Bromide

Bromide

SCHEMBL2353262

Br.CN(C)c1ccc(N)cc1

nearest known ligand 0.94

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 2/20 0.44
ADRA2B known ✓ P18089 2/20 0.44
ADRA2C known ✓ P18825 2/20 0.44
ACHE known ✓ P22303 1/20 0.43
ALDH1A1 P00352 8/20 0.94
CYP3A4 P08684 5/20 0.94
MAPK1 P28482 5/20 0.94
TDP1 Q9NUW8 4/20 0.94
ALOX15 P16050 3/20 0.94
TP53 P04637 2/20 0.94
TSHR P16473 6/20 0.65
HSD17B10 Q99714 2/20 0.65
L3MBTL1 Q9Y468 2/20 0.50
PSMD14 O00487 1/20 0.50
RECQL P46063 1/20 0.50
GFER P55789 1/20 0.50
NOS1 P29475 1/20 0.48
MAPT P10636 3/20 0.47
MEN1 O00255 2/20 0.47
KMT2A Q03164 2/20 0.47

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 SCHEMBL20661275 0.97 ALDH1A1 (0.89) ALDH1A1CYP3A4MAPK1TDP1ALOX15
SCHEMBL15246 0.97 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPK1TDP1ALOX15
SCHEMBL8468934 0.97 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPK1TDP1ALOX15
Hydrochloric Acid SCHEMBL309541 0.94 ALDH1A1 (0.94) ALDH1A1CYP3A4MAPK1TDP1ALOX15
Hydrochloric Acid SCHEMBL971113 0.94 ALDH1A1 (0.94) ALDH1A1CYP3A4MAPK1TDP1ALOX15
Water SCHEMBL6142579 0.94 ALDH1A1 (0.94) ALDH1A1CYP3A4MAPK1TDP1ALOX15
Ammonia Solution, Strong SCHEMBL28575167 0.94 ALDH1A1 (0.94) ALDH1A1CYP3A4MAPK1TDP1ALOX15
SCHEMBL4356329 0.94 ALDH1A1 (0.94) ALDH1A1CYP3A4MAPK1TDP1ALOX15
Hydrochloric Acid SCHEMBL9805647 0.92 ALDH1A1 (0.89) ALDH1A1CYP3A4MAPK1TDP1ALOX15
Benzene SCHEMBL28123318 0.92 ALDH1A1 (0.89) ALDH1A1CYP3A4MAPK1TDP1ALOX15

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-8680113-B2 BMI-1 protein expression modulators PTC THERAPEUTICS, INC. (US) 2014-03-25 US disclosed
US-20110190239-A1 BMI-1 PROTEIN EXPRESSION MODULATORS PTC THERAPEUTICS, INC. (US) 2011-08-04 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-20110190239-A1 BMI-1 PROTEIN EXPRESSION MODULATORS BMI1, CREBBP, BAZ2A ADRA2A 4808/4885ADRA2B 4630/4885ADRA2C 4782/4885

“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.