Bromide

Bromide

SCHEMBL20840237

Br.Cc1cnc(C(=O)O)c(O)c1

nearest known ligand 0.47

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4

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
ACHE known ✓ P22303 1/20 0.34
HCAR2 Q8TDS4 1/20 0.47
ALDH1A1 P00352 2/20 0.41
EGLN1 Q9GZT9 6/20 0.40
VEGFA P15692 2/20 0.40
FLT1 P17948 2/20 0.40
EGLN3 Q9H6Z9 2/20 0.40
CSNK2A1 P68400 1/20 0.38
KDM4E B2RXH2 2/20 0.38
MAPT P10636 1/20 0.38
PARP1 P09874 1/20 0.37
TPMT P51580 1/20 0.35
HCAR1 Q9BXC0 1/20 0.35
GABRP O00591 1/20 0.35
GABRD O14764 1/20 0.35
GABRA1 P14867 1/20 0.35
GABRB1 P18505 1/20 0.35
GABRG2 P18507 1/20 0.35
GABRB3 P28472 1/20 0.35
GABRA5 P31644 1/20 0.35

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
SCHEMBL14212262 0.98 HCAR2 (0.48) HCAR2ALDH1A1EGLN1VEGFAFLT1
SCHEMBL14212285 0.82 HCAR2 (0.39) HCAR2EGLN1VEGFAFLT1EGLN3
SCHEMBL7190906 0.79 HCAR2 (0.45) HCAR2ALDH1A1KDM4EMAPTPARP1
SCHEMBL1819716 0.78 GABRP (0.44) HCAR2ALDH1A1CSNK2A1KDM4EMAPT
SCHEMBL30968742 0.78 GABRP (0.44) HCAR2ALDH1A1CSNK2A1KDM4EMAPT
SCHEMBL9508588 0.78 HCAR2 (0.44) HCAR2ALDH1A1KDM4EMAPTPARP1
SCHEMBL31306918 0.77 ATM (0.53) ALDH1A1EGLN1VEGFAFLT1EGLN3
SCHEMBL28415928 0.77 CA12 (0.40) HCAR2ALDH1A1EGLN1VEGFAFLT1
SCHEMBL5637785 0.77 EGLN1 (0.66) ALDH1A1EGLN1VEGFAFLT1EGLN3
SCHEMBL1105993 0.76 MEN1 (0.43) HCAR2ALDH1A1KDM4EMAPTTPMT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20200277262-A1 N-(CYANO-SUBSTITUTED BENZYL OR PYRIDINYLMETHYL)-3-HYDROXYPICOLINAMIDE DERIVATIVES JONES BENJAMIN (US) 2020-09-03 US disclosed
EP-3676251-A1 N-(CYANO-SUBSTITUTED BENZYL OR PYRIDINYLMETHYL)-3-HYDROXYPICOLINAMIDE DERIVATIVES USEFUL AS HIF PROLYL HYDROXYLASE INHIBITORS Takeda Pharmaceutical Company Limited (JP) 2020-07-08 EP disclosed
WO-2019060850-A1 N-(CYANO-SUBSTITUTED BENZYL OR PYRIDINYLMETHYL)-3-HYDROXYPICOLINAMIDE DERIVATIVES USEFUL AS HIF PROLYL HYDROXYLASE INHIBITORS TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2019-03-28 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-20200277262-A1 N-(CYANO-SUBSTITUTED BENZYL OR PYRIDINYLMETHYL)-3-HYDROXYPICOLINAMIDE DERIVATIVES P4HA1, HRH3, HRH1 ACHE 1379/4885HCAR2 134/4885ALDH1A1 1144/4885

“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.