Bromide

Bromide

SCHEMBL15201212

Br.Oc1ccc(N2CCN3c4ccccc4-c4ccccc4C23)cc1

nearest known ligand 0.37

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
▸ MAPT P10636 6/20 0.36
▸ MAPK1 P28482 2/20 0.36
▸ GPR3 P46089 1/20 0.35
▸ ALDH1A1 P00352 4/20 0.35
▸ CYP1A2 P05177 1/20 0.35
▸ CYP3A4 P08684 1/20 0.35
▸ ALOX15 P16050 1/20 0.35
▸ HIF1A Q16665 1/20 0.35
▸ GAA P10253 4/20 0.33
▸ MEN1 O00255 3/20 0.33
▸ KMT2A Q03164 3/20 0.33
▸ KDM4E B2RXH2 2/20 0.33
▸ NPSR1 Q6W5P4 1/20 0.33
▸ POLB P06746 1/20 0.33
▸ L3MBTL1 Q9Y468 2/20 0.33
▸ ESR1 P03372 1/20 0.33
▸ ESR2 Q92731 1/20 0.33
▸ SMN1; SMN2 Q16637 1/20 0.33
▸ LMNA P02545 1/20 0.32
▸ ATM Q13315 1/20 0.32

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 SCHEMBL1863432 0.88 MAPT (0.44) MAPTMAPK1GPR3ALDH1A1CYP1A2
SCHEMBL5260413 0.86 MAPT (0.45) MAPTMAPK1GPR3ALDH1A1CYP1A2
Bromide SCHEMBL1867530 0.82 RAB9A (0.42) MAPTALDH1A1GAAMEN1KMT2A
Bromide SCHEMBL1868452 0.82 KDM4E (0.38) MAPTGPR3ALDH1A1CYP1A2CYP3A4
SCHEMBL5260851 0.80 RAB9A (0.43) MAPTALDH1A1GAAMEN1KMT2A
SCHEMBL5258131 0.80 KDM4E (0.39) MAPTGPR3ALDH1A1CYP1A2CYP3A4
Bromide SCHEMBL1862498 0.73 GPR3 (0.37) GPR3ALDH1A1CYP1A2CYP3A4ALOX15
Bromide SCHEMBL1861609 0.72 GPR3 (0.37) MAPTMAPK1GPR3ALDH1A1CYP1A2
Bromide SCHEMBL1862922 0.72 GPR3 (0.39) GPR3ALDH1A1CYP1A2CYP3A4ALOX15
SCHEMBL5259651 0.71 GPR3 (0.38) GPR3ALDH1A1CYP1A2CYP3A4ALOX15

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-2814611-B1 APPARATUS AND METHODS FOR THE PREPARATION OF REACTION VESSELS WITH A 3D-PRINTER UNIV GLASGOW COURT (GB) 2020-06-17 — — EP disclosed
US-9643152-B2 Methods for the preparation of reaction vessels THE UNIVERSITY COURT OF THE UNIVERSITY OF GLASGOW (GB) 2017-05-09 — — US disclosed
US-20150010461-A1 APPARATUS AND METHODS FOR THE PREPARATION OF REACTION VESSELS Deepmatter Ltd. (GB) 2015-01-08 — — US disclosed
EP-2814611-A1 APPARATUS AND METHODS FOR THE PREPARATION OF REACTION VESSELS WITH A 3D -PRINTER THE UNIVERSITY COURT OF THE UNIVERSITY OF GLASGOW (GB) 2014-12-24 — — EP disclosed
WO-2013121230-A1 APPARATUS AND METHODS FOR THE PREPARATION OF REACTION VESSELS WITH A 3D -PRINTER THE UNIVERSITY COURT OF THE UNIVERSITY OF GLASGOW (GB) 2013-08-22 — — WO 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-20150010461-A1 APPARATUS AND METHODS FOR THE PREPARATION OF REACTION VESSELS FLT4, HTR3D, PTGIS MAPT 3166/4885MAPK1 2942/4885GPR3 887/4885

“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.

Send feedback