Bromide

Bromide

SCHEMBL6132265

Br.Br.c1cc2c(cc1CC1CNCCN1)OCCO2

nearest known ligand 0.41

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
SLC6A3 known ✓ Q01959 2/20 0.36
SLC6A2 known ✓ P23975 1/20 0.36
HRH3 Q9Y5N1 1/20 0.40
CYP2D6 P10635 3/20 0.38
LTA4H P09960 1/20 0.37
CYP3A4 P08684 2/20 0.36
SLC6A1 P30531 1/20 0.36
KDM1A O60341 1/20 0.36
MAOA P21397 1/20 0.36
MAOB P27338 1/20 0.36
CHRM4 P08173 1/20 0.36
DRD2 P14416 1/20 0.36
HTR7 P34969 1/20 0.36
LMNA P02545 4/20 0.35
ALDH1A1 P00352 3/20 0.35
GAA P10253 2/20 0.35
HSD17B10 Q99714 2/20 0.35
HTT P42858 2/20 0.35
USP2 O75604 1/20 0.35
HPGD P15428 1/20 0.35

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
SCHEMBL28742028 0.99 HRH3 (0.41) HRH3CYP2D6LTA4HCYP3A4SLC6A3
SCHEMBL6968326 0.90 CYP3A4 (0.46) HRH3CYP2D6CYP3A4SLC6A3SLC6A2
Hydrochloric Acid SCHEMBL6132969 0.89 CYP3A4 (0.45) HRH3CYP2D6CYP3A4SLC6A3SLC6A2
Bromide SCHEMBL8113670 0.78 HRH3 (0.37) HRH3LTA4H
SCHEMBL5191962 0.76 ALDH1A1 (0.48) ALDH1A1HSD17B10HTTUSP2HPGD
SCHEMBL27557499 0.72 SLC6A4 (0.50) HRH3CYP2D6LTA4HCYP3A4SLC6A3
Bromide SCHEMBL6132738 0.71 ESR1 (0.45) HRH3LTA4HDRD2GAATP53
Bromide SCHEMBL6132729 0.71 HRH3 (0.40) HRH3LTA4HDRD2GAA
SCHEMBL27090452 0.71 POLB (0.47) CYP2D6CYP3A4SLC6A3SLC6A2SLC6A1
SCHEMBL27075574 0.71 POLB (0.47) CYP2D6CYP3A4SLC6A3SLC6A2SLC6A1

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 3 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

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 SLC6A3 478/4885SLC6A2 406/4885HRH3 229/4885
US-20030114668-A1 AROYL-PIPERAZINE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS TACHYKININ ANTAGONISTS TACR1, NPSR1, SSTR2 SLC6A3 440/4885SLC6A2 515/4885HRH3 31/4885

“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.