Bromide

Bromide

SCHEMBL813697

CCc1cccc(CC)c1NC(C)CN(C)CC(C)Nc1c(CC)cccc1CC.[Br-].[Br-].[Co+2]

nearest known ligand 0.37

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
HTT P42858 2/20 0.37
ALOX15 P16050 2/20 0.36
CYP2C19 P33261 2/20 0.36
TSHR P16473 1/20 0.36
HIF1A Q16665 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
ADRA2A P08913 1/20 0.36
ADRA2B P18089 1/20 0.36
ADRA2C P18825 1/20 0.36
KCNH2 Q12809 2/20 0.36
SCN5A Q14524 2/20 0.36
ANPEP P15144 1/20 0.35
GABRA1 P14867 2/20 0.35
GABRB2 P47870 2/20 0.35
CACNA1C Q13936 1/20 0.35
CLCN2 P51788 1/20 0.34
KDM4E B2RXH2 1/20 0.34
ALDH1A1 P00352 1/20 0.34
MAPT P10636 1/20 0.34
HPGD P15428 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 SCHEMBL812576 0.97 ADRA2A (0.39) HTTALOX15CYP2C19TSHRHIF1A
Bromide SCHEMBL813715 0.81 ALDH1A1 (0.30) CYP2C19ALDH1A1CYP1A2
Bromide SCHEMBL813723 0.81 HTT (0.38) HTTALOX15CYP2C19TSHRHIF1A
SCHEMBL15494163 0.80 ANPEP (0.43) HTTALOX15CYP2C19TSHRHIF1A
Bromide SCHEMBL813987 0.79 MEN1 (0.36) HTTCYP2C19ADRA2AADRA2BADRA2C
Hydrochloric Acid SCHEMBL813553 0.78 ALDH1A1 (0.30) CYP2C19ALDH1A1CYP1A2
Hydrochloric Acid SCHEMBL813477 0.77 HTT (0.38) HTTALOX15CYP2C19TSHRHIF1A
Bromide SCHEMBL813163 0.77 SMN1; SMN2 (0.44) TSHRHIF1ATDP1GABRA1GABRB2
SCHEMBL28705440 0.77 GABRA1 (0.43) HTTALOX15CYP2C19TSHRHIF1A
Bromide SCHEMBL815490 0.75 MAPT (0.43) ALOX15CYP2C19TDP1KDM4EALDH1A1

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 HTT 2677/4885ALOX15 1394/4885CYP2C19 2901/4885

“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.