Bromide

SCHEMBL5014150

C[N+](C)(C)CCCOc1ccc(C2=C(c3ccc(OCCC[N+](C)(C)C)cc3)C3=NC2=CC2=NC(=CC4=NC(=CC5=NC(=C3)C=C5)C=C4)C=C2)cc1.[Br-].[Br-]

nearest known ligand 0.00

Known targets — ChEMBL curated mechanism

ACHE CHKA CHRM1 CHRM2 CHRM3 CHRM4 CHRM5 CHRNA1 CHRNB1 CHRND CHRNE CHRNG HRH2 OPRM1

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.

Compound	similarity	top predicted	shared targets
Hydrochloric Acid SCHEMBL5014143	0.98	CYP3A4 (0.32)	—
SCHEMBL23036930	0.84	RARB (0.39)	—
SCHEMBL28246175	0.84	RARB (0.39)	—
Bromide SCHEMBL5014264	0.81	—	—
SCHEMBL2327446	0.80	CHRNB4 (0.30)	—
Hydrochloric Acid SCHEMBL27620956	0.80	CHRNB4 (0.30)	—
Hydrochloric Acid SCHEMBL584419	0.79	CYP3A4 (0.32)	—
Hydrochloric Acid SCHEMBL5165803	0.77	CYP3A4 (0.31)	—
SCHEMBL5013694	0.72	—	—
SCHEMBL28049799	0.72	SENP1 (0.30)	—

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.

Patent	Title	Assignee	Published	Priority	Filing	Country	Status
EP-1963333-A1	PROCESS FOR THE PREPARATION OF PORPHYRIN DERIVATIVES AS ANTIMICROBIAL AGENTS BY PHOTODYNAMIC THERAPY (PDT)	Destiny Pharma Limited (GB)	2008-09-03	—	—	EP	claimed
WO-2007074340-A1	PROCESS FOR THE PREPARATION OF PORPHYRIN DERIVATIVES AS ANTIMICROBIAL AGENTS BY PHOTODYNAMIC THERAPY (PDT)	DESTINY PHARMA LIMITED (GB)	2007-07-05	—	—	WO	claimed