Bromide

Bromide

SCHEMBL4448810

Br.Br.N=C(N)SCc1ccc(Cl)cc1Oc1cc([N+](=O)[O-])ccc1CSC(=N)N

nearest known ligand 0.53

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
IDO1 P14902 8/20 0.53
HTT P42858 3/20 0.53
CYP1A2 P05177 6/20 0.52
CYP2D6 P10635 3/20 0.52
CYP2C9 P11712 3/20 0.52
HPGD P15428 2/20 0.52
ALOX15 P16050 2/20 0.52
HIF1A Q16665 1/20 0.42
LMNA P02545 2/20 0.41
ALDH1A1 P00352 2/20 0.41
GAA P10253 1/20 0.41
CYP2C19 P33261 1/20 0.40
MAPT P10636 2/20 0.39
NPSR1 Q6W5P4 1/20 0.39
PRMT1 Q99873 1/20 0.39
MEN1 O00255 1/20 0.38
TP53 P04637 1/20 0.38
MAPK1 P28482 1/20 0.38
RECQL P46063 1/20 0.38
KMT2A Q03164 1/20 0.38

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
SCHEMBL3690757 0.99 CYP1A2 (0.53) IDO1HTTCYP1A2CYP2D6CYP2C9
Bromide SCHEMBL4442756 0.94 IDO1 (0.50) IDO1HTTCYP1A2CYP2D6CYP2C9
SCHEMBL3687161 0.93 CYP1A2 (0.50) IDO1HTTCYP1A2CYP2D6CYP2C9
SCHEMBL3680878 0.90 CYP1A2 (0.48) IDO1HTTCYP1A2CYP2D6CYP2C9
Bromide SCHEMBL4437753 0.88 IDO1 (0.51) IDO1HTTCYP1A2CYP2D6CYP2C9
Bromide SCHEMBL4448815 0.88 CYP1A2 (0.42) IDO1HTTCYP1A2CYP2D6CYP2C9
SCHEMBL3680100 0.87 IDO1 (0.52) IDO1HTTCYP1A2CYP2D6CYP2C9
SCHEMBL3690762 0.86 CYP1A2 (0.43) IDO1HTTCYP1A2CYP2D6CYP2C9
Bromide SCHEMBL4442761 0.84 HPGD (0.41) IDO1HTTCYP1A2CYP2D6CYP2C9
SCHEMBL3687166 0.83 HPGD (0.42) IDO1HTTCYP1A2CYP2D6CYP2C9

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
EP-2061754-A1 BIARYL AND BIHETEROARYL COMPOUNDS USEFUL IN TREATING IRON DISORDERS XENON PHARMACEUTICALS INC. (CA) 2009-05-27 EP disclosed
WO-2008115999-A1 BIARYL AND BIHETEROARYL COMPOUNDS USEFUL IN TREATING IRON DISORDERS XENON PHARMACEUTICALS INC. (CA) 2008-09-25 WO disclosed
US-20080234384-A1 BIARYL AND BIHETEROARYL COMPOUNDS USEFUL IN TREATING IRON DISORDERS XENON PHARMACEUTICALS INC. (CA) 2008-09-25 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 (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-20080234384-A1 BIARYL AND BIHETEROARYL COMPOUNDS USEFUL IN TREATING IRON DISORDERS FECH, SLC10A1, SLC40A1 IDO1 269/4885HTT 1363/4885CYP1A2 71/4885

“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.