Bromide

Bromide

SCHEMBL2196188

COc1ccc(Cn2cc[n+](C)c2)cc1.[Br-]

nearest known ligand 0.45

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 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.45
KDM4E B2RXH2 1/20 0.45
ALDH1A1 P00352 1/20 0.45
ALOX15 P16050 1/20 0.45
CMA1 P23946 1/20 0.45
HSP90AA1 P07900 2/20 0.43
GSK3A P49840 1/20 0.42
GSK3B P49841 1/20 0.42
CYP19A1 P11511 2/20 0.42
SIGMAR1 Q99720 1/20 0.41
SMN1; SMN2 Q16637 3/20 0.41
MEN1 O00255 1/20 0.39
APAF1 O14727 1/20 0.39
NPC1 O15118 1/20 0.39
PLA2G1B P04054 1/20 0.39
MAPK1 P28482 1/20 0.39
HTT P42858 1/20 0.39
RAB9A P51151 1/20 0.39
KMT2A Q03164 1/20 0.39
NPSR1 Q6W5P4 1/20 0.39

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
SCHEMBL1009269 0.98 MAPT (0.46) MAPTKDM4EALDH1A1ALOX15CMA1
SCHEMBL16674128 0.86 PON1 (0.46) MAPTALDH1A1HSP90AA1CYP19A1SMN1; SMN2
Bromide SCHEMBL2194865 0.82 LPO (0.55) MAPTKDM4EALDH1A1CMA1SIGMAR1
Bromide SCHEMBL9661601 0.82 MAPT (0.49) MAPTALDH1A1ALOX15HSP90AA1GSK3A
SCHEMBL12220255 0.81 PON1 (0.43) MAPTHSP90AA1CYP19A1SMN1; SMN2MEN1
Iodide SCHEMBL11084422 0.81 MAPT (0.45) MAPTKDM4EALDH1A1ALOX15CMA1
SCHEMBL1011073 0.80 LPO (0.56) MAPTKDM4EALDH1A1CMA1SIGMAR1
Bromide SCHEMBL2194611 0.80 HSP90AA1 (0.48) KDM4EALDH1A1HSP90AA1CYP19A1SIGMAR1
SCHEMBL1046806 0.80 PON1 (0.36) MAPTHSP90AA1CYP19A1SMN1; SMN2MEN1
Bromide SCHEMBL1179197 0.80 PON1 (0.49) MAPTCMA1HSP90AA1CYP19A1SIGMAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8980875-B2 Platinum-N-heterocyclic carbene derivatives, preparation thereof and therapeutic use thereof CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2015-03-17 US disclosed
US-20130338128-A1 PLATINUM-N-HETEROCYCLIC CARBENE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2013-12-19 US disclosed
US-8481522-B2 Platinum-N-heterocyclic carbene derivatives, preparation thereof and therapeutic use thereof SANOFI (FR) 2013-07-09 US disclosed
US-20110172199-A1 PLATINUM-N-HETEROCYCLIC CARBENE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF SANOFI-AVENTIS (FR) 2011-07-14 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 (2 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-20130338128-A1 PLATINUM-N-HETEROCYCLIC CARBENE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF SCO2, C3AR1, IDH1 MAPT 4712/4885KDM4E 4803/4885ALDH1A1 1989/4885
US-20110172199-A1 PLATINUM-N-HETEROCYCLIC CARBENE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF SCO2, C3AR1, IDH1 MAPT 4712/4885KDM4E 4803/4885ALDH1A1 1989/4885

“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.