Bromide

Bromide

SCHEMBL8071608

CCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC.[Br-]

nearest known ligand 0.94

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 16)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 12/20 0.94
HTT P42858 2/20 0.94
HSP90AA1 P07900 2/20 0.79
RAD52 P43351 2/20 0.79
KMT2A Q03164 1/20 0.74
ALDH1A1 P00352 1/20 0.67
TP53 P04637 1/20 0.67
CYP3A4 P08684 1/20 0.67
ALOX15 P16050 1/20 0.67
TSHR P16473 1/20 0.67
ALOX12 P18054 1/20 0.67
SMN1; SMN2 Q16637 1/20 0.67
HIF1A Q16665 1/20 0.67
HSD17B10 Q99714 1/20 0.67
PLA2G1B P04054 1/20 0.64
ATG4B Q9Y4P1 1/20 0.64

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 SCHEMBL18334663 1.00 DNM1 (0.94) DNM1HTTHSP90AA1RAD52KMT2A
Bromide SCHEMBL10855468 1.00 DNM1 (0.94) DNM1HTTHSP90AA1RAD52KMT2A
Bromide SCHEMBL18141261 1.00 DNM1 (0.94) DNM1HTTHSP90AA1RAD52KMT2A
Bromide SCHEMBL5490891 1.00 DNM1 (0.94) DNM1HTTHSP90AA1RAD52KMT2A
Bromide SCHEMBL11340296 1.00 DNM1 (0.94) DNM1HTTHSP90AA1RAD52KMT2A
Bromide SCHEMBL8110085 1.00 DNM1 (0.94) DNM1HTTHSP90AA1RAD52KMT2A
Bromide SCHEMBL22397860 1.00 DNM1 (0.94) DNM1HTTHSP90AA1RAD52KMT2A
Bromide SCHEMBL22397869 1.00 DNM1 (0.94) DNM1HTTHSP90AA1RAD52KMT2A
Bromide SCHEMBL21986903 1.00 DNM1 (0.94) DNM1HTTHSP90AA1RAD52KMT2A
Bromide SCHEMBL18140617 1.00 DNM1 (0.94) DNM1HTTHSP90AA1RAD52KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10428194-B2 Modified acrylic resin cured product, and laminate thereof, and production methods therefor MITSUI CHEMICALS, INC. (JP) 2019-10-01 US disclosed
EP-3263635-B1 MODIFIED ACRYLIC RESIN CURED PRODUCT, AND LAMINATE THEREOF, AND PRODUCTION METHODS THEREFOR MITSUI CHEMICALS INC (JP) 2019-09-18 EP disclosed
US-20180163056-A1 HYDROPHILIC CURABLE COMPOSITIONS MITSUI CHEMICALS, INC. (JP) 2018-06-14 US disclosed
US-20180036995-A1 HYDROPHILIC MONOLAYER FILM WITH OPTICAL FUNCTIONALITY AND STACK OF THE SAME MITSUI CHEMICALS, INC. (JP) 2018-02-08 US disclosed
US-20180030230-A1 MODIFIED ACRYLIC RESIN CURED PRODUCT, AND LAMINATE THEREOF, AND PRODUCTION METHODS THEREFOR MITSUI CHEMICALS, INC. (JP) 2018-02-01 US disclosed
EP-3270192-A1 HYDROPHILIC SINGLE-LAYER FILM HAVING OPTICAL FUNCTIONALITY, AND LAMINATE THEREOF Mitsui Chemicals, Inc. (JP) 2018-01-17 EP disclosed
EP-3263635-A1 MODIFIED ACRYLIC RESIN CURED PRODUCT, AND LAMINATE THEREOF, AND PRODUCTION METHODS THEREFOR Mitsui Chemicals, Inc. (JP) 2018-01-03 EP disclosed
EP-3081578-A1 COMPOSITION FOR HYDROPHILIC CURED PRODUCT Mitsui Chemicals, Inc. (JP) 2016-10-19 EP disclosed
EP-1015537-A1 NO-RUB HARD SURFACE CLEANER ALBEMARLE CORPORATION (US) 2000-07-05 EP disclosed
US-5922669-A AN AQUEOUS SOLUTION COMPRISING A NONIONIC SURFACTANT MIXTURE OF AN ALCOHOL ETHOXYLATE AND AN ALKYLDIMETHYLAMINE OXIDE ALBEMARLE CORPORATION (US) 1999-07-13 US disclosed
WO-1999013036-A1 NO-RUB HARD SURFACE CLEANER ALBEMARLE CORPORATION (US) 1999-03-18 WO disclosed