Mianserin

Mianserin

SCHEMBL340474

CN1CCN2c3ccccc3Cc3ccccc3C2C1.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 Mianserin. 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
DRD3 known ✓ P35462 8/20 0.97
HTR2A known ✓ P28223 7/20 0.97
DRD2 known ✓ P14416 7/20 0.97
HTR1A known ✓ P08908 6/20 0.97
HTR2C known ✓ P28335 5/20 0.97
HTR2B known ✓ P41595 5/20 0.97
DRD4 known ✓ P21917 4/20 0.97
HTR1D known ✓ P28221 3/20 0.97
ADRA2A known ✓ P08913 3/20 0.97
DRD1 known ✓ P21728 3/20 0.97
ADRA1A known ✓ P35348 3/20 0.97
CHRM2 known ✓ P08172 2/20 0.97
CHRM1 known ✓ P11229 2/20 0.97
ADRA2B known ✓ P18089 2/20 0.97
ADRA2C known ✓ P18825 2/20 0.97
HTR7 known ✓ P34969 2/20 0.97
HRH1 known ✓ P35367 2/20 0.97
HTR3A known ✓ P46098 2/20 0.97
SLC6A2 known ✓ P23975 2/20 0.97
SLC6A4 known ✓ P31645 2/20 0.97

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
Mianserin SCHEMBL29366576 1.00 MEN1 (1.00) MEN1TP53CYP3A4KMT2AHPGD
Mianserin SCHEMBL29182002 0.99 MEN1 (0.97) MEN1TP53CYP3A4KMT2AHPGD
Mianserin SCHEMBL353397 0.98 DRD3 (1.00) MEN1TP53CYP3A4KMT2AHPGD
Mianserin SCHEMBL29356897 0.98 DRD3 (1.00) MEN1TP53CYP3A4KMT2AHPGD
Mianserin SCHEMBL9122085 0.98 DRD3 (1.00) MEN1TP53CYP3A4KMT2AHPGD
Mianserin SCHEMBL23326358 0.98 DRD3 (1.00) MEN1TP53CYP3A4KMT2AHPGD
Mianserin SCHEMBL18020 0.98 DRD3 (1.00) MEN1TP53CYP3A4KMT2AHPGD
Mianserin SCHEMBL11336834 0.97 HTR2A (0.97) MEN1TP53CYP3A4KMT2AHPGD
Mianserin SCHEMBL8344416 0.97 DRD3 (0.97) MEN1TP53CYP3A4KMT2AHPGD
Mianserin SCHEMBL9752060 0.97 DRD3 (0.97) MEN1TP53CYP3A4KMT2AHPGD

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 1590 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250381110-A1 SKIN CARE COMPOSITION AND METHOD OF USING THE SAME PROCTER & GAMBLE (US) 2025-12-18 US claimed
CN-119899192-A Synthesis method of mianserin hydrochloride 仁和堂药业有限公司 2025-04-29 CN claimed
CN-117777146-B Mirabilin hydrochloride monohydrate crystal form I and preparation method thereof 仁和堂药业有限公司 2025-02-14 CN claimed
CN-119176757-A Preparation method of mianserin hydrochloride intermediate and derivative thereof 四川青木制药有限公司 2024-12-24 CN claimed
CN-118852173-A Novel mianserin hydrochloride crystal form and preparation method thereof 南京桦冠生物技术有限公司 2024-10-29 CN claimed
CN-117820319-A Novel crystal form of mianserin hydrochloride and preparation method thereof 仁和堂药业有限公司 2024-04-05 CN claimed
CN-117777144-A Mirabilin hydrochloride novel crystal form II and preparation method thereof 仁和堂药业有限公司 2024-03-29 CN claimed
CN-117777146-A Novel crystal form I of mianserin hydrochloride monohydrate and preparation method thereof 仁和堂药业有限公司 2024-03-29 CN claimed
EP-4232004-A1 FRACTAL FORMULATIONS Nanogyre Sprl (BE) 2023-08-30 EP claimed
US-11344496-B2 Methods for preparing stabilized amorphous drug formulations using acoustic fusion MERCK SHARP & DOHME CORP. (US) 2022-05-31 US claimed
US-20050181049-A1 Composition and method for enhancing bioavailability ALZA CORPORATION 2005-08-18 US claimed
WO-2005051358-A1 COMPOSITION AND METHOD FOR ENHANCING BIOAVAILABILITY ALZA CORPORATION (US) 2005-06-09 WO claimed
WO-2005004855-A1 TREATMENT OF PREMATURE EJACULATION WORLDWIDE PE PATENT HOLDCO PTY LTD (AU) 2005-01-20 WO claimed
US-20040185097-A1 Controlled release modifying complex and pharmaceutical compositions thereof GLENMARK PHARMACEUTICALS LTD. 2004-09-23 US claimed
WO-2004076675-A2 GLUTAMATE TRANSPORT MODULATORY COMPOUNDS AND METHODS JOHNS HOPKINS UNIVERSITY (US) 2004-09-10 WO claimed
WO-2004066910-A2 CONTROLLED RELEASE MODIFYING COMPLEX AND PHARMACEUTICAL COMPOSITIONS THEREOF GLENMARK PHARMACEUTICALS LTD. (US) 2004-08-12 WO claimed
US-20040063612-A1 Neuroprotective agents CARBOMER, INC. 2004-04-01 US claimed
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 US claimed
EP-0651638-A1 PHARMACEUTICAL COMPOSITION AND METHOD OF TREATMENT FOR SEROTONIN DEPLETION ILLNESS IVY, Mary Elisabeth (ZA) 1995-05-10 EP claimed
WO-1994002138-A1 PHARMACEUTICAL COMPOSITION AND METHOD OF TREATMENT FOR SEROTONIN DEPLETION ILLNESS IVY, MARY, ELIZABETH (ZA) 1994-02-03 WO 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 (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-20250381110-A1 SKIN CARE COMPOSITION AND METHOD OF USING THE SAME SQSTM1, BECN1, CUTA DRD3 4375/4885HTR2A 2503/4885DRD2 4671/4885
US-11344496-B2 Methods for preparing stabilized amorphous drug formulations using acoustic fusion PDE8B, RPS27A, PDE8A DRD3 3802/4885HTR2A 4310/4885DRD2 4027/4885
US-20040063612-A1 Neuroprotective agents GAP43, NLN, NOS3 DRD3 2809/4885HTR2A 1077/4885DRD2 2801/4885

“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.