Bromide

Bromide

SCHEMBL5865072

Br.O=[N+]([O-])c1cc(O)c2ncccc2c1

nearest known ligand 0.97

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
ADRA2B known ✓ P18089 1/20 0.48
ADRA2C known ✓ P18825 1/20 0.48
CHRM3 known ✓ P20309 1/20 0.48
HTR3A known ✓ P46098 1/20 0.48
ADRA1A known ✓ P35348 1/20 0.47
MAPT P10636 8/20 0.97
KDM4E B2RXH2 7/20 0.97
RAB9A P51151 5/20 0.97
NPC1 O15118 4/20 0.97
SMN1; SMN2 Q16637 3/20 0.97
HTT P42858 2/20 0.97
CASP6 P55212 2/20 0.97
TDP1 Q9NUW8 2/20 0.97
PKM P14618 1/20 0.97
NFKB1 P19838 1/20 0.97
NFKB2 Q00653 1/20 0.97
RELA Q04206 1/20 0.97
HSP90AA1 P07900 2/20 0.57
HSP90AB1 P08238 1/20 0.57
L3MBTL1 Q9Y468 4/20 0.51

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
SCHEMBL2167844 0.98 MAPT (1.00) MAPTKDM4ERAB9ANPC1SMN1; SMN2
Hydrochloric Acid SCHEMBL1786218 0.85 MAPT (0.74) MAPTKDM4ERAB9ANPC1SMN1; SMN2
SCHEMBL8545403 0.82 MAPT (0.67) MAPTKDM4ERAB9ANPC1SMN1; SMN2
SCHEMBL4329054 0.81 MAPT (0.69) MAPTKDM4ERAB9ANPC1SMN1; SMN2
SCHEMBL13977911 0.79 MAPT (0.68) MAPTKDM4ERAB9ANPC1SMN1; SMN2
SCHEMBL31067261 0.79 MAPT (0.68) MAPTKDM4ERAB9ANPC1SMN1; SMN2
SCHEMBL3113854 0.79 MAPT (0.68) MAPTKDM4ERAB9ANPC1SMN1; SMN2
SCHEMBL15007822 0.79 MAPT (0.68) MAPTKDM4ERAB9ANPC1SMN1; SMN2
Oxyquinoline SCHEMBL10906631 0.77 MAPT (0.64) MAPTKDM4ERAB9ANPC1SMN1; SMN2
SCHEMBL6071988 0.77 MAPT (0.60) MAPTKDM4ERAB9ANPC1SMN1; SMN2

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
US-7064117-B2 Anti-cancer 2,3-dihydro-1H-pyrrolo[3,2-f]quinoline complexes of cobalt and chromium AUCKLAND UNISERVICES LIMITED (NZ) 2006-06-20 US disclosed
US-20050038249-A1 Anti-cancer 2,3-dihydro-1H-pyrrole[3,2-f] quinoline compolexes of cobalt and chromium AUCKLAND UNISERVICES LIMITED (NZ) 2005-02-17 US disclosed
EP-1363908-A4 ANTI-CANCER 2,3-DIHYDRO-1H-PYRROLO 3,2-f]QUINOLINE COMPLEXES OF COBALT AND CHROMIUM AUCKLAND UNISERVICES LTD (NZ) 2004-05-06 EP disclosed
EP-1363908-A1 ANTI-CANCER 2,3-DIHYDRO-1H-PYRROLO 3,2-f]QUINOLINE COMPLEXES OF COBALT AND CHROMIUM Auckland Uniservices Limited (NZ) 2003-11-26 EP disclosed
WO-2002059122-A1 ANTI-CANCER 2,3-DIHYDRO-1H-PYRROLO[3,2-f]QUINOLINE COMPLEXES OF COBALT AND CHROMIUM AUCKLAND UNISERVICES LIMITED (NZ) 2002-08-01 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-20050038249-A1 Anti-cancer 2,3-dihydro-1H-pyrrole[3,2-f] quinoline compolexes of cobalt and chromium CA2, HIF1AN, PPOX ADRA2B 3737/4885ADRA2C 2183/4885CHRM3 2335/4885

“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.