Benzylimidazole

Benzylimidazole

SCHEMBL411827

Cl.c1ccc(Cn2ccnc2)cc1

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

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CYP19A1 known ✓ P11511 6/20 0.96
CYP11B1 P15538 16/20 0.96
CYP11B2 P19099 13/20 0.96
CYP1A2 P05177 1/20 0.96
POLB P06746 1/20 0.96
CYP3A4 P08684 1/20 0.96
CYP2D6 P10635 1/20 0.96
MAPT P10636 1/20 0.96
TBXAS1 P24557 1/20 0.96
QPCT Q16769 1/20 0.96
CYP4Z1 Q86W10 1/20 0.96
QPCTL Q9NXS2 1/20 0.96
CYP17A1 P05093 1/20 0.77
CYP2A6 P11509 1/20 0.67
CYP2B6 P20813 1/20 0.67

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
Benzylimidazole SCHEMBL414 0.98 CYP11B1 (1.00) CYP11B1CYP11B2CYP19A1CYP1A2POLB
SCHEMBL22063900 0.98 CYP11B1 (1.00) CYP11B1CYP11B2CYP19A1CYP1A2POLB
Benzylimidazole SCHEMBL3786782 0.96 CYP11B1 (0.96) CYP11B1CYP11B2CYP19A1CYP1A2POLB
Benzylimidazole SCHEMBL29239318 0.96 CYP11B1 (0.96) CYP11B1CYP11B2CYP19A1CYP1A2POLB
Benzylimidazole SCHEMBL31453527 0.96 CYP11B1 (0.96) CYP11B1CYP11B2CYP19A1CYP1A2POLB
Benzylimidazole SCHEMBL16237308 0.96 CYP11B1 (0.96) CYP11B1CYP11B2CYP19A1CYP1A2POLB
Benzylimidazole SCHEMBL27803894 0.92 CYP11B1 (0.89) CYP11B1CYP11B2CYP19A1CYP1A2POLB
Benzylimidazole SCHEMBL28764644 0.91 CYP11B1 (0.86) CYP11B1CYP11B2CYP19A1CYP1A2POLB
Benzylimidazole SCHEMBL27535101 0.91 CYP11B1 (0.86) CYP11B1CYP11B2CYP19A1CYP1A2POLB
Benzylimidazole SCHEMBL7942345 0.90 CYP11B1 (0.77) CYP11B1CYP11B2CYP19A1CYP1A2POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109957286-A Ink and its preparation method and application 深圳市百柔新材料技术有限公司 2019-07-02 CN claimed
CN-108136366-A molecularly imprinted polymer 相位全息成像PHI有限公司 2018-06-08 CN claimed
US-20120020915-A1 Compounds and Methods for Treating Cancer and Diseases of the Central Nervous System QUEENS UNIVERSITY AT KINGSTON (CA) 2012-01-26 US claimed
US-20110319459-A1 Compounds and Methods for Treating Cancer and Diseases of the Central Nervous System OSTA BIOTECHNOLOGIES (CA) 2011-12-29 US claimed
EP-2173740-A1 HEME-OXYGENASE INHIBITORS AND USE OF THE SAME IN THE TREATMENT OF CANCER AND DISEASES OF THE CENTRAL NERVOUS SYSTEM Osta Biotechnologies (CA) 2010-04-14 EP claimed
US-20090176831-A1 Compounds and Methods for Treating Cancer and Diseases of the Central Nervous System OSTA BIOTECHNOLOGIES (CA) 2009-07-09 US claimed
WO-2008151437-A1 HEME-OXYGENASE INHIBITORS AND USE OF THE SAME IN THE TREATMENT OF CANCER AND DISEASES OF THE CENTRAL NERVOUS SYSTEM OSTA BIOTECHNOLOGIES (CA) 2008-12-18 WO claimed
EP-1094706-A1 PROCESS FOR THE BIOCIDAL TREATMENT OF SURFACES RHODIA CHIMIE (FR) 2001-05-02 EP claimed
WO-2000002449-A1 PROCESS FOR THE BIOCIDAL TREATMENT OF SURFACES RHODIA CHIMIE (FR) 2000-01-20 WO claimed
US-20250270537-A1 METHODS FOR NUCLEIC ACID CAPTURE ZYMO RESEARCH CORPORATION (US) 2025-08-28 US disclosed
US-20220186207-A1 METHODS FOR NUCLEIC ACID CAPTURE ZYMO RES CORPORATION (US) 2022-06-16 US disclosed
US-11236325-B2 Methods for nucleic acid capture ZYMO RESEARCH CORPORATION (US) 2022-02-01 US disclosed
US-11214715-B2 Ionic polymers and their use as wet-adhesives and coatings ACatechol, Inc. (US) 2022-01-04 US disclosed
CN-107427869-B Heavy metal fixing agent for treating ash and method for treating ash using same 栗田工业株式会社 2021-02-02 CN disclosed
EP-1324821-A2 EMULSION COMPRISING A BLEND OF CATIONIC, ANIONIC AND BRIDGING SURFACTANS, OIL AND WATER STEPAN COMPANY (US) 2003-07-09 EP disclosed
EP-1320354-A2 SHAMPOO AND BODY WASH COMPOSITION STEPAN COMPANY (US) 2003-06-25 EP disclosed
WO-2002022083-A2 EMULSION COMPRISING A BLEND OF CATIONIC, ANIONIC AND BRIDGING SURFACTANTS, OIL AND WATER STEPAN COMPANY (US) 2002-03-21 WO disclosed
WO-2002022105-A2 SHAMPOO AND BODY WASH COMPOSITION STEPAN COMPANY (US) 2002-03-21 WO disclosed
EP-0056664-B1 ADDITION POLYMERS AND METAL COMPLEXES THEREOF EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1986-11-12 EP disclosed
US-4032596-A QUATERNARY AMMONIUM SALTS, FREE RADICAL CATALYSTS AIR PRODUCTS AND CHEMICALS, INC. (US) 1977-06-28 US 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 (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-20110319459-A1 Compounds and Methods for Treating Cancer and Diseases of the Central Nervous System TXNRD2, HMOX1, HMOX2 CYP19A1 884/4885CYP11B1 61/4885CYP11B2 68/4885
US-20120020915-A1 Compounds and Methods for Treating Cancer and Diseases of the Central Nervous System HMOX1, HMOX2, CYC1 CYP19A1 641/4885CYP11B1 63/4885CYP11B2 60/4885
US-20090176831-A1 Compounds and Methods for Treating Cancer and Diseases of the Central Nervous System HMOX1, HMOX2, CYC1 CYP19A1 614/4885CYP11B1 55/4885CYP11B2 52/4885

“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.