Bromide

Bromide

SCHEMBL8466957

Br.CCCCCCCCCCCCN(C)CCCCCCl

nearest known ligand 0.62

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
CHRM2 known ✓ P08172 1/20 0.42
TSHR P16473 4/20 0.62
ALDH1A1 P00352 1/20 0.62
DNM1 Q05193 3/20 0.54
S1PR2 O95136 1/20 0.48
S1PR1 P21453 1/20 0.48
S1PR3 Q99500 1/20 0.48
S1PR5 Q9H228 1/20 0.48
TDP1 Q9NUW8 1/20 0.46
GGPS1 O95749 4/20 0.44
FDPS P14324 1/20 0.44
AGTR1 P30556 1/20 0.44
OPRM1 P35372 1/20 0.44
PDE3A Q14432 1/20 0.44
MAPT P10636 1/20 0.43
LMNA P02545 1/20 0.42
TP53 P04637 1/20 0.42
HTT P42858 1/20 0.42
HBB P68871 1/20 0.42
KDM5A P29375 2/20 0.41

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
Methylamine SCHEMBL6265466 0.93 TSHR (0.59) TSHRALDH1A1DNM1S1PR2S1PR1
SCHEMBL7265266 0.93 TSHR (0.57) TSHRALDH1A1DNM1S1PR2S1PR1
Methylamine SCHEMBL2024601 0.91 TSHR (0.56) TSHRALDH1A1DNM1S1PR2S1PR1
Methylamine SCHEMBL6303494 0.91 TSHR (0.56) TSHRALDH1A1DNM1S1PR2S1PR1
SCHEMBL10957981 0.88 MAPT (0.60) TSHRALDH1A1DNM1S1PR2S1PR1
SCHEMBL26685916 0.88 MAPT (0.60) TSHRALDH1A1DNM1S1PR2S1PR1
SCHEMBL11825151 0.88 TSHR (0.50) TSHRALDH1A1DNM1S1PR2S1PR1
SCHEMBL31325281 0.87 MAPT (0.56) TSHRALDH1A1DNM1S1PR2S1PR1
Bromide SCHEMBL5531256 0.87 DNM1 (0.68) TSHRDNM1S1PR2S1PR1S1PR3
Bromide SCHEMBL3059787 0.87 DNM1 (0.68) TSHRDNM1S1PR2S1PR1S1PR3

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
US-5969090-A QUATERNIZED CROSSLINKED HYDROCARBON AMINE POLYMER GELTEX PHARMACEUTICALS, INC. (US) 1999-10-19 US disclosed
US-5900475-A MODIFIED POLYALLYLAMINE; ANTICHOLESTEROL AGENT GELTEX PHARMACEUTICALS, INC. (US) 1999-05-04 US disclosed
EP-0830390-A1 HYDROPHOBIC HETEROATOM-CONTAINING SEQUESTRANT FOR CHOLESTEROL DEPLETION GELTEX PHARMACEUTICALS, INC. (US) 1998-03-25 EP disclosed
WO-1996039449-A1 HYDROPHOBIC HETEROATOM-CONTAINING SEQUESTRANT FOR CHOLESTEROL DEPLETION GELTEX PHARMACEUTICALS, INC. (US) 1996-12-12 WO disclosed