Bromide

Bromide

SCHEMBL143506

CN(C)CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]

nearest known ligand 0.58

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
▸ CHRM2 known ✓ P08172 2/20 0.46
▸ CHRM4 known ✓ P08173 1/20 0.46
▸ CHRM5 known ✓ P08912 1/20 0.46
▸ CHRM1 known ✓ P11229 1/20 0.46
▸ CHRM3 known ✓ P20309 1/20 0.46
▸ HRH2 known ✓ P25021 1/20 0.46
▸ OPRM1 known ✓ P35372 1/20 0.46
▸ HIF1A Q16665 1/20 0.58
▸ HTR2A P28223 4/20 0.57
▸ HRH1 P35367 4/20 0.57
▸ CYP1A2 P05177 2/20 0.46
▸ CYP2D6 P10635 2/20 0.46
▸ TSHR P16473 2/20 0.46
▸ LMNA P02545 2/20 0.46
▸ SLC6A2 P23975 2/20 0.46
▸ SLC6A4 P31645 2/20 0.46
▸ SCN1A P35498 2/20 0.46
▸ SCN2A Q99250 2/20 0.46
▸ SCN3A Q9NY46 2/20 0.46
▸ ADRA2A P08913 1/20 0.46

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
SCHEMBL8532850 0.96 HIF1A (0.58) HIF1AHTR2AHRH1CYP1A2CYP2D6
Iodide SCHEMBL9549744 0.96 HIF1A (0.58) HIF1AHTR2AHRH1CYP1A2CYP2D6
Hydrochloric Acid SCHEMBL9549567 0.96 HIF1A (0.58) HIF1AHTR2AHRH1CYP1A2CYP2D6
Water SCHEMBL8528580 0.96 HIF1A (0.58) HIF1AHTR2AHRH1CYP1A2CYP2D6
SCHEMBL8972950 0.90 HIF1A (0.52) HIF1AHTR2AHRH1CYP1A2CYP2D6
Bromide SCHEMBL190865 0.88 HTR2A (0.60) HIF1AHTR2AHRH1CYP1A2CYP2D6
Bicarbonate SCHEMBL8973196 0.87 TSHR (0.52) HIF1AHTR2AHRH1CYP1A2CYP2D6
Phosphoric Acid SCHEMBL8972371 0.87 HTR2A (0.50) HIF1AHTR2AHRH1CYP1A2CYP2D6
Bromide SCHEMBL8909571 0.86 HTR2A (0.53) HIF1AHTR2AHRH1CYP1A2CYP2D6
Bromide SCHEMBL246032 0.86 HTR2A (0.58) HIF1AHTR2AHRH1CYP1A2CYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114097785-A Polysaccharide-based photothermal sterilization material and application thereof in seed protection and grain storage 中国科学院化学研究所 2022-03-01 — — CN claimed
US-8808403-B2 Process for solid electrolytic capacitors using polymer slurries KEMET ELECTRONICS CORPORATION (US) 2014-08-19 — — US claimed
US-20120201803-A1 3-SUBSTITUTED COMPOUNDS FOR REDUCING URIC ACID WELLSTAT THERAPEUTICS CORPORATION (US) 2012-08-09 — — US claimed
WO-2012037362-A2 PROCESS FOR SOLID ELECTROLYTIC CAPACITORS USING POLYMER SLURRIES KEMET ELECTRONICS CORPORATION (US) 2012-03-22 — — WO claimed
US-20120063063-A1 PROCESS FOR SOLID ELECTROLYTIC CAPACITORS USING POLYMER SLURRIES KEMET ELECTRONICS CORPORATION (US) 2012-03-15 — — US claimed
US-7709168-B2 Phosphonium containing charge transport layer photoconductors XEROX CORPORATION (US) 2010-05-04 — — US claimed
US-20090092915-A1 PHOSPHONIUM CONTAINING CHARGE TRANSPORT LAYER PHOTOCONDUCTORS XEROX CORPORATION (US) 2009-04-09 — — US claimed
US-20090092914-A1 PHOSPHONIUM CONTAINING PHOTOGENERATING LAYER PHOTOCONDUCTORS XEROX CORPORATION (US) 2009-04-09 — — US claimed
US-6248161-B1 Preparation of permanent color inks from water-soluble colorants using specific phosphonium salts HEWLETT-PACKARD COMPANY 2001-06-19 — — US claimed
EP-0743574-B1 Migration imaging members XEROX CORP (US) 2000-12-27 — — EP claimed
EP-0743573-B1 Method for obtaining image contrast migration imaging members XEROX CORP (US) 2000-09-06 — — EP claimed
EP-0615853-B1 Recording sheets containing phosphonium compounds XEROX CORP (US) 1996-10-16 — — EP claimed
JP-4213319-A — — None — — JP disclosed
WO-2026087965-A1 COMPOSITION COMPRISING EPOXY RESIN WITH CONSTRAINED AROMATIC RINGS AND PHOTOBASE 3M INNOVATIVE PROPERTIES COMPANY (US) 2026-04-30 — — WO disclosed
WO-2025200154-A1 TWO-PART EPOXY COMPOSITION COMPRISING THIOL CURATIVE, AND CATALYST 3M INNOVATIVE PROPERTIES COMPANY (US) 2025-10-02 — — WO disclosed
CN-114729133-B Method for forming fiber reinforced composite material and epoxy resin composition used therein 东丽株式会社 2024-09-20 — — CN disclosed
US-4324792-A SKIN DISORDERS, HAY FEVER, ASTHMA GLAXO GROUP LIMITED (GB) 1982-04-13 — — US disclosed
WO-1981001407-A1 NOVEL HALOPHENYL-PYRIDYL-ALLYLAMINE DERIVATIVES ASTRA LAEKEMEDEL AB (SE) 1981-05-28 — — WO disclosed
EP-0029420-A1 Novel halophenyl-pyridyl-allylamine derivatives, processes and intermediates as well as pharmaceutical preparations thereof Astra Läkemedel Aktiebolag (SE) 1981-05-27 — — EP disclosed
WO-1979000023-A1 A NOVEL PROCESS FOR PREPARATION OF A THERAPEUTICALLY ACTIVE PYRIDINE COMPOUND ASTRA LAEKEMEDEL AB (SE) 1979-01-25 — — WO 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-20120201803-A1 3-SUBSTITUTED COMPOUNDS FOR REDUCING URIC ACID XDH, NLRP3, ASIC3 CHRM2 3297/4885CHRM4 2637/4885CHRM5 3326/4885

“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.

Send feedback