCHEMBL249560 0.79 ADRB2 (0.58) KDM4ETDP1MAPTRECQLKMT2A
SCHEMBL11279641 0.79 SLC6A4 (0.59) KDM4ETDP1MAPTRECQLKMT2A
Oxilofrine SCHEMBL5174274 0.79 KMT2A (0.68) KDM4ETDP1MAPTKMT2ATSHR
Oxilofrine SCHEMBL29354826 0.79 KMT2A (0.68) KDM4ETDP1MAPTKMT2ATSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2806034-B1 Compounds and uses thereof to induce an immunogenic cancer cell death in a subject ROUSSY INST GUSTAVE (FR) 2017-06-28 — — EP disclosed
EP-2806034-A1 Compounds and uses thereof to induce an immunogenic cancer cell death in a subject Institut Gustave Roussy (FR) 2014-11-26 — — EP disclosed
US-8865653-B2 Method of treatment for immunogenic treatment resistant cancer INSTITUT GUSTAVE ROUSSY (FR) 2014-10-21 — — US disclosed
US-8828944-B2 Compounds and uses thereof to induce an immunogenic cancer cell death in a subject INSTITUT GUSTAVE ROUSSY (FR) 2014-09-09 — — US disclosed
US-20130156790-A1 COMPOUNDS AND USES THEREOF TO INDUCE AN IMMUNOGENIC CANCER CELL DEATH IN A SUBJECT INSTITUT GUSTAVE ROUSSY (FR) 2013-06-20 — — US disclosed
US-20130052160-A1 COMPOUNDS AND USES THEREOF TO INDUCE AN IMMUNOGENIC CANCER CELL DEATH IN A SUBJECT INSTITUT GUSTAVE ROUSSY (FR) 2013-02-28 — — US disclosed
EP-2561088-A1 COMPOUNDS AND USES THEREOF TO INDUCE AN IMMUNOGENIC CANCER CELL DEATH IN A SUBJECT Institut Gustave Roussy (FR) 2013-02-27 — — EP disclosed
WO-2012007783-A1 KITS AND METHODS FOR DETECTING THE ABILITY TO INDUCE AN IMMUNOGENIC CANCER CELL DEATH IN A SUBJECT INSTITUT GUSTAVE ROUSSY (FR) 2012-01-19 — — WO disclosed
WO-2011131246-A1 COMPOUNDS AND USES THEREOF TO INDUCE AN IMMUNOGENIC CANCER CELL DEATH IN A SUBJECT INSTITUT GUSTAVE ROUSSY (FR) 2011-10-27 — — WO disclosed
WO-2011131472-A1 COMPOUNDS AND USES THEREOF TO INDUCE AN IMMUNOGENIC CANCER CELL DEATH IN A SUBJECT INSTITUT GUSTAVE ROUSSY (FR) 2011-10-27 — — WO disclosed
WO-1994000432-A1 ANORECTIC EPINEPHRINE DERIVATIVES THE UNITED STATES OF AMERICA, REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 1994-01-06 — — WO disclosed
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