Bromide

Bromide

SCHEMBL813373

Cc1cc(C)c(NCCCNCCNc2c(C)cc(C)cc2C)c(C)c1.[Br-].[Br-].[Co+2]

nearest known ligand 0.40

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

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 13)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 1/20 0.32
RAPGEF4 Q8WZA2 11/20 0.40
ALDH1A1 P00352 2/20 0.36
MAPT P10636 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
L3MBTL1 Q9Y468 1/20 0.36
TP53 P04637 1/20 0.33
ALOX15 P16050 1/20 0.33
LMNA P02545 1/20 0.33
GAA P10253 1/20 0.31
DRD2 P14416 1/20 0.31
DRD4 P21917 1/20 0.31
DRD3 P35462 1/20 0.31

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
Hydrochloric Acid SCHEMBL812894 0.96 RAPGEF4 (0.40) RAPGEF4ALDH1A1MAPTTDP1L3MBTL1
Bromide SCHEMBL813517 0.96 RAPGEF4 (0.43) RAPGEF4ALDH1A1MAPTTDP1L3MBTL1
Hydrochloric Acid SCHEMBL813568 0.92 RAPGEF4 (0.43) RAPGEF4ALDH1A1MAPTTDP1L3MBTL1
Bromide SCHEMBL813610 0.92 RAPGEF4 (0.46) RAPGEF4ALDH1A1MAPTLMNAGAA
Hydrochloric Acid SCHEMBL815781 0.88 RAPGEF4 (0.46) RAPGEF4ALDH1A1MAPTLMNAGAA
Hydrochloric Acid SCHEMBL813865 0.88 RAPGEF4 (0.46) RAPGEF4ALDH1A1MAPTLMNAGAA
SCHEMBL812880 0.88 RAPGEF4 (0.50) RAPGEF4ALDH1A1MAPTLMNAGAA
SCHEMBL814154 0.86 RAPGEF4 (0.48) RAPGEF4ALDH1A1MAPTLMNAGAA
SCHEMBL813197 0.86 RAPGEF4 (0.48) RAPGEF4ALDH1A1MAPTLMNAGAA
SCHEMBL816160 0.86 RAPGEF4 (0.48) RAPGEF4ALDH1A1MAPTLMNAGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8058372-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2011-11-15 US disclosed
US-20080319147-A1 Catalyst Composition II EXXONMOBIL CHEMICAL PATENTS INC. 2008-12-25 US disclosed
US-7371803-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2008-05-13 US disclosed
US-20070066776-A1 Catalyst composition II SOLAN GREGORY A 2007-03-22 US disclosed
US-7189791-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2007-03-13 US disclosed
EP-1641842-A2 POLYMERIZATION AND OLIGOMERIZATION CATALYST WITH TRIDENTATE OR TETRADENTATE LIGAND Exxonmobil Chemical Patents Inc. (US) 2006-04-05 EP disclosed
US-20040266961-A1 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. 2004-12-30 US disclosed
WO-2004106390-A2 POLYMERIZATION AND OLIGOMERIZATION CATALYST WITH TRIDENTATE OR TETRADENTATE LIGAND EXXONMOBIL CHEMICAL PATENTS INC. (US) 2004-12-09 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-20040266961-A1 Catalyst composition II MLX, CBX2, BMX CHRM2 293/4885RAPGEF4 4437/4885ALDH1A1 4593/4885

“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.