Bromide

Bromide

SCHEMBL9167271

Br.CCCCCCCCCCCCCCOc1ccc(C(=O)Nc2cccc(CN3C=CSC3)c2)cc1

nearest known ligand 0.57

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 13)

geneUniProtsupporting neighboursconfidence
NR1H4 Q96RI1 7/20 0.57
MAPT P10636 2/20 0.48
TP53 P04637 2/20 0.48
THRB P10828 1/20 0.48
PARP1 P09874 2/20 0.48
SMN1; SMN2 Q16637 2/20 0.46
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
KDM4E B2RXH2 1/20 0.46
RAB9A P51151 1/20 0.46
PLK1 P53350 2/20 0.45
LMNA P02545 1/20 0.44
STAT3 P40763 1/20 0.44

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 SCHEMBL9165334 0.92 NR1H4 (0.59) NR1H4MAPTTHRBSMN1; SMN2MEN1
Bromide SCHEMBL9166719 0.91 MEN1 (0.51) NR1H4MAPTTHRBPARP1SMN1; SMN2
Bromide SCHEMBL9165002 0.91 THRB (0.53) NR1H4MAPTTP53THRBSMN1; SMN2
Bromide SCHEMBL9167526 0.90 THRB (0.58) NR1H4MAPTTHRBSMN1; SMN2MEN1
Bromide SCHEMBL9162050 0.90 NAMPT (0.46) NR1H4SMN1; SMN2MEN1KMT2ARAB9A
Bromide SCHEMBL9159971 0.89 SMN1; SMN2 (0.48) NR1H4MAPTTP53SMN1; SMN2MEN1
Bromide SCHEMBL9169422 0.89 L3MBTL1 (0.56) NR1H4MAPTSMN1; SMN2MEN1KMT2A
Bromide SCHEMBL9167052 0.89 L3MBTL1 (0.56) NR1H4MAPTSMN1; SMN2MEN1KMT2A
Bromide SCHEMBL9167155 0.89 NLRP3 (0.46) NR1H4MAPTSMN1; SMN2MEN1KMT2A
Bromide SCHEMBL9162576 0.88 ACKR3 (0.44) NR1H4THRBPARP1

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