Benzylimidazole

Benzylimidazole

SCHEMBL3786782

I.c1ccc(Cn2ccnc2)cc1

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHRM1CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNG

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
CYP11B1 P15538 16/20 0.96
CYP11B2 P19099 13/20 0.96
CYP19A1 P11511 6/20 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 SCHEMBL31453527 0.96 CYP11B1 (0.96) CYP11B1CYP11B2CYP19A1CYP1A2POLB
Benzylimidazole SCHEMBL29239318 0.96 CYP11B1 (0.96) CYP11B1CYP11B2CYP19A1CYP1A2POLB
Benzylimidazole SCHEMBL16237308 0.96 CYP11B1 (0.96) CYP11B1CYP11B2CYP19A1CYP1A2POLB
Benzylimidazole SCHEMBL411827 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 SCHEMBL28970402 0.89 CYP11B1 (0.83) 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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7855285-B2 Methods for selective N-9 glycosylation of purines BRIGHAM YOUNG UNIVERSITY (US) 2010-12-21 US disclosed
US-20080207891-A1 Methods For Selective N-9 Glycosylation of Purines BRIGHAM YOUNG UNIVERSITY (US) 2008-08-28 US disclosed
EP-1895841-A2 METHODS FOR SELECTIVE N-9 GLYCOSYLATION OF PURINES Brigham Young University (US) 2008-03-12 EP disclosed
WO-2006138396-A2 METHODS FOR SELECTIVE N-9 GLYCOSYLATION OF PURINES BRIGHAM YOUNG UNIVERSITY, TRANSFER TECHNOLOGY OFFICE (US) 2006-12-28 WO 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-20080207891-A1 Methods For Selective N-9 Glycosylation of Purines PNP, SLC29A2, SLC28A2 CYP11B1 2369/4885CYP11B2 2059/4885CYP19A1 4818/4885

“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.