Bromide

Bromide

SCHEMBL9167155

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

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 20)

geneUniProtsupporting neighboursconfidence
NLRP3 Q96P20 2/20 0.46
P2RY14 Q15391 1/20 0.46
MMP7 P09237 1/20 0.44
MMP10 P09238 1/20 0.44
MMP13 P45452 2/20 0.43
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
MEN1 O00255 1/20 0.42
KMT2A Q03164 1/20 0.42
ALDH1A1 P00352 1/20 0.42
LMNA P02545 1/20 0.42
MDH1 P40925 1/20 0.41
EPHX2 P34913 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 SCHEMBL9165386 0.93 FAAH (0.44) NR1H4CYP2D6EPHX2ACKR3
Bromide SCHEMBL9159971 0.92 SMN1; SMN2 (0.48) NR1H4SMN1; SMN2HIF1AMEN1KMT2A
Bromide SCHEMBL9166558 0.90 MAPT (0.48) SMN1; SMN2KDM4ECYP1A2CYP2D6PDE4A
Bromide SCHEMBL9167424 0.90 MAPT (0.48) SMN1; SMN2KDM4ECYP1A2CYP2D6PDE4A
Bromide SCHEMBL9162050 0.89 NAMPT (0.46) NR1H4SMN1; SMN2MEN1KMT2ANPC1
Bromide SCHEMBL9167271 0.89 NR1H4 (0.57) NR1H4SMN1; SMN2KDM4EMEN1KMT2A
Bromide SCHEMBL9161733 0.88 ACKR3 (0.41) NR1H4MEN1KMT2AEPHX2ACKR3
Bromide SCHEMBL9167554 0.88 LMNA (0.43) NLRP3P2RY14MMP13SMN1; SMN2KDM4E
Bromide SCHEMBL9165638 0.88 SMN1; SMN2 (0.48) NR1H4SMN1; SMN2CYP2D6MDH1NPC1
Bromide SCHEMBL9171679 0.88 MEN1 (0.44) MMP7MMP10CYP2D6MEN1KMT2A

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