Bromide

Bromide

SCHEMBL4469358

Br.c1ccc2sc(-c3ccc(C45CCCN(CC4)C5)cn3)cc2c1

nearest known ligand 0.45

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
CHRM2 known ✓ P08172 2/20 0.36
CHRM3 known ✓ P20309 2/20 0.36
SIGMAR1 known ✓ Q99720 2/20 0.34
KDM1A O60341 1/20 0.45
CYP11B1 P15538 1/20 0.42
CYP11B2 P19099 1/20 0.42
IKBKB O14920 1/20 0.37
CHUK O15111 1/20 0.37
IKBKG Q9Y6K9 1/20 0.37
DCK P27707 1/20 0.37
CHRM4 P08173 2/20 0.36
CHRM5 P08912 2/20 0.36
CHRM1 P11229 2/20 0.36
CCNC P24863 2/20 0.36
CDK8 P49336 2/20 0.36
CYP3A4 P08684 1/20 0.36
GSK3A P49840 1/20 0.36
GSK3B P49841 1/20 0.36
PRKCQ Q04759 1/20 0.36
KCNH2 Q12809 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
SCHEMBL4473736 0.99 KDM1A (0.46) KDM1ACYP11B1CYP11B2IKBKBCHUK
SCHEMBL2678642 0.97 KDM1A (0.47) KDM1ACYP11B1CYP11B2IKBKBCHUK
SCHEMBL2677931 0.94 KDM1A (0.49) KDM1ACYP11B1CYP11B2IKBKBCHUK
Bromide SCHEMBL4474311 0.80 KDM1A (0.43) KDM1ACYP11B1CYP11B2IKBKBCHUK
Bromide SCHEMBL4460367 0.79 PTPN11 (0.33) CHRM2CHRM4CHRM5CHRM1CHRM3
SCHEMBL4467652 0.79 KDM1A (0.43) KDM1ACYP11B1CYP11B2IKBKBCHUK
Bromide SCHEMBL4469527 0.78 KDM1A (0.40) KDM1ACYP11B1CYP11B2CCNCCDK8
Bromide SCHEMBL4460467 0.78 HPGDS (0.42) CYP11B1CYP11B2
Bromide SCHEMBL4471147 0.78 HSD11B1 (0.39)
SCHEMBL5218727 0.77 HPGDS (0.43) CYP11B1CYP11B2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7585974-B2 Derivatives of 5-(pyridin-3-yl)-1-azabicyclo[3.2.1]octane, their preparation and their therapeutic application SANOFI-AVENTIS (FR) 2009-09-08 US claimed
US-20070185137-A1 Derivatives of 5-(pyridin-3-yl)-1-azabicyclo[3.2.1]octane, their preparation and their therapeutic application SANOFI-AVENTIS (FR) 2007-08-09 US claimed
EP-1465893-B1 DERIVATIVES OF 5-(PYRIDIN-3-YL)-1-AZABICYCLO (3.2.1) OCTANE, THE PREPARATION THEREOF AND THE APPLICATION OF SAME IN THERAPEUTICS SANOFI AVENTIS (FR) 2007-02-28 EP 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-20070185137-A1 Derivatives of 5-(pyridin-3-yl)-1-azabicyclo[3.2.1]octane, their preparation and their therapeutic application PAICS, CYC1, AADAC CHRM2 93/4885CHRM3 118/4885SIGMAR1 552/4885

“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.