Bromide

Bromide

SCHEMBL31050231

Br.NCCNN

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
SCHEMBL466511 0.96
Hydrogen Sulfide SCHEMBL10900451 0.92
Ethylenediamine SCHEMBL28594538 0.92
Hydrochloric Acid SCHEMBL28094416 0.92
Water SCHEMBL28108822 0.92
Ethylenediamine SCHEMBL8121893 0.92 CA12 (0.47)
Ethane SCHEMBL3074989 0.88
Propane SCHEMBL3075180 0.85
Butane SCHEMBL3061276 0.82
Sulfuric Acid SCHEMBL25412843 0.77 LMNA (0.45)

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-118702640-A Synthesis method for synthesizing N-substituted oxazolidine-2-ketone by ionic liquid catalysis 东华理工大学 2024-09-27 CN claimed
CN-118702640-A Synthesis method for synthesizing N-substituted oxazolidine-2-ketone by ionic liquid catalysis 东华理工大学 2024-09-27 CN disclosed