Bromide

Bromide

SCHEMBL2158161

CCCCCCCCCCCCCC[N+](C)(C)CCC[Si](OC)(OC)OC.[Br-]

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

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.

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.96
DNM1 Q05193 10/20 0.59
HTT P42858 5/20 0.58
HSP90AA1 P07900 1/20 0.52
RAD52 P43351 1/20 0.52
KMT2A Q03164 2/20 0.48
SMN1; SMN2 Q16637 3/20 0.44
RAB9A P51151 2/20 0.44
MEN1 O00255 1/20 0.44
GAA P10253 1/20 0.44
MAPT P10636 1/20 0.44

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
Bromide SCHEMBL29706404 1.00 LMNA (0.96) LMNADNM1HTTHSP90AA1RAD52
Bromide SCHEMBL1494723 1.00 LMNA (0.96) LMNADNM1HTTHSP90AA1RAD52
Bromide SCHEMBL28429574 1.00 LMNA (0.96) LMNADNM1HTTHSP90AA1RAD52
Bromide SCHEMBL28430194 1.00 LMNA (0.96) LMNADNM1HTTHSP90AA1RAD52
Bromide SCHEMBL29712384 1.00 LMNA (0.96) LMNADNM1HTTHSP90AA1RAD52
SCHEMBL13388580 0.98 LMNA (1.00) LMNADNM1HTTHSP90AA1RAD52
SCHEMBL1123475 0.98 LMNA (1.00) LMNADNM1HTTHSP90AA1RAD52
SCHEMBL31255930 0.98 LMNA (1.00) LMNADNM1HTTHSP90AA1RAD52
SCHEMBL2710518 0.98 LMNA (1.00) LMNADNM1HTTHSP90AA1RAD52
SCHEMBL10608031 0.98 LMNA (1.00) LMNADNM1HTTHSP90AA1RAD52

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 36 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119708953-A Long-acting low-surface-energy coating with high recoating performance, and preparation method and application thereof 四川大学 2025-03-28 CN claimed
CN-116262623-A Metal modified hierarchical porous high-silicon Y molecular sieve and preparation method and application thereof 中国科学院大连化学物理研究所 2023-06-16 CN claimed
CN-111303637-A Preparation method of medical organic silicon rubber composition 孟令芝 2020-06-19 CN claimed
CN-111286203-A Medical organic silicon rubber composition 孟令芝 2020-06-16 CN claimed
US-6323260-B1 AMINOHYDROCARBONSILOXANE MOIETY COMPRISING BOTH SILICON AND NITROGEN. BAYER INC. (CA) 2001-11-27 US claimed
EP-1131379-A1 PROCESS FOR HYDROPHOBICIZING PARTICLES, AND THEIR USE IN DISPERSIONS Bayer Inc. (CA) 2001-09-12 EP claimed
WO-2000031178-A1 PROCESS FOR HYDROPHOBICIZING PARTICLES, AND THEIR USE IN DISPERSIONS BAYER INC. (CA) 2000-06-02 WO claimed
CN-119708953-A Long-acting low-surface-energy coating with high recoating performance, and preparation method and application thereof 四川大学 2025-03-28 CN disclosed
CN-116262623-A Metal modified hierarchical porous high-silicon Y molecular sieve and preparation method and application thereof 中国科学院大连化学物理研究所 2023-06-16 CN disclosed
EP-2880102-B1 PARTICULATE METAL OXIDE PARTICLES COMPRISING A METAL OXIDE CORE AND A COATING LAYER COMPRISING AN INORGANIC MATERIAL, A SILANE COUPLING AGENT AND/OR A HYDROPHOBIZING AGENT. CRODA INT PLC (GB) 2022-06-29 EP disclosed
US-10869826-B2 Particulate metal oxide particles comprising a metal oxide core and a coating layer comprising an inorganic material, a silane coupling agent and/or a hydrophobizing agent CRODA INTERNATIONAL PLC 2020-12-22 US disclosed
CN-111303637-A Preparation method of medical organic silicon rubber composition 孟令芝 2020-06-19 CN disclosed
CN-111286203-A Medical organic silicon rubber composition 孟令芝 2020-06-16 CN disclosed
US-6407153-B1 Silica-containing rubber compositions BAYER INC. (CA) 2002-06-18 US disclosed
EP-1208145-A2 PROCESS FOR PREPARATION OF RUBBER SILICA MASTERBATCHES BASED ON THE USE OF POLYMER LATICES Bayer Inc. (CA) 2002-05-29 EP disclosed
US-6323260-B1 AMINOHYDROCARBONSILOXANE MOIETY COMPRISING BOTH SILICON AND NITROGEN. BAYER INC. (CA) 2001-11-27 US disclosed
US-20010009948-A1 Elastomeric butyl compounds with improved chemical bonding between the butyl elastomer and the filler BAYER INC. (CA) 2001-07-26 US disclosed
WO-2001010946-A2 PROCESS FOR PREPARATION OF RUBBER SILICA MASTERBATCHES BASED ON THE USE OF POLYMER LATICES BAYER INC. (CA) 2001-02-15 WO disclosed
EP-0983317-A1 PROCESS FOR HYDROPHOBICIZING PARTICLES, AND THEIR USE AS FILLERS IN POLYMER MASTERBATCHES Bayer Inc. (CA) 2000-03-08 EP disclosed
WO-1998053004-A1 PROCESS FOR HYDROPHOBICIZING PARTICLES, AND THEIR USE AS FILLERS IN POLYMER MASTERBATCHES BAYER INC. (CA) 1998-11-26 WO disclosed