Bromide

Bromide

SCHEMBL869439

CCOc1cc2ncc(C#N)c(Nc3ccc(OCc4ccccn4)c(Cl)c3)c2cc1NC(=O)/C=C/C[N+](C)(C)Cc1c([N+](=O)[O-])ncn1C.[Br-]

nearest known ligand 0.68

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
HRH2 known ✓ P25021 1/20 0.68
EGFR P00533 13/20 0.68
ERBB2 P04626 8/20 0.68
STK3 Q13188 7/20 0.68
STK4 Q13043 5/20 0.68
BTK Q06187 2/20 0.68
SRC P12931 2/20 0.68
KDR P35968 2/20 0.68
STK25 O00506 1/20 0.68
MAP2K7 O14733 1/20 0.68
CHEK1 O14757 1/20 0.68
GAK O14976 1/20 0.68
EPHB6 O15197 1/20 0.68
ABCC4 O15439 1/20 0.68
MAP3K13 O43283 1/20 0.68
NUAK1 O60285 1/20 0.68
STK17B O94768 1/20 0.68
STK10 O94804 1/20 0.68
PRKD3 O94806 1/20 0.68
ABCB11 O95342 1/20 0.68

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
SCHEMBL17503056 1.00 EGFR (0.68) EGFRERBB2STK3STK4BTK
Trifluoroacetic Acid SCHEMBL868416 0.97 EGFR (0.65) EGFRERBB2STK3STK4BTK
Bromide SCHEMBL867611 0.89 EGFR (0.67) EGFRERBB2STK3STK4BTK
SCHEMBL17503010 0.89 EGFR (0.67) EGFRERBB2STK3STK4BTK
Trifluoroacetic Acid SCHEMBL17503023 0.87 EGFR (0.63) EGFRERBB2STK3STK4BTK
SCHEMBL4540604 0.86 EGFR (0.82) EGFRERBB2STK3STK4BTK
SCHEMBL4540611 0.86 EGFR (0.82) EGFRERBB2STK3STK4BTK
SCHEMBL2386955 0.86 EGFR (0.83) EGFRERBB2STK3STK4BTK
SCHEMBL29801718 0.86 EGFR (0.83) EGFRERBB2STK3STK4BTK
SCHEMBL2386963 0.86 EGFR (0.83) EGFRERBB2STK3STK4BTK

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-3031807-A1 PRODRUG FORMS OF KINASE INHIBITORS AND THEIR USE IN THERAPY Auckland UniServices Limited (NZ) 2016-06-15 EP disclosed
EP-2406262-B1 PRODRUG FORMS OF KINASE INHIBITORS AND THEIR USE IN THERAPY AUCKLAND UNISERVICES LTD (NZ) 2016-02-17 EP disclosed
US-20160002222-A1 PRODRUG FORMS OF KINASE INHIBITORS AND THEIR USE IN THERAPY AUCKLAND UNISERVICES LIMITED (NZ) 2016-01-07 US disclosed
US-9073916-B2 Prodrug forms of kinase inhibitors and their use in therapy AUCKLAND UNISERVICES LIMITED (NZ) 2015-07-07 US disclosed
US-20120077811-A1 PRODRUG FORMS OF KINASE INHIBITORS AND THEIR USE IN THERAPY AUCKLAND UNISERVICES LIMITED (NZ) 2012-03-29 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-20120077811-A1 PRODRUG FORMS OF KINASE INHIBITORS AND THEIR USE IN THERAPY NTRK3, TK1, TNNI3K HRH2 1027/4885EGFR 48/4885ERBB2 7/4885
US-20160002222-A1 PRODRUG FORMS OF KINASE INHIBITORS AND THEIR USE IN THERAPY NTRK3, TK1, TNNI3K HRH2 1090/4885EGFR 41/4885ERBB2 7/4885

“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.