Bromide

Bromide

SCHEMBL1856525

Br.NCc1cccc(-c2ccccc2)c1

nearest known ligand 0.67

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 16)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 3/20 0.67
LOXL2 Q9Y4K0 1/20 0.64
AGXT P21549 1/20 0.59
CFD P00746 4/20 0.54
AOC3 Q16853 3/20 0.51
CSNK2A1 P68400 2/20 0.50
PNMT P11086 1/20 0.50
ENPP2 Q13822 1/20 0.50
HRH3 Q9Y5N1 1/20 0.50
PLG P00747 1/20 0.49
PLAU P00749 1/20 0.49
F11 P03951 1/20 0.49
KLKB1 P03952 1/20 0.49
F7 P08709 1/20 0.49
TPSB2 P20231 1/20 0.49
MAOA P21397 1/20 0.48

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
SCHEMBL43554 0.98 TAAR1 (0.70) TAAR1LOXL2AGXTCFDAOC3
SCHEMBL29400616 0.98 TAAR1 (0.70) TAAR1LOXL2AGXTCFDAOC3
Hydrochloric Acid SCHEMBL29793666 0.95 TAAR1 (0.67) TAAR1LOXL2AGXTCFDAOC3
Hydrochloric Acid SCHEMBL1237399 0.95 TAAR1 (0.67) TAAR1LOXL2AGXTCFDAOC3
SCHEMBL27799749 0.95 TAAR1 (0.67) TAAR1LOXL2AGXTCFDAOC3
SCHEMBL28247640 0.95 TAAR1 (0.74) TAAR1LOXL2AGXTCFDAOC3
SCHEMBL3791745 0.91 LOXL2 (0.60) TAAR1LOXL2AGXTCFDCSNK2A1
SCHEMBL3794460 0.88 TAAR1 (0.70) TAAR1LOXL2AGXTCFDPNMT
Benzylamine SCHEMBL11416949 0.88 LOXL2 (0.74) TAAR1LOXL2AGXTCFDAOC3
Biphenyl SCHEMBL27410798 0.88 TAAR1 (0.84) TAAR1LOXL2AGXTCSNK2A1PNMT

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-1470102-B1 SUBSTITUTED METHYLENE AMIDE DERIVATIVES AS MODULATORS OF PROTEIN TYROSINE PHOSPHATASES (PTPS) MERCK SERONO SA (CH) 2011-05-25 EP disclosed
US-7592477-B2 Substituted methylene amide derivatives as modulators of protein tyrosine phosphatases (PTPs) LABORATOIRES SERONO SA (CH) 2009-09-22 US disclosed
US-20050124656-A1 Substituted methylene amide derivatives as modulators of protein tyrosine phosphatases(ptps) APPLIED RESEARCH SYSTEMS ARS (NL) 2005-06-09 US disclosed
EP-1470102-A1 SUBSTITUTED METHYLENE AMIDE DERIVATIVES AS MODULATORS OF PROTEIN TYROSINE PHOSPHATASES (PTPS) Applied Research Systems ARS Holding N.V. (AN) 2004-10-27 EP disclosed
WO-2003064376-A1 SUBSTITUTED METHYLENE AMIDE DERIVATIVES AS MODULATORS OF PROTEIN TYROSINE PHOSPHATASES (PTPS) APPLIED RESEARCH SYSTEMS ARS HOLDING N.V. (AN) 2003-08-07 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-20050124656-A1 Substituted methylene amide derivatives as modulators of protein tyrosine phosphatases(ptps) PTPRS, PTPA, PTPMT1 TAAR1 1657/4885LOXL2 2570/4885AGXT 647/4885

“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.