Bromide

Bromide

SCHEMBL5087237

CCCCC[N+](C)(CCCCC)CCCCC.[Br-]

nearest known ligand 0.63

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 15)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 10/20 0.63
ALDH1A1 P00352 1/20 0.61
TP53 P04637 1/20 0.61
CYP3A4 P08684 1/20 0.61
ALOX15 P16050 1/20 0.61
TSHR P16473 1/20 0.61
ALOX12 P18054 1/20 0.61
SMN1; SMN2 Q16637 1/20 0.61
HIF1A Q16665 1/20 0.61
HSD17B10 Q99714 1/20 0.61
SLC22A1 O15245 2/20 0.59
SLC22A2 O15244 1/20 0.59
HTT P42858 1/20 0.58
HSP90AA1 P07900 1/20 0.57
RAD52 P43351 1/20 0.57

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 SCHEMBL7152946 0.97 DNM1 (0.68) DNM1ALDH1A1TP53CYP3A4ALOX15
Bromide SCHEMBL10695829 0.97 DNM1 (0.68) DNM1ALDH1A1TP53CYP3A4ALOX15
Bromide SCHEMBL240975 0.97 DNM1 (0.68) DNM1ALDH1A1TP53CYP3A4ALOX15
Bromide SCHEMBL853784 0.97 DNM1 (0.68) DNM1ALDH1A1TP53CYP3A4ALOX15
Bromide SCHEMBL1697452 0.97 DNM1 (0.68) DNM1ALDH1A1TP53CYP3A4ALOX15
Bromide SCHEMBL4347940 0.97 DNM1 (0.68) DNM1ALDH1A1TP53CYP3A4ALOX15
Bromide SCHEMBL1306021 0.97 DNM1 (0.68) DNM1ALDH1A1TP53CYP3A4ALOX15
Bromide SCHEMBL5086721 0.97 DNM1 (0.68) DNM1ALDH1A1TP53CYP3A4ALOX15
Bromide SCHEMBL20504226 0.97 DNM1 (0.68) DNM1ALDH1A1TP53CYP3A4ALOX15
Bromide SCHEMBL28857902 0.97 DNM1 (0.68) DNM1ALDH1A1TP53CYP3A4ALOX15

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9587182-B2 Synergistic formulations of functionalized copolymers and ionic liquids for dehydrated and desalted of medium, heavy and extra heavy crude oils INSTITUTO MEXICANO DEL PETROLEO (MX) 2017-03-07 US claimed
US-9650577-B2 Synergistic formulations of functionalized copolymers and ionic liquids for dehydrated and desalted of medium, heavy and extra heavy crude oils INSTITUTO MEXICANO DEL PETROLEO (MX) 2017-05-16 US disclosed
US-9587182-B2 Synergistic formulations of functionalized copolymers and ionic liquids for dehydrated and desalted of medium, heavy and extra heavy crude oils INSTITUTO MEXICANO DEL PETROLEO (MX) 2017-03-07 US disclosed
US-20150087729-A1 SYNERGISTIC FORMULATIONS OF FUNCTIONALIZED COPOLYMERS AND IONIC LIQUIDS FOR DEHYDRATED AND DESALTED OF MEDIUM, HEAVY AND EXTRA HEAVY CRUDE OILS MEXICANO INST PETROL (MX) 2015-03-26 US disclosed
US-20120261312-A1 SYNERGISTIC FORMULATIONS OF FUNCTIONALIZED COPOLYMERS AND IONIC LIQUIDS FOR DEHYDRATED AND DESALTED OF MEDIUM, HEAVY AND EXTRA HEAVY CRUDE OILS INSTITUTO MEXICANO DEL PETROLEO (MX) 2012-10-18 US disclosed
US-20080214386-A1 Stability; easily separated from solution; surface treatment of catalyst with Group seven compound; reacting epoxide with carbon dioxide NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2008-09-04 US disclosed
EP-0268261-A1 Process for producing 1-hydrocarbyl mercaptans PHILLIPS PETROLEUM COMPANY (US) 1988-05-25 EP disclosed