Bromide

Bromide

SCHEMBL10529486

Cc1ccccc1C(=O)C[n+]1ccn(C)c1.[Br-]

nearest known ligand 0.45

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 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 4/20 0.45
MEN1 O00255 3/20 0.45
RECQL P46063 1/20 0.45
ERCC5 P28715 1/20 0.42
FEN1 P39748 1/20 0.42
POLB P06746 1/20 0.41
CTNNB1 P35222 2/20 0.40
WNT3A P56704 2/20 0.40
HPGD P15428 3/20 0.40
ALDH1A1 P00352 3/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
PABPC1 P11940 1/20 0.38
ATM Q13315 1/20 0.38
L3MBTL1 Q9Y468 2/20 0.37
NPC1 O15118 1/20 0.37
RAB9A P51151 1/20 0.37
KDM4E B2RXH2 1/20 0.37
MAPK1 P28482 1/20 0.37
GAA P10253 1/20 0.36
ELANE P08246 1/20 0.36

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
SCHEMBL10531099 0.99 ERCC5 (0.43) KMT2AMEN1RECQLERCC5FEN1
Bromide SCHEMBL10526865 0.83 POLB (0.48) KMT2AMEN1RECQLPOLBALDH1A1
Bromide SCHEMBL27671525 0.82 KMT2A (0.42) KMT2AMEN1RECQLPOLBHPGD
SCHEMBL10526750 0.82 POLB (0.46) KMT2AMEN1POLBALDH1A1SMN1; SMN2
Iodide SCHEMBL10529424 0.81 POLB (0.42) KMT2AMEN1RECQLPOLBHPGD
Bromide SCHEMBL3844583 0.81 KMT2A (0.67) KMT2AMEN1RECQLPOLBALDH1A1
Hydrochloric Acid SCHEMBL10528498 0.81 POLB (0.45) KMT2AMEN1POLBALDH1A1SMN1; SMN2
SCHEMBL20527505 0.81 ALDH1A1 (0.47) KMT2APOLBCTNNB1WNT3AHPGD
SCHEMBL16624840 0.79 KMT2A (0.64) KMT2AMEN1RECQLPOLBALDH1A1
Hydrochloric Acid SCHEMBL10526733 0.78 KMT2A (0.62) KMT2AMEN1RECQLPOLBALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0182533-B1 3-(2-ARYL-2-OXOETHYL)-IMIDAZOLIUM SALTS AS HYPOGLYCEMIC AGENTS ELI LILLY AND COMPANY (US) 1989-09-20 EP claimed
US-4609670-A ANTIDIABETIC AGENTS ELI LILLY AND COMPANY (US) 1986-09-02 US claimed
EP-0182533-A2 3-(2-Aryl-2-oxoethyl)-imidazolium salts as hypoglycemic agents ELI LILLY AND COMPANY (US) 1986-05-28 EP claimed
EP-0182533-B1 3-(2-ARYL-2-OXOETHYL)-IMIDAZOLIUM SALTS AS HYPOGLYCEMIC AGENTS ELI LILLY AND COMPANY (US) 1989-09-20 EP disclosed
US-4683312-A ANTIDIABETIC AGENTS ELI LILLY AND COMPANY (US) 1987-07-28 US disclosed
US-4609670-A ANTIDIABETIC AGENTS ELI LILLY AND COMPANY (US) 1986-09-02 US disclosed
EP-0182533-A2 3-(2-Aryl-2-oxoethyl)-imidazolium salts as hypoglycemic agents ELI LILLY AND COMPANY (US) 1986-05-28 EP disclosed