Bromide

Bromide

SCHEMBL962121

Br.C=CCSC(N)=Nc1cc(OC)c(-n2cnc(C)n2)cc1F

nearest known ligand 0.33

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
PSEN1 known ✓ P49768 10/20 0.33
PSEN2 known ✓ P49810 10/20 0.33
APH1B known ✓ Q8WW43 10/20 0.33
NCSTN known ✓ Q92542 10/20 0.33
APH1A known ✓ Q96BI3 10/20 0.33
PSENEN known ✓ Q9NZ42 10/20 0.33
NOS3 P29474 2/20 0.31
NOS1 P29475 2/20 0.31
NOS2 P35228 2/20 0.31
ALDH1A1 P00352 1/20 0.31
MAPT P10636 1/20 0.31
HTT P42858 1/20 0.31
CYP3A4 P08684 2/20 0.30
CYP2C8 P10632 1/20 0.30
CYP2D6 P10635 1/20 0.30
CYP2C9 P11712 1/20 0.30
UGT1A1 P22309 1/20 0.30
CYP2C19 P33261 1/20 0.30
KCNH2 Q12809 1/20 0.30
SLCO1B1 Q9Y6L6 1/20 0.30

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
SCHEMBL12918206 0.99 PSEN1 (0.34) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL12918124 0.84 PSEN1 (0.33) PSEN1PSEN2APH1BNCSTNAPH1A
Iodide SCHEMBL965215 0.83 PSEN1 (0.33) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL962357 0.76 PSEN1 (0.35) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL964617 0.71 PSEN1 (0.34) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL513196 0.70 PSEN1 (0.37) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL961727 0.67 PSEN1 (0.37) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL12918137 0.65 HTR3E (0.40) PSEN1PSEN2APH1BNCSTNAPH1A
Iodide SCHEMBL965905 0.64 HTR3E (0.39) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL12918204 0.64 HTR3E (0.33) NOS3NOS1NOS2

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
EP-2379553-B1 BICYCLIC COMPOUNDS FOR THE REDUCTION OF BETA-AMYLOID PRODUCTION BRISTOL MYERS SQUIBB CO (US) 2013-06-26 EP disclosed
US-8349880-B2 Bicyclic compounds for the reduction of beta-amyloid production BRISTOL-MYERS SQUIBB COMPANY (US) 2013-01-08 US disclosed
US-20110015175-A1 Bicyclic Compounds for the Reduction of Beta-Amyloid Production BRISTOL-MYERS SQUIBB COMPANY 2011-01-20 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 (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-20110015175-A1 Bicyclic Compounds for the Reduction of Beta-Amyloid Production APP, BACE1, APBA1 PSEN1 6/4885PSEN2 7/4885APH1B 13/4885

“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.