Prozapine

Prozapine

SCHEMBL365642

Cl.c1ccc(C(CCN2CCCCCC2)c2ccccc2)cc1

nearest known ligand 0.69

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

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
KCNA3 known ✓ P22001 1/20 0.62
SIGMAR1 known ✓ Q99720 1/20 0.53
ALDH1A1 P00352 2/20 0.64
CCR2 P41597 4/20 0.59
CYP2D6 P10635 1/20 0.58
OPRL1 P41146 1/20 0.57
MEN1 O00255 1/20 0.53
KMT2A Q03164 1/20 0.53
CYP3A4 P08684 1/20 0.51

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
Fenpiprane SCHEMBL11585426 1.00 ALDH1A1 (0.64) ALDH1A1KCNA3CCR2CYP2D6OPRL1
Fenpiprane SCHEMBL24507 0.98 ALDH1A1 (0.66) ALDH1A1KCNA3CCR2CYP2D6OPRL1
Prozapine SCHEMBL25765 0.98 ALDH1A1 (0.66) ALDH1A1KCNA3CCR2CYP2D6OPRL1
Hydrochloric Acid SCHEMBL29267226 0.90 CYP3A4 (0.66) ALDH1A1KCNA3CCR2CYP2D6OPRL1
Hydrochloric Acid SCHEMBL30517299 0.90 CYP3A4 (0.66) ALDH1A1KCNA3CCR2CYP2D6OPRL1
SCHEMBL67164 0.87 SIGMAR1 (0.66) ALDH1A1SIGMAR1
Hydrochloric Acid SCHEMBL8665657 0.84 CYP3A4 (0.51) ALDH1A1CCR2CYP2D6SIGMAR1MEN1
Hydrochloric Acid SCHEMBL5756120 0.84 ALDH1A1 (0.51) ALDH1A1CCR2CYP2D6SIGMAR1MEN1
Diisopromine SCHEMBL28142824 0.83 ALDH1A1 (0.51) ALDH1A1KCNA3CCR2CYP2D6OPRL1
Hydrochloric Acid SCHEMBL6938293 0.83 ALDH1A1 (0.51) ALDH1A1KCNA3CCR2CYP2D6OPRL1

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