Losoxantrone

Losoxantrone

SCHEMBL6685621

Cl.O=C1c2c(O)cccc2-c2nn(CCNCCO)c3ccc(NCCNCCO)c1c23

nearest known ligand 0.98

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 Losoxantrone. 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
TOP2A known ✓ P11388 10/20 0.98
CACNA1F known ✓ O60840 1/20 0.50
EGFR known ✓ P00533 1/20 0.50
ESR1 known ✓ P03372 1/20 0.50
ERBB2 known ✓ P04626 1/20 0.50
CHRM2 known ✓ P08172 1/20 0.50
CHRM4 known ✓ P08173 1/20 0.50
CHRM1 known ✓ P11229 1/20 0.50
SLC6A2 known ✓ P23975 1/20 0.50
HRH2 known ✓ P25021 1/20 0.50
HTR2C known ✓ P28335 1/20 0.50
ADRA1A known ✓ P35348 1/20 0.50
PTGS2 known ✓ P35354 1/20 0.50
DRD3 known ✓ P35462 1/20 0.50
OPRK1 known ✓ P41145 1/20 0.50
HTR2B known ✓ P41595 1/20 0.50
CACNA1D known ✓ Q01668 1/20 0.50
KCNH2 known ✓ Q12809 1/20 0.50
CACNA1S known ✓ Q13698 1/20 0.50
CACNA1C known ✓ Q13936 1/20 0.50

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
Losoxantrone SCHEMBL29409658 1.00 TOP2A (0.98) TOP2AMEN1USP2LMNATP53
Losoxantrone SCHEMBL5170 0.99 TOP2A (0.96) TOP2AMEN1USP2LMNATP53
Losoxantrone SCHEMBL61319 0.99 TOP2A (1.00) TOP2AMEN1USP2LMNATP53
Losoxantrone SCHEMBL29360703 0.99 TOP2A (1.00) TOP2AMEN1USP2LMNATP53
Losoxantrone SCHEMBL27927741 0.96 TOP2A (0.94) TOP2AMEN1USP2LMNATP53
SCHEMBL10800466 0.94 TOP2A (0.90) TOP2AMEN1USP2LMNATP53
Losoxantrone SCHEMBL27975856 0.93 TOP2A (0.88) TOP2AMEN1USP2LMNATP53
SCHEMBL22877226 0.92 TOP2A (0.87) TOP2AMEN1USP2LMNATP53
SCHEMBL18689529 0.92 TOP2A (0.87) TOP2AMEN1USP2LMNATP53
SCHEMBL10805434 0.91 TOP2A (0.86) TOP2AMEN1USP2LMNATP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040204357-A1 Modulator of the megalin-mediated uptake of radiotherapeutics and/or radiodiagnostics into kidney cells and their use in therapy and diagnostics SCHERING AG (DE) 2004-10-14 US disclosed
WO-2004084953-A1 MODULATORS OF THE MEGALIN-MEDIATED UPTAKE OF RADIOTHERAPEUTICS AND/OR RADIODIAGNOSTICS INTO KIDNEY CELLS AND THEIR USE IN THERAPY AND DIAGNOSTICS SCHERING AG (DE) 2004-10-07 WO disclosed
US-20040052730-A1 Methods and systems for assessing biological materials using optical and spectroscopic detection techniques CYTOSCAN SCIENCES, L.L.C. 2004-03-18 US disclosed
US-6573063-B2 Administering a contrast agent to a viable sample, acquiring a test data set and comparing to a comparison data set to assess the response CYTOSCAN SCIENCES, LLC 2003-06-03 US disclosed
US-6319682-B1 DETECTING CHLORIDE CHANNEL MODULATORS; MIX CELL AND HYDROGEN ION CONCENTRATION ADJUSTER, EVALUATE AND RECORD CELL ACTIVITY, INCUBATE CELLS WITH MODULATOR AND EVALUATE CELL ACTIVITY, COMPARE TO CONTROL CYTOSCAN SCIENCES, L.L.C. 2001-11-20 US disclosed