Bromide

Bromide

SCHEMBL2073135

C[N+](C)(C)CCCOc1ccccc1N.[Br-]

nearest known ligand 0.62

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
CHRM2 known ✓ P08172 1/20 0.35
CHRM1 known ✓ P11229 1/20 0.35
ACHE known ✓ P22303 1/20 0.35
CYP1A2 P05177 1/20 0.62
CYP2C9 P11712 1/20 0.62
CYP2C19 P33261 1/20 0.62
ALDH1A1 P00352 4/20 0.53
TDP1 Q9NUW8 2/20 0.44
ADRA2B P18089 1/20 0.44
PTGS1 P23219 1/20 0.44
APP P05067 1/20 0.41
LMNA P02545 2/20 0.40
RECQL P46063 1/20 0.40
KDM4E B2RXH2 3/20 0.38
SCN1A P35498 2/20 0.36
SCN2A Q99250 2/20 0.36
SCN3A Q9NY46 2/20 0.36
CHRNB4 P30926 1/20 0.36
CHRNA3 P32297 1/20 0.36
CHRNA7 P36544 1/20 0.36

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
SCHEMBL12844852 0.89 CYP1A2 (0.61) CYP1A2CYP2C9CYP2C19ALDH1A1TDP1
SCHEMBL10386552 0.80 CYP1A2 (0.76) CYP1A2CYP2C9CYP2C19ALDH1A1TDP1
SCHEMBL10387995 0.80 CYP1A2 (0.76) CYP1A2CYP2C9CYP2C19ALDH1A1TDP1
SCHEMBL10804708 0.78 CYP1A2 (0.73) CYP1A2CYP2C9CYP2C19ALDH1A1TDP1
SCHEMBL865680 0.78 CYP1A2 (0.73) CYP1A2CYP2C9CYP2C19ALDH1A1TDP1
SCHEMBL23493022 0.78 CYP1A2 (0.73) CYP1A2CYP2C9CYP2C19ALDH1A1TDP1
SCHEMBL29502067 0.78 CYP1A2 (0.73) CYP1A2CYP2C9CYP2C19ALDH1A1TDP1
SCHEMBL23493019 0.78 CYP1A2 (0.73) CYP1A2CYP2C9CYP2C19ALDH1A1TDP1
SCHEMBL23493031 0.78 CYP1A2 (0.73) CYP1A2CYP2C9CYP2C19ALDH1A1TDP1
SCHEMBL3358175 0.78 CYP1A2 (0.73) CYP1A2CYP2C9CYP2C19ALDH1A1TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1851215-B1 WATER-SOLUBLE TETRAZOLIUM SALTS BAYER HEALTHCARE LLC (US) 2013-12-18 EP disclosed
US-7897331-B2 Process of using a tetrazolium salt BAYER HEALTHCARE LLC (US) 2011-03-01 US disclosed
US-20100255506-A1 PROCESS OF USING A TETRAZOLIUM SALT BAYER HEALTHCARE LLC (US) 2010-10-07 US disclosed
US-7767822-B2 Water-soluble tetrazolium salts BAYER HEALTHCARE LLC (US) 2010-08-03 US disclosed
US-20080125471-A1 Water-Soluble Tetrazolium Salts ASCENSIA DIABETES CARE HOLDINGS AG (CH) 2008-05-29 US disclosed
EP-1851215-A1 WATER-SOLUBLE TETRAZOLIUM SALTS Bayer Healthcare, LLC (US) 2007-11-07 EP disclosed
WO-2006076619-A1 WATER-SOLUBLE TETRAZOLIUM SALTS BAYER HEALTHCARE LLC (US) 2006-07-20 WO 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-20080125471-A1 Water-Soluble Tetrazolium Salts TST, AASDHPPT, APRT CHRM2 4713/4885CHRM1 4376/4885ACHE 2850/4885

“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.