Bromide

Bromide

SCHEMBL197090

CCCCCCCCCCCCCCCC[P+](CCCC)(CCCC)CCCC.[Br-]

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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
OPRM1 known ✓ P35372 1/20 0.39
DNM1 Q05193 7/20 1.00
TSHR P16473 2/20 0.50
THRB P10828 1/20 0.50
BDKRB2 P30411 3/20 0.46
ALDH1A1 P00352 1/20 0.43
TP53 P04637 1/20 0.43
CYP3A4 P08684 1/20 0.43
ALOX15 P16050 1/20 0.43
ALOX12 P18054 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
HIF1A Q16665 1/20 0.43
HSD17B10 Q99714 1/20 0.43
LMNA P02545 1/20 0.42
CA2 P00918 1/20 0.39

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 SCHEMBL5091347 1.00 DNM1 (1.00) DNM1TSHRTHRBBDKRB2ALDH1A1
Bromide SCHEMBL5093099 1.00 DNM1 (1.00) DNM1TSHRTHRBBDKRB2ALDH1A1
Bromide SCHEMBL1517962 1.00 DNM1 (1.00) DNM1TSHRTHRBBDKRB2ALDH1A1
Bromide SCHEMBL422617 1.00 DNM1 (1.00) DNM1TSHRTHRBBDKRB2ALDH1A1
Bromide SCHEMBL3216257 1.00 DNM1 (1.00) DNM1TSHRTHRBBDKRB2ALDH1A1
Bromide SCHEMBL1023018 1.00 DNM1 (1.00) DNM1TSHRTHRBBDKRB2ALDH1A1
Bromide SCHEMBL5086746 1.00 DNM1 (1.00) DNM1TSHRTHRBBDKRB2ALDH1A1
Bromide SCHEMBL3112034 1.00 DNM1 (1.00) DNM1TSHRTHRBBDKRB2ALDH1A1
Bromide SCHEMBL9574841 1.00 DNM1 (1.00) DNM1TSHRTHRBBDKRB2ALDH1A1
Bromide SCHEMBL5086682 1.00 DNM1 (1.00) DNM1TSHRTHRBBDKRB2ALDH1A1

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

Appears in 3065 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120682125-B 1-Hydroxy-1-sodium sulfonate structural compound based on cinnamaldehyde derivative, and preparation method and application thereof 中国农业大学 2026-05-15 CN claimed
EP-4713317-A1 A PROCESS FOR PURIFICATION OF ETHOFUMESATE Adama Agan Ltd. (IL) 2026-03-25 EP claimed
EP-4638452-A1 PROCESS FOR THE PREPARATION OF 7-(4-CHLOROBENZYL)-1-(3-HYDROXYPROPYL)-3-METHYL-8-(3-(TRIFLUOROMETHOXY)-PHENOXY)-3,7-DIHYDRO-1H-PURINE-2,6-DIONE Boehringer Ingelheim International GmbH (DE) 2025-10-29 EP claimed
US-12344784-B2 Stabilized perovskite quantum dot material QUANTUM ADVANCED SOLUTIONS LIMITED (GB) 2025-07-01 US claimed
CN-111718716-B Nanostructure with inorganic ligands for electroluminescent devices 昭荣化学工业株式会社 2025-06-10 CN claimed
US-20250154401-A1 REDUCED-POLYMER-LOADING, HIGH-TEMPERATURE FRACTURING FLUIDS AND METHODS AND SYSTEMS RELATED THERETO SAUDI ARABIAN OIL COMPANY (SA) 2025-05-15 US claimed
CN-119706808-A Two-dimensional fluorine-doped carbon nano sheet and preparation and application thereof 中国科学院大连化学物理研究所 2025-03-28 CN claimed
CN-119666830-A Visual array sensor constructed based on oxidation reaction of nano porphyrin and oxidant on different-level West lake Longjing at different production areas and application thereof 中南民族大学 2025-03-21 CN claimed
US-12209218-B2 Reduced-polymer-loading, high-temperature fracturing fluids and methods and systems related thereto SAUDI ARABIAN OIL COMPANY (SA) 2025-01-28 US claimed
CN-119264033-A Synthesis method of oxygen-18 substituted Abediterol precursor 中国科学技术大学 2025-01-07 CN claimed
US-4451679-A RUTHENIUM COMPOUNDS, PHOSPHONIUM OR QUATERNARY AMMONIUM COMPOUNDS TEXACO INC. (US) 1984-05-29 US claimed
US-4451680-A RUTHENIUM COMPOUND, BIDENTATE OR MULTIDENTATE PHOSPHINE, PHOSPHONIUM COMPOUND TEXACO INC. (US) 1984-05-29 US claimed
EP-0074272-A1 Process for the preparation of hydroxybenzaldehydes SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1983-03-16 EP claimed
EP-0004460-B1 IMPROVED SYNTHESIS OF 1,4-DIAZA-2-CYCLOALKANONE AND SUBSTITUTED DERIVATIVES THEREOF The B.F. GOODRICH Company (US) 1983-03-09 EP claimed
US-4359429-A Mercaptoacetonitrile synthesis W. R. GRACE & CO. (US) 1982-11-16 US claimed
US-4338290-A HYDROGEN IODIDE ACID CATALYST NATIONAL DISTILLERS & CHEMICAL CORP. (US) 1982-07-06 US claimed
US-4200761-A Process for preparing N-cyano-N'methyl-N\"-{2-[(4-methyl-5-imidazolyl)-methylthio]-ethyl} guanidine LEK, TOVARNA FARMACEVTSKIH IN KEMICNIH IZDELKOV, N.SOL.O. (YU) 1980-04-29 US claimed
US-4191702-A PHASE TRANSFER AGENT ELF UNION (FR) 1980-03-04 US claimed
US-4140516-A Encapsulation process employing phase transfer catalysts STAUFFER CHEMICAL COMPANY (US) 1979-02-20 US claimed
US-4092306-A Oxidation of hydrazones to the corresponding diazo compounds in the presence of a phase transfer and an oxidation catalyst which is iodine, an iodide or an iodonium salt GLAXO LABORATORIES LIMITED (EN) 1978-05-30 US claimed