Primaperone

Primaperone

SCHEMBL364809

Cl.O=C(CCCN1CCCCC1)c1ccc(F)cc1

nearest known ligand 0.97

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 Primaperone. 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
HTR1A known ✓ P08908 5/20 0.68
DRD3 known ✓ P35462 5/20 0.68
DRD1 known ✓ P21728 3/20 0.68
ADRA2A known ✓ P08913 2/20 0.68
ADRA1A known ✓ P35348 2/20 0.68
OPRM1 known ✓ P35372 2/20 0.68
KCNH2 known ✓ Q12809 2/20 0.68
HRH3 known ✓ Q9Y5N1 2/20 0.68
CHRM2 known ✓ P08172 1/20 0.68
SLC6A4 known ✓ P31645 2/20 0.67
SLC6A3 known ✓ Q01959 2/20 0.67
DRD2 known ✓ P14416 6/20 0.65
DRD4 known ✓ P21917 4/20 0.64
HTR2A known ✓ P28223 3/20 0.64
HTR2C known ✓ P28335 3/20 0.64
HRH1 known ✓ P35367 3/20 0.64
SIGMAR1 known ✓ Q99720 2/20 0.64
CHRM1 known ✓ P11229 1/20 0.64
HTR2B known ✓ P41595 1/20 0.64
HTR6 known ✓ P50406 1/20 0.64

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
Primaperone SCHEMBL310299 0.98 TSHR (0.74) TSHRHTR1ADRD3DRD1ADRA2A
SCHEMBL4496558 0.97 TSHR (0.76) TSHRHTR1ADRD3DRD1ADRA2A
SCHEMBL11755100 0.89 ALDH1A1 (0.71) TSHRHTR1AADRA1AKCNH2HRH3
Primaperone SCHEMBL30110541 0.88 TSHR (0.68) TSHRHTR1ADRD3DRD1ADRA2A
SCHEMBL7350313 0.87 ALDH1A1 (0.68) TSHRHTR1ADRD3DRD1ADRA2A
Hydrochloric Acid SCHEMBL7375876 0.87 TSHR (0.60) TSHRHTR1ADRD3DRD1ADRA2A
Hydrochloric Acid SCHEMBL7376357 0.87 TSHR (0.60) TSHRHTR1ADRD3DRD1ADRA2A
Hydrochloric Acid SCHEMBL16986196 0.87 TSHR (1.00) TSHRHTR1ADRD3DRD1ADRA2A
Hydrochloric Acid SCHEMBL16986155 0.85 TSHR (0.72) TSHRHTR1ADRD3DRD1ADRA2A
Hydrochloric Acid SCHEMBL10788566 0.85 TSHR (0.72) TSHRHTR1ADRD3DRD1ADRA2A

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 13 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
US-20150266864-A1 HETEROAROMATIC COMPOUNDS, METHOD FOR PREPARING THE COMPOUNDS, PHARMACEUTICAL COMPOSITIONS, USES AND METHOD FOR TREATING ACUTE AND CHRONIC PAIN CRISTÁLIA PRODUTOS QUÍMICOS FARMACÊUTICOS LTDA (BR) 2015-09-24 US disclosed
EP-2905278-A1 HETEROAROMATIC COMPOUNDS, METHOD FOR PREPARING THE COMPOUNDS, PHARMACEUTICAL COMPOSITIONS, USES AND METHOD FOR TREATING ACUTE AND CHRONIC PAIN Cristália Produtos Químicos Farmacêuticos LTDA. (BR) 2015-08-12 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
US-4086234-A Process for the preparation of tertiary amines G. D. SEARLE & CO. (US) 1978-04-25 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20150266864-A1 HETEROAROMATIC COMPOUNDS, METHOD FOR PREPARING THE COMPOUNDS, PHARMACEUTICAL COMPOSITIONS, USES AND METHOD FOR TREATING ACUTE AND CHRONIC PAIN TRPV1, AP1G1, INA HTR1A 670/4885DRD3 2293/4885DRD1 2316/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.