Bromide

Bromide

SCHEMBL7246358

Fc1cc2ccc(C[P+](c3ccccc3)(c3ccccc3)c3ccccc3)nc2cc1F.[Br-]

nearest known ligand 0.34

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 8)

geneUniProtsupporting neighboursconfidence
SNCA P37840 2/20 0.34
CYSLTR2 Q9NS75 2/20 0.34
CYSLTR1 Q9Y271 2/20 0.34
HIF1A Q16665 1/20 0.33
PDE10A Q9Y233 3/20 0.32
APP P05067 1/20 0.32
CYP1A2 P05177 1/20 0.31
TERT O14746 1/20 0.30

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 SCHEMBL4485285 0.79 CYP1A2 (0.49) SNCACYSLTR2CYSLTR1HIF1APDE10A
Bromide SCHEMBL7086028 0.79 NR4A2 (0.40) SNCAPDE10ACYP1A2
Hydrochloric Acid SCHEMBL2401263 0.76 CYP1A2 (0.49) CYSLTR2CYSLTR1HIF1APDE10ACYP1A2
Hydrochloric Acid SCHEMBL8071622 0.74 CYP1A2 (0.47) CYSLTR2CYSLTR1PDE10ACYP1A2
Bromide SCHEMBL8128341 0.70 PPARA (0.33) SNCAHIF1APDE10AAPP
SCHEMBL4061337 0.70 CCR1 (0.48) CYSLTR2CYSLTR1PDE10AAPPTERT
SCHEMBL6089466 0.70 TERT (0.37) CYSLTR2CYSLTR1PDE10AAPPTERT
Hydrochloric Acid SCHEMBL7512828 0.69 ALDH1A1 (0.41) CYSLTR2CYSLTR1HIF1APDE10AAPP
Bromide SCHEMBL19994660 0.68 SNCA (0.44) SNCAHIF1ACYP1A2
Bromide SCHEMBL9086038 0.68 SNCA (0.38) SNCAHIF1AAPPCYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030216571-A1 Antiallergens; antiinflammatory agents UBE INDUSTRIES, LTD. (JP) 2003-11-20 US disclosed
EP-1254897-A1 TRICYCLIC COMPOUNDS Ube Industries, Ltd. (JP) 2002-11-06 EP disclosed
EP-0699188-A1 QUINOLINE DERIVATIVES AS LEUKOTRIENE ANTAGONISTS MERCK FROSST CANADA INC. (CA) 1996-03-06 EP disclosed
US-5438141-A Antiasthmatic agents, antiallergens MERCK FROSST CANADA, INC. (CA) 1995-08-01 US disclosed
WO-1994027968-A1 QUINOLINE DERIVATIVES AS LEUKOTRIENE ANTAGONISTS MERCK FROSST CANADA INC. (CA) 1994-12-08 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 (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-20030216571-A1 Antiallergens; antiinflammatory agents CYSLTR2, CYSLTR1, LTC4S SNCA 4671/4885CYSLTR2 1/4885CYSLTR1 2/4885

“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.