Bromide

Bromide

SCHEMBL9168409

CCCCCCCCCCCCCCOc1ccc(CC(=O)Nc2cccc(C[n+]3ccsc3C)c2)cc1.[Br-]

nearest known ligand 0.46

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 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 1/20 0.46
NLRP3 Q96P20 2/20 0.46
P2RY14 Q15391 1/20 0.46
NR1H4 Q96RI1 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
KDM4E B2RXH2 1/20 0.43
CYP1A2 P05177 1/20 0.43
CYP2D6 P10635 1/20 0.43
PDE4A P27815 1/20 0.43
HIF1A Q16665 1/20 0.43
HDAC10 Q969S8 1/20 0.43
HDAC6 Q9UBN7 1/20 0.43
MDH1 P40925 1/20 0.41
NPC1 O15118 1/20 0.41
HPGD P15428 1/20 0.41
RAB9A P51151 1/20 0.41
MMP7 P09237 1/20 0.41
MMP10 P09238 1/20 0.41
USP2 O75604 1/20 0.40
LMNA P02545 1/20 0.40

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 SCHEMBL9164522 0.93 PLA2G4B (0.44) MAPTNR1H4
Bromide SCHEMBL9163765 0.92 SMN1; SMN2 (0.48) MAPTNR1H4SMN1; SMN2HIF1AMDH1
Bromide SCHEMBL9169340 0.90 MAPT (0.55) MAPTSMN1; SMN2KDM4ECYP1A2CYP2D6
Bromide SCHEMBL9167259 0.89 MAPT (0.44) MAPTNR1H4SMN1; SMN2NPC1RAB9A
Bromide SCHEMBL9168042 0.89 NR1H4 (0.57) MAPTNR1H4SMN1; SMN2LMNA
Bromide SCHEMBL9168383 0.88 MAPT (0.41) MAPTNR1H4
Bromide SCHEMBL9171763 0.88 MAPT (0.46) MAPT
Bromide SCHEMBL9159649 0.88 SMN1; SMN2 (0.48) NR1H4SMN1; SMN2MDH1NPC1RAB9A
Bromide SCHEMBL9159837 0.88 KMT2A (0.42) MAPTSMN1; SMN2LMNAHTT
Bromide SCHEMBL9169337 0.88 SMN1; SMN2 (0.53) MAPTSMN1; SMN2KDM4EHPGDUSP2

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