Bromide

Bromide

SCHEMBL4364815

Br.C=CCN1C=CN(CCCCC)C1

nearest known ligand 0.33

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4

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 8)

geneUniProtsupporting neighboursconfidence
SIGMAR1 known ✓ Q99720 1/20 0.30
TSHR P16473 2/20 0.33
ALDH1A1 P00352 2/20 0.32
CYP1A2 P05177 1/20 0.32
CYP2D6 P10635 1/20 0.32
CYP2C19 P33261 1/20 0.32
GUSB P08236 2/20 0.30
EBP Q15125 1/20 0.30

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 SCHEMBL4362539 0.98 TSHR (0.36) TSHRALDH1A1CYP1A2CYP2D6CYP2C19
Bromide SCHEMBL29249978 0.98 TSHR (0.36) TSHRALDH1A1CYP1A2CYP2D6CYP2C19
SCHEMBL1680335 0.98 TSHR (0.34) TSHRALDH1A1GUSBEBPSIGMAR1
Hydrochloric Acid SCHEMBL28958784 0.96 TSHR (0.33) TSHRALDH1A1GUSBEBPSIGMAR1
SCHEMBL15901603 0.96 TSHR (0.38) TSHRALDH1A1CYP1A2CYP2D6CYP2C19
SCHEMBL2693560 0.96 TSHR (0.38) TSHRALDH1A1CYP1A2CYP2D6CYP2C19
SCHEMBL3398654 0.96 TSHR (0.38) TSHRALDH1A1CYP1A2CYP2D6CYP2C19
SCHEMBL4358564 0.96 TSHR (0.38) TSHRALDH1A1CYP1A2CYP2D6CYP2C19
Hydrochloric Acid SCHEMBL28380752 0.95 TSHR (0.36) TSHRALDH1A1CYP1A2CYP2D6CYP2C19
Iodide SCHEMBL2894608 0.95 TSHR (0.36) TSHRALDH1A1CYP1A2CYP2D6CYP2C19

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
EP-1721900-B1 NOVEL IMIDAZOLIUM COMPOUND KANTO KAGAKU (JP) 2014-06-11 EP disclosed
US-7517999-B2 needs no complicated operations for dissolution and has excellent handleability and a high ionic conductivity, electrolytes; 1-butyl-3-allylimidazolium bromide KANTO KAGAKU KABUSHIKI KAISHA (JP) 2009-04-14 US disclosed
US-20070191612-A1 Needs no complicated operations for dissolution and has excellent handleability and a high ionic conductivity, electrolytes; 1-butyl-3-allylimidazolium bromide HIROYUKI OHNO (JP) 2007-08-16 US disclosed
CN-1922152-A Novel imidazolium compound KANTO KAGAKU (JP) 2007-02-28 CN disclosed
EP-1721900-A1 NOVEL IMIDAZOLIUM COMPOUND Kanto Kagaku Kabushiki Kaisha (JP) 2006-11-15 EP 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-20070191612-A1 Needs no complicated operations for dissolution and has excellent handleability and a high ionic conductivity, electrolytes; 1-butyl-3-allylimidazolium bromide SLC26A3, KCNJ11, SLC26A4 SIGMAR1 2593/4885TSHR 1992/4885ALDH1A1 538/4885

“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.