Bromide

Bromide

SCHEMBL6132729

Br.Br.Cc1ccc(CC2CNCCN2)cc1O

nearest known ligand 0.40

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
ACHE known ✓ P22303 1/20 0.37
HRH3 Q9Y5N1 1/20 0.40
LTA4H P09960 1/20 0.37
PARP1 P09874 1/20 0.36
MEN1 O00255 1/20 0.35
ABL1 P00519 1/20 0.35
ALPL P05186 1/20 0.35
GAA P10253 1/20 0.35
KMT2A Q03164 1/20 0.35
RIN1 Q13671 1/20 0.35
DRD2 P14416 1/20 0.35
DRD4 P21917 1/20 0.35
CDK4 P11802 1/20 0.32
CCND1 P24385 1/20 0.32
CDK2 P24941 1/20 0.32
TSHR P16473 1/20 0.32
CASP1 P29466 1/20 0.32
ESR1 P03372 1/20 0.31
ESR2 Q92731 1/20 0.31
TRPA1 O75762 1/20 0.30

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
SCHEMBL27484596 0.99 HRH3 (0.41) HRH3LTA4HACHEPARP1MEN1
Hydrochloric Acid SCHEMBL27595304 0.97 HRH3 (0.40) HRH3LTA4HACHEPARP1MEN1
Bromide SCHEMBL6132738 0.89 ESR1 (0.45) HRH3LTA4HPARP1MEN1ABL1
Hydrochloric Acid SCHEMBL27536111 0.86 ESR1 (0.45) HRH3LTA4HPARP1MEN1ABL1
SCHEMBL27472173 0.81 HRH3 (0.41) HRH3LTA4HPARP1MEN1ABL1
SCHEMBL27484227 0.81 LTA4H (0.41) HRH3LTA4HPARP1MEN1ABL1
SCHEMBL28746746 0.81 HRH3 (0.43) HRH3LTA4HPARP1
Bromide SCHEMBL6132805 0.81 HRH3 (0.41) HRH3LTA4HMEN1KMT2A
SCHEMBL27471263 0.78 SSTR1 (0.41) HRH3LTA4HPARP1DRD4
Hydrochloric Acid SCHEMBL6132984 0.78 HRH3 (0.39) HRH3LTA4HPARP1

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-6924278-B2 Heterocyclic carboxy amines such as (2R)-1-[3,5-Bis(trifluoromethyl)benzoyl]-4-[4-((3S)-3-ethylmorpholino)-2-butynyl]-2-[(1H-indol-3-yl)methyl]piperazine, used as substance P and neurokinin antagonist for prophylaxis of diseases FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2005-08-02 US disclosed
US-20050027121-A1 Aroyl-piperazine derivatives, their preparation and their use as tachykinin antagonists FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2005-02-03 US disclosed
US-20030114668-A1 AROYL-PIPERAZINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS TACHYKININ ANTAGONISTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2003-06-19 US disclosed
EP-0993457-A1 AROYL-PIPERAZINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS TACHYKININ ANTAGONISTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2000-04-19 EP disclosed
WO-1998057954-A1 AROYL-PIPERAZINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS TACHYKININ ANTAGONISTS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1998-12-23 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 (2 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-20050027121-A1 Aroyl-piperazine derivatives, their preparation and their use as tachykinin antagonists TAC3, TACR1, SSTR5 ACHE 525/4885HRH3 229/4885LTA4H 911/4885
US-20030114668-A1 AROYL-PIPERAZINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS TACHYKININ ANTAGONISTS TACR1, NPSR1, SSTR2 ACHE 960/4885HRH3 31/4885LTA4H 561/4885

“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.