Bromide

Bromide

SCHEMBL19405463

C[Si](C)([O-])c1ccccc1F.[Br-].[Mg+2]

nearest known ligand 0.37

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 20)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.37
NOTUM Q6P988 2/20 0.34
NPC1 O15118 5/20 0.33
RAB9A P51151 5/20 0.33
SMN1; SMN2 Q16637 3/20 0.33
GAA P10253 2/20 0.33
ALDH1A1 P00352 4/20 0.32
L3MBTL1 Q9Y468 3/20 0.32
PKM P14618 2/20 0.32
MEN1 O00255 3/20 0.32
KMT2A Q03164 3/20 0.32
NFKB1 P19838 2/20 0.32
NFKB2 Q00653 2/20 0.32
RELA Q04206 2/20 0.32
KDM4E B2RXH2 2/20 0.32
MGAM O43451 1/20 0.32
SI P14410 1/20 0.32
MGAM2 Q2M2H8 1/20 0.32
MAPK1 P28482 1/20 0.32
NFE2L2 Q16236 1/20 0.31

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
Hydrochloric Acid SCHEMBL19583281 0.95 ACHE (0.37) ACHENOTUMNPC1RAB9ASMN1; SMN2
Bromide SCHEMBL19405535 0.86 ACHE (0.37) ACHENOTUMNPC1RAB9ASMN1; SMN2
Bromide SCHEMBL19405421 0.83 BCAT1 (0.33) ACHEGAAMGAMSIMGAM2
Hydrochloric Acid SCHEMBL19405531 0.82 ACHE (0.37) ACHENOTUMNPC1RAB9ASMN1; SMN2
Bromide SCHEMBL19405493 0.81 ACHE (0.35) ACHENPC1RAB9AGAAALDH1A1
Hydrochloric Acid SCHEMBL19405486 0.78 BCAT1 (0.33) ACHE
Hydrochloric Acid SCHEMBL19405604 0.76 ACHE (0.35) ACHENPC1RAB9AALDH1A1L3MBTL1
SCHEMBL8932025 0.75 ACHE (0.43) ACHENOTUMNPC1RAB9ASMN1; SMN2
Bromide SCHEMBL19405391 0.74 TSHR (0.41) ACHENOTUMNPC1RAB9ASMN1; SMN2
Bromide SCHEMBL19405466 0.74 CES2 (0.33) ACHE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10367231-B2 Magnesium-containing electrolytic solution FUJIFILM WAKO PURE CHEMICAL CORPORATION (JP) 2019-07-30 US disclosed
EP-3226340-B1 MAGNESIUM-CONTAINING ELECTROLYTIC SOLUTION FUJIFILM WAKO PURE CHEMICAL CORP (JP) 2018-11-07 EP disclosed
US-20170331154-A1 MAGNESIUM-CONTAINING ELECTROLYTIC SOLUTION WAKO PURE CHEMICAL INDUSTRIES, LTD. (JP) 2017-11-16 US disclosed
EP-3226340-A1 MAGNESIUM-CONTAINING ELECTROLYTIC SOLUTION Wako Pure Chemical Industries, Ltd. (JP) 2017-10-04 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-10367231-B2 Magnesium-containing electrolytic solution CA1, CA3, CA2 ACHE 188/4885NOTUM 1219/4885NPC1 4052/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.