Bromide

Bromide

SCHEMBL6061034

Cc1cccc([P+](Cc2ccccc2)(c2cccc(C)c2)c2cccc(C)c2)c1.[Br-]

nearest known ligand 0.47

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 19)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.39
SNCA P37840 2/20 0.47
TAAR1 Q96RJ0 4/20 0.40
SLC6A2 P23975 2/20 0.39
MAOA P21397 1/20 0.39
SLC6A4 P31645 1/20 0.39
SLC6A3 Q01959 1/20 0.39
SIGMAR1 Q99720 1/20 0.39
CYP2A6 P11509 1/20 0.39
ADORA2A P29274 1/20 0.39
ADORA1 P30542 1/20 0.39
IDO1 P14902 2/20 0.39
PPARG P37231 1/20 0.38
PPARA Q07869 1/20 0.38
ACP3 P15309 1/20 0.38
NPSR1 Q6W5P4 1/20 0.37
POLB P06746 1/20 0.37
ALDH1A1 P00352 1/20 0.37
TP53 P04637 1/20 0.37

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
Hydrochloric Acid SCHEMBL6061532 0.96 SNCA (0.44) SNCATAAR1SLC6A2MAOASLC6A4
Iodide SCHEMBL6061684 0.96 SNCA (0.44) SNCATAAR1SLC6A2MAOASLC6A4
Bromide SCHEMBL2646998 0.93 SNCA (0.47) SNCATAAR1SLC6A2MAOASLC6A4
Bromide SCHEMBL7197866 0.89 SNCA (0.43) SNCATAAR1ACHEIDO1ALDH1A1
Hydrochloric Acid SCHEMBL29427125 0.89 SNCA (0.44) SNCATAAR1SLC6A2MAOASLC6A4
Hydrochloric Acid SCHEMBL2447879 0.89 SNCA (0.44) SNCATAAR1SLC6A2MAOASLC6A4
Phosphoric Acid SCHEMBL7197899 0.89 ACP3 (0.43) SNCAPPARGPPARAACP3POLB
Acetic Acid SCHEMBL8750035 0.87 SNCA (0.41) SNCAPPARGPPARAACP3POLB
Acetic Acid SCHEMBL7193257 0.86 SNCA (0.41) SNCAPPARGPPARAACP3POLB
Hydrochloric Acid SCHEMBL7199763 0.85 SNCA (0.41) SNCATAAR1ACHEIDO1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-1993004122-A1 POLYESTER COMPOSITIONS CONTAINING PHOSPHONIUM COMPOUNDS THE DOW CHEMICAL COMPANY (US) 1993-03-04 WO claimed
US-20060229400-A1 Powder coating matting agent comprising ester amide condensation product FLETCHER TIM 2006-10-12 US disclosed
US-20050288450-A1 Coating matting agent comprising amide condensation product FLETCHER TIM 2005-12-29 US disclosed
EP-1509561-A1 POWDER COATING MATTING AGENT COMPRISING ESTER AMIDE CONDENSATION PRODUCT Grace GmbH & Co. KG (DE) 2005-03-02 EP disclosed
WO-2003102048-A1 POWDER COATING MATTING AGENT COMPRISING ESTER AMIDE CONDENSATION PRODUCT GRACE GMBH & CO. KG (DE) 2003-12-11 WO disclosed
EP-0624173-B2 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 2003-04-09 EP disclosed
EP-0624173-B1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS DOW CHEMICAL CO (US) 1997-04-02 EP disclosed
EP-0624173-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS. DOW CHEMICAL CO (US) 1994-11-17 EP disclosed
US-5360886-A Alklyphenylphosphine or phosphonium catalyst THE DOW CHEMICAL COMPANY (US) 1994-11-01 US disclosed
US-5310853-A Epoxy resins THE DOW CHEMICAL COMPANY (US) 1994-05-10 US disclosed
WO-1993015126-A1 PRECATALYZED CATALYST COMPOSITIONS, PROCESS FOR PREPARING RESINS THE DOW CHEMICAL COMPANY (US) 1993-08-05 WO disclosed
US-5202407-A Phosphonium or phosphine catalyst having at least three alkylphenyl groups attached to phosphorus atom THE DOW CHEMICAL COMPANY (US) 1993-04-13 US disclosed
WO-1993004122-A1 POLYESTER COMPOSITIONS CONTAINING PHOSPHONIUM COMPOUNDS THE DOW CHEMICAL COMPANY (US) 1993-03-04 WO disclosed