Bromide

Bromide

SCHEMBL4463474

Br.Cc1noc(C)c1-c1ccc(C23C=CCN(CC2)C3)cn1

nearest known ligand 0.36

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
CYP1A2 P05177 11/20 0.36
ALDH1A1 P00352 6/20 0.36
TSHR P16473 5/20 0.36
MAPK1 P28482 2/20 0.36
CYP2C9 P11712 2/20 0.36
USP2 O75604 2/20 0.35
CLK4 Q9HAZ1 5/20 0.33
CYP3A4 P08684 5/20 0.33
CYP2C19 P33261 4/20 0.33
HSD17B10 Q99714 4/20 0.33
CYP2D6 P10635 4/20 0.33
ALOX15 P16050 4/20 0.33
MEN1 O00255 2/20 0.33
KMT2A Q03164 2/20 0.33
HSD11B1 P28845 1/20 0.33
ROCK1 Q13464 1/20 0.33
CDC42BPB Q9Y5S2 1/20 0.33
OPRM1 P35372 1/20 0.32
OPRL1 P41146 1/20 0.32
BRD4 O60885 3/20 0.31

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
SCHEMBL5220520 0.99 CYP1A2 (0.37) CYP1A2ALDH1A1TSHRMAPK1CYP2C9
Bromide SCHEMBL4464997 0.79 PTPN11 (0.31)
SCHEMBL4475112 0.78 CHRNA7 (0.37) ROCK1
Bromide SCHEMBL4467487 0.77 CYP11B1 (0.36) ALDH1A1MAPK1MEN1KMT2A
SCHEMBL5219651 0.77 PTPN11 (0.32)
SCHEMBL4461401 0.77 ALOX5AP (0.31)
SCHEMBL4473796 0.77 CYP1A2 (0.39) CYP1A2ALDH1A1TSHRMAPK1CYP2C9
Bromide SCHEMBL4466117 0.77 HSD11B1 (0.37) HSD11B1
Bromide SCHEMBL4479130 0.76 CYP11B1 (0.35) CYP1A2ALDH1A1CYP3A4CYP2C19HSD17B10
SCHEMBL5218539 0.76 CYP11B1 (0.36) ALDH1A1MAPK1HSD17B10MEN1KMT2A

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 CYP1A2 152/4885ALDH1A1 323/4885TSHR 452/4885

“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.