Bromide

Bromide

SCHEMBL422617

CCCCCCCCCCCCCCCCCC[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 SCHEMBL197090 1.00 DNM1 (1.00) DNM1TSHRTHRBBDKRB2ALDH1A1
Bromide SCHEMBL1517962 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

Claimed or disclosed in 279 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116948547-A Novel white reinforced photovoltaic backboard base film, preparation method and application thereof 宁波勤邦新材料科技股份有限公司 2023-10-27 CN claimed
CN-114561034-A Antimicrobial modified sulfonated styrene-based polymer compound and preparation method thereof 中国科学院长春应用化学研究所 2022-05-31 CN claimed
CN-102675707-A Quaternary phosphonium salt montmorillonoid enhanced polyolefin nanocomposite and preparation method thereof UNIV HENAN SCIENCE & TECH 2012-09-19 CN claimed
CN-101268055-B Process for preparing 5-fluoro-1, 3-dialkyl-1H-pyrazole-4-carbonyl fluorides BAYER CROPSCIENCE AG 2011-02-16 CN claimed
US-7714144-B2 5-chloro-1,3-dimethyl-1H-pyrazole-4-carbonyl chloride are initially charged in polyethylene glycol dimethyl ether, potassium fluoride and tetraphenylphosphonium bromide as phase tranfer catalyst and sulfolane to produce 5-fluoro-1,3-dimethyl-1H-pyrazole-4-carbonyl fluoride BAYER CROPSCIENCE AG (DE) 2010-05-11 US claimed
US-20090306401-A1 Method For The Production of 5-Fluoro-1,3-Dialkyl-1H-Pyrazol-4-Carbonyl Fluorides BAYER CROPSCIENCE AG (DE) 2009-12-10 US claimed
EP-1483333-B1 THERMOPLASTIC MOULDING MATERIAL AND MOULDED BODIES PRODUCED THEREFROM TICONA GMBH (DE) 2008-12-31 EP claimed
EP-1928839-B1 METHOD FOR THE PRODUCTION OF 5-FLUORO-1,3-DIALKYL-1H-PYRAZOL-4-CARBONYL FLUORIDES BAYER CROPSCIENCE AG (DE) 2008-12-31 EP claimed
CN-101268055-A Process for preparing 5-fluoro-1, 3-dialkyl-1H-pyrazole-4-carbonyl fluorides BAYER CROPSCIENCE AG (DE) 2008-09-17 CN claimed
EP-1483330-B1 POLYOXYMETHYLENE MOLDING COMPOUND AND MOLDED BODY PRODUCED THEREFROM TICONA GMBH (DE) 2008-05-21 EP claimed
US-5463148-A Process for the preparation of chlorofluoronitrobenzenes HOECHST AKTIENGESELLSCHAFT (DE) 1995-10-31 US claimed
EP-0536175-B1 PROCESS FOR PRODUCING CHLOROFLUORONITRO BENZENES AND DIFLUORONITRO BENZENES HOECHST AG (DE) 1995-09-20 EP claimed
EP-0635303-A1 Catalyst for nucleophilic aromatic substitutions HOECHST AKTIENGESELLSCHAFT (DE) 1995-01-25 EP claimed
EP-0615858-A1 Transparent recording sheets XEROX CORPORATION (US) 1994-09-21 EP claimed
EP-0615853-A1 Recording sheets containing phosphonium compounds XEROX CORPORATION (US) 1994-09-21 EP claimed
US-5330823-A Transparent recording sheets XEROX CORPORATION (US) 1994-07-19 US claimed
EP-0536175-A1 PROCESS FOR PRODUCING CHLOROFLUORONITRO BENZENES AND DIFLUORONITRO BENZENES. HOECHST AG (DE) 1993-04-14 EP claimed
EP-0523671-A2 Process for the preparation of chlorofluoronitrobenzenes HOECHST AKTIENGESELLSCHAFT (DE) 1993-01-20 EP claimed
WO-1992000270-A1 PROCESS FOR PRODUCING CHLOROFLUORONITRO BENZENES AND DIFLUORONITRO BENZENES HOECHST AKTIENGESELLSCHAFT (DE) 1992-01-09 WO claimed
US-4496643-A PHOSPHONIUM, ARSONIUM, OR STIBONIUM COMPOUND IN BINDER AS TONER AND FLUOROCARBON CARRIER COATED PARTICLES EASTMAN KODAK COMPANY (US) 1985-01-29 US claimed

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-20090306401-A1 Method For The Production of 5-Fluoro-1,3-Dialkyl-1H-Pyrazol-4-Carbonyl Fluorides CYP4X1, DHX35, AOX1 OPRM1 4295/4885DNM1 793/4885TSHR 2562/4885

“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.