Bromide

Bromide

SCHEMBL320970

Br.NCCNC(=O)Nc1ccc(O)c(Cl)c1

nearest known ligand 0.55

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4

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
MEN1 O00255 2/20 0.55
KMT2A Q03164 2/20 0.55
LMNA P02545 4/20 0.50
MAPT P10636 3/20 0.50
CA2 P00918 3/20 0.50
CA1 P00915 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
EPHX2 P34913 3/20 0.48
NPC1 O15118 2/20 0.48
RAB9A P51151 2/20 0.48
HPGD P15428 1/20 0.48
MAPK1 P28482 1/20 0.48
EPHX1 P07099 1/20 0.47
ALDH1A1 P00352 2/20 0.46
CNR1 P21554 1/20 0.45
ERCC1 P07992 1/20 0.45
ERCC4 Q92889 1/20 0.45
HSD17B10 Q99714 2/20 0.44
GOT1 P17174 1/20 0.44
SLC2A1 P11166 1/20 0.44

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
SCHEMBL27761103 0.81 EPHX2 (0.67) MEN1KMT2AMAPTCA2CA1
Bromide SCHEMBL320987 0.81 ALDH1A1 (0.60) MEN1KMT2ALMNAMAPTSMN1; SMN2
Hydrochloric Acid SCHEMBL322141 0.81 MEN1 (0.49) MEN1KMT2ALMNAMAPTCA2
SCHEMBL4348602 0.80 EPHX2 (0.74) MEN1KMT2AMAPTCA2CA1
SCHEMBL13272730 0.79 KDM4C (0.55) MEN1KMT2AMAPTEPHX2HPGD
SCHEMBL4341839 0.79 CNR1 (0.68) MEN1KMT2ALMNAMAPTCA2
SCHEMBL19472661 0.79 MAPT (0.62) MEN1KMT2ALMNAMAPTCA2
SCHEMBL21621109 0.78 EPHX2 (0.62) MEN1KMT2ALMNAMAPTCA2
SCHEMBL7757105 0.76 TERT (0.54) MEN1KMT2ALMNAMAPTCA2
SCHEMBL5958601 0.76 EPHX2 (0.53) MEN1KMT2ALMNAMAPTCA2

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
US-20130261178-A1 PHENOXYPROPANOL DERIVATIVES AND THEIR USE IN TREATING CARDIAC AND CARDIOVASCULAR DISEASES MISTRY SHAILESH (GB) 2013-10-03 US disclosed
EP-2590937-A1 PHENOXYPROPANOL DERIVATIVES AND THEIR USE IN TREATING CARDIAC AND CARDIOVASCULAR DISEASES The University Of Nottingham (GB) 2013-05-15 EP disclosed
WO-2012004549-A1 PHENOXYPROPANOL DERIVATIVES AND THEIR USE IN TREATING CARDIAC AND CARDIOVASCULAR DISEASES THE UNIVERSITY OF NOTTINGHAM (GB) 2012-01-12 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-20130261178-A1 PHENOXYPROPANOL DERIVATIVES AND THEIR USE IN TREATING CARDIAC AND CARDIOVASCULAR DISEASES NR3C2, NPR3, ADRB3 MEN1 4434/4885KMT2A 4656/4885LMNA 615/4885

“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.