Bromide

Bromide

SCHEMBL814498

Cc1cccc(C)c1NCCCN(C)CCNc1c(C)cccc1C.[Br-].[Br-].[Co+2]

nearest known ligand 0.42

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 19)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 4/20 0.42
HRH2 known ✓ P25021 1/20 0.33
BCHE P06276 3/20 0.42
RAD52 P43351 2/20 0.39
NPC1 O15118 1/20 0.39
POLB P06746 1/20 0.39
SLC2A1 P11166 1/20 0.39
APOBEC3A P31941 1/20 0.39
RAB9A P51151 1/20 0.39
KMT2A Q03164 1/20 0.39
APOBEC3G Q9HC16 1/20 0.39
BRD4 O60885 2/20 0.37
ATAD2 Q6PL18 2/20 0.37
EGFR P00533 1/20 0.37
TERT O14746 2/20 0.33
HRH1 P35367 1/20 0.33
HRH3 Q9Y5N1 1/20 0.33
MAPT P10636 1/20 0.32
HTT P42858 1/20 0.32

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 SCHEMBL813752 0.97 ACHE (0.42) ACHEBCHERAD52NPC1POLB
Bromide SCHEMBL813718 0.97 ACHE (0.44) ACHEBCHERAD52NPC1POLB
Hydrochloric Acid SCHEMBL812522 0.93 ACHE (0.44) ACHEBCHERAD52NPC1POLB
Bromide SCHEMBL814465 0.93 MAPT (0.36) ACHEBCHERAD52NPC1POLB
Hydrochloric Acid SCHEMBL813716 0.90 MAPT (0.36) ACHEBCHERAD52NPC1POLB
Hydrochloric Acid SCHEMBL813091 0.90 MAPT (0.36) ACHEBCHERAD52NPC1POLB
SCHEMBL813393 0.89 MAPT (0.39) ACHEBCHERAD52NPC1POLB
SCHEMBL815855 0.88 MAPT (0.38) ACHEBCHERAD52NPC1POLB
SCHEMBL811896 0.88 MAPT (0.38) ACHEBCHERAD52NPC1POLB
SCHEMBL813365 0.88 MAPT (0.38) ACHEBCHERAD52NPC1POLB

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 6 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
US-20040266961-A1 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. 2004-12-30 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-20040266961-A1 Catalyst composition II MLX, CBX2, BMX ACHE 3557/4885HRH2 1276/4885BCHE 3414/4885

“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.