Bromide

Bromide

SCHEMBL7596648

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

nearest known ligand 0.36

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
ACHE known ✓ P22303 3/20 0.33
SPHK2 Q9NRA0 1/20 0.36
KMT2A Q03164 3/20 0.35
BRD4 O60885 1/20 0.35
TERT O14746 2/20 0.34
MAOB P27338 2/20 0.34
CYP1A2 P05177 1/20 0.34
TSHR P16473 1/20 0.34
NFKB1 P19838 1/20 0.34
MEN1 O00255 2/20 0.34
BLM P54132 1/20 0.34
PMP22 Q01453 1/20 0.34
APOBEC3A P31941 1/20 0.34
CTDSP1 Q9GZU7 1/20 0.34
APOBEC3G Q9HC16 1/20 0.34
PLAU P00749 1/20 0.33
MAPT P10636 4/20 0.33
SMN1; SMN2 Q16637 2/20 0.33
BCHE P06276 2/20 0.33
HDAC3 O15379 1/20 0.33

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
SCHEMBL13596778 0.99 SPHK2 (0.36) SPHK2KMT2ABRD4TERTMAOB
SCHEMBL13596779 0.89 SPHK2 (0.35) SPHK2KMT2ABRD4TERTMAOB
Bromide SCHEMBL8908921 0.88 KMT2A (0.34) KMT2ABRD4MEN1ACHEMAPT
Bromide SCHEMBL8909862 0.86 KMT2A (0.37) KMT2ABRD4ACHEMAPTSMN1; SMN2
SCHEMBL13596780 0.83 KDM4E (0.42) SPHK2KMT2ABRD4MEN1ACHE
SCHEMBL17898189 0.81 PPARA (0.45) TSHRACHEMAPTTP53KDM4E
Bromide SCHEMBL8908965 0.81 TTR (0.37) KMT2AACHEMAPTSMN1; SMN2TP53
SCHEMBL12907529 0.80 TTR (0.38) KMT2AACHEMAPTSMN1; SMN2TP53
SCHEMBL12907508 0.76 GAA (0.37) KMT2AMEN1MAPTSMN1; SMN2KDM4E
SCHEMBL6254465 0.75 L3MBTL1 (0.42) KMT2AMEN1ACHEMAPTSMN1; 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
EP-0361817-B1 Nucleophilic polysubstituted aryl acridinium esters, conjugates, production and uses thereof BAYER AG (US) 2002-08-28 EP disclosed
US-6080591-A USEFUL IN BIOLOGICAL ASSAYS FOR DETERMINATION OF VITAMIN B12, FOLATE, CORTISOL, ESTRADIOL, AND THROMBOXANE B2 BAYER CORPORATION (US) 2000-06-27 US disclosed
US-5663074-A INCUBATION OF FOLATE WITH AMINE REACTIVE COMPOUND, ACTIVATION AND INCUBATION THE ACRIDINIUM ESTER-FOLATE CONJUGATE CHIRON DIAGNOSTICS CORPORATION (US) 1997-09-02 US disclosed
US-5538901-A ANALYSIS CIBA CORNING DIAGNOSTICS CORP. (US) 1996-07-23 US disclosed
EP-0661270-A1 Nucleophilic polysubstituted aryl acridinium esters, conjugates, production and uses thereof Ciba Corning Diagnostics Corp. (US) 1995-07-05 EP disclosed
US-5241070-A Biological analysis CIBA CORNING DIAGNOSTICS CORP. (US) 1993-08-31 US disclosed