Bromide

Bromide

SCHEMBL7044939

CCOC(=O)C1=C(C[n+]2ccccc2)N(c2ccccc2)C(C[n+]2ccccc2)=C(C(=O)OCC)C1c1ccccc1.[Br-].[Br-]

nearest known ligand 0.54

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 17)

geneUniProtsupporting neighboursconfidence
GAA P10253 3/20 0.54
KDM4E B2RXH2 2/20 0.54
ADORA3 P0DMS8 1/20 0.48
SIRT3 Q9NTG7 4/20 0.46
MAPT P10636 4/20 0.46
HTT P42858 2/20 0.46
HPGD P15428 2/20 0.46
MEN1 O00255 1/20 0.46
TSHR P16473 1/20 0.46
KMT2A Q03164 1/20 0.46
GLA P06280 1/20 0.44
ALDH1A1 P00352 3/20 0.44
NPSR1 Q6W5P4 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
POLB P06746 1/20 0.41
TP53 P04637 1/20 0.41
ALOX12 P18054 1/20 0.41

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
Iodide SCHEMBL9511466 0.75 ADORA3 (0.62) GAAKDM4EADORA3HPGDTSHR
Bromide SCHEMBL7044891 0.75 PPARG (0.44) GAAKDM4EMAPTTSHRALDH1A1
Bromide SCHEMBL7047317 0.75 PPARG (0.44) GAAKDM4EMAPTTSHRALDH1A1
Bromide SCHEMBL7047729 0.72 ADORA3 (0.52) GAAKDM4EADORA3SIRT3MAPT
SCHEMBL26880568 0.71 KDM4E (1.00) GAAKDM4EADORA3SIRT3MAPT
SCHEMBL11451540 0.70 KDM4E (0.67) GAAKDM4EADORA3SIRT3MAPT
SCHEMBL11818299 0.70 KDM4E (0.76) GAAKDM4EADORA3SIRT3MAPT
SCHEMBL3027412 0.69 ADORA3 (0.89) GAAKDM4EADORA3MAPTHPGD
SCHEMBL8024613 0.69 ALDH1A1 (0.67) GAAKDM4EADORA3SIRT3MAPT
Bromide SCHEMBL7044932 0.68 PPARG (0.46) KDM4EADORA3TSHRALDH1A1POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030064954-A1 Cationic amphiphilic 1,4-dihydropyridine derivatives useful for delivery of nucleotide containing compounds SPONDULI SERVICES, LTD. (AU) 2003-04-03 US 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-20030064954-A1 Cationic amphiphilic 1,4-dihydropyridine derivatives useful for delivery of nucleotide containing compounds ACIN1, DNA2, KPNA1 GAA 1302/4885KDM4E 2990/4885ADORA3 278/4885

“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.