Bromide

Bromide

SCHEMBL583319

Br.CC1CN(C(=O)OC(C)(C)C)CCN(C(=O)OC(C)(C)C)CCNCCN1CC(=O)OC(C)(C)C

nearest known ligand 0.43

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 13)

geneUniProtsupporting neighboursconfidence
NR1H2 P55055 1/20 0.39
SETD7 Q8WTS6 1/20 0.37
GPR119 Q8TDV5 6/20 0.37
USP2 O75604 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.37
DDB1 Q16531 1/20 0.36
CRBN Q96SW2 1/20 0.36
MEN1 O00255 2/20 0.36
KMT2A Q03164 2/20 0.36
ALDH1A1 P00352 1/20 0.36
MAPT P10636 1/20 0.36
HPGD P15428 1/20 0.35
EPHX2 P34913 1/20 0.35

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
SCHEMBL18986043 0.96 NR1H2 (0.39) NR1H2SETD7GPR119USP2SMN1; SMN2
SCHEMBL3783647 0.89 NR1H2 (0.39) NR1H2SETD7GPR119USP2SMN1; SMN2
Bromide SCHEMBL6428393 0.81 SETD7 (0.43) NR1H2SETD7GPR119USP2SMN1; SMN2
SCHEMBL3315088 0.80 NR1H2 (0.40) NR1H2SETD7GPR119USP2SMN1; SMN2
SCHEMBL3319602 0.80 NR1H2 (0.40) NR1H2SETD7GPR119USP2SMN1; SMN2
SCHEMBL9282186 0.80 SETD7 (0.43) NR1H2SETD7GPR119USP2SMN1; SMN2
SCHEMBL15347416 0.78 SLC6A9 (0.43) NR1H2SETD7GPR119USP2SMN1; SMN2
SCHEMBL1673065 0.78 SLC6A9 (0.43) NR1H2SETD7GPR119USP2SMN1; SMN2
SCHEMBL17152994 0.78 PLA2G10 (0.35)
SCHEMBL13567937 0.78 GPR119 (0.39) NR1H2SETD7GPR119USP2SMN1; SMN2

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-8138332-B2 Synthesis of cyclen derivatives GE HEALTHCARE AS (NO) 2012-03-20 US disclosed
EP-1877389-B1 SYNTHESIS OF CYCLEN DERIVATIVES GE HEALTHCARE AS (NO) 2012-02-15 EP disclosed
US-20090216011-A1 Synthesis of cyclen derivatives AXELSSON OSKAR 2009-08-27 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-20090216011-A1 Synthesis of cyclen derivatives DCTN3, TET3, CCDC47 NR1H2 4334/4885SETD7 1125/4885GPR119 4683/4885

“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.