Bromide

Bromide

SCHEMBL31252190

O=C(NCCCn1cc(F)[n+](CCCC[n+]2cc(F)n(CCCCn3cnc(F)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 20)

geneUniProtsupporting neighboursconfidence
▸ HTT P42858 1/20 0.36
▸ LMNA P02545 1/20 0.35
▸ SMN1; SMN2 Q16637 1/20 0.35
▸ QPCT Q16769 1/20 0.34
▸ TGM2 P21980 1/20 0.34
▸ KEAP1 Q14145 3/20 0.33
▸ NFE2L2 Q16236 3/20 0.33
▸ L3MBTL1 Q9Y468 2/20 0.33
▸ MAPT P10636 1/20 0.33
▸ ANPEP P15144 1/20 0.32
▸ CA1 P00915 1/20 0.32
▸ CA2 P00918 1/20 0.32
▸ GHSR Q92847 1/20 0.32
▸ SLC40A1 Q9NP59 1/20 0.32
▸ DPP8 Q6V1X1 1/20 0.31
▸ DPP7 Q9UHL4 1/20 0.31
▸ KAT2B Q92831 1/20 0.31
▸ FOLH1 Q04609 1/20 0.31
▸ MMP2 P08253 1/20 0.31
▸ MMP9 P14780 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 SCHEMBL31252115 0.81 HTT (0.36) HTTLMNASMN1; SMN2QPCTTGM2
SCHEMBL31252144 0.80 HTT (0.54) HTTLMNASMN1; SMN2QPCTTGM2
Bromide SCHEMBL31252155 0.80 HTT (0.46) HTTLMNASMN1; SMN2TGM2KEAP1
Bromide SCHEMBL31252188 0.79 HTT (0.34) HTTLMNASMN1; SMN2QPCTTGM2
Bromide SCHEMBL31252103 0.79 HTT (0.46) HTTLMNASMN1; SMN2TGM2KEAP1
Bromide SCHEMBL31252279 0.70 HTT (0.44) HTTLMNASMN1; SMN2TGM2KEAP1
SCHEMBL31252012 0.70 HTT (0.55) HTTLMNASMN1; SMN2QPCTTGM2
Bromide SCHEMBL31252065 0.69 HTT (0.46) HTTLMNASMN1; SMN2TGM2KEAP1
Bromide SCHEMBL31252086 0.69 HTT (0.46) HTTLMNASMN1; SMN2TGM2KEAP1
SCHEMBL31252099 0.68 HTT (0.51) HTTLMNASMN1; SMN2QPCTTGM2

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
Send feedback