Bromide

Bromide

SCHEMBL11569593

Br.C[C@]1(OC(N)=O)CC[C@H](N)CC1

nearest known ligand 0.43

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 3)

geneUniProtsupporting neighboursconfidence
SCN1A P35498 1/20 0.30
SCN2A Q99250 1/20 0.30
SCN3A Q9NY46 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
SCHEMBL21591911 0.98 SCN1A (0.31) SCN1ASCN2ASCN3A
SCHEMBL11567957 0.82 SLC1A2 (0.32) SCN1ASCN2ASCN3A
SCHEMBL28363969 0.82 SCN1A (0.31) SCN1ASCN2ASCN3A
SCHEMBL11085265 0.82 SLC1A2 (0.32) SCN1ASCN2ASCN3A
SCHEMBL8648894 0.80
SCHEMBL6822711 0.78
SCHEMBL6822712 0.78
Hydrochloric Acid SCHEMBL28676586 0.78
SCHEMBL29049006 0.77 APLNR (0.30)
SCHEMBL12332047 0.76 CYP19A1 (0.40) SCN1ASCN2ASCN3A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0001774-A1 Derivatives of BPTI (basic pancreatic trypsin-inhibitor), process for their preparation and their use as medicines BAYER AG (DE) 1979-05-16 EP disclosed