Bromide

Bromide

SCHEMBL3314015

CCCCc1ccc(CCCC[n+]2ccc(C)cc2)cc1.[Br-]

nearest known ligand 0.67

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
CHKA known ✓ P35790 2/20 0.55
CHRM2 known ✓ P08172 2/20 0.44
CHRM5 known ✓ P08912 2/20 0.44
CHRM1 known ✓ P11229 2/20 0.44
CHRM3 known ✓ P20309 2/20 0.44
ACHE known ✓ P22303 2/20 0.44
CHRM4 known ✓ P08173 1/20 0.44
HTT P42858 5/20 0.67
KMT2A Q03164 4/20 0.57
MEN1 O00255 3/20 0.57
MAPT P10636 3/20 0.57
RAD52 P43351 3/20 0.57
MAPK1 P28482 1/20 0.57
NPSR1 Q6W5P4 1/20 0.57
CHRNA7 P36544 2/20 0.50
CHRNA10 Q9GZZ6 2/20 0.50
CHRNA9 Q9UGM1 2/20 0.50
TP53 P04637 2/20 0.48
CYP1A2 P05177 1/20 0.48
CYP2D6 P10635 1/20 0.48

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
SCHEMBL13334099 0.98 HTT (0.69) HTTKMT2AMEN1MAPTRAD52
SCHEMBL4405443 0.91 HTT (0.61) HTTKMT2AMEN1MAPTRAD52
SCHEMBL13361695 0.89 HTT (0.60) HTTKMT2AMEN1MAPTRAD52
Bromide SCHEMBL9362559 0.85 HTT (0.91) HTTKMT2AMEN1MAPTRAD52
SCHEMBL16405358 0.84 CHRM2 (0.62) HTTKMT2AMEN1MAPTRAD52
Bromide SCHEMBL8659288 0.83 KMT2A (0.64) HTTKMT2AMEN1MAPTRAD52
Bromide SCHEMBL1502789 0.83 HTT (0.96) HTTKMT2AMEN1MAPTRAD52
Bromide SCHEMBL9362504 0.83 HTT (0.96) HTTKMT2AMEN1MAPTRAD52
Bromide SCHEMBL1502820 0.83 HTT (0.96) HTTKMT2AMEN1MAPTRAD52
Miripirium SCHEMBL10323639 0.83 HTT (0.96) HTTKMT2AMEN1MAPTRAD52

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20140371266-A1 Mono Quaternary Ammonium Salts and Methods for Modulating Neuronal Nicotinic Acetylcholine Receptors UNIV KENTUCKY RES FOUND (US) 2014-12-18 US claimed
US-8846937-B2 Mono quaternary ammonium salts and methods for modulating neuronal nicotinic acetylcholine receptors UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 2014-09-30 US claimed
US-20100113511-A1 Mono Quaternary Ammonium Salts and Methods for Modulating Neuronal Nicotinic Acetylcholine Receptors UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 2010-05-06 US claimed
WO-2007149392-A1 MONO QUATERNARY AMMONIUM SALTS AND METHODS FOR MODULATING NEURONAL NICOTINIC ACETYLCHOLINE RECEPTORS UNIVERSITY OF KENTUCKY (US) 2007-12-27 WO claimed
US-9550753-B2 Mono quaternary ammonium salts and methods for modulating neuronal nicotinic acetylcholine receptors UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 2017-01-24 US disclosed
US-20140371266-A1 Mono Quaternary Ammonium Salts and Methods for Modulating Neuronal Nicotinic Acetylcholine Receptors UNIV KENTUCKY RES FOUND (US) 2014-12-18 US disclosed
US-8846937-B2 Mono quaternary ammonium salts and methods for modulating neuronal nicotinic acetylcholine receptors UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 2014-09-30 US disclosed
US-20100113511-A1 Mono Quaternary Ammonium Salts and Methods for Modulating Neuronal Nicotinic Acetylcholine Receptors UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 2010-05-06 US disclosed
WO-2007149392-A1 MONO QUATERNARY AMMONIUM SALTS AND METHODS FOR MODULATING NEURONAL NICOTINIC ACETYLCHOLINE RECEPTORS UNIVERSITY OF KENTUCKY (US) 2007-12-27 WO 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 (2 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-20100113511-A1 Mono Quaternary Ammonium Salts and Methods for Modulating Neuronal Nicotinic Acetylcholine Receptors CHRNA2, CHRNA4, CHRNA5 CHKA 272/4885CHRM2 20/4885CHRM5 18/4885
US-20140371266-A1 Mono Quaternary Ammonium Salts and Methods for Modulating Neuronal Nicotinic Acetylcholine Receptors CHRNA2, CHRNA4, CHRNA5 CHKA 271/4885CHRM2 20/4885CHRM5 18/4885

“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.