Bromide

Bromide

SCHEMBL9169340

CCCCCCCCCCCCCCOc1ccc(CC(=O)Nc2ccc(C[n+]3ccsc3C)cc2)cc1.[Br-]

nearest known ligand 0.55

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 17)

geneUniProtsupporting neighboursconfidence
MAPT P10636 1/20 0.55
GAA P10253 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
SMN1; SMN2 Q16637 3/20 0.46
KDM4E B2RXH2 1/20 0.46
CYP1A2 P05177 1/20 0.46
CYP2D6 P10635 1/20 0.46
PDE4A P27815 1/20 0.46
HIF1A Q16665 1/20 0.46
HDAC10 Q969S8 1/20 0.46
HDAC6 Q9UBN7 1/20 0.46
LMNA P02545 2/20 0.45
NPC1 O15118 1/20 0.44
HPGD P15428 1/20 0.44
RAB9A P51151 1/20 0.44
FAAH O00519 7/20 0.43
ALDH1A1 P00352 1/20 0.43

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 SCHEMBL9164007 0.92 MAPT (0.50) MAPTGAAL3MBTL1FAAH
Bromide SCHEMBL9168409 0.90 MAPT (0.46) MAPTSMN1; SMN2KDM4ECYP1A2CYP2D6
Bromide SCHEMBL9171763 0.90 MAPT (0.46) MAPT
Bromide SCHEMBL9163199 0.89 LMNA (0.50) MAPTSMN1; SMN2KDM4ELMNANPC1
Bromide SCHEMBL9166126 0.88 MAPT (0.47) MAPTGAAL3MBTL1FAAH
Bromide SCHEMBL9160351 0.86 ALDH1A1 (0.42) MAPTSMN1; SMN2LMNANPC1RAB9A
Bromide SCHEMBL9168069 0.86 EPHX2 (0.50) MAPTSMN1; SMN2KDM4ELMNAHPGD
Bromide SCHEMBL9167606 0.86 MAPT (0.42) MAPTSMN1; SMN2LMNAALDH1A1
Bromide SCHEMBL9162237 0.86 MAPT (0.42) MAPTSMN1; SMN2LMNAFAAHALDH1A1
Bromide SCHEMBL9165825 0.86 EPHX2 (0.50) MAPTSMN1; SMN2KDM4ELMNAHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5432189-A Bis-aryl amide and urea antagonists of platelet activating factor AMERICAN CYANAMID COMPANY (US) 1995-07-11 US disclosed
US-5350759-A Bis-aryl urea compounds WISSNER ALLAN (US) 1994-09-27 US disclosed
US-5231182-A Platelet activating factor inhibitor AMERICAN CYANAMID COMPANY (US) 1993-07-27 US disclosed
US-5225425-A Respiratory system disorders AMERICAN CYANAMID COMPANY (US) 1993-07-06 US disclosed
US-5128351-A BIS-ARYL AMIDE AND UREA ANTAGONISTS OF PLATELET ACTIVATING FACTOR AMERICAN CYANAMID COMPANY (US) 1992-07-07 US disclosed
US-5077409-A Reducing hydroxy bis-aryl amide, acylating, hydrolyzing, sulfonating, halogenating, alkylating with nitrogen heterocycle AMERICAN CYANAMID COMPANY (US) 1991-12-31 US disclosed