Bromide

Bromide

SCHEMBL5565403

O=[N+]([O-])c1ccc(C[n+]2cc(-c3ccccc3)cc(N3CCOCC3)n2)cc1.[Br-]

nearest known ligand 0.46

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
NPC1 O15118 3/20 0.46
KMT2A Q03164 3/20 0.45
MEN1 O00255 2/20 0.45
ALDH1A1 P00352 6/20 0.45
CYP2C9 P11712 2/20 0.45
CYP1A2 P05177 1/20 0.45
HPGD P15428 1/20 0.45
LMNA P02545 3/20 0.44
THRB P10828 1/20 0.44
RCE1 Q9Y256 1/20 0.43
RAB9A P51151 4/20 0.43
MAPT P10636 1/20 0.43
KCNJ1 P48048 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
SLC29A1 Q99808 1/20 0.43
MAPK1 P28482 1/20 0.42
PIK3CA P42336 1/20 0.40
CYP3A4 P08684 1/20 0.39
CYP2C19 P33261 1/20 0.39
HTT P42858 1/20 0.39

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 SCHEMBL5565800 0.87 HTT (0.48) KMT2AALDH1A1HPGDLMNAMAPT
Bromide SCHEMBL5565101 0.84 HTT (0.43) KMT2AALDH1A1HPGDLMNAMAPT
Bromide SCHEMBL5561271 0.81 CNR2 (0.46) NPC1ALDH1A1LMNARAB9AMAPT
Bromide SCHEMBL5560141 0.81 MAPT (0.41) KMT2AMEN1ALDH1A1HPGDLMNA
Bromide SCHEMBL5564744 0.81 CNR2 (0.44) KMT2AMEN1ALDH1A1CYP2C9CYP1A2
SCHEMBL6017175 0.80 CNR2 (0.47) NPC1ALDH1A1LMNARAB9AMAPT
Hydrochloric Acid SCHEMBL5564730 0.79 ALDH1A1 (0.45) NPC1KMT2AMEN1ALDH1A1CYP2C9
Bromide SCHEMBL5564610 0.79 ABL1 (0.43) ALDH1A1MAPTPIK3CAHTT
Bromide SCHEMBL5565311 0.78 HTT (0.41) KMT2AALDH1A1LMNAMAPTMAPK1
Bromide SCHEMBL5565848 0.78 CNR2 (0.46) ALDH1A1CYP2C9CYP1A2LMNARAB9A

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-7300932-B2 Pyrrolo[1,2-b]pyridazine derivatives JAPAN TOBACCO INC. (JP) 2007-11-27 US disclosed
EP-1653969-A4 PYRROLO 1,2-B PYRIDAZINE DERIVATIVES JAPAN TOBACCO INC (JP) 2006-12-20 EP disclosed
EP-1653969-A2 PYRROLO 1,2-B PYRIDAZINE DERIVATIVES Japan Tabacco Inc. (JP) 2006-05-10 EP disclosed
US-20050070545-A1 For treatment or prevention of metabolic and cell proliferative diseases; modifying lipid metabolism TULARIK INC. (US) 2005-03-31 US disclosed
WO-2005013907-A2 PYRROLO[1,2-B]PYRIDAZINE DERIVATIVES JAPAN TOBACCO INC. (JP) 2005-02-17 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050070545-A1 For treatment or prevention of metabolic and cell proliferative diseases; modifying lipid metabolism PC, ACACB, ACAT1 NPC1 172/4885KMT2A 1671/4885MEN1 1029/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.