Methoxyphenamine

Methoxyphenamine

SCHEMBL208636

CNC(C)Cc1ccccc1OC.Cl

nearest known ligand 0.61

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 Methoxyphenamine. 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 0.51
SLC18A2 known ✓ Q05940 1/20 0.48
SIGMAR1 known ✓ Q99720 1/20 0.48
SLC6A2 known ✓ P23975 1/20 0.47
SLC6A4 known ✓ P31645 1/20 0.47
SLC6A3 known ✓ Q01959 1/20 0.47
KCNH2 known ✓ Q12809 1/20 0.47
CHRM2 known ✓ P08172 3/20 0.46
CHRM4 known ✓ P08173 2/20 0.46
CHRM5 known ✓ P08912 2/20 0.46
CHRM1 known ✓ P11229 2/20 0.46
CHRM3 known ✓ P20309 2/20 0.46
ALDH1A1 P00352 1/20 0.51
MAPT P10636 1/20 0.51
IDO1 P14902 1/20 0.49
TAAR1 Q96RJ0 2/20 0.48
CYP2D6 P10635 2/20 0.47
CYP3A4 P08684 1/20 0.47
CYP2C9 P11712 1/20 0.47
CYP2C19 P33261 1/20 0.47

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
Methoxyphenamine SCHEMBL29379229 1.00 ALDH1A1 (0.51) ALDH1A1GAAMAPTIDO1TAAR1
Methoxyphenamine SCHEMBL29390678 0.98 TAAR1 (0.50) ALDH1A1GAAMAPTIDO1TAAR1
Methoxyphenamine SCHEMBL14655868 0.98 TAAR1 (0.50) ALDH1A1GAAMAPTIDO1TAAR1
Methoxyphenamine SCHEMBL218289 0.98 TAAR1 (0.50) ALDH1A1GAAMAPTIDO1TAAR1
Methoxyphenamine SCHEMBL2751759 0.98 TAAR1 (0.50) ALDH1A1GAAMAPTIDO1TAAR1
Methoxyphenamine SCHEMBL6625653 0.84 ALDH1A1 (0.53) ALDH1A1GAAMAPTCYP2D6CYP3A4
SCHEMBL20545745 0.83 ALDH1A1 (0.53) ALDH1A1GAACYP2D6CYP3A4CYP2C19
SCHEMBL4031642 0.81 IDO1 (0.51) ALDH1A1GAAMAPTIDO1CYP2D6
SCHEMBL11743782 0.81 SIGMAR1 (0.53) ALDH1A1GAAMAPTIDO1TAAR1
SCHEMBL878976 0.79 IDO1 (0.53) ALDH1A1GAAMAPTIDO1TAAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-217735854-U Vacuum pump is used in production of methoxamine hydrochloride 常州瑞明药业有限公司 2022-11-04 CN claimed
CN-114685290-A Preparation method of methoxyphenamine hydrochloride 杭州国瑞生物科技有限公司 2022-07-01 CN claimed
US-20200131431-A1 CHEMICAL ADDITIVES AND SURFACTANT COMBINATIONS FOR FAVORABLE WETTABILITY ALTERATION AND IMPROVED HYDROCARBON RECOVERY FACTORS ALCHEMY SCIENCES INC (US) 2020-04-30 US claimed
CN-209848351-U A rotary evaporator for producing methoxamine hydrochloride 常州瑞明药业有限公司 2019-12-27 CN claimed
CN-110144640-A A kind of processing method of degradable fishing net 巢湖市翔宇渔具有限公司 2019-08-20 CN claimed
CN-110004162-A A kind of carbonyl reductase, gene and its application on methoxyphenamine hydrochloride key intermediate 长兴制药股份有限公司 2019-07-12 CN claimed
CN-105669469-B A kind of synthetic method of methoxyphenamine hydrochloride 常州瑞明药业有限公司 2018-05-18 CN claimed
CN-106699576-A Method for synthesizing methoxyphenamine hydrochloride 常州瑞明药业有限公司 2017-05-24 CN claimed
CN-104306375-B Compound methoxyphenamine capsule and preparation method thereof 东北制药集团沈阳第制药有限公司 2017-01-11 CN claimed
CN-104306375-A Compound methoxyphenamine capsule and preparation method thereof NORTHEAST PHARMACEUTICAL GROUP SHENYANG NO 1 PHARMACEUTICAL CO LTD 2015-01-28 CN claimed
CN-1479628-A Use of CYP206 inhibitors in combination therapies �Ʒ� 2004-03-03 CN claimed
US-20030236298-A1 1,3-bis-(substituted-phenyl)-2-propen-1-ones and their use to treat VCAM-1 mediated disorders ATHEROGENICS PHARMACEUTICALS, INC. 2003-12-25 US claimed
CN-1118701-C Method for detecting composition of carena, methoxyphenamine hydrochloride, narcotine, etc at same time UNIV FUDAN (CN) 2003-08-20 CN 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
CN-1294519-A Pharmaceutical composition containing a compound having an activity of promoting the absorption of an active ingredient INPHARMA SA (CH) 2001-05-09 CN claimed
CN-1273361-A Method for detecting composition of carena, methoxyphenamine hydrochloride, narcotine, etc at same time UNIV FUDAN (CN) 2000-11-15 CN 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
EP-0189861-A2 Percutaneous absorption accelerator for ionic water-soluble medicine SHOWA DENKO KABUSHIKI KAISHA (JP) 1986-08-06 EP claimed

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-20030236298-A1 1,3-bis-(substituted-phenyl)-2-propen-1-ones and their use to treat VCAM-1 mediated disorders VCAM1, ICAM1, ITGB1 GAA 684/4885SLC18A2 3139/4885SIGMAR1 2292/4885

“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.