Bromide

Bromide

SCHEMBL20185959

Br.Br.CCCCCCCC/C=C\CCCCCCCC(=O)OCCNCCNCCOC(=O)CCCCCCC/C=C\CCCCCCCC

nearest known ligand 0.58

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 20)

geneUniProtsupporting neighboursconfidence
EPHX2 P34913 4/20 0.58
DGKA P23743 2/20 0.57
MGLL Q99685 1/20 0.57
MAPT P10636 2/20 0.56
ALDH1A1 P00352 1/20 0.56
THRB P10828 1/20 0.56
CNR1 P21554 1/20 0.56
CNR2 P34972 1/20 0.56
FAAH O00519 2/20 0.52
PRKCE Q02156 1/20 0.52
PRKCQ Q04759 1/20 0.52
PRKCD Q05655 1/20 0.52
PRKCA P17252 1/20 0.52
GMNN O75496 1/20 0.50
USP2 O75604 1/20 0.50
LMNA P02545 1/20 0.50
CYP1A2 P05177 1/20 0.50
POLB P06746 1/20 0.50
CYP2C9 P11712 1/20 0.50
ALOX15 P16050 1/20 0.50

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
SCHEMBL12232837 0.98 EPHX2 (0.60) EPHX2DGKAMGLLMAPTALDH1A1
SCHEMBL18209370 0.98 EPHX2 (0.60) EPHX2DGKAMGLLMAPTALDH1A1
Hydrochloric Acid SCHEMBL20185950 0.97 EPHX2 (0.58) EPHX2DGKAMGLLMAPTALDH1A1
SCHEMBL12179613 0.97 EPHX2 (0.61) EPHX2DGKAMGLLMAPTALDH1A1
SCHEMBL14760438 0.97 EPHX2 (0.61) EPHX2DGKAMGLLMAPTALDH1A1
Hydrochloric Acid SCHEMBL20185982 0.94 MGLL (0.61) EPHX2DGKAMGLLMAPTALDH1A1
SCHEMBL17586415 0.94 EPHX2 (0.57) EPHX2DGKAMGLLMAPTALDH1A1
SCHEMBL12179602 0.93 MGLL (0.68) EPHX2DGKAMGLLMAPTALDH1A1
SCHEMBL14759657 0.93 MGLL (0.68) EPHX2DGKAMGLLMAPTALDH1A1
SCHEMBL6072564 0.92 CNR2 (0.64) EPHX2DGKAMGLLMAPTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107801395-B Process for preparing amphiphilic imidazolinium compounds 拜耳动物保健有限责任公司 2022-02-22 CN disclosed
EP-3292106-B1 PROCESS FOR THE PREPARATION OF AMPHIPHILIC IMIDAZOLINIUM COMPOUNDS BAYER ANIMAL HEALTH GMBH (DE) 2021-10-27 EP disclosed
US-10479768-B2 Process for the preparation of amphiphilic imidazolinium compounds BAYER ANIMAL HEALTH GMBH (DE) 2019-11-19 US disclosed
US-20180148415-A1 IMPROVED PROCESS FOR THE PREPARATION OF AMPHIPHILIC IMIDAZOLINIUM COMPOUNDS ELANCO ANIMAL HEALTH GMBH (DE) 2018-05-31 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 (2 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-10479768-B2 Process for the preparation of amphiphilic imidazolinium compounds IPO8, IPO9, IPO7 EPHX2 1872/4885DGKA 99/4885MGLL 198/4885
US-20180148415-A1 IMPROVED PROCESS FOR THE PREPARATION OF AMPHIPHILIC IMIDAZOLINIUM COMPOUNDS IPO8, IPO9, IPO7 EPHX2 2297/4885DGKA 62/4885MGLL 142/4885

“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.