Bromide

Bromide

SCHEMBL2970790

Br.N#Cc1cccc(-c2csc(C3CCNCC3)n2)c1

nearest known ligand 0.57

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 0.57
CPT2 P23786 1/20 0.47
CPT1A P50416 1/20 0.47
CPT1B Q92523 1/20 0.47
ALDH1A1 P00352 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
USP30 Q70CQ3 2/20 0.43
L3MBTL1 Q9Y468 2/20 0.43
MEN1 O00255 1/20 0.43
GAA P10253 1/20 0.43
KMT2A Q03164 1/20 0.43
UCHL1 P09936 1/20 0.43
PLAT P00750 1/20 0.43
IDO1 P14902 2/20 0.42
XDH P47989 1/20 0.41
CYP1A2 P05177 2/20 0.41
CYP1A1 P04798 1/20 0.41
CYP1B1 Q16678 1/20 0.41
CYP2C19 P33261 1/20 0.40
HSD17B10 Q99714 1/20 0.40

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
SCHEMBL4260528 0.99 HPGDS (0.58) HPGDSCPT2CPT1ACPT1BALDH1A1
Bromide SCHEMBL2984507 0.85 HPGDS (0.55) HPGDSCPT2CPT1AGAA
SCHEMBL4270370 0.83 HPGDS (0.56) HPGDSCPT2CPT1AGAA
Bromide SCHEMBL2986096 0.82 HPGDS (0.62) HPGDSALDH1A1SMN1; SMN2L3MBTL1MEN1
Bromide SCHEMBL2973216 0.82 HPGDS (0.76) HPGDSALDH1A1SMN1; SMN2L3MBTL1MEN1
SCHEMBL3772059 0.81 HPGDS (0.64) HPGDSALDH1A1SMN1; SMN2L3MBTL1MEN1
SCHEMBL10040499 0.81 HPGDS (0.60) HPGDSALDH1A1SMN1; SMN2L3MBTL1MEN1
SCHEMBL2975771 0.81 CPT2 (0.52) HPGDSCPT2CPT1ACPT1BALDH1A1
SCHEMBL2979635 0.81 ALDH1A1 (0.50) HPGDSCPT2CPT1ACPT1BALDH1A1
SCHEMBL2297392 0.80 HPGDS (0.78) HPGDSALDH1A1SMN1; SMN2L3MBTL1MEN1

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
US-20070043083-A1 Thiazolyl piperidine derivatives HOFFMANN-LA ROCHE INC. 2007-02-22 US disclosed
WO-2007020213-A2 THIAZOLYL PIPERIDINE DERIVATIVES USEFUL AS H3 RECEPTOR MODULATORS F. HOFFMANN-LA ROCHE AG (CH) 2007-02-22 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-20070043083-A1 Thiazolyl piperidine derivatives HRH3, HRH4, H1-3 HPGDS 658/4885CPT2 1357/4885CPT1A 766/4885

“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.