Bromide

Bromide

SCHEMBL7878893

CC(C)C1=C([Zr+2](C2=C(C(C)C)C=CC2)=[Si](C)C)CC=C1.[Br-].[Br-]

nearest known ligand 0.00

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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.

⚠ 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
Hydrochloric Acid SCHEMBL616016 0.69
Hydrochloric Acid SCHEMBL9066709 0.69
Bromide SCHEMBL7885917 0.65
SCHEMBL28014004 0.64
SCHEMBL9750871 0.64
SCHEMBL7923511 0.63
SCHEMBL714797 0.63
Bromide SCHEMBL7886678 0.63
Bromide SCHEMBL7878867 0.63
Hydrochloric Acid SCHEMBL7885912 0.61

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-6175025-B1 Process for synthesizing metallocene compounds ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 2001-01-16 US disclosed