Clofexamide

Clofexamide

SCHEMBL365077

CCN(CC)CCNC(=O)COc1ccc(Cl)cc1.Cl

nearest known ligand 0.78

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 Clofexamide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 1/20 0.78
CYP1A2 P05177 2/20 0.76
CYP2D6 P10635 1/20 0.76
KDM4E B2RXH2 1/20 0.53
HTT P42858 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.52
PKM P14618 1/20 0.51
MEN1 O00255 4/20 0.50
KMT2A Q03164 4/20 0.50
CYP2C9 P11712 1/20 0.50
CYP2C19 P33261 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
ALDH1A1 P00352 1/20 0.49
L3MBTL1 Q9Y468 1/20 0.49
RAB9A P51151 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
Clofexamide SCHEMBL1604514 0.99 CYP1A2 (0.78) CYP3A4CYP1A2CYP2D6KDM4EHTT
Hydrochloric Acid SCHEMBL11539142 0.96 CYP3A4 (0.73) CYP3A4CYP1A2CYP2D6KDM4EHTT
Mefexamide SCHEMBL364170 0.88 CYP3A4 (1.00) CYP3A4CYP1A2CYP2D6KDM4ESMN1; SMN2
Mefexamide SCHEMBL126334 0.86 CYP1A2 (1.00) CYP3A4CYP1A2CYP2D6KDM4ESMN1; SMN2
Clofexamide SCHEMBL28469628 0.85 CYP1A2 (0.60) CYP3A4CYP1A2CYP2D6KDM4EHTT
Mefexamide SCHEMBL1650022 0.84 CYP1A2 (0.95) CYP3A4CYP1A2CYP2D6KDM4ESMN1; SMN2
SCHEMBL7002893 0.82 CYP1A2 (0.73) CYP3A4CYP1A2CYP2D6KDM4ESMN1; SMN2
Clofexamide SCHEMBL30139614 0.81 CYP1A2 (0.54) CYP3A4CYP1A2CYP2D6KDM4EHTT
SCHEMBL11371588 0.81 NPC1 (0.61) CYP3A4CYP1A2CYP2D6KDM4ESMN1; SMN2
SCHEMBL29889090 0.80 TSHR (0.61) CYP3A4CYP1A2CYP2D6KDM4EHTT

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 10 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-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-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