Bromide

Bromide

SCHEMBL7197342

COc1cccc(C[P+](c2ccccc2C)(c2ccccc2C)c2ccccc2C)c1.[Br-]

nearest known ligand 0.51

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 16)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 1/20 0.43
CHRM1 known ✓ P11229 1/20 0.43
CHRM3 known ✓ P20309 1/20 0.43
TAAR1 Q96RJ0 3/20 0.51
IDO1 P14902 2/20 0.45
AGXT P21549 2/20 0.45
MAOB P27338 2/20 0.44
SIGMAR1 Q99720 2/20 0.43
SCN8A Q9UQD0 1/20 0.43
IDH1 O75874 1/20 0.42
CMA1 P23946 1/20 0.42
AOC3 Q16853 1/20 0.41
MAPT P10636 1/20 0.41
CASR P41180 1/20 0.41
MEN1 O00255 1/20 0.41
KMT2A Q03164 1/20 0.41

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 SCHEMBL7195761 0.97 TAAR1 (0.51) TAAR1IDO1AGXTMAOBSIGMAR1
Iodide SCHEMBL7197231 0.97 TAAR1 (0.51) TAAR1IDO1AGXTMAOBSIGMAR1
Phosphoric Acid SCHEMBL7197200 0.90 TAAR1 (0.46) TAAR1IDO1AGXTMAOBSCN8A
Acetic Acid SCHEMBL8750052 0.89 TAAR1 (0.44) TAAR1IDH1MAPTMEN1KMT2A
Succinic Acid SCHEMBL7195815 0.87 TAAR1 (0.43) TAAR1IDH1MAPTMEN1KMT2A
Acetic Acid SCHEMBL7195824 0.87 MTNR1A (0.45) TAAR1IDH1MEN1KMT2A
Bromide SCHEMBL7195760 0.83 L3MBTL1 (0.47) IDO1SIGMAR1SCN8AMAPT
Phosphoric Acid SCHEMBL9318697 0.82 MAOB (0.39) TAAR1IDO1AGXTMAOBSCN8A
Phosphoric Acid SCHEMBL9318706 0.81 MAOB (0.38) TAAR1MAOBIDH1MAPTMEN1
Bromide SCHEMBL3110986 0.80 TAAR1 (0.56) TAAR1IDO1AGXTMAOBSIGMAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
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
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