Bromide

Bromide

SCHEMBL4362535

C=CCn1cc[n+](CCCCCCCC)c1.[Br-]

nearest known ligand 0.48

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 1/20 0.43
CHRM4 known ✓ P08173 1/20 0.43
CHRM5 known ✓ P08912 1/20 0.43
CHRM1 known ✓ P11229 1/20 0.43
CHRM3 known ✓ P20309 1/20 0.43
ACHE known ✓ P22303 1/20 0.43
HSP90AA1 P07900 2/20 0.44
KMT2A Q03164 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
MEN1 O00255 1/20 0.44
EGFR P00533 1/20 0.43
LMNA P02545 1/20 0.43
PLA2G1B P04054 1/20 0.43
ERBB2 P04626 1/20 0.43
LCK P06239 1/20 0.43
FYN P06241 1/20 0.43
ADRA2A P08913 1/20 0.43
ADORA3 P0DMS8 1/20 0.43
TSHR P16473 1/20 0.43
ALOX12 P18054 1/20 0.43

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 SCHEMBL29770293 1.00 HSP90AA1 (0.44) HSP90AA1KMT2ASMN1; SMN2MEN1EGFR
SCHEMBL15901858 0.98 MEN1 (0.42) HSP90AA1KMT2ASMN1; SMN2MEN1CHRM2
SCHEMBL2693562 0.98 MEN1 (0.42) HSP90AA1KMT2ASMN1; SMN2MEN1CHRM2
SCHEMBL4358559 0.98 MEN1 (0.42) HSP90AA1KMT2ASMN1; SMN2MEN1CHRM2
SCHEMBL3398646 0.98 MEN1 (0.42) HSP90AA1KMT2ASMN1; SMN2MEN1CHRM2
SCHEMBL23698403 0.98 MEN1 (0.42) HSP90AA1KMT2ASMN1; SMN2MEN1CHRM2
Bromide SCHEMBL4364809 0.98 MEN1 (0.42) HSP90AA1KMT2ASMN1; SMN2MEN1
Hydrochloric Acid SCHEMBL2900812 0.97 MEN1 (0.43) HSP90AA1KMT2ASMN1; SMN2MEN1CHRM2
Iodide SCHEMBL2894605 0.97 SMN1; SMN2 (0.42) HSP90AA1KMT2ASMN1; SMN2MEN1LMNA
SCHEMBL1680333 0.97 MEN1 (0.40) HSP90AA1KMT2ASMN1; SMN2MEN1CHRM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1721900-B1 NOVEL IMIDAZOLIUM COMPOUND KANTO KAGAKU (JP) 2014-06-11 EP disclosed
US-7517999-B2 needs no complicated operations for dissolution and has excellent handleability and a high ionic conductivity, electrolytes; 1-butyl-3-allylimidazolium bromide KANTO KAGAKU KABUSHIKI KAISHA (JP) 2009-04-14 US disclosed
US-20070191612-A1 Needs no complicated operations for dissolution and has excellent handleability and a high ionic conductivity, electrolytes; 1-butyl-3-allylimidazolium bromide HIROYUKI OHNO (JP) 2007-08-16 US disclosed
EP-1721900-A1 NOVEL IMIDAZOLIUM COMPOUND Kanto Kagaku Kabushiki Kaisha (JP) 2006-11-15 EP 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-20070191612-A1 Needs no complicated operations for dissolution and has excellent handleability and a high ionic conductivity, electrolytes; 1-butyl-3-allylimidazolium bromide SLC26A3, KCNJ11, SLC26A4 CHRM2 1811/4885CHRM4 2877/4885CHRM5 4079/4885

“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.