Bromide

Bromide

SCHEMBL142841

Br.NCCc1ccc(O)c(S(N)(=O)=O)c1

nearest known ligand 0.58

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
ADRA2A known ✓ P08913 3/20 0.58
SLC6A2 known ✓ P23975 3/20 0.58
SLC6A3 known ✓ Q01959 2/20 0.58
HTR1A known ✓ P08908 2/20 0.58
ADRB2 known ✓ P07550 1/20 0.58
ADRA1D known ✓ P25100 1/20 0.58
ADRA1A known ✓ P35348 1/20 0.58
ADRA1B known ✓ P35368 1/20 0.58
HTR3A known ✓ P46098 1/20 0.44
TAAR1 Q96RJ0 5/20 0.58
MAPK1 P28482 3/20 0.58
KDM4E B2RXH2 3/20 0.58
DRD2 P14416 3/20 0.58
DRD1 P21728 3/20 0.58
TDP1 Q9NUW8 3/20 0.58
MAPT P10636 2/20 0.58
DRD4 P21917 2/20 0.58
DRD5 P21918 2/20 0.58
DRD3 P35462 2/20 0.58
RECQL P46063 2/20 0.58

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
SCHEMBL113163 0.98 TAAR1 (0.60) TAAR1MAPK1KDM4EADRA2ASLC6A2
SCHEMBL11669534 0.84 BACE1 (0.57) TAAR1MAPK1KDM4EADRA2ASLC6A2
SCHEMBL8173017 0.82 KDM4E (0.40) TAAR1MAPK1KDM4EADRA2ASLC6A2
SCHEMBL28873594 0.79 CA2 (0.53) CA12CA1CA2CA4CA6
SCHEMBL111618 0.79 CA12 (0.52) TAAR1MAPK1KDM4EADRA2ASLC6A2
SCHEMBL3769908 0.79 CA12 (0.52) TAAR1MAPK1KDM4EADRA2ASLC6A2
Dopamine SCHEMBL3114891 0.78 KDM4E (0.81) TAAR1MAPK1KDM4EADRA2ASLC6A2
Dopamine SCHEMBL9241925 0.78 KDM4E (0.81) TAAR1MAPK1KDM4EADRA2ASLC6A2
Dopamine SCHEMBL30960386 0.77 KDM4E (0.95) TAAR1MAPK1KDM4EADRA2ASLC6A2
Dopamine SCHEMBL3769932 0.77 KDM4E (0.95) TAAR1MAPK1KDM4EADRA2ASLC6A2

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-20120058984-A1 PYRIMIDINE DERIVATIVES USED AS ITK INHIBITORS GLAXO GROUP LIMITED (GB) 2012-03-08 US disclosed
EP-2408769-A1 PYRIMIDINE DERIVATIVES USED AS ITK INHIBITORS Glaxo Group Limited (GB) 2012-01-25 EP disclosed
WO-2010106016-A1 PYRIMIDINE DERIVATIVES USED AS ITK INHIBITORS GLAXO GROUP LIMITED (GB) 2010-09-23 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-20120058984-A1 PYRIMIDINE DERIVATIVES USED AS ITK INHIBITORS DTYMK, ITK, DCK ADRA2A 4644/4885SLC6A2 3554/4885SLC6A3 3822/4885

“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.