Bromide

Bromide

SCHEMBL3324489

Clc1cc[n+](Cc2ccccc2)c2ccccc12.[Br-]

nearest known ligand 0.56

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 11)

geneUniProtsupporting neighboursconfidence
CHKA known ✓ P35790 9/20 0.54
KDM4E B2RXH2 1/20 0.51
NPC1 O15118 1/20 0.51
MITF O75030 1/20 0.51
ALDH1A1 P00352 1/20 0.51
GLA P06280 1/20 0.51
GAA P10253 1/20 0.51
HPGD P15428 1/20 0.51
HTT P42858 1/20 0.51
RAB9A P51151 1/20 0.51
SMN1; SMN2 Q16637 1/20 0.51

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 SCHEMBL1461850 0.79 KDM4E (0.68) CHKAKDM4ENPC1RAB9A
SCHEMBL1363019 0.77 KDM4E (0.69) CHKAKDM4ENPC1MITFALDH1A1
SCHEMBL4625936 0.77 KDM4E (0.44) CHKAKDM4ENPC1ALDH1A1HTT
SCHEMBL10136900 0.76 KDM4E (0.80) CHKAKDM4ENPC1MITFALDH1A1
Bromide SCHEMBL21436708 0.76 CHKA (0.50) CHKAKDM4ENPC1MITFALDH1A1
Water SCHEMBL14740255 0.72 CHKA (0.88) CHKA
Hydrochloric Acid SCHEMBL17845876 0.72 KDM4E (0.51) CHKAKDM4ENPC1MITFALDH1A1
Hydrochloric Acid SCHEMBL10548962 0.72 KDM4E (0.51) CHKAKDM4ENPC1MITFALDH1A1
Bromide SCHEMBL17075096 0.72 CHKA (0.47) CHKAKDM4ENPC1MITFALDH1A1
Bromide SCHEMBL18334837 0.72 CHKA (0.58) CHKA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2607431-B1 Cyanine dye compounds LIFE TECHNOLOGIES CORP (US) 2016-08-24 EP disclosed
EP-1720944-B1 CYANINE DYE COMPOUNDS LIFE TECHNOLOGIES CORP (US) 2013-07-17 EP disclosed
EP-2607431-A1 Cyanine dye compounds Life Technologies Corporation (US) 2013-06-26 EP disclosed
US-7842811-B2 Cyanine dye compounds Life Technologies Corporation (US) 2010-11-30 US disclosed
US-20100120051-A1 CYANINE DYE COMPOUNDS Life Technologies Corporation (US) 2010-05-13 US disclosed
US-7655409-B2 Have negatively charged substituent for fluorescent staining of DNA; used to distinguish DNA present in a sample from RNA Life Technologies Corporation (US) 2010-02-02 US disclosed
US-20090047683-A1 CYANINE DYE COMPOUNDS INVITROGEN CORPORATION (US) 2009-02-19 US disclosed
US-7446202-B2 Cyanine dye compounds MOLECULAR PROBES, INC. (US) 2008-11-04 US disclosed
EP-1720944-A2 CYANINE DYE COMPOUNDS Molecular Probes Inc. (US) 2006-11-15 EP disclosed
US-20050214810-A1 Cyanine dye compounds MOLECULAR PROBES, INC. 2005-09-29 US disclosed
WO-2005056689-A2 CYANINE DYE COMPOUNDS MOLECULAR PROBES, INC. (US) 2005-06-23 WO 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-20050214810-A1 Cyanine dye compounds POLL, XPA, DUT CHKA 803/4885KDM4E 801/4885NPC1 2613/4885

“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.