Bromide

Bromide

SCHEMBL9167396

Br.CCCCCCCCCCCCCCCCOc1ccc(CN(C(C)=O)c2cccc(Cc3cccnc3)c2)cc1

nearest known ligand 0.48

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 20)

geneUniProtsupporting neighboursconfidence
NFKB1 P19838 2/20 0.48
NFKB2 Q00653 2/20 0.48
RELA Q04206 2/20 0.48
LMNA P02545 2/20 0.48
NPC1 O15118 1/20 0.48
POLB P06746 1/20 0.48
MAPT P10636 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.48
LTA4H P09960 1/20 0.46
GRM2 Q14416 2/20 0.44
L3MBTL1 Q9Y468 1/20 0.44
FAAH O00519 1/20 0.43
LTB4R2 Q9NPC1 1/20 0.43
TSPO P30536 2/20 0.43
TSHR P16473 2/20 0.43
CYP1A2 P05177 1/20 0.43
CYP2C9 P11712 1/20 0.43
CYP2C19 P33261 1/20 0.43
KMT2A Q03164 1/20 0.42
PSMB5 P28074 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
Bromide SCHEMBL9165138 0.93 GRM2 (0.44) NFKB1NFKB2RELALMNANPC1
Bromide SCHEMBL9159782 0.93 GRM2 (0.44) NFKB1NFKB2RELALMNANPC1
Bromide SCHEMBL9169053 0.92 NFKB1 (0.47) NFKB1NFKB2RELALMNANPC1
Bromide SCHEMBL9166803 0.92 LTA4H (0.51) NFKB1NFKB2RELALMNANPC1
Bromide SCHEMBL9169046 0.92 LTA4H (0.51) NFKB1NFKB2RELALMNANPC1
Bromide SCHEMBL9162203 0.87 LTA4H (0.46) NFKB1NFKB2RELALMNANPC1
Bromide SCHEMBL9167534 0.87 LTA4H (0.46) NFKB1NFKB2RELALMNANPC1
Bromide SCHEMBL9169245 0.87 TP53 (0.44) LMNAMAPTLTA4HGRM2L3MBTL1
Bromide SCHEMBL9169207 0.87 CYP3A4 (0.41) NFKB1NFKB2RELALMNANPC1
Bromide SCHEMBL9168018 0.87 L3MBTL1 (0.41) NFKB1NFKB2RELALMNANPC1

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