Bromide

Bromide

SCHEMBL2984287

Br.COc1ccc(-c2csc(C3CCNCC3)n2)cc1OC

nearest known ligand 0.54

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
HPGDS O60760 1/20 0.51
TLR9 Q9NR96 4/20 0.47
TLR7 Q9NYK1 4/20 0.47
TLR8 Q9NR97 3/20 0.47
RAB9A P51151 6/20 0.47
NPC1 O15118 5/20 0.47
MAPT P10636 5/20 0.47
SMN1; SMN2 Q16637 2/20 0.47
MEN1 O00255 7/20 0.47
KMT2A Q03164 7/20 0.47
ALDH1A1 P00352 2/20 0.47
HTT P42858 2/20 0.47
KDM4E B2RXH2 1/20 0.47
MAPK1 P28482 2/20 0.46
ALOX15 P16050 1/20 0.46
HSD17B10 Q99714 1/20 0.46
PKM P14618 1/20 0.46
PLAT P00750 1/20 0.43
GAA P10253 1/20 0.42
CYP1A1 P04798 1/20 0.42

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
SCHEMBL4261970 0.99 HPGDS (0.52) HPGDSTLR9TLR7TLR8RAB9A
Tert-Butyl Formate SCHEMBL28309477 0.88 TLR9 (0.45) HPGDSTLR9TLR7TLR8RAB9A
Bromide SCHEMBL2972856 0.84 NPC1 (0.62) HPGDSRAB9ANPC1MAPTSMN1; SMN2
SCHEMBL4257174 0.82 RAB9A (0.60) HPGDSRAB9ANPC1MAPTSMN1; SMN2
Bromide SCHEMBL2987437 0.82 HPGDS (0.56) HPGDSRAB9ANPC1SMN1; SMN2ALDH1A1
SCHEMBL4262042 0.81 HPGDS (0.57) HPGDSRAB9ANPC1SMN1; SMN2MEN1
SCHEMBL2981891 0.80 MAPT (0.50) TLR9TLR7TLR8RAB9ANPC1
Bromide SCHEMBL2983628 0.79 HPGDS (0.57) HPGDSRAB9ANPC1MAPTSMN1; SMN2
SCHEMBL2978630 0.79 MAPT (0.49) TLR9TLR7TLR8RAB9ANPC1
Bromide SCHEMBL2981940 0.79 HPGDS (0.52) HPGDSMEN1KMT2APLATCYP1A2

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-7786143-B2 Thiazolyl piperidine derivatives HOFFMAN-LA ROCHE INC. (US) 2010-08-31 US disclosed
EP-1945635-B1 THIAZOLYL PIPERIDINE DERIVATIVES USEFUL AS H3 RECEPTOR MODULATORS HOFFMANN LA ROCHE (CH) 2009-05-06 EP disclosed
EP-1945635-A2 THIAZOLYL PIPERIDINE DERIVATIVES USEFUL AS H3 RECEPTOR MODULATORS F.HOFFMANN-LA ROCHE AG (CH) 2008-07-23 EP disclosed
WO-2007020213-A2 THIAZOLYL PIPERIDINE DERIVATIVES USEFUL AS H3 RECEPTOR MODULATORS F. HOFFMANN-LA ROCHE AG (CH) 2007-02-22 WO disclosed
US-20070043083-A1 Thiazolyl piperidine derivatives HOFFMANN-LA ROCHE INC. 2007-02-22 US 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-20070043083-A1 Thiazolyl piperidine derivatives HRH3, HRH4, H1-3 HPGDS 658/4885TLR9 321/4885TLR7 343/4885

“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.