Bromide

Bromide

SCHEMBL262065

CCN(CC)C(N(CC)CC)=[N+](CC)CC.[Br-]

nearest known ligand 0.33

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
CHRM1 known ✓ P11229 1/20 0.32
ACHE known ✓ P22303 1/20 0.32
OPRM1 known ✓ P35372 1/20 0.32
EHMT2 Q96KQ7 3/20 0.33
EHMT1 Q9H9B1 3/20 0.33
ABCB11 O95342 2/20 0.33
HTT P42858 2/20 0.33
GSDMD P57764 2/20 0.33
CA12 O43570 2/20 0.33
CA1 P00915 2/20 0.33
CA2 P00918 2/20 0.33
CA4 P22748 2/20 0.33
CA9 Q16790 2/20 0.33
CYP2E1 P05181 1/20 0.33
PTGS1 P23219 1/20 0.33
LMNA P02545 2/20 0.32
PHGDH O43175 1/20 0.32
PLIN1 O60240 1/20 0.32
GMNN O75496 1/20 0.32
TRPA1 O75762 1/20 0.32

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
SCHEMBL1119578 0.97 EHMT2 (0.35) EHMT2EHMT1ABCB11HTTGSDMD
Hydrochloric Acid SCHEMBL27913333 0.94 EHMT2 (0.33) EHMT2EHMT1ABCB11HTTGSDMD
Iodide SCHEMBL7033668 0.94 EHMT2 (0.33) EHMT2EHMT1ABCB11HTTGSDMD
Hydrochloric Acid SCHEMBL261161 0.94 EHMT2 (0.33) EHMT2EHMT1ABCB11HTTGSDMD
Fluoride Ion SCHEMBL4607229 0.94 EHMT2 (0.33) EHMT2EHMT1ABCB11HTTGSDMD
SCHEMBL7032131 0.87
SCHEMBL7035110 0.85 TSHR (0.39) LMNAALDH1A1TSHR
SCHEMBL8717245 0.85 CA12 (0.37) CA12CA1CA2CA9ALDH1A1
Hydrochloric Acid SCHEMBL25405995 0.83 CA12 (0.36) CA12CA1CA2CA9TSHR
Acetic Acid SCHEMBL261148 0.83 CA1 (0.36) CA1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114621178-A Preparation process of fluoroethylene carbonate 内蒙古源宏精细化工有限公司 2022-06-14 CN claimed
EP-2292627-B1 Aqueous catalytic process for the preparation of thiocarboxylate silane MOMENTIVE PERFORMANCE MAT INC (US) 2016-03-30 EP claimed
EP-1869057-B1 AQUEOUS CATALYTIC PROCESS FOR THE PREPARATION OF THIOCARBOXYLATE SILANE MOMENTIVE PERFORMANCE MAT INC (US) 2012-12-19 EP claimed
US-8013173-B2 Method of purifying dianhydrides, the dianhydrides formed thereby, and polyetherimides formed therefrom SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2011-09-06 US claimed
EP-1960408-B1 PROCESS FOR THE PRODUCTION OF MERCAPTOALKYLALKOXYSILANES MOMENTIVE PERFORMANCE MAT INC (US) 2011-07-20 EP claimed
EP-2292627-A1 Aqueous catalytic process for the preparation of thiocarboxylate silane Momentive Performance Materials Inc. (US) 2011-03-09 EP claimed
EP-2280963-A1 METHOD OF PURIFYING DIANHYDRIDES, THE DIANHYDRIDES FORMED THEREBY, AND POLYETHERIMIDES FORMED THEREFROM SABIC Innovative Plastics IP B.V. (NL) 2011-02-09 EP claimed
EP-2271611-A1 METHODS FOR PREPARING OXYDIPHTHALIC ANHYDRIDES SABIC Innovative Plastics IP B.V. (NL) 2011-01-12 EP claimed
WO-2009120215-A9 METHODS FOR PREPARING OXYDIPHTHALIC ANHYDRIDES SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2010-11-11 WO claimed
US-7674920-B2 Methods for preparing oxydiphthalic anhydrides, oxydiphthalic anhydrides prepared thereby, and polyetherimides derived therefrom SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2010-03-09 US claimed
US-5898080-A Method for preparing diaryl carbonates employing hexaalkylguanidinium halides GENERAL ELECTRIC COMPANY (US) 1999-04-27 US claimed
US-5807965-A Interfacial copolyestercarbonate method using catalyst comprising hexaalkylguanidinium salt and tertiary amine GENERAL ELECTRIC COMPANY (US) 1998-09-15 US claimed
US-5760272-A REACTING A HYDROXYAROMATIC COMPOUND WITH OXYGEN AND CARBON MONOXIDE IN PRESENCE OF A CATALYST MIXTURE GENERAL ELECTRIC COMPANY (US) 1998-06-02 US claimed
EP-0816414-A2 Preparation of polyether polymers GENERAL ELECTRIC COMPANY (US) 1998-01-07 EP claimed
US-5663275-A POLYETHERIMIDES, HIGH MOLECULAR WEIGHT, ENGINEERING RESINS GENERAL ELECTRIC COMPANY (US) 1997-09-02 US claimed
US-5438114-A Heating with a primary amine in the presence of a non-metal containing catalyst of tertiary amine, tertiary phosphine, quaternary ammonium salt, quaternary phosphonium salt or hexaalkylguanidium salt or heterocyclic analog thereof GENERAL ELECTRIC COMPANY (US) 1995-08-01 US claimed
EP-0642544-A1 PHASE TRANSFER CATALYZED PREPARATION OF AROMATIC POLYETHER POLYMERS GENERAL ELECTRIC COMPANY (US) 1995-03-15 EP claimed
WO-1994022939-A1 PHASE TRANSFER CATALYZED PREPARATION OF AROMATIC POLYETHER POLYMERS GENERAL ELECTRIC COMPANY (US) 1994-10-13 WO claimed
US-5229482-A Phase transfer catalyzed preparation of aromatic polyether polymers GENERAL ELECTRIC COMPANY (US) 1993-07-20 US claimed
US-5132423-A Nucleophilic substitution reaction of alkali hydroxy- or mercaptoaromatic compound and heterocyclic substituted imide GENERAL ELECTRIC COMPANY (US) 1992-07-21 US claimed