Bromide

Bromide

SCHEMBL31252115

O=C(NCCCn1cc(Cl)[n+](CCCC[n+]2cc(Cl)n(CCCCn3cnc(Cl)c3)c2)c1)OCc1ccccc1.[Br-].[Br-]

nearest known ligand 0.36

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 18)

geneUniProtsupporting neighboursconfidence
▸ HTT P42858 1/20 0.36
▸ KAT2B Q92831 1/20 0.35
▸ TGM2 P21980 1/20 0.34
▸ KEAP1 Q14145 3/20 0.33
▸ NFE2L2 Q16236 3/20 0.33
▸ SMN1; SMN2 Q16637 2/20 0.33
▸ LMNA P02545 1/20 0.33
▸ QPCT Q16769 1/20 0.33
▸ L3MBTL1 Q9Y468 2/20 0.33
▸ MAPT P10636 1/20 0.33
▸ MMP2 P08253 2/20 0.32
▸ MMP9 P14780 2/20 0.32
▸ ANPEP P15144 1/20 0.32
▸ CA1 P00915 1/20 0.32
▸ CA2 P00918 1/20 0.32
▸ STING1 Q86WV6 2/20 0.32
▸ DPP8 Q6V1X1 1/20 0.31
▸ DPP7 Q9UHL4 1/20 0.31

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 SCHEMBL31252190 0.81 HTT (0.36) HTTKAT2BTGM2KEAP1NFE2L2
Bromide SCHEMBL31252086 0.80 HTT (0.46) HTTKAT2BTGM2KEAP1NFE2L2
SCHEMBL31252012 0.79 HTT (0.55) HTTKAT2BTGM2KEAP1NFE2L2
Bromide SCHEMBL31252188 0.78 HTT (0.34) HTTTGM2KEAP1NFE2L2SMN1; SMN2
Bromide SCHEMBL31252103 0.70 HTT (0.46) HTTKAT2BTGM2KEAP1NFE2L2
Bromide SCHEMBL31252155 0.69 HTT (0.46) HTTKAT2BTGM2KEAP1NFE2L2
Bromide SCHEMBL31252065 0.69 HTT (0.46) HTTKAT2BTGM2KEAP1NFE2L2
Bromide SCHEMBL31252066 0.69 HTT (0.46) HTTKAT2BTGM2KEAP1NFE2L2
SCHEMBL31252144 0.69 HTT (0.54) HTTKAT2BTGM2KEAP1NFE2L2
SCHEMBL31252088 0.67 HTT (0.54) HTTKAT2BTGM2KEAP1NFE2L2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4720162-A1 MAIN CHAIN CATIONIC OLIGO(IMIDAZOLIUM) FORMS N-HETEROCYCLIC CARBENE FOR EFFECTIVE BACTERIAL KILLING IN COMPLEX ENVIRONMENT Nanyang Technological University (SG) 2026-04-08 — — EP disclosed
WO-2024248739-A1 MAIN CHAIN CATIONIC OLIGO(IMIDAZOLIUM) FORMS N-HETEROCYCLIC CARBENE FOR EFFECTIVE BACTERIAL KILLING IN COMPLEX ENVIRONMENT NANYANG TECHNOLOGICAL UNIVERSITY (SG) 2024-12-05 — — WO disclosed
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