Bromide

Bromide

SCHEMBL813161

CCc1cc(CC)c(NCCN(CCNc2c(CC)cc(CC)cc2CC)Cc2ccccn2)c(CC)c1.[Br-].[Br-].[Co+2]

nearest known ligand 0.46

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 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 2/20 0.46
MAPT P10636 2/20 0.46
SMN1; SMN2 Q16637 2/20 0.46
LIN28A Q9H9Z2 1/20 0.46
KDM4E B2RXH2 2/20 0.41
TSHR P16473 2/20 0.41
POLB P06746 2/20 0.41
HTT P42858 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40
KMT2A Q03164 3/20 0.37
MEN1 O00255 2/20 0.37
RAB9A P51151 2/20 0.36
APP P05067 1/20 0.36
NPC1 O15118 1/20 0.36
LMNA P02545 1/20 0.36
CYP2C19 P33261 2/20 0.35
ALDH1A1 P00352 1/20 0.35
HRH3 Q9Y5N1 1/20 0.35
KCNA5 P22460 1/20 0.35
CYP2D6 P10635 1/20 0.34

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 SCHEMBL813155 0.99 TDP1 (0.47) TDP1MAPTSMN1; SMN2LIN28AKDM4E
Hydrochloric Acid SCHEMBL815188 0.98 TDP1 (0.48) TDP1MAPTSMN1; SMN2LIN28AKDM4E
Hydrochloric Acid SCHEMBL812656 0.96 TDP1 (0.47) TDP1MAPTSMN1; SMN2LIN28AKDM4E
Hydrochloric Acid SCHEMBL813191 0.96 TDP1 (0.47) TDP1MAPTSMN1; SMN2LIN28AKDM4E
SCHEMBL815611 0.96 TDP1 (0.47) TDP1MAPTSMN1; SMN2LIN28AKDM4E
Hydrochloric Acid SCHEMBL812978 0.96 TDP1 (0.47) TDP1MAPTSMN1; SMN2LIN28AKDM4E
Hydrochloric Acid SCHEMBL814149 0.96 TDP1 (0.47) TDP1MAPTSMN1; SMN2LIN28AKDM4E
Bromide SCHEMBL813346 0.96 TDP1 (0.42) TDP1MAPTSMN1; SMN2LIN28AKDM4E
Hydrochloric Acid SCHEMBL812951 0.94 TDP1 (0.43) TDP1MAPTSMN1; SMN2LIN28AKDM4E
Bromide SCHEMBL812886 0.93 TDP1 (0.43) TDP1MAPTSMN1; SMN2LIN28AKDM4E

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 TDP1 3897/4885MAPT 1902/4885SMN1; SMN2 1110/4885

“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.