Bromide

Bromide

SCHEMBL4763493

Br.[Br-].[H+].c1ccc(P(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.80

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 0.30
TDP1 Q9NUW8 3/20 0.80
CYP3A4 P08684 1/20 0.80
ESR1 P03372 4/20 0.57
ESR2 Q92731 4/20 0.57
KDM4E B2RXH2 1/20 0.44
GAA P10253 1/20 0.44
NPSR1 Q6W5P4 1/20 0.34
DRD1 P21728 2/20 0.33
ALDH1A1 P00352 2/20 0.33
LMNA P02545 2/20 0.30
MAPT P10636 1/20 0.30
HTT P42858 1/20 0.30
TSHR P16473 3/20 0.30
CA1 P00915 2/20 0.30
CA2 P00918 2/20 0.30
CA9 Q16790 2/20 0.30
CA12 O43570 1/20 0.30
GLA P06280 1/20 0.30
CA3 P07451 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
Bromide SCHEMBL3145494 0.97 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Bromide SCHEMBL64729 0.93 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Bromide SCHEMBL1409552 0.93 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Bromide SCHEMBL71504 0.93 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Bromide SCHEMBL3314443 0.93 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Bromide SCHEMBL28046864 0.93 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
SCHEMBL11170638 0.93 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Bromide SCHEMBL64728 0.93 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Bromide SCHEMBL1409549 0.93 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Bromide SCHEMBL624311 0.93 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E

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
EP-1979343-A2 BICYCLIC HETEROARYL COMPOUNDS AS PDE10 INHIBITORS Pfizer Products Inc. (US) 2008-10-15 EP disclosed
WO-2007077490-A2 BICYCLIC HETEROARYL COMPOUNDS AS PDE10 INHIBITORS PFIZER PRODUCTS INC. (US) 2007-07-12 WO disclosed
US-20070155779-A1 BICYCLIC HETEROARYL COMPOUNDS AS PDE10 INHIBITORS PFIZER INC 2007-07-05 US disclosed
US-4605675-A Polyene compounds useful in the treatment of allergic responses USV PHARMACEUTICAL CORP. (US) 1986-08-12 US disclosed
US-4387250-A Phosphonium salts, process for their preparation and use of same as starting materials for preparing unsaturated bicyclic compounds FIRMENICH SA (CH) 1983-06-07 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-20070155779-A1 BICYCLIC HETEROARYL COMPOUNDS AS PDE10 INHIBITORS PDE12, PDE10A, PDE7A ACHE 27/4885TDP1 42/4885CYP3A4 548/4885

“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.