Bromide

Bromide

SCHEMBL6746472

Br.N=c1n(CC(=O)c2ccc(O)cc2)c2ccccc2n1Cc1ccccc1

nearest known ligand 0.72

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
MAPT P10636 8/20 0.72
KMT2A Q03164 6/20 0.72
MITF O75030 5/20 0.72
KDM4E B2RXH2 3/20 0.72
HTT P42858 2/20 0.72
SMN1; SMN2 Q16637 5/20 0.71
MEN1 O00255 2/20 0.71
TDP1 Q9NUW8 1/20 0.71
F2R P25116 1/20 0.64
NPSR1 Q6W5P4 4/20 0.62
ALDH1A1 P00352 1/20 0.61
XBP1 P17861 1/20 0.61
OXTR P30559 1/20 0.61
AVPR1A P37288 1/20 0.61
BLM P54132 1/20 0.61
LMNA P02545 2/20 0.61
L3MBTL1 Q9Y468 1/20 0.61
TP53 P04637 1/20 0.60
TSHR P16473 1/20 0.58
NPC1 O15118 1/20 0.58

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 SCHEMBL6748462 0.92 MAPT (0.82) MAPTKMT2AMITFKDM4EHTT
Bromide SCHEMBL6752864 0.90 MAPT (0.72) MAPTKMT2AMITFKDM4EHTT
Bromide SCHEMBL6746416 0.88 MAPT (0.71) MAPTKMT2AMITFKDM4EHTT
SCHEMBL5460666 0.87 MAPT (0.69) MAPTKMT2AMITFKDM4EHTT
SCHEMBL14470550 0.87 MAPT (0.88) MAPTKMT2AMITFKDM4EHTT
Bromide SCHEMBL6750274 0.85 MAPT (0.67) MAPTKMT2AMITFKDM4EHTT
Bromide SCHEMBL6752895 0.84 F2R (0.70) MAPTKMT2AMITFKDM4EHTT
Bromide SCHEMBL6750417 0.83 MAPT (0.61) MAPTKMT2AMITFKDM4EHTT
Bromide SCHEMBL6751209 0.83 KMT2A (0.64) MAPTKMT2AMITFKDM4EHTT
Bromide SCHEMBL6752701 0.83 NPSR1 (0.58) MAPTKMT2AMITFKDM4EHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040242627-A1 2-Iminoimidazole derivatives (1) EISAI R&D MANAGEMENT CO., LTD. (JP) 2004-12-02 US disclosed
US-20040191629-A1 Anode of sulfur; cathode of lithium silicide; molten metal compound as electrolytes SANYO ELECTRIC CO., LTD. 2004-09-30 US disclosed
EP-1394152-A1 2-IMINOIMIDAZOLE DERIVATIVES (1) Eisai Co., Ltd. (JP) 2004-03-03 EP disclosed
US-20020151714-A1 PROCESS FOR PREPARING 1,4-DISUBSTITUTED PIPERIDINE COMPOUNDS CILAG AG (CH) 2002-10-17 US disclosed
US-6322722-B1 BUTYLENE OXIDE DERIVATIVE AND HYDROCARBON BLOWING AGENT; PRODUCES LOW DENSITY, WITHOUT HIGHER CONCENTRATION OF WATER THE DOW CHEMICAL COMPANY 2001-11-27 US disclosed
US-5942530-A Method for treating pain ELI LILLY AND COMPANY (US) 1999-08-24 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-20040242627-A1 2-Iminoimidazole derivatives (1) H1-2, H1-0, H1-3 MAPT 4077/4885KMT2A 340/4885MITF 3456/4885

“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.