Bromide

Bromide

SCHEMBL7367229

Br.O=[N+]([O-])c1cc(-c2csc(Nc3cccnc3)n2)cc(O)c1O

nearest known ligand 0.60

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 19)

geneUniProtsupporting neighboursconfidence
MAPK1 P28482 2/20 0.60
MAPT P10636 8/20 0.58
ALDH1A1 P00352 5/20 0.58
CLK1 P49759 1/20 0.57
NPC1 O15118 7/20 0.56
L3MBTL1 Q9Y468 1/20 0.56
MEN1 O00255 9/20 0.56
KMT2A Q03164 9/20 0.56
RAB9A P51151 4/20 0.56
PKM P14618 2/20 0.53
GAA P10253 2/20 0.53
VCP P55072 1/20 0.53
GLA P06280 1/20 0.53
LMNA P02545 2/20 0.50
ALOX12 P18054 1/20 0.50
NPSR1 Q6W5P4 1/20 0.50
NCOA3 Q9Y6Q9 1/20 0.49
HTT P42858 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.48

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
SCHEMBL7369662 0.87 CSNK2A1 (0.61) MAPK1MAPTALDH1A1NPC1L3MBTL1
Bromide SCHEMBL7368418 0.82 MAPT (0.47) MAPK1MAPTALDH1A1NPC1L3MBTL1
SCHEMBL7371604 0.80 MAPT (0.62) MAPK1MAPTALDH1A1NPC1L3MBTL1
SCHEMBL22560267 0.76 MAPK1 (1.00) MAPK1MAPTALDH1A1CLK1NPC1
Bromide SCHEMBL7674933 0.75 MAPK1 (0.82) MAPK1MAPTALDH1A1CLK1NPC1
SCHEMBL7554938 0.75 MAPT (0.91) MAPK1MAPTALDH1A1CLK1NPC1
SCHEMBL7366431 0.75 LARS1 (0.57) MAPK1MAPTALDH1A1CLK1NPC1
SCHEMBL7557437 0.74 MAPK1 (0.84) MAPK1MAPTALDH1A1CLK1NPC1
Bromide SCHEMBL7406302 0.74 MEN1 (0.56) MAPK1MAPTALDH1A1NPC1L3MBTL1
Bromide SCHEMBL7691671 0.73 MAPK1 (0.82) MAPK1MAPTALDH1A1CLK1NPC1

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5633371-A ENZYME INHIBITORS; TREATMENT OF DEPRESSION AND PARKINSON*S DISEASE HOFFMANN-LA ROCHE INC. (US) 1997-05-27 US disclosed
US-5476875-A Catechol derivatives HOFFMAN-LA ROCHE INC. (US) 1995-12-19 US disclosed
US-5389653-A Inhibitors of the enzyme catechol-O-methyltransferase; useful as co-medication in treatment of Parkinson's disease HOFFMAN-LA ROCHE INC. (US) 1995-02-14 US disclosed
US-5236952-A Inhibit the enzyme catechol-O-methyltransferase; for treatment of Parkinson's disease administered with L-dopa HOFFMANN-LA ROCHE INC. (US) 1993-08-17 US disclosed
EP-0237929-B1 3,5-DISUBSTITUTED PYROCATECHOL DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 1993-06-02 EP disclosed