Bromide

Bromide

SCHEMBL5088657

Br.Nc1ccc(Cc2ccccc2)c(Cc2ccccc2)c1Cc1ccccc1

nearest known ligand 0.46

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 9)

geneUniProtsupporting neighboursconfidence
HTR2A P28223 1/20 0.42
CALM1 P0DP23 1/20 0.42
BCL2 P10415 1/20 0.41
BCL2L1 Q07817 1/20 0.41
ALOX5 P09917 1/20 0.40
CTRC Q99895 3/20 0.37
HPGD P15428 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
DHFR P00374 1/20 0.36

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
SCHEMBL1704793 0.98 CALM1 (0.44) HTR2ACALM1BCL2BCL2L1ALOX5
Iodide SCHEMBL5087629 0.96 HTR2A (0.42) HTR2ACALM1BCL2BCL2L1ALOX5
Hydrochloric Acid SCHEMBL5088464 0.96 HTR2A (0.42) HTR2ACALM1BCL2BCL2L1ALOX5
SCHEMBL11406170 0.94 CALM1 (0.44) HTR2ACALM1BCL2BCL2L1ALOX5
SCHEMBL1498780 0.87 CALM1 (0.55) HTR2ACALM1SMN1; SMN2
SCHEMBL1046166 0.85 CALM1 (0.58) HTR2ACALM1BCL2BCL2L1ALOX5
SCHEMBL25231432 0.84 HTR2A (0.42) HTR2ACALM1BCL2BCL2L1ALOX5
SCHEMBL30539480 0.84 HTR2A (0.42) HTR2ACALM1BCL2BCL2L1ALOX5
SCHEMBL5840210 0.82 HTR2A (0.38) HTR2ACALM1ALOX5
SCHEMBL398862 0.82 HTR2A (0.48) HTR2ACALM1BCL2BCL2L1ALOX5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080214386-A1 Stability; easily separated from solution; surface treatment of catalyst with Group seven compound; reacting epoxide with carbon dioxide NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2008-09-04 US disclosed
EP-0634407-B1 Process for production of tris(tribromophenoxy)-s-triazine DAI ICHI KOGYO SEIYAKU CO LTD (JP) 2001-10-10 EP disclosed
US-6075142-A CATALYTICALLY REACTING CYANURIC CHLORIDE AND AQUEOUS TRIBROMOPHENOLATE SOLUTION CONTAINING A REDUCING AGENT AND A PHASE TRANSFER CATALYST TO FORM TRIS/TRIBROMOPHENOXY/-S-TRAIZINE DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 2000-06-13 US disclosed
EP-0735084-B1 Flame retardant thermoplastic styrenic resin composition DAI ICHI KOGYO SEIYAKU CO LTD (JP) 2000-01-12 EP disclosed
EP-0633253-B1 Process for production of tris(tribromophenoxy)-s-triazine DAI ICHI KOGYO SEIYAKU CO LTD (JP) 1999-09-01 EP disclosed
US-5907040-A REACTION OF CYANURIC CHLORIDE WITH BROMOPHENOL AND TERT-AMINECATALYSTS DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1999-05-25 US disclosed
US-5696302-A INTERMEDIATES FOR PRODUCING TRIS(TRIBROMOPHENOXY)-S-TRIAZINE DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1997-12-09 US disclosed
EP-0735084-A1 Flame retardant thermoplastic styrenic resin composition DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1996-10-02 EP disclosed
US-5498714-A FROM CYANURIC CHLORIDE AND TRIBROMOPHENOLATE, PHASE TRANSFER AGENT, REDUCING AGENT TO PREVENT POLYMERIZATION DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1996-03-12 US disclosed
EP-0634407-A1 Process for production of tris(tribromophenoxy)-s-triazine DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1995-01-18 EP disclosed
EP-0633253-A1 Process for production of tris(tribromophenoxy)-s-triazine DAI-ICHI KOGYO SEIYAKU CO., LTD. (JP) 1995-01-11 EP disclosed