Bromide

Bromide

SCHEMBL7058827

Cc1c(CCO)sc[n+]1CC(=O)c1cccs1.Cc1sc[n+](CC(=O)N2CCCCCC2)c1C.Cc1sc[n+](CC(=O)N2CCN(c3ccccc3)CC2)c1C.Cc1sc[n+](CC(=O)N2CCSCC2)c1C.Cc1sc[n+](CC(=O)c2cccs2)c1C.[Br-].[Br-].[Br-].[Br-].[Br-]

nearest known ligand 0.39

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
OPRM1 known ✓ P35372 1/20 0.33
MAPT P10636 12/20 0.39
MEN1 O00255 5/20 0.39
KMT2A Q03164 5/20 0.39
L3MBTL1 Q9Y468 4/20 0.39
POLB P06746 3/20 0.39
KDM4E B2RXH2 3/20 0.39
GAA P10253 2/20 0.39
PKM P14618 2/20 0.39
RECQL P46063 1/20 0.39
ALDH1A1 P00352 7/20 0.37
NPC1 O15118 2/20 0.35
RAB9A P51151 2/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
CYP2C19 P33261 1/20 0.35
GFER P55789 2/20 0.34
PLA2G1B P04054 1/20 0.34
ATG4B Q9Y4P1 1/20 0.34
THRB P10828 1/20 0.33
OPRD1 P41143 1/20 0.33

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 SCHEMBL5015370 0.90 KMT2A (0.39) MAPTMEN1KMT2AL3MBTL1POLB
Bromide SCHEMBL7057614 0.88 HTR1A (0.43) MEN1KMT2APOLBKDM4EALDH1A1
Bromide SCHEMBL6423648 0.87 MAPT (0.36) MAPTMEN1KMT2AL3MBTL1POLB
Bromide SCHEMBL3846461 0.77 MAPT (0.51) MAPTMEN1KMT2AL3MBTL1POLB
SCHEMBL5069508 0.76 MAPT (0.52) MAPTMEN1KMT2AL3MBTL1POLB
Bromide SCHEMBL3846652 0.76 OPRM1 (0.45) MAPTMEN1KMT2AL3MBTL1POLB
SCHEMBL5070440 0.75 TKT (0.44) MAPTMEN1KMT2APOLBALDH1A1
Hydrochloric Acid SCHEMBL3846488 0.74 TKT (0.44)
Bromide SCHEMBL7050342 0.74 NPC1 (0.32) L3MBTL1NPC1RAB9ASMN1; SMN2
Bromide SCHEMBL3851290 0.71 KMT2A (0.48) KMT2AKDM4EALDH1A1NPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1128830-A4 REVERSING ADVANCED GLYCOSYLATION CROSS-LINKS USING HETEROCYCLIC-SUBSTITUTED THIAZOLIUM SALTS ALTEON INC (US) 2004-03-31 EP disclosed
EP-1128830-A1 REVERSING ADVANCED GLYCOSYLATION CROSS-LINKS USING HETEROCYCLIC-SUBSTITUTED THIAZOLIUM SALTS Alteon, Inc. (US) 2001-09-05 EP disclosed
WO-2000027395-A1 REVERSING ADVANCED GLYCOSYLATION CROSS-LINKS USING HETEROCYCLIC-SUBSTITUTED THIAZOLIUM SALTS ALTEON, INC. (US) 2000-05-18 WO disclosed