Bromide

Bromide

SCHEMBL9810690

Br.FC(F)(F)[Zn]

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
SCHEMBL2992041 0.93
Hydrochloric Acid SCHEMBL1452996 0.86
Iodide SCHEMBL11020380 0.86
SCHEMBL6837252 0.67
SCHEMBL5359711 0.63
SCHEMBL668190 0.62
Hydrogen Sulfide SCHEMBL25252062 0.57
Bromide SCHEMBL28527082 0.57
Bromide SCHEMBL5108256 0.57
Bromide SCHEMBL30294169 0.57

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103275052-A Method for synthesizing isoflavone by nickel-catalyzed Negishi cross coupling reaction at room temperature UNIV SHAANXI NORMAL 2013-09-04 CN disclosed
US-5013829-A Stable congener of 2',3'-dideoxyadenosine UNIVERSITY OF IOWA RESEARCH FOUNDATION (US) 1991-05-07 US disclosed