Bromide

Bromide

SCHEMBL5945895

Br.Cc1ccc(N2CCN(C)CC2)c2c1CCC(NC(=O)c1ccc(N3CCOCC3)cc1)C2

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 19)

geneUniProtsupporting neighboursconfidence
USP30 Q70CQ3 1/20 0.48
MAPK14 Q16539 4/20 0.47
DRD2 P14416 5/20 0.46
HTR2A P28223 5/20 0.46
DRD3 P35462 5/20 0.46
BRD4 O60885 1/20 0.45
AR P10275 2/20 0.43
HDAC3 O15379 2/20 0.43
HDAC8 Q9BY41 2/20 0.43
MEN1 O00255 1/20 0.42
KMT2A Q03164 1/20 0.42
KCNH2 Q12809 1/20 0.42
SCN5A Q14524 1/20 0.42
SCN9A Q15858 1/20 0.42
NPC1 O15118 2/20 0.42
RAB9A P51151 2/20 0.42
TP53 P04637 1/20 0.42
PKM P14618 1/20 0.42
MAPK1 P28482 1/20 0.42

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 SCHEMBL7990792 1.00 USP30 (0.48) USP30MAPK14DRD2HTR2ADRD3
Bromide SCHEMBL5945892 1.00 USP30 (0.48) USP30MAPK14DRD2HTR2ADRD3
Bromide SCHEMBL7990796 1.00 USP30 (0.48) USP30MAPK14DRD2HTR2ADRD3
SCHEMBL29358671 0.99 USP30 (0.49) USP30MAPK14DRD2HTR2ADRD3
SCHEMBL3828127 0.99 USP30 (0.49) USP30MAPK14DRD2HTR2ADRD3
SCHEMBL5106853 0.99 USP30 (0.49) USP30MAPK14DRD2HTR2ADRD3
Hydrochloric Acid SCHEMBL7786685 0.98 USP30 (0.48) USP30MAPK14DRD2HTR2ADRD3
Hydrochloric Acid SCHEMBL7244869 0.98 USP30 (0.48) USP30MAPK14DRD2HTR2ADRD3
SCHEMBL7240506 0.98 USP30 (0.48) USP30MAPK14DRD2HTR2ADRD3
Hydrochloric Acid SCHEMBL7786681 0.98 USP30 (0.48) USP30MAPK14DRD2HTR2ADRD3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20060034911-A1 New oral immediated release dosage form ASTRAZENECA AB (SE) 2006-02-16 US claimed
US-6706710-B2 SEROTONIN H5-HT1B- RECEPTOR ANTAGONIST, FOR TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS SUCH AS DEPRESSION, ANXIETY, ETC. ASTRAZENECA AB (SE) 2004-03-16 US claimed
US-6291458-B1 Morpholinobenzamide salts ASTRAZENECA AB (SE) 2001-09-18 US claimed
US-20060034911-A1 New oral immediated release dosage form ASTRAZENECA AB (SE) 2006-02-16 US disclosed
EP-1572158-A1 A NEW ORAL IMMEDIATED RELEASE DOSAGE FORM AstraZeneca AB (SE) 2005-09-14 EP disclosed
WO-2004110447-A1 USE OF TETRAHYDRONAPHTALENE DERIVATIVES FOR TREATMENT OF GI DISORDERS ASTRAZENECA AB (SE) 2004-12-23 WO disclosed
WO-2004052342-A1 A NEW ORAL IMMEDIATED RELEASE DOSAGE FORM ASTRAZENECA AB (SE) 2004-06-24 WO disclosed
US-6706710-B2 SEROTONIN H5-HT1B- RECEPTOR ANTAGONIST, FOR TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS SUCH AS DEPRESSION, ANXIETY, ETC. ASTRAZENECA AB (SE) 2004-03-16 US disclosed
EP-1305303-A1 NOVEL FORM OF (R)- i N /i - 5-METHYL-8-(4-METHYLPIPERAZIN-1-YL)-1,2,3,4-TETRAHYDRO-2-NAPHTHYL]-4-MORPHOLINOBENZAMIDE AstraZeneca AB (SE) 2003-05-02 EP disclosed
WO-2002008212-A1 NOVEL FORM OF (R)-N-[5-METHYL-8-(4-METHYLPIPERAZIN-1-YL)-1,2,3,4-TETRAHYDRO-2-NAPHTHYL]-4-MORPHOLINOBENZAMIDE ASTRAZENECA AB (SE) 2002-01-31 WO disclosed
EP-1149083-A1 MORPHOLINOBENZAMIDE SALTS AstraZeneca AB (SE) 2001-10-31 EP disclosed
US-6291458-B1 Morpholinobenzamide salts ASTRAZENECA AB (SE) 2001-09-18 US disclosed
WO-2000043378-A1 NEW MORPHOLINOBENZAMIDE SALTS ASTRAZENECA AB (SE) 2000-07-27 WO disclosed