Nalorphine

Nalorphine

SCHEMBL149571

C=CCN1CC[C@]23c4c5ccc(O)c4O[C@H]2[C@@H](O)C=C[C@H]3[C@H]1C5.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
OPRM1 known ✓ P35372 7/20 0.98
OPRK1 known ✓ P41145 6/20 0.98
OPRD1 known ✓ P41143 4/20 0.98
SIGMAR1 known ✓ Q99720 1/20 0.98
ADRA2A known ✓ P08913 1/20 0.71
MRGPRX2 Q96LB1 2/20 0.71
SLC22A1 O15245 1/20 0.71
ARRB1 P49407 1/20 0.71

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
Nalorphine SCHEMBL12030798 0.99 OPRM1 (1.00) OPRM1OPRK1OPRD1SIGMAR1MRGPRX2
Nalorphine SCHEMBL6908593 0.99 OPRM1 (1.00) OPRM1OPRK1OPRD1SIGMAR1MRGPRX2
Nalorphine SCHEMBL19199030 0.99 OPRM1 (1.00) OPRM1OPRK1OPRD1SIGMAR1MRGPRX2
Nalorphine SCHEMBL14124636 0.99 OPRM1 (1.00) OPRM1OPRK1OPRD1SIGMAR1MRGPRX2
Nalorphine SCHEMBL12230555 0.99 OPRM1 (1.00) OPRM1OPRK1OPRD1SIGMAR1MRGPRX2
Nalorphine SCHEMBL17771837 0.99 OPRM1 (1.00) OPRM1OPRK1OPRD1SIGMAR1MRGPRX2
Nalorphine SCHEMBL38920 0.99 OPRM1 (1.00) OPRM1OPRK1OPRD1SIGMAR1MRGPRX2
Nalorphine SCHEMBL12091243 0.99 OPRM1 (1.00) OPRM1OPRK1OPRD1SIGMAR1MRGPRX2
Nalorphine SCHEMBL16015635 0.99 OPRM1 (1.00) OPRM1OPRK1OPRD1SIGMAR1MRGPRX2
Nalorphine SCHEMBL1883694 0.98 OPRM1 (0.98) OPRM1OPRK1OPRD1SIGMAR1MRGPRX2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120282255-A1 METHODS AND COMPOSITIONS FOR THE TREATMENT OF ALCOHOLISM AND ALCOHOL DEPENDENCE SUMMIT BIOSCIENCES, INC. 2012-11-08 US claimed
EP-1754712-A2 Transcobalamin binding conjugates useful for treating abnormal cellular proliferation MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2007-02-21 EP claimed
US-20060166862-A1 Transcobalamin receptor binding conjugates useful for treating abnormal cellular proliferation REGENTS OF THE UNIVERSITY OF MINNESOTA 2006-07-27 US claimed
US-7008444-B2 Method of controlling body temperature while reducing shivering RADIANT MEDICAL, INC. (US) 2006-03-07 US claimed
EP-1334114-A2 TRANSCOBALAMIN BINDING CONJUGATES USEFUL FOR TREATING ABNORMAL CELLULAR PROLIFERATION MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH (US) 2003-08-13 EP claimed
US-20020151525-A1 Transcobalamin receptor binding conjugates useful for treating abnormal cellular proliferation COLLINS DOUGLAS A (US) 2002-10-17 US claimed
WO-2002055530-A2 TRANSCOBALAMIN BINDING CONJUGATES USEFUL FOR TREATING ABNORMAL CELLULAR PROLIFERATION MAYO FOUNDATION (US) 2002-07-18 WO claimed
EP-0046270-B1 NOVEL DERIVATIVES OF BIO-AFFECTING PHENOLIC COMPOUNDS AND PHARMACEUTICAL COMPOSITION CONTAINING THEM INTERx RESEARCH CORPORATION (US) 1986-05-21 EP claimed
JP-57004991-A None JP disclosed
EP-3946547-B1 DEVICES AND METHODS FOR DELIVERING PHARMACEUTICAL COMPOSITIONS PINOVA THERAPEUTICS INC (US) 2026-03-25 EP disclosed
EP-3890700-B1 ORAL THIN FILMS UNIV STRATHCLYDE (GB) 2026-02-11 EP disclosed
US-12539280-B2 Oral thin films UNIVERSITY OF STRATHCLYDE (GB) 2026-02-03 US disclosed
US-20250058094-A1 DEVICES AND METHODS FOR DELIVERY OF PHARMACEUTICAL COMPOSITIONS PINOVA THERAPEUTICS INC. 2025-02-20 US disclosed
US-12194263-B2 Devices and methods for delivery of pharmaceutical compositions Pocket Naloxone Corp. (US) 2025-01-14 US disclosed
WO-1982003768-A1 NOVEL METHOD OF ADMINISTERING NARCOTIC ANTAGONISTS AND ANALGESICS AND NOVEL DOSAGE FORMS CONTAINING SAME UNIV KENTUCKY (US) 1982-11-11 WO disclosed
EP-0046270-A1 Novel derivatives of bio-affecting phenolic compounds and pharmaceutical composition containing them INTERx RESEARCH CORPORATION (US) 1982-02-24 EP disclosed
JP-S574991-A CYCLOPROPYLMETHYLNORMORPHINE-6-SULFURIC ESTER SANKYO CO LTD 1982-01-11 JP disclosed
US-4269843-A NONHABIT-FORMING; ANTAGONIST, ANTAGONISM SRI INTERNATIONAL (US) 1981-05-26 US disclosed
US-4218454-A N-αMethylcyclopropylmethyl derivatives of normorphine and noroodeine, and analgesic compositions and methods employing the normorphine derivatives SRI INTERNATIONAL (US) 1980-08-19 US disclosed
US-3957788-A ANALGESICS, ANTI-TUSSIVES, ANTIINFLAMMATORY AGENTS DAINIPPON PHARMACEUTICAL CO., LTD. (JA) 1976-05-18 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 (3 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-12539280-B2 Oral thin films ABCB11, SLC6A1, OPRK1 OPRM1 6/4885OPRK1 3/4885OPRD1 4/4885
US-20060166862-A1 Transcobalamin receptor binding conjugates useful for treating abnormal cellular proliferation PCNA, MKI67, SLC19A1 OPRM1 2385/4885OPRK1 1860/4885OPRD1 3315/4885
US-20020151525-A1 Transcobalamin receptor binding conjugates useful for treating abnormal cellular proliferation PCNA, MKI67, SLC19A1 OPRM1 2385/4885OPRK1 1860/4885OPRD1 3315/4885

“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.