Bromide

Bromide

SCHEMBL145264

CC[N+](C)(C)CCOC.[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 10)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 2/20 0.44
HSP90AA1 P07900 1/20 0.44
RAD52 P43351 1/20 0.44
HTT P42858 1/20 0.40
KMT2A Q03164 1/20 0.40
CHRNB4 P30926 1/20 0.34
CHRNA3 P32297 1/20 0.34
CHRNA7 P36544 1/20 0.34
BBOX1 O75936 3/20 0.33
ESR1 P03372 1/20 0.33

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
SCHEMBL119566 0.97
Iodide SCHEMBL2430929 0.94 DNM1 (0.40) DNM1HSP90AA1RAD52HTTKMT2A
Water SCHEMBL142997 0.94 DNM1 (0.40) DNM1HSP90AA1RAD52HTTKMT2A
Hydrochloric Acid SCHEMBL16594014 0.94 DNM1 (0.40) DNM1HSP90AA1RAD52HTTKMT2A
SCHEMBL1277047 0.87 DNM1 (0.36) DNM1HSP90AA1RAD52HTTKMT2A
Bromide SCHEMBL3389321 0.85 DNM1 (0.38) DNM1HSP90AA1RAD52HTTKMT2A
Bromide SCHEMBL30869348 0.85 DNM1 (0.33) DNM1HTT
SCHEMBL1277012 0.82 DNM1 (0.36) DNM1HSP90AA1RAD52HTTKMT2A
SCHEMBL12583479 0.82 HTT (0.32) DNM1HTT
Acetic Acid SCHEMBL2761986 0.82 BBOX1 (0.48) DNM1HSP90AA1RAD52HTTKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2834251-B1 IONIC COMPOUNDS HAVING A SILYLOXY GROUP HYDRO QUEBEC (CA) 2019-11-13 EP disclosed
US-9969757-B2 Ionic compounds having a silyloxy group HYDRO-QUEBEC (CA) 2018-05-15 US disclosed
US-20150093655-A1 IONIC COMPOUNDS HAVING A SILYLOXY GROUP HYDRO-QUEBEC (CA) 2015-04-02 US disclosed
EP-2834251-A1 IONIC COMPOUNDS HAVING A SILYLOXY GROUP Hydro-Québec (CA) 2015-02-11 EP disclosed
WO-2013149349-A1 IONIC COMPOUNDS HAVING A SILYLOXY GROUP HYDRO-QUéBEC (CA) 2013-10-10 WO disclosed
US-20120058057-A1 Anti-dandruff Agents MERCK PATENT GMBH (DE) 2012-03-08 US disclosed
WO-2010136105-A2 AMMONIUMCARBOXYLATES MERCK PATENT GMBH (DE) 2010-12-02 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-20150093655-A1 IONIC COMPOUNDS HAVING A SILYLOXY GROUP EPCAM, ILK, VIM DNM1 2791/4885HSP90AA1 4015/4885RAD52 4711/4885
US-20120058057-A1 Anti-dandruff Agents POLR1C, ETF1, PIK3C3 DNM1 128/4885HSP90AA1 2834/4885RAD52 4562/4885

“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.