Bromide

Bromide

SCHEMBL3602837

Br.CCOC(=O)c1ccccc1N1CC2CNCCN2C1=O

nearest known ligand 0.42

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
ADRA1D known ✓ P25100 1/20 0.39
ADRA1A known ✓ P35348 1/20 0.39
ADRA1B known ✓ P35368 1/20 0.39
HTR1A known ✓ P08908 1/20 0.38
HSD17B10 Q99714 4/20 0.42
MAPT P10636 3/20 0.42
GAA P10253 2/20 0.42
SMN1; SMN2 Q16637 2/20 0.42
MAPK1 P28482 1/20 0.42
OPRM1 P35372 1/20 0.42
TSHR P16473 2/20 0.41
KMT2A Q03164 3/20 0.40
ALDH1A1 P00352 5/20 0.40
HTR2C P28335 4/20 0.39
HTR2A P28223 3/20 0.39
HTR2B P41595 3/20 0.39
HPGD P15428 3/20 0.38
KDM4E B2RXH2 2/20 0.38
L3MBTL1 Q9Y468 2/20 0.38
GLA P06280 1/20 0.38

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
SCHEMBL17062423 0.82 HTR2C (0.43) GAAHTR2CHTR2AHTR2BL3MBTL1
SCHEMBL4264273 0.80 ALDH1A1 (0.44) HSD17B10MAPTGAASMN1; SMN2MAPK1
Hydrochloric Acid SCHEMBL3607612 0.79 ALDH1A1 (0.43) HSD17B10MAPTGAASMN1; SMN2MAPK1
Hydrochloric Acid SCHEMBL3608533 0.79 HTR2C (0.50) HTR2CHTR2AHTR2BCASP1CASP7
SCHEMBL4266773 0.78 ALOX5 (0.49) SMN1; SMN2ALDH1A1HTR2CHTR2AHTR2B
Hydrochloric Acid SCHEMBL3593426 0.78 ALOX5 (0.48) SMN1; SMN2ALDH1A1HTR2CHTR2AHTR2B
Bromide SCHEMBL3602839 0.77 MAPT (0.42) HSD17B10MAPTGAASMN1; SMN2MAPK1
SCHEMBL3606991 0.76 SCN9A (0.49) HSD17B10MAPTGAASMN1; SMN2MAPK1
Bromide SCHEMBL3596621 0.74 HTR2C (0.46) HTR2CHTR2AHTR2B
Bromide SCHEMBL3614413 0.73 HTR2C (0.41) OPRM1HTR2CHTR2AHTR2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100004249-A1 Bicyclic heterocyclic compound and use thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2010-01-07 US disclosed
EP-2039695-A1 BICYCLIC HETEROCYCLIC COMPOUND AND USE THEREOF Takeda Pharmaceutical Company Limited (JP) 2009-03-25 EP 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-20100004249-A1 Bicyclic heterocyclic compound and use thereof HTR2C, HTR5A, HTR2A ADRA1D 417/4885ADRA1A 384/4885ADRA1B 277/4885

“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.