Bromide

Bromide

SCHEMBL4380424

Cn1cc[n+](C[n+]2ccn(C)c2)c1.[Br-].[Br-]

nearest known ligand 0.31

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

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 8)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.30
ALDH1A1 P00352 1/20 0.31
GAA P10253 1/20 0.31
BCHE P06276 1/20 0.30
MEN1 O00255 1/20 0.30
HSP90AA1 P07900 1/20 0.30
KMT2A Q03164 1/20 0.30
SMN1; SMN2 Q16637 1/20 0.30

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
SCHEMBL988006 0.97
Iodide SCHEMBL4384951 0.95 ALDH1A1 (0.31) ALDH1A1GAA
Bromide SCHEMBL21777064 0.84 ALDH1A1 (0.33) ALDH1A1GAA
Bromide SCHEMBL2214550 0.84 ALDH1A1 (0.33) ALDH1A1GAA
Bromide SCHEMBL28087169 0.82 MEN1 (0.33) MEN1HSP90AA1KMT2ASMN1; SMN2
Bromide SCHEMBL28437156 0.82 MEN1 (0.33) MEN1HSP90AA1KMT2ASMN1; SMN2
Bromide SCHEMBL193042 0.82
SCHEMBL173392 0.81
SCHEMBL6114516 0.81
Water SCHEMBL4948873 0.80 MEN1 (0.32) MEN1HSP90AA1KMT2ASMN1; 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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2035526-B1 USE IN OLEDS OF TRANSITION METAL CARBENE COMPLEXES THAT CONTAIN NO CYCLOMETALLATION VIA NON-CARBENES UDC IRELAND LTD (IE) 2021-11-17 EP disclosed
US-8940904-B2 Use of transition metal-carbene complexes which do not comprise any cyclometallation via non-carbenes in OLEDs BASF SE (DE) 2015-01-27 US disclosed
US-8247574-B2 Use of PT -and PD-BIS- and tetra-carbon complexes with bridged carbon ligands in OLEDs BASF SE (DE) 2012-08-21 US disclosed
US-20090326237-A1 USE OF PT-AND PD-BIS-AND TETRA-CARBON COMPLEXES WITH BRIDGED CARBON LIGANDS IN OLEDS BASF SE (DE) 2009-12-31 US disclosed
EP-2044169-B1 USE OF PT- AND PD-BIS- AND TETRA-CARBON COMPLEXES WITH BRIDGED CARBON LIGANDS IN OLEDS BASF SE (DE) 2009-11-25 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-20090326237-A1 USE OF PT-AND PD-BIS-AND TETRA-CARBON COMPLEXES WITH BRIDGED CARBON LIGANDS IN OLEDS PDCD1, PDCD1LG2, CD274 ACHE 3341/4885ALDH1A1 911/4885GAA 3359/4885

“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.