Bromide

Bromide

SCHEMBL8468244

Br.[LiH].[LiH].[LiH]

nearest known ligand 0.00

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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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 SCHEMBL27921875 1.00
Bromide SCHEMBL480167 1.00
Bromide SCHEMBL7172901 1.00
Bromide SCHEMBL19991772 0.82
Bromide SCHEMBL22158250 0.82
Bromide SCHEMBL3304853 0.82
Bromide SCHEMBL22158109 0.82
Bromide SCHEMBL22158174 0.82
Bromide SCHEMBL10389902 0.82
Bromide SCHEMBL9356814 0.82

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
US-6008404-A REACTING AN ALCOHOL OR POLYOL WITH AN ESTER OF A METHACRYLATE OR ACRYLATE IN PRESENCE OF TRANSESTERIFICATION CATALYST AND AN ALKALI METAL BROMIDE SALT TO PRODUCE ALCOHOL OR POLYOL ESTER OF ACRYLATE/METHACRYLATE FREE OF POLYMERIC DERIVATIVE CIBA SPECIALTY CHEMICALS CORPORATION (US) 1999-12-28 US disclosed