Bromide

Bromide

SCHEMBL7045704

CCCCCCCCCCCCCCCC/C=C/OC(=O)C1=C(C[n+]2ccccc2)NC(C[n+]2ccccc2)=C(C(=O)O/C=C/CCCCCCCCCCCCCCCC)C1c1ccccc1.[Br-].[Br-]

nearest known ligand 0.35

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

The experimentally established mechanism targets of Bromide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
SOAT2 O75908 1/20 0.35
SOAT1 P35610 1/20 0.35
EPHX2 P34913 4/20 0.35
FAAH O00519 3/20 0.35
CNR1 P21554 1/20 0.35
CNR2 P34972 1/20 0.35
ADORA3 P0DMS8 1/20 0.34
PPARG P37231 3/20 0.34
CES1 P23141 1/20 0.33
DAGLA Q9Y4D2 1/20 0.33
CACNA1B Q00975 1/20 0.33
CACNA1F O60840 1/20 0.33
CACNA1D Q01668 1/20 0.33
CACNA1S Q13698 1/20 0.33
CACNA1C Q13936 1/20 0.33
DUSP3 P51452 1/20 0.33
PTPN7 P35236 1/20 0.33
KDM4E B2RXH2 1/20 0.33
ALDH1A1 P00352 1/20 0.33

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
Bromide SCHEMBL7041639 0.83 PPARG (0.46) ADORA3PPARGCACNA1FCACNA1DCACNA1S
Bromide SCHEMBL7044895 0.83 PPARG (0.46) ADORA3PPARGCACNA1FCACNA1DCACNA1S
SCHEMBL6552826 0.71 SOAT2 (0.49) SOAT2SOAT1EPHX2FAAHCNR1
SCHEMBL6552841 0.71 SOAT2 (0.49) SOAT2SOAT1EPHX2FAAHCNR1
SCHEMBL6552573 0.71 SOAT2 (0.49) SOAT2SOAT1EPHX2FAAHCNR1
SCHEMBL6552788 0.71 SOAT2 (0.49) SOAT2SOAT1EPHX2FAAHCNR1
SCHEMBL6552638 0.71 SOAT2 (0.49) SOAT2SOAT1EPHX2FAAHCNR1
SCHEMBL21528269 0.71 SOAT2 (0.49) SOAT2SOAT1EPHX2FAAHCNR1
SCHEMBL22439055 0.71 SOAT2 (0.49) SOAT2SOAT1EPHX2FAAHCNR1
SCHEMBL6551288 0.69 LMNA (0.47) SOAT2SOAT1EPHX2FAAHCNR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030064954-A1 Cationic amphiphilic 1,4-dihydropyridine derivatives useful for delivery of nucleotide containing compounds SPONDULI SERVICES, LTD. (AU) 2003-04-03 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 (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-20030064954-A1 Cationic amphiphilic 1,4-dihydropyridine derivatives useful for delivery of nucleotide containing compounds ACIN1, DNA2, KPNA1 SOAT2 1325/4885SOAT1 1174/4885EPHX2 2925/4885

“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.