Bromide

Bromide

SCHEMBL5565848

Clc1cccc(C[n+]2cc(-c3ccccc3)cc(N3CCOCC3)n2)c1.[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
CNR2 P34972 1/20 0.46
HTT P42858 2/20 0.43
ALDH1A1 P00352 2/20 0.43
LMNA P02545 1/20 0.43
PIK3CB P42338 3/20 0.43
PIK3CD O00329 1/20 0.43
PIK3CA P42336 1/20 0.43
MAPT P10636 4/20 0.41
CDK1 P06493 1/20 0.40
CDK2 P24941 1/20 0.40
SMG1 Q96Q15 1/20 0.40
CYP1A2 P05177 1/20 0.40
CYP3A4 P08684 1/20 0.40
CYP2C9 P11712 1/20 0.40
CYP2C19 P33261 1/20 0.40
TSHR P16473 1/20 0.39
MAPK1 P28482 1/20 0.39
NPSR1 Q6W5P4 1/20 0.39
HSD17B10 Q99714 1/20 0.39
STK4 Q13043 2/20 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 0.90 HTT (0.48) HTTALDH1A1LMNAPIK3CBPIK3CA
Bromide SCHEMBL5559706 0.89 MAPT (0.46) CNR2HTTALDH1A1LMNAPIK3CB
Bromide SCHEMBL5564744 0.88 CNR2 (0.44) CNR2HTTALDH1A1LMNAPIK3CB
Bromide SCHEMBL5565311 0.87 HTT (0.41) CNR2HTTALDH1A1LMNAPIK3CB
Bromide SCHEMBL5559268 0.84 CYP1A2 (0.47) HTTALDH1A1LMNAMAPTSMG1
Bromide SCHEMBL5565101 0.82 HTT (0.43) HTTALDH1A1LMNAPIK3CBMAPT
Bromide SCHEMBL5560418 0.82 HTT (0.43) HTTALDH1A1LMNAPIK3CBPIK3CD
Bromide SCHEMBL5559995 0.82 HTT (0.45) HTTALDH1A1LMNAPIK3CBPIK3CA
Bromide SCHEMBL5559239 0.80 ALDH1A1 (0.59) HTTALDH1A1LMNAPIK3CBMAPT
Hydrochloric Acid SCHEMBL5565412 0.80 ALDH1A1 (0.47) HTTALDH1A1LMNAPIK3CBMAPT

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 CNR2 3754/4885HTT 894/4885ALDH1A1 978/4885

“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.