Bromide

Bromide

SCHEMBL3229156

Br.Br.CCCCC(CCCCN)C(N)(CCCC)CCCC.CCCCC(CCCCN)C(N)(CCCC)CCCC

nearest known ligand 0.43

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4

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 16)

geneUniProtsupporting neighboursconfidence
DNM1 Q05193 8/20 0.43
ALDH1A1 P00352 2/20 0.39
MEN1 O00255 1/20 0.39
KMT2A Q03164 1/20 0.39
TSHR P16473 1/20 0.39
EPHX1 P07099 1/20 0.39
FDPS P14324 2/20 0.34
TDP1 Q9NUW8 1/20 0.33
DPP8 Q6V1X1 1/20 0.33
DPP9 Q86TI2 1/20 0.33
DPP7 Q9UHL4 1/20 0.33
CYP3A4 P08684 1/20 0.33
GNAI3 P08754 1/20 0.33
GNAO1 P09471 1/20 0.33
GNAI1 P63096 1/20 0.33
OPRM1 P35372 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
Bromide SCHEMBL3219480 0.98 DNM1 (0.46) DNM1ALDH1A1MEN1KMT2ATSHR
Bromide SCHEMBL3231148 0.91 DNM1 (0.52) DNM1ALDH1A1MEN1KMT2ATSHR
Bromide SCHEMBL3217136 0.90 FDPS (0.35) DNM1ALDH1A1MEN1KMT2ATSHR
Bromide SCHEMBL3916851 0.90 FDPS (0.41) DNM1ALDH1A1FDPSTDP1CYP3A4
Bromide SCHEMBL5087902 0.90 FDPS (0.35) DNM1ALDH1A1FDPSTDP1OPRM1
Bromide SCHEMBL5138211 0.88 FDPS (0.44) DNM1FDPSCYP3A4OPRM1
Bromide SCHEMBL5085195 0.88 FDPS (0.44) DNM1FDPSCYP3A4OPRM1
Bromide SCHEMBL5087215 0.88 FDPS (0.44) DNM1FDPSCYP3A4OPRM1
Bromide SCHEMBL5089308 0.88 FDPS (0.44) DNM1FDPSCYP3A4OPRM1
Bromide SCHEMBL5091596 0.88 FDPS (0.44) DNM1FDPSCYP3A4OPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6251354-B1 RECOVERING METAL NITRATE AND SEPARATION GENERAL ELECTRIC CO. 2001-06-26 US claimed
US-5068353-A Etherification of phthalimide with an alkali metal diphenoxide in the presence of a catalytic phase transfer agent and a solvent GENERAL ELECTRIC COMPANY (US) 1991-11-26 US claimed
EP-0273159-B1 SYNTHESIS OF AROMATIC BIS(ETHER PHTHALIMIDE) COMPOUNDS GENERAL ELECTRIC COMPANY (US) 1991-08-14 EP claimed
EP-0141692-B1 BIS-QUATERNARY SALTS AS PHASE TRANSFER CATALYSTS FOR AROMATIC ETHER IMIDE PREPARATION GENERAL ELECTRIC COMPANY (US) 1989-10-25 EP claimed
US-4554357-A NUCLEOPHILIC DISPLACEMENT GENERAL ELECTRIC COMPANY (US) 1985-11-19 US claimed
EP-0141692-A1 Bis-quaternary salts as phase transfer catalysts for aromatic ether imide preparation GENERAL ELECTRIC COMPANY (US) 1985-05-15 EP claimed
US-7834134-B2 Polyarylethers, blends and methods for making GENERAL ELECTRIC COMPANY (US) 2010-11-16 US disclosed
US-20100041837-A1 POLYARYLETHERS, BLENDS AND METHODS FOR MAKING GENERAL ELECTRIC COMPANY 2010-02-18 US disclosed
US-20100041838-A1 POLYARYLETHERS, BLENDS AND METHODS FOR MAKING BL TECHNOLOGIES, INC. 2010-02-18 US disclosed
US-6251354-B1 RECOVERING METAL NITRATE AND SEPARATION GENERAL ELECTRIC CO. 2001-06-26 US disclosed
EP-0611764-B1 Method of preparing aromatic ether bisimides GEN ELECTRIC (US) 1999-09-22 EP disclosed
US-5068353-A Etherification of phthalimide with an alkali metal diphenoxide in the presence of a catalytic phase transfer agent and a solvent GENERAL ELECTRIC COMPANY (US) 1991-11-26 US disclosed
EP-0273159-B1 SYNTHESIS OF AROMATIC BIS(ETHER PHTHALIMIDE) COMPOUNDS GENERAL ELECTRIC COMPANY (US) 1991-08-14 EP disclosed
EP-0141692-B1 BIS-QUATERNARY SALTS AS PHASE TRANSFER CATALYSTS FOR AROMATIC ETHER IMIDE PREPARATION GENERAL ELECTRIC COMPANY (US) 1989-10-25 EP disclosed
EP-0273159-A1 Synthesis of aromatic bis(ether phthalimide) compounds GENERAL ELECTRIC COMPANY (US) 1988-07-06 EP disclosed
US-4554357-A NUCLEOPHILIC DISPLACEMENT GENERAL ELECTRIC COMPANY (US) 1985-11-19 US disclosed
US-4554357-A NUCLEOPHILIC DISPLACEMENT GENERAL ELECTRIC COMPANY (US) 1985-11-19 US disclosed
EP-0141692-A1 Bis-quaternary salts as phase transfer catalysts for aromatic ether imide preparation GENERAL ELECTRIC COMPANY (US) 1985-05-15 EP disclosed
EP-0141692-A1 Bis-quaternary salts as phase transfer catalysts for aromatic ether imide preparation GENERAL ELECTRIC COMPANY (US) 1985-05-15 EP disclosed