Bromide

Bromide

SCHEMBL186788

CCCCOC(=O)C(OC(=O)C[n+]1ccn(C)c1)c1ccccc1.[Br-]

nearest known ligand 0.39

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 19)

geneUniProtsupporting neighboursconfidence
CHRM4 known ✓ P08173 1/20 0.34
CHRM1 known ✓ P11229 1/20 0.34
CHRM3 known ✓ P20309 1/20 0.34
TSHR P16473 3/20 0.36
L3MBTL1 Q9Y468 3/20 0.36
ALOX15 P16050 1/20 0.36
SMN1; SMN2 Q16637 3/20 0.36
NPC1 O15118 2/20 0.36
RAB9A P51151 2/20 0.36
LMNA P02545 1/20 0.36
TDP1 Q9NUW8 2/20 0.36
MEN1 O00255 2/20 0.36
KMT2A Q03164 2/20 0.36
HSP90AA1 P07900 1/20 0.36
ALDH1A1 P00352 2/20 0.35
HSD17B10 Q99714 1/20 0.35
CYP3A4 P08684 1/20 0.34
MAPK1 P28482 1/20 0.34
POLB P06746 1/20 0.34

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 SCHEMBL187505 1.00 TSHR (0.36) TSHRL3MBTL1ALOX15SMN1; SMN2NPC1
SCHEMBL15896800 0.99 TSHR (0.37) TSHRL3MBTL1ALOX15SMN1; SMN2NPC1
SCHEMBL15896807 0.99 TSHR (0.37) TSHRL3MBTL1ALOX15SMN1; SMN2NPC1
SCHEMBL15896790 0.99 TSHR (0.37) TSHRL3MBTL1ALOX15SMN1; SMN2NPC1
SCHEMBL805649 0.96 NPC1 (0.41) TSHRSMN1; SMN2NPC1RAB9ALMNA
SCHEMBL15897200 0.96 NPC1 (0.41) TSHRSMN1; SMN2NPC1RAB9ALMNA
SCHEMBL15897085 0.96 NPC1 (0.41) TSHRSMN1; SMN2NPC1RAB9ALMNA
Bromide SCHEMBL187292 0.90 MMP8 (0.37) TSHRSMN1; SMN2NPC1LMNAMEN1
Bromide SCHEMBL187478 0.90 MMP8 (0.37) TSHRSMN1; SMN2NPC1LMNAMEN1
SCHEMBL803862 0.89 MMP8 (0.38) TSHRSMN1; SMN2NPC1LMNAMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8785655-B2 Ionic liquid solvents DUBLIN CITY UNIVERSITY (IE) 2014-07-22 US claimed
US-20120071661-A1 Ionic Liquid Solvents DUBLIN CITY UNIVERSITY (IE) 2012-03-22 US claimed
EP-2401258-A1 IONIC LIQUID SOLVENTS Dublin City University (IE) 2012-01-04 EP claimed
WO-2010097412-A1 IONIC LIQUID SOLVENTS DUBLIN CITY UNIVERSITY (IE) 2010-09-02 WO claimed
US-8785655-B2 Ionic liquid solvents DUBLIN CITY UNIVERSITY (IE) 2014-07-22 US disclosed
US-20120071661-A1 Ionic Liquid Solvents DUBLIN CITY UNIVERSITY (IE) 2012-03-22 US 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-20120071661-A1 Ionic Liquid Solvents EBP, PAICS, HACD3 CHRM4 1404/4885CHRM1 289/4885CHRM3 1004/4885

“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.