N-Benzylmethylamine

N-Benzylmethylamine

SCHEMBL237384

CNCc1ccccc1.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 N-Benzylmethylamine. 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 0.50
SIGMAR1 known ✓ Q99720 2/20 0.46
MAPT P10636 3/20 1.00
CYP3A4 P08684 2/20 1.00
KDM4E B2RXH2 1/20 1.00
ATM Q13315 1/20 0.54
TAAR1 Q96RJ0 1/20 0.54
MEN1 O00255 2/20 0.54
KMT2A Q03164 2/20 0.54
IDO1 P14902 2/20 0.52
THRB P10828 1/20 0.52
TDP1 Q9NUW8 1/20 0.52
LOXL2 Q9Y4K0 1/20 0.50
CALM1 P0DP23 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.48
HTT P42858 1/20 0.46
ADH1B P00325 1/20 0.46
ADH1C P00326 1/20 0.46
ADH1A P07327 1/20 0.46
ADH7 P40394 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
N-Benzylmethylamine SCHEMBL27370226 1.00 MAPT (1.00) MAPTCYP3A4KDM4EATMTAAR1
N-Benzylmethylamine SCHEMBL28173950 1.00 MAPT (1.00) MAPTCYP3A4KDM4EATMTAAR1
N-Benzylmethylamine SCHEMBL23581071 0.97 MAPT (0.95) MAPTCYP3A4KDM4EATMTAAR1
N-Benzylmethylamine SCHEMBL11638857 0.97 MAPT (0.95) MAPTCYP3A4KDM4EATMTAAR1
N-Benzylmethylamine SCHEMBL2271 0.97
N-Benzylmethylamine SCHEMBL11696446 0.97 CYP3A4 (0.94) MAPTCYP3A4KDM4EATMTAAR1
SCHEMBL24334039 0.97 CYP3A4 (0.94) MAPTCYP3A4KDM4EATMTAAR1
N-Benzylmethylamine SCHEMBL4609847 0.97 CYP3A4 (0.94) MAPTCYP3A4KDM4EATMTAAR1
N-Benzylmethylamine SCHEMBL8083805 0.94
N-Benzylmethylamine SCHEMBL9346326 0.94 CYP3A4 (0.90) MAPTCYP3A4KDM4EATMTAAR1

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 1923 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122081951-A Corrosion inhibitor for circulating water of coastal high-chlorine environment steel mill and preparation method thereof 2026-05-26 CN claimed
US-12614726-B2 Dispersion and stabilization of MXene materials and MXene materials for energy storage applications DREXEL UNIVERSITY (US) 2026-04-28 US claimed
CN-118375018-A Paving method of high-viscosity asphalt ultrathin cover layer 深圳市路桥建设集团有限公司 2024-07-23 CN claimed
CN-114191332-B Hair mask with shape memory function and preparation method thereof 上海自然堂集团有限公司 2024-04-02 CN claimed
CN-117736369-A Reverse microemulsion thickener, preparation method and non-crosslinked recyclable fracturing fluid 陕西延长石油(集团)有限责任公司 2024-03-22 CN claimed
US-20240058434-A1 NANOEMULSION UNIVERSAL INFLUENZA VACCINE BLUEWILLOW BIOLOGICS, INC. (US) 2024-02-22 US claimed
WO-2023200764-A1 NANOEMULSION UNIVERSAL INFLUENZA VACCINE BLUEWILLOW BIOLOGICS, INC. (US) 2023-10-19 WO claimed
CN-116832227-A Preparation method and application of substrate surface adhesion electrostatic complex coating 征鸿诺瓦医疗科技(深圳)有限公司 2023-10-03 CN claimed
WO-2023133143-A1 INTRANASAL POLYSACCHARIDE CONJUGATE NANOEMULSION VACCINES AND METHODS OF USING THE SAME BLUEWILLOW BIOLOGICS, INC. (US) 2023-07-13 WO claimed
US-11648337-B2 Drug-coated balloon catheters for body lumens UROTRONIC, INC. (US) 2023-05-16 US claimed
US-5374536-A Adding known quantity of microbe contaminated water, nutrient, oxidation-reduction indicator to series of sample wells, adding serial dilution of first and second microbiocides, incubating, comparing color change NALCO CHEMICAL COMPANY (US) 1994-12-20 US claimed
EP-0615857-A1 Recording sheets containing monoammonium compounds XEROX CORPORATION (US) 1994-09-21 EP claimed
US-5320902-A Suitable for use in ink jet printing XEROX CORPORATION (US) 1994-06-14 US claimed
WO-1994012460-A1 PROCESS FOR PREPARING SUBSTANTIALLY PURE ENANTIOMERS OF PHENYLPROPIONIC ACIDS THE BOOTS COMPANY PLC (GB) 1994-06-09 WO claimed
EP-0505023-A1 Synergistic, additive or antagonistic product selection test for biocides NALCO CHEMICAL COMPANY (US) 1992-09-23 EP claimed
EP-0358856-A2 Novel insecticidal dibenzoyl-tert-butylcarbanonitrile compounds and method for the preparation thereof AMERICAN CYANAMID COMPANY (US) 1990-03-21 EP claimed
US-4857550-A Novel insecticidal dibenzoyl-tert-butylcarbazonitrile compounds and method for the preparation thereof AMERICAN CYANAMID COMPANY (US) 1989-08-15 US claimed
US-4800235-A MICROBIOCIDES NALCO CHEMICAL COMPANY (US) 1989-01-24 US claimed
EP-0252278-A2 Disinfecting agents and their use in disinfecting the skin and mucous membranes Henkel Kommanditgesellschaft auf Aktien (DE) 1988-01-13 EP claimed
US-4076765-A MOLDING MATERIALS, CONSTRUCTION MATERIALS SUMITOMO CHEMICAL COMPANY, LIMITED (JA) 1978-02-28 US 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-12614726-B2 Dispersion and stabilization of MXene materials and MXene materials for energy storage applications SLC10A6, SLC9A2, SLC6A19 GAA 4182/4885SIGMAR1 158/4885MAPT 3721/4885

“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.