Bromide

Bromide

SCHEMBL786345

CCCCOC(=O)C(OC(=O)C[n+]1ccn(C)c1)c1ccc2c(c1)OCO2.[Br-]

nearest known ligand 0.37

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 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.37
HPGD P15428 1/20 0.37
KMT2A Q03164 3/20 0.36
MEN1 O00255 2/20 0.36
KDM4E B2RXH2 1/20 0.36
MAPT P10636 1/20 0.36
RAB9A P51151 1/20 0.36
SMN1; SMN2 Q16637 1/20 0.36
USP2 O75604 1/20 0.36
ALPG P10696 1/20 0.36
TAS1R3 Q7RTX0 4/20 0.36
TAS1R1 Q7RTX1 4/20 0.36
EDNRA P25101 1/20 0.35
OGA O60502 2/20 0.35
TSHR P16473 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
SCHEMBL15896801 0.99 ALDH1A1 (0.38) ALDH1A1HPGDKMT2AMEN1KDM4E
Bromide SCHEMBL786195 0.91 KMT2A (0.40) ALDH1A1HPGDKMT2AMEN1KDM4E
SCHEMBL15896809 0.90 KMT2A (0.39) ALDH1A1HPGDKMT2AMEN1KDM4E
SCHEMBL15897079 0.88 EDNRA (0.46) KMT2AMEN1RAB9ASMN1; SMN2TAS1R3
Hydrochloric Acid SCHEMBL786185 0.87 EDNRA (0.46) KMT2AMEN1RAB9ASMN1; SMN2TAS1R3
SCHEMBL803601 0.86 ALDH1A1 (0.44) ALDH1A1HPGDKMT2AMEN1KDM4E
Bromide SCHEMBL187505 0.82 TSHR (0.36) ALDH1A1KMT2AMEN1RAB9ASMN1; SMN2
Bromide SCHEMBL186788 0.82 TSHR (0.36) ALDH1A1KMT2AMEN1RAB9ASMN1; SMN2
SCHEMBL15896807 0.81 TSHR (0.37) ALDH1A1KMT2AMEN1RAB9ASMN1; SMN2
SCHEMBL15896790 0.81 TSHR (0.37) ALDH1A1KMT2AMEN1RAB9ASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8785655-B2 Ionic liquid solvents DUBLIN CITY UNIVERSITY (IE) 2014-07-22 US claimed
US-20120071661-A1 Ionic Liquid Solvents DUBLIN CITY UNIVERSITY (IE) 2012-03-22 US claimed

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-20120071661-A1 Ionic Liquid Solvents EBP, PAICS, HACD3 ALDH1A1 834/4885HPGD 1134/4885KMT2A 3968/4885

“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.