Bromide

Bromide

SCHEMBL7045709

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

nearest known ligand 0.43

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 11)

geneUniProtsupporting neighboursconfidence
CACNA1B Q00975 10/20 0.43
ADORA3 P0DMS8 1/20 0.38
SOAT2 O75908 1/20 0.36
SOAT1 P35610 1/20 0.36
CACNA1F O60840 1/20 0.36
CACNA1D Q01668 1/20 0.36
CACNA1S Q13698 1/20 0.36
CACNA1C Q13936 1/20 0.36
KDM4E B2RXH2 1/20 0.35
GAA P10253 1/20 0.35
PPARG P37231 2/20 0.35

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 SCHEMBL7045704 0.87 SOAT2 (0.35) CACNA1BADORA3SOAT2SOAT1CACNA1F
Bromide SCHEMBL7044582 0.86 PPARG (0.46) ADORA3CACNA1FCACNA1DCACNA1SCACNA1C
Bromide SCHEMBL7041639 0.86 PPARG (0.46) ADORA3CACNA1FCACNA1DCACNA1SCACNA1C
Bromide SCHEMBL7044895 0.86 PPARG (0.46) ADORA3CACNA1FCACNA1DCACNA1SCACNA1C
Bromide SCHEMBL7047729 0.73 ADORA3 (0.52) ADORA3CACNA1DKDM4EGAA
SCHEMBL7044561 0.71 ALDH1A1 (0.51) ADORA3CACNA1FCACNA1DCACNA1SCACNA1C
SCHEMBL7048693 0.71 ALDH1A1 (0.51) ADORA3CACNA1FCACNA1DCACNA1SCACNA1C
SCHEMBL15869137 0.71 LMNA (0.53) SOAT2SOAT1KDM4EPPARG
Bromide SCHEMBL7046534 0.71 KDM4E (0.46) CACNA1FCACNA1DCACNA1SCACNA1CKDM4E
SCHEMBL30211175 0.70 LMNA (0.54) SOAT2SOAT1KDM4EPPARG

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 CACNA1B 1089/4885ADORA3 278/4885SOAT2 1325/4885

“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.