Bromide

Bromide

SCHEMBL18154059

CCC[n+]1cccc2ccccc21.[Br-]

nearest known ligand 0.71

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 18)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 16/20 0.71
BCHE P06276 16/20 0.71
KDM4E B2RXH2 1/20 0.69
MEN1 O00255 1/20 0.69
RGS12 O14924 1/20 0.69
NPC1 O15118 1/20 0.69
USP2 O75604 1/20 0.69
LMNA P02545 1/20 0.69
HSP90AA1 P07900 1/20 0.69
THRB P10828 1/20 0.69
MAPK1 P28482 1/20 0.69
HTT P42858 1/20 0.69
RAD52 P43351 1/20 0.69
RAB9A P51151 1/20 0.69
KMT2A Q03164 1/20 0.69
MCL1 Q07820 1/20 0.69
SMN1; SMN2 Q16637 1/20 0.69
NPSR1 Q6W5P4 1/20 0.69

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
SCHEMBL1128342 0.98 KDM4E (0.71) BCHEACHEKDM4EMEN1RGS12
Hydrochloric Acid SCHEMBL5144187 0.96 KDM4E (0.69) BCHEACHEKDM4EMEN1RGS12
Iodide SCHEMBL29889034 0.96 KDM4E (0.74) BCHEACHEKDM4EMEN1RGS12
Iodide SCHEMBL4618173 0.96 KDM4E (0.74) BCHEACHEKDM4EMEN1RGS12
Bromide SCHEMBL28780721 0.89 KDM4E (0.81) BCHEACHEKDM4EMEN1RGS12
SCHEMBL1017312 0.86 KDM4E (0.83) BCHEACHEKDM4EMEN1RGS12
SCHEMBL29560554 0.86 KDM4E (0.83) BCHEACHEKDM4EMEN1RGS12
Bromide SCHEMBL3360044 0.85 KDM4E (0.93) BCHEACHEKDM4EMEN1RGS12
Bromide SCHEMBL3359102 0.85 KDM4E (0.93) BCHEACHEKDM4EMEN1RGS12
Bromide SCHEMBL3359702 0.85 KDM4E (0.93) BCHEACHEKDM4EMEN1RGS12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10787745-B2 Corrosion inhibition SCHLUMBERGER TECHNOLOGY CORPORATION (US) 2020-09-29 US disclosed
US-20180135187-A1 Corrosion Inhibition SCHLUMBERGER TECHNOLOGY CORPORATION 2018-05-17 US disclosed
US-20170335467-A1 CORROSION INHIBITION SCHLUMBERGER TECHNOLOGY CORPORATION (US) 2017-11-23 US disclosed
EP-3227470-A1 CORROSION INHIBITION Services Pétroliers Schlumberger (FR) 2017-10-11 EP disclosed
WO-2016167837-A1 CORROSION INHIBITION SCHLUMBERGER CANADA LIMITED (CA) 2016-10-20 WO disclosed
US-20150322070-A1 PIPERIDINE INHIBITORS OF JANUS KINASE 3 AUSPEX PHARMACEUTICALS, INC. 2015-11-12 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-20150322070-A1 PIPERIDINE INHIBITORS OF JANUS KINASE 3 JAK2, JAK3, PAK3 ACHE 3892/4885BCHE 3748/4885KDM4E 568/4885
US-20180135187-A1 Corrosion Inhibition SOD1, AOC1, NOX1 ACHE 837/4885BCHE 3671/4885KDM4E 1455/4885

“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.