Bromide

Bromide

SCHEMBL4532368

Br.OCC1CN(Cc2ccccc2)CC(O)C1c1ccc(O)cc1

nearest known ligand 0.63

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 11)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.41
GBA1 P04062 8/20 0.63
FUCA1 P04066 2/20 0.52
PYGL P06737 1/20 0.45
ESR1 P03372 1/20 0.44
ESR2 Q92731 1/20 0.44
GRIN2B Q13224 2/20 0.44
RORC P51449 1/20 0.42
DRD4 P21917 1/20 0.42
BCHE P06276 1/20 0.41
BACE1 P56817 1/20 0.41

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
Bromide SCHEMBL2683848 1.00 GBA1 (0.63) GBA1FUCA1PYGLESR1ESR2
Bromide SCHEMBL1943491 1.00 GBA1 (0.63) GBA1FUCA1PYGLESR1ESR2
SCHEMBL6953561 0.99 GBA1 (0.64) GBA1FUCA1PYGLESR1ESR2
SCHEMBL5329691 0.99 GBA1 (0.64) GBA1FUCA1PYGLESR1ESR2
SCHEMBL7447584 0.88 FUCA1 (0.63) GBA1FUCA1ESR1ESR2GRIN2B
SCHEMBL6042485 0.88 FUCA1 (0.63) GBA1FUCA1ESR1ESR2GRIN2B
SCHEMBL6042482 0.88 FUCA1 (0.63) GBA1FUCA1ESR1ESR2GRIN2B
SCHEMBL6042917 0.87 GBA1 (0.63) GBA1FUCA1PYGLRORC
SCHEMBL6043347 0.85 GBA1 (0.60) GBA1FUCA1PYGLGRIN2BRORC
SCHEMBL500739 0.80 GBA1 (0.82) GBA1FUCA1PYGL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20090270380-A1 3,4,5-Substituted Piperidines as Renin Inhibitors NOVARTIS AG (CH) 2009-10-29 US disclosed
US-20060079533-A1 Methods of treating alzheimer's disease NIEMAN JAMES A 2006-04-13 US disclosed
CN-1147471-C Renin inhibitors - 2004-04-28 CN disclosed
WO-2002076440-A2 METHODS OF TREATING ALZHEIMER'S DISEASE WITH PIPERIDIN DERIVATES ELAN PHARMACEUTICALS, INC. (US) 2002-10-03 WO disclosed
CN-1349503-A renin inhibitors HOFFMANN LA ROCHE (CH) 2002-05-15 CN disclosed
EP-1175400-A1 RENIN INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2002-01-30 EP disclosed
US-6150526-A Piperidine derivative having renin inhibiting activity HOFFMANN-LA ROCHE INC. (US) 2000-11-21 US disclosed
WO-2000064873-A1 RENIN INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2000-11-02 WO disclosed
US-6051712-A PREVENTION OF HIGH BLOOD PRESSURE AND CARDIAC INSUFFICIENCY, AS WELL AS GLAUCOMA, CARDIAC INFARCT, KIDNEY INSUFFICIENCY AND RESTENOSIS HOFFMANN-LA ROCHE INC. (US) 2000-04-18 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-20090270380-A1 3,4,5-Substituted Piperidines as Renin Inhibitors REN, AGTR1, AGTR2 ACHE 833/4885GBA1 1611/4885FUCA1 2031/4885
US-20060079533-A1 Methods of treating alzheimer's disease BACE1, PSEN1, PSEN2 ACHE 7/4885GBA1 158/4885FUCA1 605/4885

“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.