Bromide

Bromide

SCHEMBL8909862

Cc1cc(C(=O)NCCOP(=O)(O)O)cc(C)c1OC(=O)c1c2ccccc2[n+](C)c2ccccc12.[Br-]

nearest known ligand 0.37

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 18)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 3/20 0.35
KMT2A Q03164 2/20 0.37
BRD4 O60885 1/20 0.34
NPC1 O15118 2/20 0.34
RAB9A P51151 2/20 0.34
RECQL P46063 1/20 0.34
MAPT P10636 4/20 0.33
SMN1; SMN2 Q16637 4/20 0.33
TP53 P04637 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
HPGD P15428 2/20 0.32
POLB P06746 2/20 0.32
LMNA P02545 1/20 0.32
BCHE P06276 1/20 0.31
FGFR1 P11362 1/20 0.31
PDGFRA P16234 1/20 0.31
FLT1 P17948 1/20 0.31
KDR P35968 1/20 0.31

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 SCHEMBL8908921 0.88 KMT2A (0.34) KMT2AACHEBRD4MAPTSMN1; SMN2
Bromide SCHEMBL7596648 0.86 SPHK2 (0.36) KMT2AACHEBRD4MAPTSMN1; SMN2
SCHEMBL13596778 0.85 SPHK2 (0.36) KMT2AACHEBRD4MAPTSMN1; SMN2
Bromide SCHEMBL8908965 0.78 TTR (0.37) KMT2AACHENPC1RAB9ARECQL
SCHEMBL17898189 0.78 PPARA (0.45) ACHEMAPTTP53HPGDLMNA
SCHEMBL12907529 0.77 TTR (0.38) KMT2AACHENPC1RAB9ARECQL
SCHEMBL13596779 0.75 SPHK2 (0.35) KMT2ABRD4NPC1RAB9AMAPT
SCHEMBL13979959 0.74 SRC (0.32) MAPTTP53POLBLMNA
SCHEMBL6254465 0.72 L3MBTL1 (0.42) KMT2AACHEMAPTSMN1; SMN2TP53
Bromide SCHEMBL4190244 0.72 GAA (0.36) KMT2AACHERECQLMAPTSMN1; SMN2

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-5656500-A LIPOSOMES COUPLED TO MOLECULES WITH BIOLOGICAL ACTIVITY SELECTED FROM ANTIGENS, ANTIBODIES, AND NUCLEIC ACIDS, THESE CONJUGATE ENCAPSULATE HYDROPHILIC POLYSUBSTITUTED ARYL ACRIDINIUM ESTERS CHIRON DIAGNOSTICS CORPORATION (US) 1997-08-12 US disclosed
US-5595875-A DNA, RNA, IMMUNOASSAY, CHEMILUMINESCENCE CIBA CORNING DIAGNOSTICS CORP. (US) 1997-01-21 US disclosed
EP-0353971-B1 Acridinium esters and method for detection of an analyte using acridinium esters and liposomes CIBA CORNING DIAGNOSTICS CORP (US) 1996-02-07 EP disclosed
US-5449556-A Chemiluminescent markers CIBA CORNING DIAGNOSTICS CORP. (US) 1995-09-12 US disclosed
US-5227489-A Hydrophilic chemiluminescent markers CIBA CORNING DIAGNOSTICS CORP. (US) 1993-07-13 US disclosed
EP-0353971-A2 Acridinium esters and method for detection of an analyte using acridinium esters and liposomes Ciba Corning Diagnostics Corp. (US) 1990-02-07 EP disclosed