Bromide

Bromide

SCHEMBL2695097

O=C(C[n+]1ccc(Br)cc1)c1ccccc1.[Br-]

nearest known ligand 0.70

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 16)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 1/20 0.70
KMT2A Q03164 6/20 0.68
MEN1 O00255 4/20 0.65
ALDH1A1 P00352 6/20 0.62
KDM4E B2RXH2 2/20 0.60
MAPT P10636 3/20 0.57
HTT P42858 3/20 0.56
SMN1; SMN2 Q16637 3/20 0.56
PABPC1 P11940 2/20 0.55
ATM Q13315 1/20 0.55
LMNA P02545 2/20 0.54
LTA4H P09960 1/20 0.54
PLA2G2A P14555 1/20 0.54
RECQL P46063 2/20 0.53
MITF O75030 1/20 0.50
NR2F2 P24468 1/20 0.50

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 SCHEMBL2691176 0.86 KDM4E (0.70) RAB9AKMT2AMEN1ALDH1A1KDM4E
Bromide SCHEMBL698678 0.85 KDM4E (0.79) RAB9AKMT2AMEN1ALDH1A1KDM4E
Bromide SCHEMBL27941533 0.85 KDM4E (0.79) RAB9AKMT2AMEN1ALDH1A1KDM4E
SCHEMBL4401836 0.84 PABPC1 (0.67) RAB9AKMT2AMEN1ALDH1A1KDM4E
SCHEMBL765905 0.83 KDM4E (0.76) RAB9AKMT2AMEN1ALDH1A1KDM4E
Bromide SCHEMBL31501128 0.82 LMNA (0.74) RAB9AKMT2AMEN1ALDH1A1KDM4E
Iodide SCHEMBL1485891 0.82 PABPC1 (0.70) RAB9AKMT2AMEN1ALDH1A1KDM4E
Bromide SCHEMBL19468787 0.82 RAB9A (1.00) RAB9AKMT2AMEN1ALDH1A1KDM4E
Bromide SCHEMBL10921414 0.82 RAB9A (0.70) RAB9AKMT2AMEN1ALDH1A1KDM4E
Ammonia Solution, Strong SCHEMBL28760030 0.81 KDM4E (0.73) RAB9AKMT2AMEN1ALDH1A1KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1858094-B1 ORGANIC COMPOUND, CHARGE TRANSPORT MATERIAL AND ORGANIC ELECTROLUMINESCENT DEVICE PIONEER CORP (JP) 2017-03-08 EP disclosed
US-8168307-B2 Organic compound, charge transport material and organic electroluminescent device PIONEER CORPORATION (JP) 2012-05-01 US disclosed
US-20090021146-A1 ORGANIC COMPOUND, CHARGE TRANSPORT MATERIAL AND ORGANIC ELECTROLUMINESCENT DEVICE PIONEER CORPORATION (JP) 2009-01-22 US disclosed
EP-1858094-A1 ORGANIC COMPOUND, CHARGE TRANSPORT MATERIAL AND ORGANIC ELECTROLUMINESCENT DEVICE Pioneer Corporation (JP) 2007-11-21 EP 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-20090021146-A1 ORGANIC COMPOUND, CHARGE TRANSPORT MATERIAL AND ORGANIC ELECTROLUMINESCENT DEVICE SLC25A21, SLCO2A1, OCIAD2 RAB9A 1941/4885KMT2A 1162/4885MEN1 1827/4885

“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.