Bromide

Bromide

SCHEMBL9568894

Br.CN1CCC=C(C(=O)O)C1

nearest known ligand 0.69

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 16)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 2/20 0.62
CHRM3 known ✓ P20309 2/20 0.62
BLM P54132 1/20 0.66
MCOLN3 Q8TDD5 1/20 0.66
LMNA P02545 2/20 0.62
CHRM4 P08173 2/20 0.62
CHRM5 P08912 2/20 0.62
CHRM1 P11229 2/20 0.62
THRB P10828 1/20 0.62
CHRNB2 P17787 1/20 0.62
CHRNA4 P43681 1/20 0.62
PMP22 Q01453 1/20 0.54
CYP1A2 P05177 1/20 0.51
CYP2D6 P10635 1/20 0.51
NFKB1 P19838 1/20 0.51
THPO P40225 1/20 0.51

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
SCHEMBL336164 0.98 CHRM2 (0.65) BLMMCOLN3LMNACHRM2CHRM4
Hydrochloric Acid SCHEMBL11584066 0.96 CHRM2 (0.62) BLMMCOLN3LMNACHRM2CHRM4
Hydrochloric Acid SCHEMBL2197726 0.96 CHRM2 (0.62) BLMMCOLN3LMNACHRM2CHRM4
Ammonia Solution, Strong SCHEMBL30785800 0.96 CHRM2 (0.62) BLMMCOLN3LMNACHRM2CHRM4
Bromide SCHEMBL10920212 0.84 BLM (0.66) BLMMCOLN3LMNACHRM2CHRM4
SCHEMBL9568926 0.82 CHRM2 (0.65) BLMMCOLN3LMNACHRM2CHRM4
SCHEMBL5203140 0.82 CHRM2 (0.65) BLMMCOLN3LMNACHRM2CHRM4
Arecoline SCHEMBL527735 0.79 BLM (1.00) BLMMCOLN3LMNACHRM2CHRM4
Hydrochloric Acid SCHEMBL1897878 0.78 CHRM2 (0.61) BLMMCOLN3LMNACHRM2CHRM4
Arecoline SCHEMBL44065 0.77 CHRM2 (1.00) BLMMCOLN3LMNACHRM2CHRM4

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-3257848-A1 COMPOUNDS AND COMPOSITIONS FOR MODULATING EGFR ACTIVITY Novartis AG (CH) 2017-12-20 EP disclosed
EP-2773635-B1 COMPOUNDS AND COMPOSITIONS FOR MODULATING EGFR ACTIVITY NOVARTIS AG (CH) 2017-08-02 EP disclosed
US-9440957-B2 Compounds and compositions for modulating EGFR Activity NOVARTIS AG (CH) 2016-09-13 US disclosed
US-20150197505-A1 Compounds and Compositions for Modulating EGFR Activity IRM LLC, A DELAWARE LIMITED LIABILITY COMPANY (BM) 2015-07-16 US disclosed
EP-0537993-A1 Nicotinic activity of a series of arecolones and isoarecolones ELI LILLY AND COMPANY (US) 1993-04-21 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-20150197505-A1 Compounds and Compositions for Modulating EGFR Activity EGFR, ERBB2, ERBB3 CHRM2 3853/4885CHRM3 3339/4885BLM 4283/4885

“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.