Bromide

Bromide

SCHEMBL7046522

COC(=O)C1=C(C[n+]2ccccc2)N(C)C(C[n+]2ccccc2)=C(C(=O)OC)C1c1ccccc1OC(F)F.[Br-].[Br-]

nearest known ligand 0.55

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
NR1I2 O75469 1/20 0.55
GAA P10253 8/20 0.43
TSHR P16473 5/20 0.43
TP53 P04637 3/20 0.43
HTT P42858 2/20 0.43
ALDH1A1 P00352 7/20 0.38
KDM4E B2RXH2 5/20 0.38
GLA P06280 4/20 0.38
HPGD P15428 4/20 0.38
CASP1 P29466 4/20 0.38
CASP7 P55210 4/20 0.38
HSD17B10 Q99714 4/20 0.38
POLB P06746 3/20 0.36
SMN1; SMN2 Q16637 2/20 0.35
MAPK1 P28482 2/20 0.35
TDP1 Q9NUW8 2/20 0.35
MEN1 O00255 1/20 0.35
KMT2A Q03164 1/20 0.35
NPSR1 Q6W5P4 2/20 0.34
ALOX15 P16050 1/20 0.34

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 SCHEMBL7046108 0.84 NR1I2 (0.62) NR1I2GAATSHRTP53HTT
Bromide SCHEMBL7046521 0.82 ALDH1A1 (0.42) TSHRHTTALDH1A1KDM4EHPGD
SCHEMBL7049245 0.77 NR1I2 (0.66) NR1I2GAATSHRTP53HTT
Riodipine SCHEMBL29389667 0.72 NR1I2 (1.00) NR1I2GAATSHRTP53ALDH1A1
Riodipine SCHEMBL636400 0.72 NR1I2 (1.00) NR1I2GAATSHRTP53ALDH1A1
SCHEMBL10893108 0.70 NR1I2 (0.91) NR1I2GAATSHRTP53ALDH1A1
SCHEMBL7049239 0.70 NR1I2 (0.70) NR1I2GAATSHRTP53HTT
SCHEMBL7045838 0.67 NR1I2 (0.65) NR1I2GAATSHRTP53HTT
SCHEMBL9806914 0.64 NR1I2 (0.76) NR1I2GAATSHRTP53ALDH1A1
SCHEMBL28371678 0.63 KDM4E (0.58) GAATSHRTP53HTTALDH1A1

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 NR1I2 2809/4885GAA 1302/4885TSHR 4680/4885

“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.