Bromide

Bromide

SCHEMBL3874747

O=C(O)Cc1ccc(C[N+]23CCC(CC2)CC3)cc1.[Br-]

nearest known ligand 0.55

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
CHKA known ✓ P35790 2/20 0.55
ACHE known ✓ P22303 1/20 0.49
CHRM2 known ✓ P08172 1/20 0.38
CHRM3 known ✓ P20309 1/20 0.38
BCHE P06276 1/20 0.49
CA2 P00918 1/20 0.44
CAMK2A Q9UQM7 1/20 0.44
AKR1B1 P15121 1/20 0.42
LMNA P02545 2/20 0.42
GAA P10253 2/20 0.42
TSHR P16473 2/20 0.42
ABCC4 O15439 1/20 0.42
PTGS1 P23219 1/20 0.42
HTT P42858 1/20 0.42
ANPEP P15144 1/20 0.39
ENPEP Q07075 1/20 0.39
ALDH1A1 P00352 2/20 0.39
HPGD P15428 2/20 0.39
HSD17B10 Q99714 2/20 0.39
FFAR1 O14842 1/20 0.39

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
SCHEMBL2912607 0.98 CHKA (0.53) CHKABCHEACHECA2CAMK2A
Bromide SCHEMBL3874382 0.80 CA2 (0.44) CA2CAMK2AAKR1B1LMNAGAA
Bromide SCHEMBL6889492 0.78 BCHE (0.68) CHKABCHEACHELMNAKMT2A
SCHEMBL2911873 0.78 CA2 (0.46) CA2CAMK2AAKR1B1LMNAGAA
SCHEMBL2344944 0.76 BCHE (0.65) CHKABCHEACHEKMT2ACHRM2
Water SCHEMBL31012149 0.74 BCHE (0.62) CHKABCHEACHEKMT2ACHRM2
SCHEMBL14031427 0.73 CHKA (0.59) CHKABCHEACHEALDH1A1HPGD
Hydrochloric Acid SCHEMBL10997929 0.72 CHKA (0.57) CHKABCHEACHELMNAALDH1A1
SCHEMBL69614 0.71 CA2 (0.79) CA2CAMK2AAKR1B1LMNAGAA
Hydrochloric Acid SCHEMBL25180348 0.69 CA2 (0.75) CA2CAMK2AAKR1B1LMNAGAA

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-7579339-B2 Ring-substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2009-08-25 US disclosed
US-7407938-B2 1,4-Diphenyl-3-(3-hydroxy-3-phenylpropyl)-2-azetidinones, e.g., 2,3,4,5,6-Pentahydroxyhexylamide of 4-(4-{4-[3-[3-(4-fluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-y]lbenzylcarbamoyl}phenoxy)benzoic acid; antilipemic agents that have intestinal absorption of less than 10%, SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2008-08-05 US disclosed
US-7390790-B2 Ring-substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2008-06-24 US disclosed
US-20070043017-A1 Ring-substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use SANOFI-AVENTIS DEUTSCHLAND GMBH 2007-02-22 US disclosed
US-20070037787-A1 1,4-Diphenyl-3-(3-hydroxy-3-phenylpropyl)-2-azetidinones, e.g., 2,3,4,5,6-Pentahydroxyhexylamide of 4-(4-{4-[3-[3-(4-fluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-y]lbenzylcarbamoyl}phenoxy)benzoic acid; antilipemic agents that have intestinal absorption of less than 10%, SANOFI-AVENTIS DEUTSCHLAND GMBH 2007-02-15 US disclosed
US-7176194-B2 Ring-substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2007-02-13 US disclosed
US-20060270613-A1 Ring-substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use SANOFI-AVENTIS DEUTSCHLAND GMBH 2006-11-30 US disclosed
US-20040082561-A1 Ring -substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2004-04-29 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 (4 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-20070043017-A1 Ring-substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use QDPR, CYP2D6, DHCR7 CHKA 2681/4885ACHE 1627/4885CHRM2 1722/4885
US-20040082561-A1 Ring -substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use QDPR, CYP2D6, DHCR7 CHKA 2914/4885ACHE 1526/4885CHRM2 1532/4885
US-20060270613-A1 Ring-substituted diphenylazetidinones, process for their preparation, medicaments comprising these compounds, and their use QDPR, CYP2D6, DHCR7 CHKA 2681/4885ACHE 1627/4885CHRM2 1722/4885
US-20070037787-A1 1,4-Diphenyl-3-(3-hydroxy-3-phenylpropyl)-2-azetidinones, e.g., 2,3,4,5,6-Pentahydroxyhexylamide of 4-(4-{4-[3-[3-(4-fluorophenyl)-3-hydroxypropyl]-2-(4-methoxyphenyl)-4-oxoazetidin-1-y]lbenzylcarbamoyl}phenoxy)benzoic acid; antilipemic agents that have intestinal absorption of less than 10%, HPD, FABP2, CYP2B6 CHKA 2528/4885ACHE 2830/4885CHRM2 1470/4885

“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.