Norchlorcyclizine

Norchlorcyclizine

SCHEMBL4649874

Cl.Cl.Clc1ccc(C(c2ccccc2)N2CCNCC2)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 Norchlorcyclizine. 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
CYP19A1 known ✓ P11511 1/20 0.83
OPRD1 known ✓ P41143 10/20 0.65
CHRM2 known ✓ P08172 2/20 0.64
HTR1A known ✓ P08908 2/20 0.64
ADRA2A known ✓ P08913 2/20 0.64
CHRM1 known ✓ P11229 2/20 0.64
DRD1 known ✓ P21728 2/20 0.64
SLC6A2 known ✓ P23975 2/20 0.64
SLC6A4 known ✓ P31645 2/20 0.64
ADRA1A known ✓ P35348 2/20 0.64
DRD3 known ✓ P35462 2/20 0.64
SLC6A3 known ✓ Q01959 2/20 0.64
KCNH2 known ✓ Q12809 2/20 0.64
HRH3 known ✓ Q9Y5N1 1/20 0.64
OPRM1 known ✓ P35372 2/20 0.57
OPRK1 known ✓ P41145 1/20 0.56
CACNA1A known ✓ O00555 1/20 0.55
CACNA2D1 known ✓ P54289 1/20 0.55
CACNB1 known ✓ Q02641 1/20 0.55
CYP2D6 P10635 3/20 0.83

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
Norchlorcyclizine SCHEMBL588155 1.00 CYP2D6 (0.83) CYP2D6CYP19A1MEN1KMT2ACYP2C19
Norchlorcyclizine SCHEMBL6556514 0.98 CYP2D6 (0.86) CYP2D6CYP19A1MEN1KMT2ACYP2C19
Norchlorcyclizine SCHEMBL467086 0.98 CYP2D6 (0.86) CYP2D6CYP19A1MEN1KMT2ACYP2C19
Norchlorcyclizine SCHEMBL588655 0.98 CYP2D6 (0.86) CYP2D6CYP19A1MEN1KMT2ACYP2C19
Norchlorcyclizine SCHEMBL7139140 0.95 CYP2D6 (0.81) CYP2D6CYP19A1MEN1KMT2ACYP2C19
Norchlorcyclizine SCHEMBL7993069 0.93 CYP2D6 (0.71) CYP2D6CYP19A1MEN1KMT2ACYP2C19
SCHEMBL5363117 0.92 CYP2D6 (0.76) CYP2D6CYP19A1MEN1KMT2ACYP2C19
SCHEMBL1137956 0.91 CYP2D6 (1.00) CYP2D6CYP19A1MEN1KMT2ACYP2C19
Norchlorcyclizine SCHEMBL7989800 0.91 CYP2D6 (0.69) CYP2D6CYP19A1MEN1KMT2ACYP2C19
Norchlorcyclizine SCHEMBL7989702 0.91 CYP2D6 (0.73) CYP2D6CYP19A1MEN1KMT2ACYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1963296-A2 OPTICALLY ACTIVE CARBAMATES, PROCESS FOR PREPARATION THEREOF AND USE THEREOF AS PHARMACEUTICAL INTERMEDIATES Egis Gyógyszergyár Nyilvánosan Múködö Részvénytársaság (HU) 2008-09-03 EP disclosed
EP-1874364-A2 SUPERABSORBER TREATED WITH METALLIC SALT AND METALLIC OXIDE AND POST-CROSSLINKED ON THE SURFACE THEREOF Evonik Stockhausen GmbH (DE) 2008-01-09 EP disclosed
WO-2007066163-A2 OPTICALLY ACTIVE CARBAMATES, PROCESS FOR PREPARATION THEREOF AND USE THEREOF AS PHARMACEUTICAL INTERMEDIATES Egis Gyógyszergyár Nyilvanosan Mukodo Reszvenytarsasag (HU) 2007-06-14 WO disclosed
WO-2006111402-A2 SUPERABSORBER TREATED WITH METALLIC SALT AND METALLIC OXIDE AND POST-CROSSLINKED ON THE SURFACE THEREOF EVONIK STOCKHAUSEN GMBH (DE) 2006-10-26 WO disclosed
EP-1236722-B1 Optically active 4-(tert-butoxycarbonyl) piperazine compound, and method for producing the same SUMITOMO CHEMICAL CO (JP) 2006-04-19 EP disclosed
US-6803465-B2 INTERMEDIATES FOR THE PRODUCTION OF ANTIALLERGIC PHARMACEUTICALS SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2004-10-12 US disclosed
US-20020128275-A1 Optically active 4-(tert-butoxycarbonyl)piperazine compound, and method for producing the same SUMITOMO CHEMICAL COMPANY, LIMITED 2002-09-12 US disclosed
EP-1236722-A1 Optically active 4-(tert-butoxycarbonyl) piperazine compound, and method for producing the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-09-04 EP 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-20020128275-A1 Optically active 4-(tert-butoxycarbonyl)piperazine compound, and method for producing the same TERT, TTI1, TBC1D15 CYP19A1 86/4885OPRD1 1514/4885CHRM2 2464/4885

“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.