Bromide

Bromide

SCHEMBL5228525

COC(=O)c1cccc([P+](Cc2ccccc2)(c2ccccc2)c2ccccc2)c1.[Br-]

nearest known ligand 0.56

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
SLC7A5 Q01650 1/20 0.56
LOXL2 Q9Y4K0 1/20 0.52
FOLH1 Q04609 1/20 0.52
SNCA P37840 2/20 0.51
CYP4F2 P78329 2/20 0.51
CYP4A11 Q02928 2/20 0.51
ALDH1A1 P00352 3/20 0.49
HPGD P15428 2/20 0.49
TSHR P16473 1/20 0.49
HIF1A Q16665 1/20 0.47
RAB9A P51151 2/20 0.47
LMNA P02545 1/20 0.45
CA1 P00915 1/20 0.43
CA2 P00918 1/20 0.43
CASR P41180 2/20 0.43
MRGPRX4 Q96LA9 1/20 0.43
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
HSD17B10 Q99714 1/20 0.43

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 SCHEMBL1532873 0.93 SLC7A5 (0.60) SLC7A5LOXL2FOLH1SNCACYP4F2
Bromide SCHEMBL31614317 0.93 SLC7A5 (0.60) SLC7A5LOXL2FOLH1SNCACYP4F2
Hydrochloric Acid SCHEMBL8123098 0.90 SLC7A5 (0.60) SLC7A5LOXL2FOLH1SNCACYP4F2
Bromide SCHEMBL9546910 0.87 SNCA (0.55) SLC7A5LOXL2SNCAALDH1A1HPGD
Bromide SCHEMBL197541 0.85 SNCA (0.61) LOXL2SNCACYP4F2CYP4A11ALDH1A1
Hydrochloric Acid SCHEMBL9493443 0.84 CA1 (0.54) SLC7A5LOXL2SNCAALDH1A1HPGD
Hydrochloric Acid SCHEMBL1509558 0.82 SNCA (0.58) LOXL2SNCACYP4F2CYP4A11ALDH1A1
Bromide SCHEMBL10773250 0.82 SNCA (0.56) LOXL2SNCACYP4A11TSHRRAB9A
Bromide SCHEMBL11685473 0.82 KDM4E (0.46) SLC7A5LOXL2FOLH1SNCAALDH1A1
Bromide SCHEMBL11094940 0.81 SLC7A5 (0.56) SLC7A5SNCACYP4F2CYP4A11ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1656138-A4 SUBSTITUTED CYCLOALKYAMINE DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL MYERS SQUIBB CO (US) 2007-04-18 EP disclosed
EP-1656138-A2 SUBSTITUTED CYCLOALKYAMINE DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY Bristol-Myers Squibb Company (US) 2006-05-17 EP disclosed
WO-2005020899-A2 SUBSTITUTED CYCLOALKYAMINE DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL-MYERS SQUIBB COMPANY (US) 2005-03-10 WO disclosed