Bromide

Bromide

SCHEMBL3884058

Cc1ccc(C(=O)C[n+]2ccccc2C)cc1.[Br-]

nearest known ligand 0.74

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 17)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 9/20 0.74
MEN1 O00255 6/20 0.67
KDM4E B2RXH2 5/20 0.67
THRB P10828 1/20 0.61
SMN1; SMN2 Q16637 2/20 0.59
MAPT P10636 2/20 0.55
ALDH1A1 P00352 3/20 0.51
LMNA P02545 1/20 0.51
HTT P42858 1/20 0.51
AHR P35869 1/20 0.51
L3MBTL1 Q9Y468 1/20 0.51
NPC1 O15118 1/20 0.50
RAB9A P51151 1/20 0.50
POLB P06746 1/20 0.49
RECQL P46063 1/20 0.48
PABPC1 P11940 1/20 0.48
ATM Q13315 1/20 0.48

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 SCHEMBL1645919 0.90 KMT2A (0.73) KMT2AMEN1KDM4ETHRBSMN1; SMN2
SCHEMBL13394254 0.88 KMT2A (0.70) KMT2AMEN1KDM4ETHRBSMN1; SMN2
Bromide SCHEMBL3884195 0.88 KMT2A (0.70) KMT2AMEN1KDM4ETHRBSMN1; SMN2
Bromide SCHEMBL1645730 0.88 KMT2A (0.70) KMT2AMEN1KDM4ETHRBSMN1; SMN2
SCHEMBL2230710 0.86 KMT2A (0.68) KMT2AMEN1KDM4ETHRBSMN1; SMN2
SCHEMBL4896174 0.86 KMT2A (0.68) KMT2AMEN1KDM4ETHRBSMN1; SMN2
Bromide SCHEMBL3885379 0.84 KMT2A (0.66) KMT2AMEN1KDM4ETHRBSMN1; SMN2
Bromide SCHEMBL6218010 0.84 KMT2A (0.65) KMT2AMEN1KDM4ETHRBSMN1; SMN2
Bromide SCHEMBL3891677 0.83 THRB (0.61) KMT2AMEN1KDM4ETHRBSMN1; SMN2
Bromide SCHEMBL3624435 0.80 KMT2A (1.00) KMT2AMEN1KDM4ESMN1; SMN2MAPT

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-8486962-B2 N-(2-Methoxy-phenyl)-2-oxo-2-(2-phenyl-indolizin-3-yl)-acetamide; antifungal agents; inhibiting Aspergillus F2G LTD. (GB) 2013-07-16 US disclosed
EP-1888063-B1 ANTIFUNGAL AGENTS F2G LTD (GB) 2009-01-14 EP disclosed
US-20080161302-A1 N-(2-Methoxy-phenyl)-2-oxo-2-(2-phenyl-indolizin-3-yl)-acetamide; antifungal agents; inhibiting Aspergillus F2G LTD. (GB) 2008-07-03 US disclosed
EP-1888063-A1 ANTIFUNGAL AGENTS F2G Ltd. (GB) 2008-02-20 EP disclosed
WO-2006123145-A1 ANTIFUNGAL AGENTS F2G LTD (GB) 2006-11-23 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-20080161302-A1 N-(2-Methoxy-phenyl)-2-oxo-2-(2-phenyl-indolizin-3-yl)-acetamide; antifungal agents; inhibiting Aspergillus NAT1, CYP1A2, CYP51A1 KMT2A 603/4885MEN1 325/4885KDM4E 1505/4885

“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.