Phenyramidol

Phenyramidol

SCHEMBL29375712

Cl.OC(CNc1ccccn1)c1ccccc1

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

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
CYP2D6 P10635 1/20 0.97
KDM4E B2RXH2 3/20 0.56
FDPS P14324 1/20 0.54
L3MBTL1 Q9Y468 2/20 0.52
FABP1 P07148 1/20 0.50
FABP6 P51161 1/20 0.50
FAAH O00519 9/20 0.49
AOC3 Q16853 3/20 0.49
CXCR4 P61073 1/20 0.47
HTT P42858 1/20 0.46
NPSR1 Q6W5P4 1/20 0.46

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
Phenyramidol SCHEMBL121004 1.00 CYP2D6 (0.97) CYP2D6KDM4EFDPSL3MBTL1FABP1
Phenyramidol SCHEMBL21963 0.98 CYP2D6 (1.00) CYP2D6KDM4EFDPSL3MBTL1FABP1
Phenyramidol SCHEMBL13310219 0.98 CYP2D6 (1.00) CYP2D6KDM4EFDPSL3MBTL1FABP1
Phenyramidol SCHEMBL29500950 0.98 CYP2D6 (1.00) CYP2D6KDM4EFDPSL3MBTL1FABP1
Phenyramidol SCHEMBL13310227 0.98 CYP2D6 (1.00) CYP2D6KDM4EFDPSL3MBTL1FABP1
Phenyramidol SCHEMBL20769334 0.97 CYP2D6 (0.97) CYP2D6KDM4EFDPSL3MBTL1FABP1
Phenyramidol SCHEMBL3446649 0.92 CYP2D6 (0.88) CYP2D6KDM4EFDPSL3MBTL1FABP1
SCHEMBL9566716 0.86 CYP2D6 (0.77) CYP2D6KDM4EFDPSFABP1FABP6
Fenyripol SCHEMBL120829 0.83 CYP2D6 (0.68) CYP2D6KDM4EL3MBTL1FAAHAOC3
Phenyramidol SCHEMBL22718457 0.83 CYP2D6 (0.71) CYP2D6KDM4EFDPSFAAHAOC3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250170161-A1 INHIBIN SUBUNIT BETA E INHIBITOR AND METHODS OF USE THEREOF RISEN (SHANGHAI) MEDICINAL TECHNOLOGY CO., LTD. (CN) 2025-05-29 US disclosed
CN-119519900-A Rate de-matching method, apparatus, device, medium and computer program product 广东杰创智能科技有限公司 2025-02-25 CN disclosed
CN-117396205-A Method for titrating Mitapilar 安吉奥斯医药品有限公司 2024-01-12 CN disclosed
CN-116568281-A Pharmaceutical preparation 安吉奥斯医药品有限公司 2023-08-08 CN disclosed
CN-109312306-B Method for producing retinal tissue 住友制药株式会社 2023-05-09 CN disclosed
CN-112824229-B Avionics function test testing system 中国商用飞机有限责任公司 2023-01-17 CN disclosed
CN-114026773-A Communication failure indication between a primary controller and a secondary controller in a secondary controlled flyback converter 赛普拉斯半导体公司 2022-02-08 CN 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-20250170161-A1 INHIBIN SUBUNIT BETA E INHIBITOR AND METHODS OF USE THEREOF INHA, IGF2BP1, IGF2BP2 CYP2D6 4711/4885KDM4E 2066/4885FDPS 1196/4885

“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.