Bromide

Bromide

SCHEMBL2978490

Br.Clc1ccc(-c2csc(C3CCNCC3)n2)cc1Cl

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
SLC6A2 known ✓ P23975 2/20 0.39
SLC6A4 known ✓ P31645 2/20 0.39
SLC6A3 known ✓ Q01959 2/20 0.39
HPGDS O60760 1/20 0.54
ABL1 P00519 3/20 0.48
AR P10275 1/20 0.44
NPC1 O15118 2/20 0.43
RAB9A P51151 2/20 0.43
MEN1 O00255 3/20 0.42
KMT2A Q03164 3/20 0.42
KDM4E B2RXH2 1/20 0.42
ALOX5 P09917 1/20 0.41
VCP P55072 1/20 0.41
ALDH1A1 P00352 3/20 0.41
GAA P10253 2/20 0.41
CYP1A2 P05177 1/20 0.41
CYP3A4 P08684 1/20 0.41
MAPT P10636 1/20 0.41
CYP2C9 P11712 1/20 0.41
CYP2C19 P33261 1/20 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
SCHEMBL4258789 0.99 HPGDS (0.55) HPGDSABL1ARNPC1RAB9A
Bromide SCHEMBL2979882 0.85 HPGDS (0.57) HPGDSNPC1RAB9AMEN1KMT2A
SCHEMBL4259512 0.83 HPGDS (0.59) HPGDSNPC1RAB9AMEN1KMT2A
Hydrochloric Acid SCHEMBL1653293 0.82 ALDH1A1 (0.58) HPGDSNPC1RAB9AMEN1KMT2A
SCHEMBL10040499 0.82 HPGDS (0.60) HPGDSABL1NPC1RAB9AMEN1
Bromide SCHEMBL2974660 0.82 HPGDS (0.54) HPGDSNPC1RAB9AMEN1KMT2A
SCHEMBL4258842 0.80 HPGDS (0.55) HPGDSNPC1RAB9AMEN1KMT2A
Bromide SCHEMBL2983628 0.80 HPGDS (0.57) HPGDSNPC1RAB9AMEN1KMT2A
Bromide SCHEMBL2984301 0.79 HPGDS (0.60) HPGDSARNPC1RAB9AMEN1
Bromide SCHEMBL2973216 0.79 HPGDS (0.76) HPGDSNPC1RAB9AMEN1KMT2A

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 SLC6A2 2750/4885SLC6A4 1585/4885SLC6A3 1432/4885

“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.