Bromide

Bromide

SCHEMBL5213747

CCCCP(=O)(CCCC)CCCC.[Br-].[Li+]

nearest known ligand 0.52

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 10)

geneUniProtsupporting neighboursconfidence
HPGD P15428 1/20 0.52
SMN1; SMN2 Q16637 1/20 0.52
TRPM8 Q7Z2W7 8/20 0.48
GABBR2 O75899 1/20 0.48
GABRR1 P24046 1/20 0.48
GABBR1 Q9UBS5 1/20 0.48
CYP3A4 P08684 2/20 0.43
LPAR3 Q9UBY5 3/20 0.42
LPAR2 Q9HBW0 1/20 0.42
TSHR P16473 2/20 0.41

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 SCHEMBL28434387 0.94 HPGD (0.52) HPGDSMN1; SMN2TRPM8GABBR2GABRR1
SCHEMBL152127 0.94 HPGD (0.56) HPGDSMN1; SMN2TRPM8GABBR2GABRR1
Water SCHEMBL32685216 0.90 HPGD (0.54) HPGDSMN1; SMN2TRPM8GABBR2GABRR1
Hydrochloric Acid SCHEMBL28443502 0.88 HPGD (0.52) HPGDSMN1; SMN2TRPM8GABBR2GABRR1
SCHEMBL11889581 0.88 HPGD (0.52) HPGDSMN1; SMN2TRPM8GABBR2GABRR1
SCHEMBL1726162 0.88 HPGD (0.52) HPGDSMN1; SMN2TRPM8GABBR2GABRR1
SCHEMBL10556882 0.88 TRPM8 (0.61) HPGDSMN1; SMN2TRPM8GABBR2GABRR1
SCHEMBL28014033 0.88 HPGD (0.52) HPGDSMN1; SMN2TRPM8GABBR2GABRR1
SCHEMBL1725975 0.88 HPGD (0.52) HPGDSMN1; SMN2TRPM8GABBR2GABRR1
SCHEMBL1725977 0.88 TRPM8 (0.61) HPGDSMN1; SMN2TRPM8GABBR2GABRR1

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 38 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0351534-B1 POLYFUNCTIONAL MONOMERS AND PROCESS FOR PRODUCTION THEREOF MITSUI TOATSU CHEMICALS, Inc. (JP) 1993-05-12 EP claimed
EP-0351534-A2 Polyfunctional monomers and process for production thereof MITSUI TOATSU CHEMICALS, Inc. (JP) 1990-01-24 EP claimed
CN-101353313-A Process to produce oxazolidinones UPJOHN CO (US) 2009-01-28 CN disclosed
CN-100387581-C Process for preparing * oxazolidinones UPJOHN CO (US) 2008-05-14 CN disclosed
CN-1319952-C Method for preparing oxazolidone amine PHARMACIA & UPJOHN CO LLC (US) 2007-06-06 CN disclosed
EP-1028940-B1 PROCESS TO PRODUCE OXAZOLIDINONES PHARMACIA & UPJOHN CO LLC (US) 2007-04-18 EP disclosed
EP-1328509-B1 METHODS OF PRODUCING OXAZOLIDINONE COMPOUNDS PHARMACIA & UPJOHN CO LLC (US) 2006-03-22 EP disclosed
US-6998420-B2 Oxazolidinone compounds PHARMACIA & UPJOHN COMPANY (US) 2006-02-14 US disclosed
US-6833453-B2 As an example, manufacturing a 5-(tert-butylcarbamoyl)-amino-methyl-oxazolidinone by condensing a carbamate with a tert-butylcarbamoyl protected derivative of glycidylamine or a 3-amino-1-halopropanol PHARMACIA & UPJOHN COMPANY 2004-12-21 US disclosed
CN-1167701-C Process for preparing oxazolidone amines �������Ŷ���Լ��������˾ 2004-09-22 CN disclosed
US-20040143131-A1 in particular,manufacturing a 5-(tert-butylcarbamoyl)-aminomethyl-oxazolidinone by condensing a carbamate with a tert-butylcarbamoyl protected derivative of glycidylamine or 3-amino-1-halopropanol, intermediates PHARMACIA & UPJOHN COMPANY 2004-07-22 US disclosed
US-20020032348-A1 Process to produce oxazolidinones PEARLMAN BRUCE ALLEN (US) 2002-03-14 US disclosed
CN-1275122-A Process for preparing oxazolidinones UPJOHN CO (US) 2000-11-29 CN disclosed
CN-1215393-A Process for preparing oxazolidinones UPJOHN CO (US) 1999-04-28 CN disclosed
EP-0351534-B1 POLYFUNCTIONAL MONOMERS AND PROCESS FOR PRODUCTION THEREOF MITSUI TOATSU CHEMICALS, Inc. (JP) 1993-05-12 EP disclosed
US-4980497-A GIVE RESINS HAVING HIGH TRANSPARENCY, SURFACE HARDNESS, AND HEAT RESISTANCE; GLAZING MATERIALS, OPTICAL LENSES AND DISC SUBSTRATES MITSUI TOATSU CHEMICALS, INC. (JP) 1990-12-25 US disclosed
EP-0351534-A2 Polyfunctional monomers and process for production thereof MITSUI TOATSU CHEMICALS, Inc. (JP) 1990-01-24 EP disclosed
EP-0050827-B1 3-(P-ALKYLSULFONYLPHENYL)-AND 3-(P-ALKYLSULFINYLPHENYL)OXAZOLIDINONE DERIVATIVES AS ANTI-BACTERIAL AGENTS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1986-04-30 EP disclosed
US-4340606-A 3-(p-Alkylsulfonylphenyl)oxazolidinone derivatives as antibacterial agents E. I. DU PONT DE NEMOURS AND COMPANY (US) 1982-07-20 US disclosed
EP-0050827-A1 3-(p-Alkylsulfonylphenyl)-and 3-(p-alkylsulfinylphenyl)oxazolidinone derivatives as anti-bacterial agents E.I. DU PONT DE NEMOURS AND COMPANY (US) 1982-05-05 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 (2 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-20040143131-A1 in particular,manufacturing a 5-(tert-butylcarbamoyl)-aminomethyl-oxazolidinone by condensing a carbamate with a tert-butylcarbamoyl protected derivative of glycidylamine or 3-amino-1-halopropanol, intermediates TET1, NAT10, TET3 HPGD 591/4885SMN1; SMN2 3257/4885TRPM8 4479/4885
US-20020032348-A1 Process to produce oxazolidinones ADH1A, ADH5, ADH1C HPGD 193/4885SMN1; SMN2 2113/4885TRPM8 4872/4885

“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.