Bromide

Bromide

SCHEMBL2675460

Fc1ccc(OCc2ccc(-c3ccc(C(F)(F)F)cc3)cc2)c(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)c1.[Br-]

nearest known ligand 0.44

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 19)

geneUniProtsupporting neighboursconfidence
PPARD Q03181 5/20 0.44
PPARG P37231 1/20 0.44
PTPN1 P18031 6/20 0.43
PTPN2 P17706 3/20 0.43
PTPN6 P29350 3/20 0.43
PTPRC P08575 1/20 0.43
PTPRB P23467 1/20 0.43
PTPN11 Q06124 1/20 0.43
RXRA P19793 2/20 0.42
RXRB P28702 2/20 0.42
RXRG P48443 2/20 0.42
PSEN1 P49768 2/20 0.41
KIFC1 Q9BW19 1/20 0.41
ALOX5 P09917 1/20 0.41
LRRK2 Q5S007 1/20 0.41
HTR2C P28335 1/20 0.39
SLC6A4 P31645 1/20 0.39
HTR2B P41595 1/20 0.39
PPARA Q07869 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
Bromide SCHEMBL2290372 0.90 PTPN1 (0.47) PPARDPPARGPTPN1PTPN2PTPN6
Bromide SCHEMBL2293962 0.87 PTPRC (0.41) PPARDPPARGPTPN1PTPN2PTPN6
Bromide SCHEMBL2296471 0.86 PPARD (0.48) PPARDPPARGALOX5PPARA
Bromide SCHEMBL2292736 0.84 HTR2A (0.38) PPARDSLC6A4PPARA
Bromide SCHEMBL2296444 0.80 FFAR1 (0.43) PPARGPTPN1SLC6A4
SCHEMBL4547677 0.79 PPARD (0.44) PPARDPPARGPTPN1PTPN2PTPN6
SCHEMBL2676421 0.79 PPARD (0.48) PPARDPPARGPTPN1PTPN2PTPN6
SCHEMBL4547681 0.79 PTPN1 (0.47) PPARDPTPN1PTPN2PTPN6PTPRC
Bromide SCHEMBL2293888 0.79 SLC1A5 (0.38) PPARDPPARGHTR2CSLC6A4HTR2B
SCHEMBL2676788 0.77 MAOB (0.51) PPARDPTPN1PTPN2PTPN6LRRK2

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-1940808-B1 DIFLUOROPHENOL DERIVATIVES AND THEIR USE BAYER IP GMBH (DE) 2013-11-27 EP disclosed
US-8173704-B2 Difluorophenol derivatives and their use BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2012-05-08 US disclosed
US-20090291993-A1 Difluorophenol Derivatives and Their Use BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2009-11-26 US disclosed
EP-1940808-A1 DIFLUOROPHENOL DERIVATIVES AND THEIR USE Bayer HealthCare AG (DE) 2008-07-09 EP disclosed
WO-2007045369-A1 DIFLUOROPHENOL DERIVATIVES AND THEIR USE BAYER HEALTHCARE AG (DE) 2007-04-26 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-20090291993-A1 Difluorophenol Derivatives and Their Use TPMT, FABP3, DPP4 PPARD 17/4885PPARG 73/4885PTPN1 143/4885

“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.