Methylephedrine

Methylephedrine

SCHEMBL68363

C[C@@H]([C@H](O)c1ccccc1)N(C)C.Cl

nearest known ligand 0.96

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 Methylephedrine. 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
GAA known ✓ P10253 1/20 0.54
ADRA2C known ✓ P18825 2/20 0.54
ADRA2A known ✓ P08913 1/20 0.54
SLC6A2 known ✓ P23975 1/20 0.53
SLC6A4 known ✓ P31645 1/20 0.53
SLC6A3 known ✓ Q01959 1/20 0.53
CHRM2 known ✓ P08172 1/20 0.50
ADRA1A known ✓ P35348 1/20 0.50
GLA known ✓ P06280 1/20 0.50
HTR2A known ✓ P28223 1/20 0.50
ALDH1A1 P00352 2/20 0.96
KDM4E B2RXH2 2/20 0.96
AOC3 Q16853 5/20 0.68
LMNA P02545 1/20 0.54
HIF1A Q16665 1/20 0.54
MEN1 O00255 2/20 0.53
KMT2A Q03164 2/20 0.53
HBB P68871 1/20 0.53
CYP2C9 P11712 2/20 0.52
MAPT P10636 1/20 0.52

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
Methylephedrine SCHEMBL7496690 0.98 KDM4E (1.00) ALDH1A1KDM4EAOC3GAAADRA2C
Methylephedrine SCHEMBL338479 0.98 KDM4E (1.00) ALDH1A1KDM4EAOC3GAAADRA2C
Methylephedrine SCHEMBL907677 0.98 KDM4E (1.00) ALDH1A1KDM4EAOC3GAAADRA2C
Methylephedrine SCHEMBL99673 0.98 KDM4E (1.00) ALDH1A1KDM4EAOC3GAAADRA2C
Methylephedrine SCHEMBL11959977 0.98 KDM4E (1.00) ALDH1A1KDM4EAOC3GAAADRA2C
Methylephedrine SCHEMBL99674 0.98 KDM4E (1.00) ALDH1A1KDM4EAOC3GAAADRA2C
Methylephedrine SCHEMBL338478 0.98 KDM4E (1.00) ALDH1A1KDM4EAOC3GAAADRA2C
Methylephedrine SCHEMBL907777 0.98 KDM4E (1.00) ALDH1A1KDM4EAOC3GAAADRA2C
Methylephedrine SCHEMBL2712293 0.98 KDM4E (1.00) ALDH1A1KDM4EAOC3GAAADRA2C
Methylephedrine SCHEMBL8083321 0.96 KDM4E (0.96) ALDH1A1KDM4EAOC3GAAADRA2C

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 1092 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250367139-A1 COMPOUND HYDROCORTISONE AND NEOMYCIN SULFATE GRANULE AND PREPARATION METHOD THEREOF HEBEI CHANGTIAN PHARMACEUTICAL CO LTD (CN) 2025-12-04 US claimed
WO-2023241662-A1 COMPOUND PARACETAMOL AND CHLORPHENAMINE MALEATE GRANULE AND PROCESS FOR PREPARING SAME 河北长天药业有限公司 2023-12-21 WO claimed
CN-110934833-B Compound paracetamol and chlorphenamine maleate granules 河北长天药业有限公司 2022-08-19 CN claimed
CN-114796280-A Compound paracetamol and chlorphenamine maleate granules and preparation process thereof 河北长天药业有限公司 2022-07-29 CN claimed
CN-108061777-B Method for detecting residual quantity of 34 illegally added medicines in weight-losing health-care food 浙江公正检验中心有限公司 2020-05-08 CN claimed
US-20170105934-A1 AQUEOUS OPHTHALMIC COMPOSITION ROHTO PHARMACEUTICAL CO., LTD. (JP) 2017-04-20 US claimed
WO-2016001937-A2 MODIFIED RELEASE PHARMACEUTICAL PREPARATIONS RUBICON RESEARCH PRIVATE LIMITED (IN) 2016-01-07 WO claimed
US-20140377328-A1 INTRAORAL SOLUBLE-TYPE FILM PREPARATION KYUKYU PHARMACEUTICAL CO., LTD. (JP) 2014-12-25 US claimed
US-20120110957-A1 METHOD FOR PREPARING RAPIDLY DISINTEGRATING FORMULATION FOR ORAL ADMINISTRATION HANMI PHARM. CO., LTD. (KR) 2012-05-10 US claimed
US-20100105783-A1 Method for preparing rapidly disintegrating formulation for oral administration and apparatus for preparing and packing the same HANMI PHARM. CO., LTD. (KR) 2010-04-29 US claimed
US-20030185886-A1 Process for the preparation of rapidly disintegrating tablet HANMI PHARM. CO., LTD. 2003-10-02 US claimed
US-6608101-B1 Inflammatory disorders; 3-(2,4-dimethoxy-5-(thien-2-yl)phenyl)-1-(4-carboxymethoxy-3,5 -dimethoxyphenyl)-2-propen-1-one; ATHEROGENICS, INC. 2003-08-19 US claimed
EP-1330448-A2 1,3-BIS-(SUBSTITUTED-PHENYL)-2-PROPEN-1-ONES AND THEIR USE TO TREAT VCAM-1 MEDIATED DISORDERS Atherogenics, Inc. (US) 2003-07-30 EP claimed
EP-1283703-A1 RAPIDLY DISINTEGRATING TABLET AND PROCESS FOR THE MANUFACTURE THEREOF Hanmi Pharm. Co., Ltd. (KR) 2003-02-19 EP claimed
US-20020001617-A1 Rapidly disintegrating tablet and process for the manufacture thereof HANMI PHARM. CO., LTD. (KR) 2002-01-03 US claimed
WO-2001098291-A2 1,3-BIS-(SUBSTITUTED-PHENYL)-2-PROPEN-1-ONES AND THEIR USE TO TREAT VCAM-1 MEDIATED DISORDERS ATHEROGENICS, INC. (US) 2001-12-27 WO claimed
WO-2001089485-A1 RAPIDLY DISINTEGRATING TABLET AND PROCESS FOR THE MANUFACTURE THEREOF HANMI PHARM. CO., LTD. (KR) 2001-11-29 WO claimed
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 US claimed
US-5700410-A Method of manufacturing wax matrices NIPPON SHINYAKU CO., LTD. (JP) 1997-12-23 US claimed
EP-0580860-B1 METHOD OF MANUFACTURING SOLID DISPERSION NIPPON SHINYAKU CO LTD (JP) 1997-10-22 EP claimed