Bromide

Bromide

SCHEMBL9026709

Br.Cc1ccc(N2CCN(CCCNc3ncc(C)cc3C(=O)N(C)C)CC2)c(OCC(F)(F)F)c1

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
Hydrochloric Acid SCHEMBL9026528 0.81 — —
Hydrochloric Acid SCHEMBL9027065 0.81 DRD2 (0.60) —
SCHEMBL9027717 0.79 DRD2 (0.69) —
Hydrochloric Acid SCHEMBL9026741 0.78 DRD2 (0.68) —
SCHEMBL9027775 0.78 — —
Oxalic Acid SCHEMBL8828479 0.76 DRD2 (0.65) —
Hydrochloric Acid SCHEMBL9026124 0.74 — —
Hydrochloric Acid SCHEMBL8828515 0.74 — —
SCHEMBL8828567 0.73 — —
Hydrochloric Acid SCHEMBL8828660 0.73 — —

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-0711757-A1 3-(4-phenylpiperazin-1-yl)propyl-amino, thio and oxy -pyridine, pyrimidine and benzene derivatives as alpha1-adrenoceptor antagonists F. Hoffmann-La Roche AG (CH) 1996-05-15 — — EP disclosed
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