Bromide

Bromide

SCHEMBL130614

C[N+]1(C)CC[C@@H](OC(=O)[C@](O)(c2cccs2)C2CCCC2)C1.[Br-]

nearest known ligand 0.69

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 9)

geneUniProtsupporting neighboursconfidence
CHRM3 known ✓ P20309 18/20 0.69
CHRM2 known ✓ P08172 13/20 0.69
CHRM1 known ✓ P11229 9/20 0.69
CHRM4 known ✓ P08173 2/20 0.69
CHRM5 known ✓ P08912 1/20 0.69
HRH1 P35367 1/20 0.69
HTR2B P41595 1/20 0.69
KCNH2 Q12809 1/20 0.69
SLC22A1 O15245 1/20 0.48

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
Bromide SCHEMBL131394 1.00 CHRM3 (0.69) CHRM3CHRM2CHRM1CHRM4CHRM5
SCHEMBL7145497 0.99 CHRM3 (0.68) CHRM3CHRM2CHRM1CHRM4CHRM5
SCHEMBL13716305 0.99 CHRM3 (0.68) CHRM3CHRM2CHRM1CHRM4CHRM5
SCHEMBL13716300 0.99 CHRM3 (0.68) CHRM3CHRM2CHRM1CHRM4CHRM5
SCHEMBL7145504 0.99 CHRM3 (0.68) CHRM3CHRM2CHRM1CHRM4CHRM5
SCHEMBL170999 0.99 CHRM3 (0.68) CHRM3CHRM2CHRM1CHRM4CHRM5
Bromide SCHEMBL7151353 0.94 CHRM3 (0.61) CHRM3CHRM2CHRM1CHRM4CHRM5
SCHEMBL7140049 0.93 CHRM3 (0.60) CHRM3CHRM2CHRM1CHRM4CHRM5
SCHEMBL7147345 0.93 CHRM3 (0.60) CHRM3CHRM2CHRM1CHRM4CHRM5
SCHEMBL7140053 0.93 CHRM3 (0.60) CHRM3CHRM2CHRM1CHRM4CHRM5

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
EP-1572641-B1 Method for production of theR,R (or S,S) configuration of glycopyrronium stereoisomers MEDA PHARMA GMBH & CO KG (DE) 2012-03-07 EP disclosed
US-7569598-B2 Process for the preparation of the R,R (or S,S) configured glycopyrronium stereoisomer MEDA PHARMA GMBH & CO. KG (DE) 2009-08-04 US disclosed
US-20060167275-A1 Process for the preparation of the r,r (or s,s) configured glycopyrronium stereoisomer PHARMACON FORSCHUNG UND BERATUNG G.M.B.H. (AT) 2006-07-27 US disclosed
EP-1572641-A1 METHOD FOR PRODUCTION OF THE R,R (OR S,S) CONFIGURATION OF GLYCOPYRRONIUM STEREOISOMERS PharmaCon Forschung und Beratung GmbH (AT) 2005-09-14 EP disclosed
WO-2004054971-A1 METHOD FOR PRODUCTION OF THE R,R (OR S,S) CONFIGURATION OF GLYCOPYRRONIUM STEREOISOMERS PHARMACON FORSCHUNG UND BERATUNG G.M.B.H. (AT) 2004-07-01 WO disclosed
EP-1369414-A1 Enantiomerically pure Arylcycloalkyl hydroxycarboxylic esters, processes for their preparation and their use as modulators of muscarinic receptors Noe, Christian R. (AT) 2003-12-10 EP 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-20060167275-A1 Process for the preparation of the r,r (or s,s) configured glycopyrronium stereoisomer GYPA, TSHR, TRHR CHRM3 151/4885CHRM2 426/4885CHRM1 423/4885

“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.