Ethylmorphine

Ethylmorphine

SCHEMBL220710

CCOc1ccc2c3c1O[C@H]1[C@@H](O)C=C[C@H]4[C@@H](C2)N(C)CC[C@@]341.Cl

nearest known ligand 0.79

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

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
OPRD1 known ✓ P41143 8/20 0.79
OPRM1 known ✓ P35372 6/20 0.79
OPRK1 known ✓ P41145 4/20 0.79
ADRB1 known ✓ P08588 1/20 0.79
PDE4D known ✓ Q08499 1/20 0.79
PDE3A known ✓ Q14432 1/20 0.79
ADRA2A known ✓ P08913 1/20 0.71
MRGPRX2 Q96LB1 4/20 0.79
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
Ethylmorphine SCHEMBL29845657 0.99 OPRM1 (0.79) OPRD1OPRM1OPRK1MRGPRX2ADRB1
Ethylmorphine SCHEMBL17747970 0.99 OPRM1 (0.79) OPRD1OPRM1OPRK1MRGPRX2ADRB1
Ethylmorphine SCHEMBL29392212 0.99 OPRD1 (0.80) OPRD1OPRM1OPRK1MRGPRX2ADRB1
Ethylmorphine SCHEMBL14516212 0.99 OPRD1 (0.80) OPRD1OPRM1OPRK1MRGPRX2ADRB1
Ethylmorphine SCHEMBL15653227 0.99 OPRD1 (0.80) OPRD1OPRM1OPRK1MRGPRX2ADRB1
Ethylmorphine SCHEMBL16922138 0.99 OPRD1 (0.80) OPRD1OPRM1OPRK1MRGPRX2ADRB1
Ethylmorphine SCHEMBL14611951 0.99 OPRD1 (0.80) OPRD1OPRM1OPRK1MRGPRX2ADRB1
Ethylmorphine SCHEMBL15757784 0.99 OPRD1 (0.80) OPRD1OPRM1OPRK1MRGPRX2ADRB1
Ethylmorphine SCHEMBL24971 0.99 OPRD1 (0.80) OPRD1OPRM1OPRK1MRGPRX2ADRB1
Ethylmorphine SCHEMBL18770594 0.99 OPRD1 (0.80) OPRD1OPRM1OPRK1MRGPRX2ADRB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210121455-A1 OPIOID RECEPTOR ANTAGONIST CONJUGATE AND USE THEREOF Shanghai Hanmai Bio-Pharma Co., Ltd. (CN) 2021-04-29 US claimed
EP-3406614-A1 OPIOID RECEPTOR ANTAGONIST CONJUGATE AND USE THEREOF Shanghai Hanmai Bio-Pharma Co., LTD. (CN) 2018-11-28 EP claimed
CN-104688767-B Application of Antaole in preparing drug-relief medicine 宁夏恩多芬科技有限公司 2017-10-24 CN claimed
CN-107033154-A Opiate receptor antagonist conjugate and its application 苏州派格生物科技有限公司 2017-08-11 CN claimed
CN-105193838-A New technology of nitrous oxide quick-acting drug treatment NINGXIA ENDORPHIN TECHNOLOGY CO LTD 2015-12-30 CN claimed
CN-104688767-A Application of Entonox in drug addiction treatment NINGBO ENDORPHELLON TECHNOLOGY CO LTD 2015-06-10 CN claimed
CN-104473927-A Polyethylene glycol and medicine molecule conjugate and preparation method thereof BEIJING JENKEM TECHNOLOGY CO LTD 2015-04-01 CN claimed
US-20060110333-A1 Composition for nasal absorption TAIHO PHARMACEUTICAL CO., LTD. (JP) 2006-05-25 US claimed
CN-1674903-A Composition for transnasal absorption TAIHO PHARMACEUTICAL CO LTD (JP) 2005-09-28 CN claimed
EP-1535615-A1 COMPOSITION FOR NASAL ABSORPTION TAIHO PHARMACEUTICAL CO., LTD. (JP) 2005-06-01 EP claimed
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 US claimed
EP-0214735-B1 CONTROLLED RELEASE PHARMACEUTICAL COMPOSITION Euroceltique S.A. (LU) 1991-08-28 EP claimed
US-4834965-A Controlled release pharmaceutical composition EUROCELTIQUE, S.A. (LU) 1989-05-30 US claimed
EP-0214735-A1 Controlled release pharmaceutical composition Euroceltique S.A. (LU) 1987-03-18 EP claimed
US-11311533-B2 Opioid receptor antagonist conjugate and use thereof Shanghai Hanmai Bio-Pharma Co., Ltd. (CN) 2022-04-26 US disclosed
US-11299587-B2 Starting material, for bulk drug or additives for drug, and bulk drug or drug using same SANYO CHEMICAL INDUSTRIES, LTD. (JP) 2022-04-12 US disclosed
US-20210363300-A1 STARTING MATERIAL FOR BULK DRUG OR ADDITIVES FOR DRUG, AND BULK DRUG OR DRUG USING SAME SANYO CHEMICAL INDUSTRIES, LTD. (JP) 2021-11-25 US disclosed
EP-0227836-A1 SUSTAINED RELEASING PATCH TEIJIN LIMITED (JP) 1987-07-08 EP disclosed
EP-0214735-A1 Controlled release pharmaceutical composition Euroceltique S.A. (LU) 1987-03-18 EP disclosed
US-4167636-A ANTITUSSIVE AGENT CHINOIN GYOGYSZER ES VEGYESZETI (HU) 1979-09-11 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-20210121455-A1 OPIOID RECEPTOR ANTAGONIST CONJUGATE AND USE THEREOF OPRL1, OPRM1, OGFR OPRD1 5/4885OPRM1 2/4885OPRK1 4/4885
US-11311533-B2 Opioid receptor antagonist conjugate and use thereof OPRL1, OPRM1, OGFR OPRD1 5/4885OPRM1 2/4885OPRK1 4/4885

“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.