Bromide

Bromide

SCHEMBL3418571

C=Cc1[nH]cc[n+]1CCCCCCCCCCCCCCCC.[Br-]

nearest known ligand 0.38

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 0.38
CHRM1 known ✓ P11229 2/20 0.38
ACHE known ✓ P22303 2/20 0.38
CHRM4 known ✓ P08173 1/20 0.38
CHRM5 known ✓ P08912 1/20 0.38
CHRM3 known ✓ P20309 1/20 0.38
OPRM1 known ✓ P35372 1/20 0.35
HTT P42858 6/20 0.38
SMN1; SMN2 Q16637 6/20 0.38
KMT2A Q03164 5/20 0.38
HSP90AA1 P07900 4/20 0.38
LMNA P02545 4/20 0.38
MEN1 O00255 4/20 0.38
RAD52 P43351 3/20 0.38
MAPT P10636 3/20 0.38
CYP1A2 P05177 2/20 0.38
CYP2D6 P10635 2/20 0.38
CYP2C19 P33261 2/20 0.38
ADRA2A P08913 2/20 0.38
ADORA3 P0DMS8 2/20 0.38

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 SCHEMBL3419365 1.00 HTT (0.38) HTTSMN1; SMN2KMT2AHSP90AA1LMNA
SCHEMBL9067234 0.98 KMT2A (0.39) HTTSMN1; SMN2KMT2AHSP90AA1LMNA
SCHEMBL15657208 0.98 KMT2A (0.39) HTTSMN1; SMN2KMT2AHSP90AA1LMNA
Iodide SCHEMBL810561 0.97 HTT (0.41) HTTSMN1; SMN2KMT2AHSP90AA1LMNA
Hydrochloric Acid SCHEMBL3419607 0.97 SMN1; SMN2 (0.38) HTTSMN1; SMN2KMT2AHSP90AA1LMNA
Hydrochloric Acid SCHEMBL8415719 0.97 SMN1; SMN2 (0.38) HTTSMN1; SMN2KMT2AHSP90AA1LMNA
Bromide SCHEMBL12500813 0.93 ALDH1A1 (0.31) TSHRCA1CA2ALDH1A1
SCHEMBL29390 0.91 ALDH1A1 (0.32) HTTSMN1; SMN2KMT2AHSP90AA1LMNA
Hydrochloric Acid SCHEMBL29697222 0.90 ALDH1A1 (0.31) TSHRCA1CA2ALDH1A1
Sulfuric Acid SCHEMBL30240028 0.83

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
WO-2010017563-A1 POLYMERIC IONIC LIQUIDS, METHODS OF MAKING AND METHODS OF USE THEREOF UNIVERSITY OF TOLEDO (US) 2010-02-11 WO claimed
WO-2013181345-A2 SYNTHESIS OF POLYMERIC IONIC LIQUIDS USING A PHOTOCHEMICAL POLYMERIZATION PROCESS THE UNIVERSITY OF TOLEDO (US) 2013-12-05 WO disclosed
WO-2010017563-A1 POLYMERIC IONIC LIQUIDS, METHODS OF MAKING AND METHODS OF USE THEREOF UNIVERSITY OF TOLEDO (US) 2010-02-11 WO disclosed
WO-2010017564-A1 BORON SELECTIVE IONIC LIQUIDS AND POLYMERIC IONIC LIQUIDS, METHODS OF MAKING AND METHODS OF USE THEREOF UNIVERSITY OF TOLEDO (US) 2010-02-11 WO disclosed