Melperone

Melperone

SCHEMBL1649537

CC1CCN(CCCC(=O)c2ccc(F)cc2)CC1.Cl

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

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 1/20 0.97
HTR1A known ✓ P08908 1/20 0.97
ADRA2A known ✓ P08913 1/20 0.97
DRD1 known ✓ P21728 1/20 0.97
ADRA1A known ✓ P35348 1/20 0.97
OPRM1 known ✓ P35372 1/20 0.97
DRD3 known ✓ P35462 1/20 0.97
KCNH2 known ✓ Q12809 1/20 0.97
HRH3 known ✓ Q9Y5N1 1/20 0.97
DRD2 known ✓ P14416 4/20 0.67
HTR2A known ✓ P28223 1/20 0.62
KMT2A Q03164 2/20 0.97
MEN1 O00255 1/20 0.97
TSHR P16473 1/20 0.73
CYP2D6 P10635 1/20 0.66
KDM4E B2RXH2 1/20 0.60
HSD17B10 Q99714 1/20 0.60

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
Melperone SCHEMBL146287 0.99 KMT2A (1.00) KMT2AMEN1CHRM2HTR1AADRA2A
Hydrochloric Acid SCHEMBL30658979 0.88 MEN1 (0.76) KMT2AMEN1CHRM2HTR1AADRA2A
SCHEMBL20254428 0.86 MEN1 (0.78) KMT2AMEN1CHRM2HTR1AADRA2A
SCHEMBL13913702 0.86 KMT2A (0.78) KMT2AMEN1CHRM2HTR1AADRA2A
Lenperone SCHEMBL11453463 0.85 MEN1 (0.72) KMT2AMEN1CHRM2HTR1AADRA2A
SCHEMBL11415059 0.85 MEN1 (0.76) KMT2AMEN1CHRM2HTR1AADRA2A
SCHEMBL4491395 0.85 KMT2A (0.76) KMT2AMEN1CHRM2HTR1AADRA2A
SCHEMBL22778808 0.85 HTR1A (0.76) KMT2AMEN1CHRM2HTR1AADRA2A
Hydrochloric Acid SCHEMBL16986196 0.85 TSHR (1.00) KMT2AMEN1CHRM2HTR1AADRA2A
Lenperone SCHEMBL121686 0.84 MEN1 (0.74) KMT2AMEN1CHRM2HTR1AADRA2A

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 51 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11278549-B2 Method of treating obesity MCMASTER UNIVERSITY (CA) 2022-03-22 US claimed
US-20190133924-A1 Alcohol-Resistant Formulations CIMA LABS INC (US) 2019-05-09 US claimed
US-20180318298-A1 Method of Treating Obesity MCMASTER UNIVERSITY (CA) 2018-11-08 US claimed
US-20150290181-A1 COMBINATION OF EFFECTIVE SUBSTANCES CAUSING SYNERGISTIC EFFECTS OF MULTIPLE TARGETING AND USE THEREOF VIVOZONE, INC. (KR) 2015-10-15 US claimed
EP-2727473-A2 COMBINATION OF EFFECTIVE SUBSTANCES CAUSING SYNERGISTIC EFFECTS OF MULTIPLE TARGETING AND USE THEREOF Vivozon, Inc. (KR) 2014-05-07 EP claimed
WO-2010077927-A1 COMPOSITIONS COMPRISING MELPERONE AND CONTROLLED-RELEASE DOSAGE FORMS EURAND, INC. (US) 2010-07-08 WO claimed
WO-2010077916-A1 COMPOSITIONS COMPRISING MELPERONE EURAND, INC. (US) 2010-07-08 WO claimed
US-20100151015-A1 Compositions Comprising Melperone and Controlled-Release Dosage Forms APTALIS PHARMATECH, INC. 2010-06-17 US claimed
US-20100151021-A1 Compositions Comprising Melperone APTALIS PHARMATECH, INC. 2010-06-17 US claimed
EP-1273301-B1 Pharmaceutical preparations based on active ingredients susceptible to illicit administration ALTERGON SA (CH) 2006-09-06 EP claimed
EP-1273301-A2 Pharmaceutical preparations based on active ingredients susceptible to illicit administration ALTERGON S.A. (CH) 2003-01-08 EP claimed
US-4344952-A Method of treating diarrhoea with gamma-piperidino-butyrophenones AB FERROSAN (SE) 1982-08-17 US claimed
US-11278549-B2 Method of treating obesity MCMASTER UNIVERSITY (CA) 2022-03-22 US disclosed
EP-2646003-B1 RAPIDLY DISPERSING GRANULES, ORALLY DISINTEGRATING TABLETS AND METHODS ADARE PHARMACEUTICALS INC (US) 2020-06-03 EP disclosed
EP-2506835-B1 COMPRESSIBLE-COATED PHARMACEUTICAL COMPOSITIONS AND TABLETS AND METHODS OF MANUFACTURE ADARE PHARMACEUTICALS INC (US) 2019-06-12 EP disclosed
US-20190133924-A1 Alcohol-Resistant Formulations CIMA LABS INC (US) 2019-05-09 US disclosed
US-5221679-A Useful for those patient who had experienced inadequate clinical response or adverse effects from, clozapine and or neuroleptic drugs CASE WESTERN RESERVE UNIVERSITY (US) 1993-06-22 US disclosed
EP-0111144-B1 SUSTAINED RELEASE SOLID DOSAGE FORMS HAVING NON-UNIFORM DISTRIBUTION OF ACTIVE INGREDIENT MERRELL DOW PHARMACEUTICALS INC. (US) 1986-12-03 EP disclosed
EP-0111144-A1 Sustained release solid dosage forms having non-uniform distribution of active ingredient MERRELL DOW PHARMACEUTICALS INC. (US) 1984-06-20 EP disclosed
US-4344952-A Method of treating diarrhoea with gamma-piperidino-butyrophenones AB FERROSAN (SE) 1982-08-17 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 (2 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-20180318298-A1 Method of Treating Obesity GPR119, HTR2A, GIPR CHRM2 370/4885HTR1A 7/4885ADRA2A 45/4885
US-11278549-B2 Method of treating obesity GPR119, HTR2A, GIPR CHRM2 370/4885HTR1A 7/4885ADRA2A 45/4885

“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.