Bromide

Bromide

SCHEMBL18154038

Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.Br.[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].[Br-].c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21.c1ccc2c(c1)ccc[n+]2CCCCCC[n+]1cccc2ccccc21

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4

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 2)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 14/20 0.96
BCHE P06276 14/20 0.96

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 SCHEMBL4891809 0.98 BCHE (1.00) BCHEACHE
Bromide SCHEMBL3599912 0.98 BCHE (1.00) BCHEACHE
Bromide SCHEMBL18154062 0.98 BCHE (1.00) BCHEACHE
Bromide SCHEMBL18154058 0.98 BCHE (1.00) BCHEACHE
Bromide SCHEMBL3597256 0.98 BCHE (1.00) BCHEACHE
Bromide SCHEMBL14937456 0.96 BCHE (1.00) BCHEACHE
SCHEMBL3596114 0.96 BCHE (1.00) BCHEACHE
SCHEMBL3604422 0.96 BCHE (1.00) BCHEACHE
SCHEMBL4887020 0.96 BCHE (1.00) BCHEACHE
SCHEMBL3603725 0.96 BCHE (1.00) BCHEACHE

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
WO-2016167837-A1 CORROSION INHIBITION SCHLUMBERGER CANADA LIMITED (CA) 2016-10-20 WO disclosed