Bromide

Bromide

SCHEMBL5833274

Br.CC1N(CCC(=O)O)c2ccccc2C1(C)C

nearest known ligand 0.42

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
DRD2 P14416 1/20 0.42
DRD4 P21917 1/20 0.42
HDAC1 Q13547 3/20 0.41
HDAC6 Q9UBN7 3/20 0.41
MEN1 O00255 3/20 0.40
KMT2A Q03164 3/20 0.40
LMNA P02545 1/20 0.40
MAPT P10636 3/20 0.38
POLB P06746 2/20 0.38
KDM4E B2RXH2 1/20 0.38
TDP1 Q9NUW8 1/20 0.38
L3MBTL1 Q9Y468 1/20 0.38
EGFR P00533 1/20 0.38
MAPK1 P28482 1/20 0.37
NPSR1 Q6W5P4 1/20 0.37
APEX1 P27695 2/20 0.36
FABP3 P05413 1/20 0.36
FABP4 P15090 1/20 0.36
FABP5 Q01469 1/20 0.36
HDAC8 Q9BY41 1/20 0.36

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 SCHEMBL28672149 1.00 DRD2 (0.42) DRD2DRD4HDAC1HDAC6MEN1
SCHEMBL29521317 0.99 DRD2 (0.43) DRD2DRD4HDAC1HDAC6MEN1
SCHEMBL5133368 0.99 DRD2 (0.43) DRD2DRD4HDAC1HDAC6MEN1
Iodide SCHEMBL3454461 0.97 DRD2 (0.42) DRD2DRD4HDAC1HDAC6MEN1
Bromide SCHEMBL7649880 0.89 GAA (0.40) DRD2DRD4HDAC1HDAC6MAPT
Bromide SCHEMBL5034614 0.89 GAA (0.40) DRD2DRD4HDAC1HDAC6MAPT
SCHEMBL14454734 0.89 FABP4 (0.41) DRD2DRD4HDAC1HDAC6MAPT
SCHEMBL25230632 0.88 GAA (0.41) DRD2DRD4HDAC1HDAC6MAPT
Iodide SCHEMBL565628 0.87 GAA (0.40) DRD2DRD4HDAC1HDAC6MAPT
Quinoline SCHEMBL28853323 0.85 L3MBTL1 (0.38) DRD2DRD4HDAC1HDAC6LMNA

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 9 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20060199949-A1 Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods CARNEGIE MELLON UNIVERSITY (US) 2006-09-07 US disclosed
US-7008798-B2 Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods CARNEGIE MELLON UNIVERSITY (US) 2006-03-07 US disclosed
US-6989275-B2 Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods CARNEGIE MELLON UNIVERSITY (US) 2006-01-24 US disclosed
US-6956032-B1 Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods CARNEGIE MELLON UNIVERSITY (US) 2005-10-18 US disclosed
US-20020146736-A1 Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods CARNEGIE MELLON UNIVERSITY 2002-10-10 US disclosed
US-20020142340-A1 Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods CARNEGIE MELLON UNIVERSITY 2002-10-03 US disclosed
US-6225050-B1 LABELING PROTEINS, CELLS, NUCLEIC ACIDS, SUGARS, CARBOHYDRATES, OR MIXTURES USING CYANINE DYE WHICH REACTS WITH AMINE, SULFHYDRYL, OR HYDROXY GROUPS OF COMPONENT CARNEGIE MELLON UNIVERSITY 2001-05-01 US disclosed
US-6048982-A OXAZOLE, THIAZOLE OR IMIDAZOLE CYANINE DYES FOR LABELS CARNEGIE MELLON UNIVERSITY (US) 2000-04-11 US disclosed
US-5627027-A Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods CARNEGIE MELLON UNIVERSITY (US) 1997-05-06 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 (3 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-20020142340-A1 Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods SHBG, IK, PTMS DRD2 1558/4885DRD4 875/4885HDAC1 4770/4885
US-20060199949-A1 Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods SHBG, IK, PTMS DRD2 1558/4885DRD4 875/4885HDAC1 4770/4885
US-20020146736-A1 Cyanine dyes as labeling reagents for detection of biological and other materials by luminescence methods SHBG, IK, PTMS DRD2 1558/4885DRD4 875/4885HDAC1 4770/4885

“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.