Bromide

Bromide

SCHEMBL19210213

CCCCCC[n+]1cc[nH]c1C.[Br-]

nearest known ligand 0.44

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
CHRM2 known ✓ P08172 2/20 0.41
CHRM1 known ✓ P11229 2/20 0.41
ACHE known ✓ P22303 2/20 0.41
CHRM4 known ✓ P08173 1/20 0.41
CHRM5 known ✓ P08912 1/20 0.41
CHRM3 known ✓ P20309 1/20 0.41
OPRM1 known ✓ P35372 1/20 0.38
HTT P42858 5/20 0.44
CA1 P00915 2/20 0.44
CA2 P00918 2/20 0.44
SMN1; SMN2 Q16637 5/20 0.41
LMNA P02545 4/20 0.41
KMT2A Q03164 3/20 0.41
HSP90AA1 P07900 3/20 0.41
RAD52 P43351 3/20 0.41
MEN1 O00255 2/20 0.41
CYP1A2 P05177 2/20 0.41
CYP2D6 P10635 2/20 0.41
CYP2C19 P33261 2/20 0.41
ADRA2A P08913 2/20 0.41

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 SCHEMBL15798390 1.00 HTT (0.44) HTTCA1CA2SMN1; SMN2LMNA
Bromide SCHEMBL9194597 1.00 HTT (0.44) HTTCA1CA2SMN1; SMN2LMNA
Bromide SCHEMBL17027655 1.00 HTT (0.44) HTTCA1CA2SMN1; SMN2LMNA
Bromide SCHEMBL8873590 1.00 HTT (0.44) HTTCA1CA2SMN1; SMN2LMNA
Bromide SCHEMBL193259 1.00 HTT (0.44) HTTCA1CA2SMN1; SMN2LMNA
Bromide SCHEMBL14894866 1.00 HTT (0.44) HTTCA1CA2SMN1; SMN2LMNA
Bromide SCHEMBL15798045 1.00 HTT (0.44) HTTCA1CA2SMN1; SMN2LMNA
Bromide SCHEMBL8750352 0.98 HTT (0.43) HTTCA1CA2SMN1; SMN2LMNA
SCHEMBL2328683 0.98 HTT (0.46) HTTCA1CA2SMN1; SMN2LMNA
SCHEMBL363480 0.98 HTT (0.46) HTTCA1CA2SMN1; SMN2LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4612750-A1 MIXED POLYHALIDE ELECTROLYTES FOR A STATIC BATTERY AND A METHOD FOR FABRICATING A STATIC BATTERY CELL EOS Energy Technology Holdings, LLC (US) 2025-09-10 EP disclosed
WO-2024097835-A1 MIXED POLYHALIDE ELECTROLYTES FOR A STATIC BATTERY AND A METHOD FOR FABRICATING A STATIC BATTERY CELL EOS Energy Technology Holdings, LLC (US) 2024-05-10 WO disclosed
EP-3459137-A2 ZINC-HALIDE BATTERY USING A DEEP EUTECTIC SOLVENT-BASED ELECTROLYTE Eos Energy Storage, LLC (US) 2019-03-27 EP disclosed
EP-3437153-A1 ELECTROLYTE FOR RECHARGEABLE ELECTROCHEMICAL CELL Eos Energy Storage, LLC (US) 2019-02-06 EP disclosed
WO-2017172878-A1 ELECTROLYTE FOR RECHARGEABLE ELECTROCHEMICAL CELL EOS ENERGY STORAGE, LLC (US) 2017-10-05 WO disclosed
EP-3204968-A1 TERMINAL ASSEMBLY FOR BIPOLAR ELECTROCHEMICAL CELL OR BATTERY Eos Energy Storage, LLC (US) 2017-08-16 EP disclosed
EP-3204977-A1 ELECTROLYTE FOR RECHARGEABLE ELECTROCHEMICAL CELL Eos Energy Storage, LLC (US) 2017-08-16 EP disclosed
EP-3204970-A2 ELECTOLYTE COMPOSITION FOR A ZINC-HALIDE BATTERY AND BIPOLAR ELECTRODE COMPRISING A TITANIUM CARBIDE COATED CATHODE BOX Eos Energy Storage, LLC (US) 2017-08-16 EP disclosed